TRIALLYLAMINE (TRALLAMN)

TRIALLYLAMINE (TRALLAMN)

TRIALLYLAMINE (TRALLLAMN)

SYNONYMS

TRIALLYLAMINE; TRALLYLAMNE; TR ALLYL AMNE; TRALLYL AMNE; TR ALLYLAMNE; TRALYLAMN; TR ALLAMN; trallylamne; TRI ALLYL AMINE ; tr allyl amne; trallyl amne; triallylamine; tri allylamine; triallyl amine; trialilamin; trialiyl amin; tr allylamne ; TRI ALLYLAMINE; TRI ALLYL AMINE ; TRIALLYL AMINE ;102-70-5;Tris(2-propenyl)amine;2-Propen-1-amine, N,N-di-2-propenyl-;Triallyl Amine;UNII-B6N19XC04R;CCRIS 4876;N,N-diallylprop-2-en-1-amine;HSDB 2904;EINECS 203-048-2;NSC 32635;UN2610;N,N-Di-2-propenyl-2-propen-1-amine;BRN 1740881;(CH2=CHCH2)3N;AI3-52705;B6N19XC04R;VPYJNCGUESNPMV-UHFFFAOYSA-N;4-04-00-01061 (Beilstein Handbook Reference);MFCD00026093;N,N-bis(prop-2-enyl)prop-2-en-1-amine;2-Propen-1-amine, N,N-di-2-propen-1-yl-;aminotri-2-propene;tri-2-propenylamine;Triallylamine; ;DTXSID5026174;N,N-Diallyl-2-propen-1-amine;CTK3J0388;MolPort-003-959-733;LS-83;N,N-Diallyl-2-propen-1-amine #;KS-00000X4Y;NSC32635;ZINC1665016;Tox21_300670;ANW-14735;n,n-di-2-propenyl-2-propen-1-amin;NSC-32635;2-Propen-1-amine,N-di-2-propenyl-;WLN: 1U2N2U1 & 2U1;AKOS015840489;FCH1113542;RTC-040015;TRA0159595;UN 2610;NCGC00248135-01;NCGC00254578-01;CAS-102-70-5;I780;KB-61994;N,N-bis(prop-2-enyl)-2-propen-1-amine;TC-040015;2-Propen-1-amine,N,N-di-2-propen-1-yl-;FT-0653420;Triallylamine [UN2610] [Flammable liquid];n pound notn-di-2-propenyl-2-propen-1-amine;Triallylamine [UN2610] [Flammable liquid];I14-4995;J-000772;InChI=1/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H;343314-28-3;44905-30-8; N,N-bis(prop-2-enyl)prop-2-en-1-amine102-70-5 [RN];203-048-2 [EINECS];2-Propen-1-amine, N,N-di-2-propen-1-yl- [ACD/Index Name];N,N-di(prop-2-en-1-yl)prop-2-en-1-amine;N,N-Diallyl-2-propen-1-amin [German] [ACD/IUPAC Name];N,N-Diallyl-2-propen-1-amine [ACD/IUPAC Name];N,N-Diallyl-2-propén-1-amine [French] [ACD/IUPAC Name];N,N-Diallylprop-2-en-1-amine;N,N-diprop-2-en-1-ylprop-2-en-1amine;Triallylamine;(CH2=CHCH2)3N;10017-56-8 [RN];105655-27-4 [RN];126068-67-5 [RN];20261-61-4 [RN];29340-81-6 [RN];2-Propen-1-amine, N, N-di-2-propenyl-;2-Propen-1-amine, N,N-di-2-propenyl-;36549-53-8 [RN];36549-54-9 [RN];36549-55-0 [RN];36659-79-7 [RN];4-04-0001061(Beilstein Handbook Reference) [Beilstein];44905-30-8 [RN];637-39-8 [RN];64114-46-1 [RN];7376-31-0 [RN];EINECS 203-048-2;H3tea;InChI=1/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H;Jsp000300;MFCD00026093 [MDL number];N,N-bis(prop-2-enyl)-2-propen-1-amine;N,N-bis(prop-2-enyl)prop-2-en-1-amine;N,N-di(prop-2-enyl)prop-2-en-1-amine;N,N-Di-2-propenyl-2-propen-1-amine;Sterolamide;Sting-Kill;Thiofaco T-35;tri-2-propenylamine;Triallylamine [UN2610] [Flammable liquid];TRIS(2-PROPENYL)AMINE;tris(prop-2-en-1-yl)amine;UN 2610;WLN: 1U2N2U1 & 2U1; triallylamine, tris 2-propenyl amine, 2-propen-1-amine, n,n-di-2-propenyl, triallyl amine, unii-b6n19xc04r; ccris 4876, n,n-diallylprop-2-en-1-amine; n,n-di-2-propenyl-2-propen-1-amine,;ch2=chch2 3n, 4-04-00-01061 beilstein handbook reference;Triallylamine;N,N-Di(prop-2-en-1-yl)prop-2-en-1-amine;2-Propen-1-amine, N,N-di-2-propen-1-yl-;102-70-5;4-04-00-01061;BRN 1740881;N,N-Di-2-propenyl-2-propen-1-amine;EINECS 203-048-2;NSC 32635;Tris(2-propenyl)amine;UNII-B6N19XC04R;343314-28-3;44905-30-8; Triallylamine;(CH2=CHCH2)3N;UN 2610;Tris(2-propenyl)amine;N,N-Diallyl-2-propen-1-amine; fluorinated 1,3,4-oxadiazoles; triallylamine; (3+2) cycloaddition; (4+2) cycloaddition; TAA;tertiaryamine;TRIALLYLAMINE;(CH2=CHCH2)3N;Trialkylamine;triallylaMate;TRIALLYAMINE HCL;Triallylamine 99%;AMINOTRI-2-PROPENE;tri-2-propenylamin; Triallylamine 102-70-5 C9H15NTriallylamine102-70-5 C9H15N;N,N-diprop-2-en-1-ylprop-2-en-1-amine;Tertiaryamine;TRIALLYAMINE HCL;Triallyl-amin;Triallylamine;tri-2-propenylamine;N,N-di(prop-2-en-1-yl)prop-2-en-1-amine;TRIALLYLAMINE:;N,N-Diallyl-2-propen-1-amine;Trialkylamine;N,N-di-2-propenyl-2-propen-1-amine;MFCD00026093;N,N,N-triallylamine;Triallyamine;N,N-Diallylprop-2-en-1-amine;2-Propen-1-amine, N,N-di-2-propen-1-yl-; triallylamine, tris 2-propenyl amine, 2-propen-1-amine, n,n-di-2-propenyl, triallyl amine, unii-b6n19xc04r, ccris 4876, n,n-diallylprop-2-en-1-amine, n,n-di-2-propenyl-2-propen-1-amine, ch2=chch2 3n, 4-04-00-01061 beilstein handbook reference; 1,1′,1”-??????(2-????);????????;???(???-2-??-1-??)???;tris(prop-2-en-1-yl)amine; 2-Propen-1-amine, N,N-di-2-propenyl-;4-04-00-01061 (Beilstein Handbook Reference);AI3-52705;BRN 1740881;CCRIS 4876;HSDB 2904;N,N-Di-2-propenyl-2-propen-1-amine;NSC 32635;Tris(2-propenyl)amine;2-Propen-1-amine, N,N-di-2-propen-1-yl-;UN2610; 2-PROPEN-1-AMINE, N,N-DI-2-PROPENYL-;Triallylamine;tertiaryamine;2-Propen-1-amine, N,N-di-2-propenyl-;Trialkylamine;AMINOTRI-2-PROPENE;N,N-di-2-propenyl-2-propen-1-amine;METATAGS:N,N-bis(prop-2-enyl)prop-2-en-1-amine; triallylamine; TRIALLYLAMINE; 102-70-5; Tris(2-propenyl)amine; 2-Propen-1-amine, N,N-di-2-propenyl-; Triallyl Amine; CCRIS 4876; N,N-diallylprop-2-en-1-amine; HSDB 2904; EINECS 203-048-2; NSC 32635; UN2610; N,N-Di-2-propenyl-2-propen-1-amine; BRN 1740881; (CH2=CHCH2)3N; AI3-52705; VPYJNCGUESNPMV-UHFFFAOYSA-N; N,N-bis(prop-2-enyl)prop-2-en-1-amine; 2-Propen-1-amine, N,N-di-2-propen-1-yl-; UNII-B6N19XC04R; aminotri-2-propene; tri-2-propenylamine; Triallylamine, 99%; ACMC-1BZCI; DSSTox_CID_6174; AC1Q28GC; DSSTox_RID_78046; DSSTox_GSID_26174; SCHEMBL20656; 4-04-00-01061 (Beilstein Handbook Reference); KSC490G8R; N,N-Diallyl-2-propen-1-amine; CTK3J0388; MolPort-003-959-733; LS-83; N,N-Diallyl-2-propen-1-amine #; NSC32635; ZINC1665016; Tox21_300670; ANW-14735; AR-1K1745; MFCD00026093; n,n-di-2-propenyl-2-propen-1-amin; NSC-32635; 2-Propen-1-amine,N-di-2-propenyl-; WLN: 1U2N2U1 & 2U1; TRALLLAMN; TRALLL AMN; triallil amin; triallil amin; tralll amn; triallil amine; triallyl amin; trallyl amn; trallyl amne; 2-Propen-1-amine, N,N-di-2-propen-1-yl- [ACD/Index Name]; N,N-di(prop-2-en-1-yl)prop-2-en-1-amine; N,N-Diallyl-2-propen-1-amin [German] [ACD/IUPAC Name]; N,N-Diallyl-2-propen-1-amine [ACD/IUPAC Name]; N,N-Diallyl-2-propén-1-amine [French] [ACD/IUPAC Name]; N,N-Diallylprop-2-en-1-amine; N,N-diprop-2-en-1-ylprop-2-en-1-amine; Triallylamine;TRIALLYLAMINE; 102-70-5; Tris(2-propenyl)amine; 2-Propen-1-amine, N,N-di-2-propenyl-; Triallyl Amine; UNII-B6N19XC04R; CCRIS 4876; N,N-diallylprop-2-en-1-amine; HSDB 2904; EINECS 203-048-2; NSC 32635; UN2610; N,N-Di-2-propenyl-2-propen-1-amine; BRN 1740881; tris(prop-2-en-1-yl)amine; (CH2=CHCH2)3N; AI3-52705; B6N19XC04R; VPYJNCGUESNPMV-UHFFFAOYSA-N; 4-04-00-01061 (Beilstein Handbook Reference); MFCD00026093; N,N-bis(prop-2-enyl)prop-2-en-1-amine; 2-Propen-1-amine, N,N-di-2-propen-1-yl-; aminotri-2-propene; tri-2-propenylamine; Triallylamine, 99%; ACMC-1BZCI; DSSTox_CID_6174; AC1Q28GC; DSSTox_RID_78046; DSSTox_GSID_26174; SCHEMBL20656; KSC490G8R; AC1L1P64; Jsp000300; CHEMBL3188834; DTXSID5026174; N,N-Diallyl-2-propen-1-amine; CTK3J0388; LS-83; N,N-Diallyl-2-propen-1-amine #; ADAL1243817; KS-00000X4Y; NSC32635; ZINC1665016; Tox21_300670; ANW-14735; n,n-di-2-propenyl-2-propen-1-amin; NSC-32635; 2-Propen-1-amine,N-di-2-propenyl-; WLN: 1U2N2U1 & 2U1; AKOS015840489; FCH1113542; RTC-040015; TRA0159595; UN 2610; NCGC00248135-01; NCGC00254578-01; CAS-102-70-5; I780; N,N-bis(prop-2-enyl)-2-propen-1-amine; TC-040015; 2-Propen-1-amine,N,N-di-2-propen-1-yl-; FT-0653420; Triallylamine [UN2610] [Flammable liquid]; n pound notn-di-2-propenyl-2-propen-1-amine; Triallylamine [UN2610] [Flammable liquid]; A800604; I14-4995; J-000772;InChI=1/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H; triallylamine (Q23779745)

 

Jump to navigationJump to search chemical compound In more languagesConfigure Language Label Description Also known as English triallylamine chemical compound Turkish No label defined No description defined Kurdish (Latin script) No label defined No description defined Kabardian No label defined No description defined All entered languages Statements instance of chemical compound 0 references image Triallylamine.png 668 × 407; 4 KB 0 references mass 137.12 atomic mass unit 1 reference chemical formula C9H05N 1 reference pKa 8.31±0.01 1 reference canonical SMILES C=CCN(CC=C)CC=C 1 reference Identifiers InChI 1S/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H2 1 reference InChIKey VPYJNCGUESNPMV-UHFFFAOYSA-N 1 reference PubChem CID 7617 1 reference CAS Registry Number 102-70-5 1 reference UNII B6N19XC04R 1 reference ZVG number 38340 0 references ID 7335 1 reference ChEMBL ID CHEMBL3188834 1 reference ECHA InfoCard ID 100.002.772 1 reference EC number 203-048-2 1 reference DSSTOX substance identifier DTXSID5026174 1 reference Wikipedia(2 entries) de Triallylaminfi Triallyyliamiini Wikibooks(0 entries) Wikinews(0 entries) Wikiquote(0 entries) Wikisource(0 entries) Wikiversity(0 entries) Wikivoyage(0 entries) Wiktionary(0 entries) Other sites(0 entries) Triallylamine(CAS RN:102-70-5 Product Number:T0332) Structure Triallylamine General Information Product Number T0332 Packing Unit Price Available Stock Quantity Portland, OR Philadelphia, PA Japan * 25mL 18.00 USD 1 9 ?20 500mL 82.00 USD Please contact us. 4 0 * Items available from stock in Japan will be delivered in 10 business days. * Please contact us if you need further information. Sales Dept Tel: +32 (0)3 735 07 00 E-mail: Sales-EU@TCIchemicals.com) * To send your quote request for bulk quantities, please click on the “Request Bulk Quotation” button. Please note that for some of our products we cannot offer bulk quantities. * TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.Request Bulk Quotation Add to Cart Purity/Analysis Method >95.0%(GC)(T) Storage Temperature M.F. / M.W. C9H15N=137.23 CAS RN 102-70-5 Related CAS RN MDL Number MFCD00026093 Packaging and Container Product DetailsSafety & Regulations Specification Purity(GC) min. 95.0 % (Neutralization titration) min. 95.0 % Data of Reference flp 39°C(lit.) bp 156°C(lit.) References Beilstein 4(4)1061 Reaxys-RN 1740881 PubChem SID 87576304 # XX5950000 EC Number 203-048-2 TRIALLYLAMINE 3 – Flammable liquid 8 – Corrosive Chemical Identifiers | Hazards | Response Recommendations | Physical Properties | Regulatory Information | Alternate Chemical Names Chemical Identifiers

 

What is this information? 

CAS Number UN/NA Number DOT Hazard Label USCG CHRIS Code

102-70-5 (TRIALLYLAMINE) 2610 Flammable Liquid Corrosive none NIOSH Pocket Guide International Chem Safety Card none none NFPA 704 data unavailable General Description A colorless liquid with a fishlike odor. Density 0.800 g / cm3 and insoluble in water. Hence floats on water. Flash point 103°F. Vapors heavier than air. May irritate skin and eyes. Used to make other chemicals. Hazards What is this information? Reactivity Alerts Strong Reducing Agent Air & Water Reactions Flammable. Insoluble in water. Fire Hazard Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a (P) may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. (ERG, 2016)

 

 

Health Hazard

Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. (ERG, 2016) Reactivity Profile TRIALLYLAMINE is a strong reducing agent that reacts violently with oxidizing agents. Corrosive towards Al and Zn [Handling Chemicals Safely 1980 p. 912] . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. Belongs to the Following Reactive Group(s) Amines, Phosphines, and Pyridines Hydrocarbons, Aliphatic Unsaturated Potentially Incompatible Absorbents Use caution: Liquids with this reactive group classification have been known to react with the absorbents listed below. More info about absorbents, including situations to watch out for… Mineral-Based & Clay-Based Absorbents Dirt/Earth Response Recommendations What is this information? Isolation and Evacuation Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: As an immediate precautionary measure, isolate spill or leak area for at least 50 meters (150 feet) in all directions. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016) Firefighting Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Some of these materials may react violently with water. SMALL FIRE: Dry chemical, CO2, water spray or alcohol-resistant foam. LARGE FIRE: Water spray, fog or alcohol-resistant foam. Move containers from fire area if you can do it without risk. Dike fire-control water for later disposal; do not scatter the material. Do not get water inside containers.

 

 

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS: Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn. (ERG, 2016)

Non-Fire Response Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Fully encapsulating, vapor-protective clothing should be worn for spills and leaks with no fire. ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor-suppressing foam may be used to reduce vapors. Absorb with earth, sand or other non-combustible material and transfer to containers (except for Hydrazine). Use clean, non-sparking tools to collect absorbed material.

 

 

LARGE SPILL: Dike far ahead of liquid spill for later disposal. Water spray may reduce vapor, but may not prevent ignition in closed spaces. (ERG, 2016)

Protective Clothing Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters’ protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. (ERG, 2016) DuPont Tychem® Suit Fabrics No information available.

First Aid

 

EYES: First check the victim for contact lenses and remove if present. Flush victim’s eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim’s eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.

INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.

INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim’s airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992) Physical Properties What is this information? Chemical Formula: C9H15N Flash Point: 103 ° F (NTP, 1992) Lower Explosive Limit (LEL): data unavailable Upper Explosive Limit (UEL): data unavailable Autoignition Temperature: data unavailable Melting Point: -94 ° F (NTP, 1992) Vapor Pressure: data unavailable Vapor Density (Relative to Air): data unavailable Specific Gravity: 0.809 at 68 ° F (NTP, 1992) Boiling Point: 311 to 313 ° F at 760 mm Hg (NTP, 1992) Molecular Weight: 137.23 (NTP, 1992) Water Solubility: 2.5 mg/mL (NTP, 1992) Ionization Potential: data unavailable IDLH: data unavailable AEGLs (Acute Exposure Guideline Levels) No AEGL information available. ERPGs (Emergency Response Planning Guidelines) No ERPG information available. PACs (Protective Action Criteria) No PAC information available. Regulatory Information What is this information? EPA Consolidated List of Lists No regulatory information available. DHS Chemical Facility Anti-Terrorism Standards (CFATS) No regulatory information available. OSHA Process Safety Management (PSM) Standard List No regulatory information available. Alternate Chemical Names What is this information? TRI-2-PROPENYLAMINE TRIALLYLAMINE TRIS(2-PROPENYL)AMINE Triallylamine 99% Synonym: TAA CAS Number 102-70-5 Linear Formula (H2C=CHCH2)3N Molecular Weight 137.22 EC Number 203-048-2 MDL number MFCD00026093 PubChem Substance ID 24900211 Triallylamine 99% SDS Specification Sheet (PDF)FTNMR (PDF) SKU-Pack Size Availability Pack Size Price (EUR) T45004-250ML Available to ship on 29.09.19 – FROM 250 ML 41.50 T45004-1L Only 4 left in stock (more on the way) – FROM 1 L 118.00 To order products, please contact your local dealer. Click here Product Recommendations 336939 Triallylphosphine 95% D9603 Diallylamine 99% 542687 Diallylmethylamine 97% 05937 N,N-Dimethylallylamine for protein sequence analysis CDS000449 N,N-Diallylamine hydrochloride AldrichCP Allylamine 98% 317748 N-Allylmethylamine 96% 336874 Allyldiphenylphosphine 95% 259470 Allyl ether 98% 241075 ?99% op PurchaseSafety & DocumentationPeer-Reviewed Papers6 Triallylamine PubChem CID: 7617 Structure: Triallylamine_small.png Triallylamine_3D_Structure.png Find Similar Structures Chemical Safety: Flammable Corrosive Acute Toxic Irritant Laboratory Chemical Safety Summary (LCSS) Datasheet Molecular Formula: C9H15N Names: TRIALLYLAMINE 102-70-5 Tris(2-propenyl)amine 2-Propen-1-amine, N,N-di-2-propenyl- Triallyl Amine More… Molecular Weight: 137.22 g/mol Dates: Modify: 2019-09-21 Create: 2005-03-26 Triallylamine appears as a colorless liquid with a fishlike odor. Density 0.800 g / cm3 and insoluble in water. Hence floats on water. Flash point 103°F. Vapors heavier than air. May irritate skin and eyes. Used to make other chemicals. from CAMEO Chemicals 1Structures HelpNew Window 1.12D Structure HelpNew Window Find Similar Structures Get Image Download Chemical Structure Depiction triallylamine.png Full screen Zoom in Zoom out from PubChem 1.23D Conformer HelpNew Window Get Image Download Interactive Chemical Structure Model Ball and Stick Sticks Wire-Frame Space-Filling Show Hydrogens Animate Full screen Zoom in Zoom out from PubChem 2Names and Identifiers HelpNew Window 2.1Computed Descriptors HelpNew Window 2.1.1IUPAC Name HelpNew Window N,N-bis(prop-2-enyl)prop-2-en-1-amine from PubChem 2.1.2InChI HelpNew Window InChI=1S/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H2 from PubChem 2.1.3InChI Key HelpNew Window VPYJNCGUESNPMV-UHFFFAOYSA-N from PubChem 2.1.4Canonical SMILES HelpNew Window C=CCN(CC=C)CC=C from PubChem 2.2Molecular Formula HelpNew Window C9H15N from PubChem 2.3Other Identifiers HelpNew Window 2.3.1CAS HelpNew Window 102-70-5 from ChemIDplus; DTP/NCI; EPA Chemicals under the TSCA; EPA DSSTox; European Chemicals Agency (ECHA); HSDB; The National Institute for Occupational Safety and Health (NIOSH) Other CAS 44905-30-8 343314-28-3 from ChemIDplus 2.3.2European Community (EC) Number HelpNew Window 203-048-2 from European Chemicals Agency (ECHA) 2.3.3NSC Number HelpNew Window 32635 from DTP/NCI 2.3.4RTECS Number HelpNew Window XX5950000 from The National Institute for Occupational Safety and Health (NIOSH) 2.3.5UN Number HelpNew Window 2610 from CAMEO Chemicals; DOT Emergency Response Guidebook; NJDOH RTK Hazardous Substance List 2.3.6UNII HelpNew Window from FDA/SPL Indexing Data 2.3.7Wikipedia HelpNew Window Triallylamine from Wikipedia 2.3.8Shipping Name/ Number DOT/UN/NA/IMO HelpNew Window UN 2610; Triallylamine from HSDB IMO 3.0; Triallylamine from HSDB 2.4Synonyms HelpNew Window Entry Terms HelpNew Window triallylamine from MeSH 2.4.2Depositor-Supplied Synonyms HelpNew Window TRIALLYLAMINE 102-70-5 Tris(2-propenyl)amine 2-Propen-1-amine, N,N-di-2-propenyl- Triallyl Amine UNII-B6N19XC04R CCRIS 4876 N,N-diallylprop-2-en-1-amine HSDB 2904 EINECS 203-048-2 NSC 32635 UN2610 N,N-Di-2-propenyl-2-propen-1-amine BRN 1740881 tris(prop-2-en-1-yl)amine (CH2=CHCH2)3N AI3-52705 B6N19XC04R VPYJNCGUESNPMV-UHFFFAOYSA-N 4-04-00-01061 (Beilstein Handbook Reference) MFCD00026093 N,N-bis(prop-2-enyl)prop-2-en-1-amine 2-Propen-1-amine, N,N-di-2-propen-1-yl- aminotri-2-propene tri-2-propenylamine Triallylamine, 99% ACMC-1BZCI DSSTox_CID_6174 AC1Q28GC DSSTox_RID_78046 DSSTox_GSID_26174 SCHEMBL20656 KSC490G8R AC1L1P64 Jsp000300 CHEMBL3188834 DTXSID5026174 N,N-Diallyl-2-propen-1-amine CTK3J0388 LS-83 N,N-Diallyl-2-propen-1-amine # ADAL1243817 KS-00000X4Y NSC32635 ZINC1665016 Tox21_300670 ANW-14735 n,n-di-2-propenyl-2-propen-1-amin NSC-32635 2-Propen-1-amine,N-di-2-propenyl- WLN: 1U2N2U1 & 2U1 AKOS015840489 FCH1113542 RTC-040015 TRA0159595 UN 2610 NCGC00248135-01 NCGC00254578-01 CAS-102-70-5 I780 N,N-bis(prop-2-enyl)-2-propen-1-amine TC-040015 2-Propen-1-amine,N,N-di-2-propen-1-yl- FT-0653420 Triallylamine [UN2610] [Flammable liquid] n pound notn-di-2-propenyl-2-propen-1-amine Triallylamine [UN2610] [Flammable liquid] A800604 I14-4995 J-000772 InChI=1/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H from PubChem 3Chemical and Physical Properties HelpNew Window 3.1Computed Properties HelpNew Window Property Name Property Value Molecular Weight 137.22 g/mol XLogP3 2.6 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 6 Exact Mass 137.120449 g/mol Monoisotopic Mass 137.120449 g/mol Topological Polar Surface Area 3.2 A^2 Heavy Atom Count 10 Formal Charge 0 Complexity 92.1 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count Triallylamine 0 Undefined Bond Stereocenter Count 0 Covalently-Bonded Unit Count 1 Compound Is Canonicalized Yes from PubChem 3.2Experimental Properties HelpNew Window 3.2.1Physical Description HelpNew Window Triallylamine appears as a colorless liquid with a fishlike odor. Density 0.800 g / cm3 and insoluble in water. Hence floats on water. Flash point 103°F. Vapors heavier than air. May irritate skin and eyes. Used to make other chemicals. from CAMEO Chemicals 3.2.2Color/Form HelpNew Window Liquid Lewis, R.J., Sr (Ed.). Hawley’s Condensed Chemical Dictionary. 13th ed. New York, NY: John Wiley & Sons, Inc. 1997., p. 1120 from HSDB Dark brown liquid State of New Jersey. Dept of Health. Right To Know Hazardous Substance list. Triallylamine. Jan 2002. Available from, as of Oct 12, 2015: http://web.doh.state.nj.us/rtkhsfs/rtkhsl.aspx from HSDB 3.2.3Odor HelpNew Window Ammonia-like State of New Jersey. Dept of Health. Right To Know Hazardous Substance list. Triallylamine. Jan 2002. Available from, as of Oct 12, 2015: http://web.doh.state.nj.us/rtkhsfs/rtkhsl.aspx from HSDB 3.2.4Boiling Point HelpNew Window 311 to 313 ° F at 760 mm Hg (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. from CAMEO Chemicals 155.5°C from EPA DSSTox 155.5 deg C Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-287 from HSDB 3.2.5Melting Point HelpNew Window -94 ° F (NTP, 1992)

National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, Triallylamine, North Carolina. from CAMEO Chemicals less than -70 deg C Clayton, G.D., F.E. Clayton (eds.) Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1090 from HSDB 3.2.6Flash Point HelpNew Window 103 ° F (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. from CAMEO Chemicals 103 DEG F OC. Sax, N.I. Dangerous Properties of Industrial Materials. 4th ed. New York: Van Nostrand Reinhold, 1975., p. 1179 from HSDB 3.2.7Solubility HelpNew Window 2.5 mg/mL (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. from CAMEO Chemicals Water Solubility 0.02 M CLAYTON,DJ & CLAYTON,FE (1993) from EPA DSSTox Triallylamine, Soluble in ethanol, ethyl ether, acetone, and benzene Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-287 from HSDB In water, 2,500 mg/l @ 25 deg C Clayton, G.D., F.E. Clayton (eds.) Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1090 from HSDB 3.2.8Density HelpNew Window 0.809 at 68 ° F (NTP, 1992) Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. from CAMEO Chemicals 0.809 @ 20 deg C Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. Triallylamine, 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-287 from HSDB 3.2.9Vapor Density HelpNew Window 4.73 (Air= 1) Clayton, G.D., F.E. Clayton (eds.) Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1090 from HSDB 3.2.10Vapor Pressure HelpNew Window 3.64 mmHg from EPA DSSTox 3.64 mm Hg @ 25 deg C Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989. from HSDB 3.2.11Octanol/Water Partition Coefficient HelpNew Window 2.59 (LogP) HANSCH,C ET AL. (1995) from EPA DSSTox Kow= 2.59 Hansch, C., Leo, A., D. Hoekman. Exploring QSAR – Hydrophobic, Electronic, and Steric Constants. Washington, DC: American Chemical Society., 1995., p. 63 from HSDB 3.2.12Decomposition HelpNew Window When heated to decomposition it emits toxic fumes of /nitrogen oxides/. Lewis, R.J. Sax’s Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 3213 from HSDB 3.2.13Viscosity HelpNew Window 2.7783X10-3 Pa.s @ 200.00 K Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989. from HSDB 3.2.14Heat of Vaporization HelpNew Window 5.4121X10+7 J/Kmol @ 200.00 K Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989. from HSDB 3.2.15Surface Tension HelpNew Window 3.5051X10-2 N/m @ 200.00 K Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Triallylamine, Washington, D.C.: Taylor and Francis, 1989. from HSDB 3.2.16Odor Threshold HelpNew Window … Recognizable @ 0.5 ppm … Clayton, G.D., F.E. Clayton (eds.) Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1135 from HSDB 3.2.17Refractive Index HelpNew Window Index of refraction: 1.4502 @ 20 deg C/D Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-287 from HSDB 3.2.18Dissociation Constants HelpNew Window pKa= 8.31 (conjugate acid) Perrin DD; Dissociation Constants of Organic Bases in Aqueous Solution, Iupac Chemical Data Series, Buttersworth, London (1965) from HSDB 3.2.19Other Experimental Properties HelpNew Window Freezing point: -70 deg C Lewis, R.J., Sr (Ed.). Hawley’s Condensed Chemical Dictionary. 13th ed. New York, NY: John Wiley & Sons, Inc. 1997., p. 1120 from HSDB Conversion units: 1 mg/l equiv to 178 ppm, 1 ppm equiv to 5.61 mg/cu m Clayton, G.D., F.E. Clayton (eds.) Triallylamine, Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1090 from HSDB 4Spectral Information HelpNew Window 4.11D NMR Spectra HelpNew Window 1D NMR Spectra NMRShiftDB Link from NMRShiftDB 4.1.11H NMR Spectra HelpNew Window Instrument Name Varian A-60 Copyright Copyright © 2009-2018 Bio-Rad Laboratories, Inc. All Rights Reserved. Thumbnail Thumbnail from SpectraBase 4.1.213C NMR Spectra HelpNew Window Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved. Thumbnail Thumbnail from SpectraBase 4.2Mass Spectrometry HelpNew Window Mass Spectrometry MASS: 715 (Atlas of Mass Spectral Data, John Wiley & Sons, New York) from HSDB 4.2.1GC-MS HelpNew Window Showing 2 of 4 View More NIST Number 113121 Library Main library Total Peaks 54 m/z Top Peak 41 m/z 2nd Highest 110 m/z 3rd Highest 39 Thumbnail Thumbnail from NIST NIST Number 3459 Library Replicate library Total Peaks 89 m/z Top Peak 41 m/z 2nd Highest 110 /z 3rd Highest 39 Thumbnail Thumbnail from NIST 4.3IR Spectra HelpNew Window IR Spectra IR: 6948 (Coblentz Society Spectral Collection) from HSDB 4.3.1FTIR Spectra HelpNew Window Technique Triallylamine CAPILLARY CELL: NEAT Source of Sample CHEM SERVICE, INC., WEST CHESTER, PENNSYLVANIA Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved. Thumbnail Thumbnail SpectraBase 4.3.2Vapor Phase IR Spectra HelpNew Window Instrument Name DIGILAB FTS-14 Vapor Phase Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved. Thumbnail Thumbnail from SpectraBase 4.4Other Spectra HelpNew Window SADTLER REF NUMBER: 15374 (IR, PRISM)

Weast, R.C. (ed.). Handbook of Chemistry and Physics. 57th ed. Cleveland: CRC Press Inc., 1976., p. C-109 from HSDB 5Related Records HelpNew Window 5.1Related Compounds with Annotation HelpNew Window 278 items View More Rows & Details Download BY Descending Compound CID Triallylamine Structure Compound CID Name Molecular Formula Molecular Weight, g/mol Structure 7616 Tripropylamine C9H21N 143.27 Structure 15342 3-Methylhepta-1,4-diene C8H14 110.2 Structure 16091 3-Bromoheptane C7H15Br 179.1 Structure 17541 Glycine, N,N-diallyl-, ethyl ester C10H17NO2 183.25 Structure 20152 Triethyl(prop-2-enyl)azanium C9H20N+ 142.26 1 2 … 56 Next from PubChem 5.2Related Compounds HelpNew Window Triallylamine Same Connectivity 2 Records Same Parent, Connectivity 21 Records Same Parent, Exact 20 Records Mixtures, Components, and Neutralized Forms 45 Records Similar Compounds 36 Records Similar Conformers 346 Records from PubChem 5.3Substances HelpNew Window 5.3.1Related Substances HelpNew Window All 130 Records Same 71 Records Mixture 59 Records from PubChem 5.3.2Substances by Category HelpNew Window 7 Categories Expanded View Download Chemical Vendors (30) Curation Efforts (8) Governmental Organizations (11) Publishers (2) NIH Initiatives (1) Research And Development (11) Subscription Services (3) Legacy Depositors (18) From PubChem Triallylamine 5.4Entrez Crosslinks HelpNew Window PubMed 1 Record from PubChem 6Chemical Vendors HelpNew Window Showing 1 Substance per Vendor View All in Entrez Download Alfa Aesar SID: 376196244 Triallylamine Purchasable Chemical: A12081 Chemical co.,ltd PubChem SID: 381030660 Purchasable Chemical: MR-1001212 VladaChem PubChem SID: 381011450 Purchasable Chemical: VL266537-50ML Tractus PubChem SID: 204357597 Purchasable Chemical: RTC-040015 TCI (Tokyo Chemical Industry) SID: 87576304 Purchasable Chemical: T0332 AKos Consulting & Solutions PubChem SID: 151979908 Purchasable Chemical: AKOS015840489 abcr GmbH triallylamine PubChem SID: 316400064 Purchasable Chemical: AB123568 Finetech Industry Limited PubChem SID: 164827204 Purchasable Chemical: FT-0653420 SynHet – Synthetic Heterocycles SID: 385263689 Purchasable : ADAL1243817 MuseChem PubChem SID: 355431327 Chemical: M067022

 

Category Category Description Categorization Type

Consumer_use Term applied when the only information the source indicates is ‘consumer’ or ‘consumer product’ ; also applied to terms that the source indicates are for consumer use, yet the descriptor term is ambivalent about usage (e.g., cleaning_washing products may be for industrial or consumer use, when the source indicates consumer use, the consumer_use term is also applied) – see appendix for full list of unambiguous consumer related terms plus ambiguous consumer related terms which if indicated are labeled with ‘consumer_use’ CPCat Cassette Triallylamine Food_contact, plastics Plastic products, industry for plastics, manufacturing of plastics, plastic additives (modifiers included when known) CPCat Cassette Manufacturing, chemical General term used only when the only information known from the source is ‘chemical,’m typically related to manufacturing of chemicals, or laboratory chemicals CPCat Cassette Manufacturing, raw_material Raw materials used in a variety of products and industries (e.g. in cosmetics, chemical manufacturing, production of metals, etc); modifiers included when known to indicate what the raw materials are used for CPCat Cassette from EPA Chemical and Products Database (CPDat) CHEMICAL INTERMEDIATE FOR ION EXCHANGE RESINS & RUBBER SRI from HSDB Lewis, R.J., Sr (Ed.). Hawley’s Condensed Chemical Dictionary. 13th ed. New York, NY: John Wiley & Sons, Inc. 1997., p. 1120 from HSDB Used as unsaturated polyester resin comonomer; crosslinking comonomer Ashford, R.D. Ashford’s Dictionary of Industrial Chemicals. London, England: Wavelength Publications Ltd., 1994., p. 900 from HSDB As an initiator for the polymerization of butadiene Gerhartz, W. (exec ed.). Ullmann’s Encyclopedia of Industrial Chemistry. 5th ed.Vol A1: Deerfield Beach, FL: VCH Publishers, 1985 to Present., p. VA1 (85) 439 from HSDB 7.3Methods of Manufacturing HelpNew Window Production: allyl chloride + ammonia (amine formation; coproduced with diallylamine/allylamine) Ashford, R.D. Ashford’s Dictionary of Industrial Chemicals. London, England: Wavelength Publications Ltd., 1994., p. 900 from HSDB 7.4Consumption Patterns HelpNew Window ESSENTIALLY 100% AS CHEMICAL INTERMEDIATE SRI from HSDB .S. Production HelpNew Window (1972) 4.54X10+5 GRAMS (ALLYLAMINES) SRI from HSDB (1975) 9.08X10+5 GRAMS (ALLYLAMINES) SRI Triallylamine from HSDB 7.6Manufacturers HelpNew Window Celanese Corp., 86 Morris Avenue, Summit, NJ 07901, (972) 443-4000; Production site: Portsmouth, VA 23703 SRI. 1999 Directory of Chemical Producers -United States. Menlo Park, CA. SRI Consulting 1999., p. 946 from HSDB 7.7General Manufacturing Information HelpNew Window EPA TSCA Commercial Activity Status triallylamine 2-Propen-1-amine, N,N-di-2-propen-1-yl-: ACTIVE https://www.epa.gov/tsca-inventory from EPA Chemicals under the TSCA 8Safety and Hazards HelpNew Window Identification HelpNew Window 8.1.1GHS Classification HelpNew Window Showing 1 of 2 View More (s) Flammable Corrosive Acute Toxic Irritant Signal Danger Hazard Statements Aggregated GHS information provided by 40 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. Triallylamine H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] H311 (40%): Toxic in contact with skin [Danger Acute toxicity, dermal] H312 (57.5%): Harmful in contact with skin [Warning Acute toxicity, dermal] H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] H331 (62.5%): Toxic if inhaled [Danger Acute toxicity, inhalation] H332 (35%): Harmful if inhaled [Warning Acute toxicity, inhalation] H412 (30%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Triallylamine Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. Precautionary Statement Codes P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P361, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) from European Chemicals Agency (ECHA) 8.1.2Health Hazard HelpNew Window Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. Triallylamine (ERG, 2016) U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals

 

 

8.1.3Fire Hazard HelpNew Window

Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a (P) may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. (ERG, 2016) Triallylamine U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals Flammable – 2nd degree, Reactive – 1st degree from NJDOH RTK Hazardous Substance List 8.1.4Fire Potential HelpNew Window MODERATE FIRE RISK… Hawley, G.G. The Condensed Chemical Dictionary. 9th ed. New York: Van Nostrand Reinhold Co., 1977., p. 874 from HSDB DANGEROUS, WHEN EXPOSED TO HEAT OR FLAME. Sax, N.I. Dangerous Properties of Industrial Materials. 4th ed. New York: Van Nostrand Reinhold, 1975., p. 1179 from HSDB liquid when exposed to heat, flame, or oxidizers. Lewis, R.J. Sax’s Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 3213 from HSDB 8.1.5Skin, Eye, and Respiratory Irritations HelpNew Window … Mucous membrane irritation or chest discomfort in some at 12.5 ppm, increasingly frequent symptoms to 50 ppm, and irritant symptoms more severe at 75 to 100 ppm … . Clayton, G.D., F.E. Clayton (eds.) Patty’s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley & Sons Inc., 1993-1994., p. 1135 from HSDB It may be very irritating to skin and eyes. of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1994., p. 1066 from HSDB An eye and severe skin irritant. , R.J. Sax’s Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 3213 from HSDB 8.2Safety and Hazard Properties HelpNew Window 8.2.1Critical Temperature & Pressure HelpNew Window Critical temperature: 592.00 K; Critical pressure: 2.4600X10+6 Pa Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989. from HSDB 8.3First Aid Measures HelpNew Window

 

 

8.3.1First Aid HelpNew Window triallylamine

EYES: First check the victim for contact lenses and remove if present. Flush victim’s eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim’s eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim’s airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. from CAMEO Chemicals 8.4Fire Fighting HelpNew Window Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Some of these materials may react violently with water. SMALL FIRE: Dry chemical, CO2, water spray or alcohol-resistant foam. LARGE FIRE: Water spray, fog or alcohol-resistant foam. Move containers from fire area if you can do it without risk. Dike fire-control water for later disposal; do not scatter the material. Do not get water inside containers. FIRE INVOLVING TANKS OR CAR/TRAILER LOADS: Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn. (ERG, 2016) triallylamine U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals 8.4.1Fire Fighting Procedures HelpNew Window FOAM, ALCOHOL FOAM, FOG.

 

Sax, N.I. Dangerous Properties of Industrial Materials. 4th ed. New York: Van Nostrand Reinhold, 1975., p. 1179 from HSDB If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped or safely confined. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use foam, dry chemical, or carbon dioxide. Keep run-off water out of sewers and water sources. Association of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1994., p. 1066 from HSDB Triallylamine 8.5Accidental Release Measures HelpNew Window 8.5.1Isolation and Evacuation HelpNew Window Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: As an immediate precautionary measure, isolate spill or leak area for at least 50 meters (150 feet) in all directions. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016) U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals 8.5.2Disposal Methods HelpNew Window SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices. from HSDB 8.5.3Preventive Measures HelpNew Window …CHARACTERISTIC AMMONIACAL ODORS & IRRITANT PROPERTIES @ LOW CONCN WOULD AFFORD ADEQUATE WARNING. …RECOMMENDED GOOD VENTILATION WHERE ALLYLAMINES WERE PRESENT & CARE TO PREVENT SKIN CONTACT. /ALLYLAMINES/ atty, F. (ed.). Industrial Hygiene and Toxicology: Volume II: Toxicology. 2nd ed. New York: Interscience Publishers, 1963., p. 2057 from HSDB Triallylamine If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Attempt to stop leak if without undue personnel hazard. Use water spray to knock-down vapors. Association of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1994., p. 1066 from HSDB Personnel protection: Avoid breathing vapors. Keep upwind. … Avoid bodily contact with the material. … Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water. … If contact with the material anticipated, wear appropriate chemical protective clothing. Association of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1994., p. 1066 from HSDB triallylamine SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place. from HSDB

8.6Handling and Storage HelpNew Window 8.6.1Nonfire Spill Response HelpNew Window Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Fully encapsulating, vapor-protective clothing should be worn for spills and leaks with no fire. ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor-suppressing foam may be used to reduce vapors. Absorb with earth, sand or other non-combustible material and transfer to containers (except for Hydrazine). Use clean, non-sparking tools to collect absorbed material. LARGE SPILL: Dike far ahead of liquid spill for later disposal. Water spray may reduce vapor, but may not prevent ignition in closed spaces. (ERG, 2016) U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals 8.6.2Storage Conditions HelpNew Window Triallylamine IN GENERAL, MATERIALS WHICH ARE TOXIC AS STORED OR WHICH CAN DECOMP INTO TOXIC COMPONENTS … SHOULD BE STORED IN A COOL, WELL-VENTILATED PLACE, OUT OF DIRECT RAYS OF THE SUN, AWAY FROM AREAS OF HIGH FIRE HAZARD, & SHOULD BE PERIODICALLY INSPECTED … . INCOMPATIBLE MATERIALS SHOULD BE ISOLATED FROM EACH OTHER. Sax, N.I. Dangerous Properties of Industrial Materials. 4th ed. New York: Van Nostrand Reinhold, 1975., p. 1179 from HSDB 8.7Exposure Control and Personal Protection HelpNew Window 8.7.1Personal Protective Equipment (PPE) HelpNew Window Personnel protection: … Wear positive pressure self-contained breathing apparatus. … Wear appropriate chemical protective gloves, boots, and goggles. Association of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1994., p. 1066 from HSDB 8.7.2Protective Equipment and Clothing HelpNew Window Triallylamine Excerpt from ERG Guide 132 [Flammable Liquids – Corrosive]: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters’ protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. (ERG, 2016) U.S. Department of Transportation, Transport Canada, and Secretariat of Communications and Transport of Mexico, with collaboration from Argentina’s Centro de Información Química para Emergencias. 2016 Emergency Response Guidebook. https://www.phmsa.dot.gov/hazmat/outreach-training/erg (accessed April 26, 2016). from CAMEO Chemicals 8.8Stability and Reactivity HelpNew Window 8.8.1Air and Water Reactions HelpNew Window

Flammable. Insoluble in water. from CAMEO Chemicals 8.8.2Reactive Group HelpNew Window Amines, Phosphines, and Pyridines Hydrocarbons, Aliphatic Unsaturated from CAMEO Chemicals 8.8.3Reactivity Alerts HelpNew Window Strong Reducing Agent CAMEO Chemicals 8.8.4Reactivity Profile HelpNew Window Triallylamine is a strong reducing agent that reacts violently with oxidizing agents. Corrosive towards Al and Zn [Handling Chemicals Safely 1980 p. 912] . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. from CAMEO Chemicals Information HelpNew Window 8.9.1DOT Emergency Guidelines HelpNew Window /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Fire or Explosion: Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a (P) may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Health: May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Public Safety: CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number listed on the inside back cover. As an immediate precautionary measure, isolate spill or leak area for at least 50 meters (150 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate closed spaces before entering. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters’ protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Evacuation: Spill: See Table 1 – Initial Isolation and Protective Action Distances for highlighted materials. For non-highlighted materials, increase, in the downwind direction, as necessary, the isolation distance shown under triallylamine “PUBLIC SAFETY”. Fire: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Fire: Some of these materials may react violently with water. Small Fire: Dry chemical, CO2, water spray or alcohol-resistant foam. Large Fire: Water spray, fog or alcohol-resistant foam. Move containers from fire area if you can do it without risk. Dike fire-control water for later disposal; do not scatter the material. Do not get water inside containers. Fire involving Tanks or Car/Trailer Loads: Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn.

U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ Spill or Leak: Fully encapsulating, vapor protective clothing should be worn for spills and leaks with no fire. ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor suppressing foam may be used to reduce vapors. Absorb with earth, sand or other non-combustible material and transfer to containers (except for Hydrazine). Use clean non-sparking tools to collect absorbed material. Large Spill: Dike far ahead of liquid spill for later disposal. Water spray may reduce vapor; but may not prevent ignition in closed spaces. U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB /GUIDE 132: FLAMMABLE LIQUIDS – CORROSIVE/ First Aid: Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.

U.S. Department of Transportation. 2012 Emergency Response Guidebook. Washington, D.C. 2012 from HSDB 8.9.2Shipment Methods and Regulations HelpNew Window No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance … and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by … /the hazardous materials regulations (49 CFR 171-177)./ 49 CFR 171.2; U.S. National Archives and Records Administration’s Electronic Code of Federal Regulations. Available from, as of February 15, 2006: http://www.ecfr.gov from HSDB The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials. International Air Transport Association. Dangerous Goods Regulations. 47th Edition. Montreal, Quebec Canada. 2006., p. 265 from HSDB The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article. International Maritime Organization. International Maritime Dangerous Goods Code. London, UK. 2004., p. 125 from HSDB 8.9.3DOT ID and Guide HelpNew Window 2610 132 from DOT Emergency Response Guidebook 8.9.4DOT Label HelpNew Window Flammable Liquid Corrosive CAMEO Chemicals 9Toxicity HelpNew Window 9.1Toxicological Information HelpNew Window 9.1.1NIOSH Toxicity Data HelpNew Window 11 items View More Rows & Details Download Measurement System Route/Organism Dose Effect Date Skin and Eye Irritation eye /rabbit 50 mg/20S rinse mild February 2008 Skin and Eye Irritation skin /rabbit 10 mg/24H open irritation test severe February 2008 Acute Toxicity Data inhalation/mammal (species unspecified) lethal concentration (50 percent kill): 2800 mg/m3 February 2008 Acute Toxicity Data inhalation/man lowest published toxic concentration: 13 ppm/5M Lung, Thorax, or Respiration: Structural or functional change in trachea or bronchi February 2008 Acute Toxicity Data inhalation/rat lethal concentration (50 percent kill): 554 ppm/8H Olfaction: Other olfaction effects; Eye: Lacrimation; Lung, Thorax, or Respiration: Dyspnea February 2008 1 Next Triallylamine from The National Institute for Occupational Safety and Health (NIOSH) 9.1.2Acute Effects HelpNew Window 8 items View More Download

Organism Test Type Route Dose Effect Reference man TCLo inhalation 13 ppm/5M (13 mg/kg) LUNGS, THORAX, OR RESPIRATION: STRUCTURAL OR FUNCTIONAL CHANGE IN TRACHEA OR BRONCHI Archives of Environmental Health., 1(343), 1960 [PMID:13714435] rat LC50 inhalation 554 ppm/8H (554 mg/kg) SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION; SENSE ORGANS AND SPECIAL SENSES: ACRIMATION: EYE; LUNGS, THORAX, OR RESPIRATION: DYSPNEA Archives of Environmental Health., 1(343), 1960 [PMID:13714435] mouse LD50 oral 492 mg/kg (492 mg/kg) BEHAVIORAL: TREMOR; LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION; GASTROINTESTINAL: OTHER CHANGES Archives of Environmental Health., 1(343), 1960 [PMID:13714435] rabbit LD50 skin 400 uL/kg (0.4 mg/kg) American Industrial Hygiene Association Journal., 23(95), 1962 [PMID:13914538] mammal (species unspecified) LC50 inhalation 2800 mg/m3 (2800 mg/kg) Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*., 14(80), 1975 1 2 Next from ChemIDplus 9.1.3Antidote and Emergency Treatment HelpNew Window Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary … . Monitor for shock and treat if necessary … . Anticipate seizures and treat if necessary … . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport … . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patent can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal … . Cover skin burns with dry sterile dressings after decontamination … . /Organic bases/Amines and related compounds/ Bronstein, A.C., P.L. Currance; Emergency Care for Hazardous Materials Exposure. 2nd ed. St. Louis, MO. Mosby Lifeline. 1994., p. 168-9 from HSDB Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious or has severe pulmonary edema. Positive-pressure ventilation techniques with a bag-valve-mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias as necessary … . Start an IV with D5W /SRP: “To keep open”, minimal flow rate/. Use lactated Ringer’s if signs of hypovolemia are present. Watch for signs of fluid overload. Administer 1% solution methylene blue if patient is symptomatic with severe hypoxia, cyanosis, and cardiac compromise not responding to oxygen. … . Consider drug therapy for pulmonary edema … . For hypotension with signs of hypovolemia, administer fluid cautiously. If patient is unresponsive to these measures, vasopressors may be helpful. Watch for signs of fluid overload … . Treat seizures with diazepam (Valium) … . Use proparacaine hydrochloride to assist eye irrigation … . / Triallylamine Organic bases/Amines and related compounds/ Bronstein, A.C., P.L. Currance; Emergency Care for Hazardous Materials Exposure. 2nd ed. St. Louis, MO. Mosby Lifeline. 1994., p. 169 from HSDB 9.1.4Human Toxicity Excerpts HelpNew Window … RECOGNIZABLE @ 0.5 PPM, MUCOUS MEMBRANE IRRITATION Trialillamin bu ters fazl (RP) HPLC metodu ile basit itril (MeCN), su ve fosforik asit içerir. Kütle Spek (MS) uyumlu uygulamalar için fosforik asidin formik asit ile deitirilmesi gerekir. Hzl UPLC uygulamalar için daha küçük 3 µm parçacklar sütunlar mevcuttur. Bu sv kromatografi yöntemi ölçeklendirilebilir ve preparatif ayrmada izolasyon safszlklar için kullanlabilir. Ayn zamanda farmakokinetik için de uygundur. Trillaminin gaz faz termal ayrm 531 ila 620 K scaklk aralnda incelenmitir. Reaksiyonda gözlenen balca ürünler propilen ve 3 – pikolindir. Dahili standart teknik kullanlarak elde edilen triallylaminin tükenmesi için birinci dereceden sabitlerin basnç ve dönüümden bamsz olduu ve Arreniusrelationsation denklem görüntüsüne uyduu tespit edildi. Tepkime homojen görünüyor, yüzeyde 15 kat deiiklik – Damarn hacim oran, hz sabitlerini deimeden brakt. Arrhenius parametreleri, propilen ve N lyalil – prop – 2 – enaldimin veren alt merkezli bir geçi durumu içeren moleküler bir eliminasyon reaksiyonu ile tutarldr. kinci ürünün 1,5 – hidrojen transferine tabi tutulmas, ardndan dihidropikolin elde etmek için bir halka kapatma reaksiyonu yaplmas önerilmektedir, bu da kendiliinden balatlan bir ayrma reaksiyonu ile 3 picoline oluumu ile reaksiyona girmektedir.

Allamin, oksitleyici malzemelerle yüksek derecede yanc ve orta derecede reaktif olan renksiz veya sarms uçucu bir svdr (HSDB 2003). Suda 9.7 pKa ile tamamen çözünür ve mukoza zarlarn tahri eden çok keskin bir amonyak benzeri bir kokuya sahiptir (Budavari ve ark. 1996; HSDB 2003; Boor ve Hysmith 1987) .2 Endüstriyel olarak kullanlr. kauçuun vulkanizasyonu ve ticari diüretikler, sedatifler ve antiseptikler dahil olmak üzere ticari ürünlerin sentezlenmesi (Benya ve Harbison 1994). Alillamin, alkil halojenürlerin (örnein allil klorür ve amonyak) aminasyonu ile üretilir ve ayrca gda maddelerinin doal bir bileenidir (Budavari ve ark. 1996; HSDB 2003). Ciddi bir solunum, göz ve cilt tahri edici olmasna ek olarak, allilamin, yüksek dozlarda oral yoldan, soluma yoluyla veya enjeksiyonla uygulandnda kardiyotoksiktir. nsan kardiyovasküler hastaln modellemek için laboratuvar hayvanlarnda kalp ve damar lezyonlarn uyarmak için kullanlmtr. Allamin kardiyotoksisitesinin, kardiyak ve vasküler dokularda akrolein ve hidrojen peroksit metabolizmas ile ilgili olduu ileri sürülmektedir (Boor ve Hysmith 1987; Ramos ve ark. 1988). Allylamine öldürücü inhalasyon toksisitesi, sçanlarda ve farelerde ve bunun ölümcül inhalasyon toksisitesinde, maymunlar, sçanlar, fareler ve tavanlar kullanlarak yaplan tek ve çoklu pozlama çalmalarnda incelenmitir. nsan gönüllüleri ve iyerindeki maruz kalmalar ile yaplan çalmalar, ksa süreli solunmaya maruz kalmann tahri edici ve toksik etkileri hakknda snrl bilgi salamtr. Alillamin koku eii s 2 pKa, asit ayrma sabitinin negatif logudur. Düük moleküler arlkl poli (alilamin), serbest radikal polimerizasyonu ile hazrlanr ve elde edilen polimer, farkl amin yüklemelerinde mezoselüler silika köpüklerine emdirilir. Elde edilen poli (alillamin) -silika kompozitlerinin, seyreltik (simüle edilmi baca gaz) ve ultradilut (simüle edilmi ortam havas) gaz aklarndan karbon dioksitin çkarlmas için etkili adsorbanlar olduu gösterilmitir. Kompozit adsorbanlarn, daha geleneksel poli (etilenimin) -silika adsorbanlarla karlatrlabilir adsorpsiyon kapasitelerine sahip olduu gösterilmitir. Poli (alillamin) ile ölçülen adsorbanlarn potansiyel avantajlar tartlmtr.

2,5-bis (triflorometil) -l, 3,4-oksadiazol ve etil 5- (triflorometil) -1,3,4-oksadiazol-2-karboksilatn siklilisyon reaksiyonlar triallylamin ile incelendi. ncelenen reaksiyonlar, oktahidro-2,7-metanofuro [3,2-c] piridin serisinin baka molekül içi sikloaddition – kafes bileikleri ürünleri verdi. Sentezlenen bileikler kuvvetli ekilde bazik özelliklere sahipti ve stabil tuzlar oluturdu.

Anilinler dioksan içinde 180 ° C’de trialitlamin ile katalitik miktarda rutenyum klorür ve trifenilfosfin ile birlikte iyi verimlerde karlk gelen 2-etil-3-metilkinolinleri vermek üzere kalay (II) klorür dihidrat varlnda reaksiyona girerler.Anilinlerin triallylamin ile rutenyum katalizli siklizasyonu, 2-etil-3-metilkinolinler verir.

Alil-, tek deerlikli organik grup için önek, -CH2 = CHCH2’dir. Alil alkol bir örnektir, CH2 = CHCH20H, berrak, keskin sv, 96 ° C’de kaynar; suda çözünebilir. Hidroliz ile allil klorürden hazrlanr. Bir alken hidrokarbon olan alil bileii, bir metilen -CH2’ye balanm bir vinil gruba (CH2 = CH-) sahiptir. Oldukça reaktif kat ba nedeniyle, alil, kaplamalarn, yaptrclarn ve elastomerlerin üretiminde kullanlan homopolimerler veya ko-polimerler oluturmak üzere kendileri veya dier monomerler ile kolayca birletirilen kat baa serbest radikal ilavesine maruz kalabilir. Serbest radikal ilavesine ek olarak, alil bileikleri, elektrofilik ilaveler, alilik ikame ve oksidasyon dahil olmak üzere çok çeitli reaksiyonlara katlabilir. Doymam bir ba olan alil, baz bileiklerde karakteristik bir koku verir. Bir örnek, siyah hardallarn ana maddesi olan alil izotiyosiyanattr. (beyaz hardal, temel olarak p-hidroksibenzil izotiyosiyanattan oluur). Alil izotiyosiyanat, hardal ya olarak adlandrlr. Alil esterleri koku, tat veya koku ile ilgilidir. Triillamin, kauçuk kimyasallar, iyon deiim reçineleri, polimerizasyon balatclar, kuaterner amonyum tuzlar, çapraz balayc ajanlarn imalatnda bir ara madde olarak kullanlr.

Asit bölgeleri ve bazik gruplar içeren çapraz balanm polimer tanecikleri, termal olarak yenilenebilir bir iyon deiimi ileminin verimli çalmas için tercih edilen yaplardr. Bu çalma, reçinelerde asidik ve bazik bölgeler arasndaki alama sorununu incelemek için tasarlanmtr. ki yaklam kullanld. lk olarak, akrilamidden hapsolmu makroradikaller hazrland ve daha sonra akrilik asit veya triallylamin ilave edildi. kinci olarak, triallylamin hidroklorürün, hidroperoksit gruplar içeren bir otoksidize poliizopropilstiren numunesine alanmas denenmitir. Bununla birlikte, hidroperoksit gruplar, kobalt naftenat mevcudiyetinde, akrilik asitin hzl ve kantitatif olarak alanmasna balasa da, hiçbir tirillamin hidroklorür grefti olumad.

Bir MOVPE ileminde ZnSe’yi kullanmak için azot hidrojen ba olmayan birkaç azot öncüsü test edildi. Bisditrimetilsilylamidozinc (ZnBTM), trimetilsillazid (TMSiN) ve trialillamin (TAN), ZnSe: N ile ditertiarbütilselenit (DTBSe), diizopropilseleni (DIPSe) ve dimetilzinc-trietilamin Numuneler fotoluminesans (PL), akm voltaj (I?V), kapasitans voltaj (C?V) ve Hall ölçümleriyle analiz edildi. Azot oluumunun ve elektriksel aktivasyonun büyüme scaklna, VI / II oranna ve dopant akna bamll incelenmitir. TMSiN ile büyütülen tabakalarn PL spektrumlarnda, yüksek dopant aklar için IN1 emisyon hattnn yan sra, Zn boluklarna bal olarak youn bir balanma-salma emisyonu gözlenmektedir. Öncüler olarak ZnBTM ve TAN ile büyütülen örnekler, eksitonik emisyonlarn genilemesini ve tabakalara azot dahil edilmesini arttrmak için IN1 emisyon hattnn enerjik konumuna doru bir kayma sergiler. Eksitonik emisyonlarn donör-alc çifti emisyonlarna kyasla younluu hâlâ devam etmektedir. ZnBTM ve TAN ile kattrlm birkaç örnein Hall ölçümleri p-tipi iletkenlii gösterse de, C?V ve ??I?V ölçümlerinin analizi numunelerin n-tipi veya yar-yaltc karakterini gösterir.

Yeni bir mesoporous polimer, mesoporous poli-trialillamin (MPTA-1), anyonik veya anyonik / iyonik olmayan kark yüzey aktif cisimlerinin organik-organik kendiliinden birlemesi yoluyla triallilaminin basit ve kolay bir yerinde in situ radikal polimerizasyonu ile sentezlenmitir. Toz XRD ve TEM görüntü analizi, bu örneklerde düzensiz solucan delii benzeri mezoporlarn varln göstermektedir. N2 sorpsiyon analizleri, bu MPTA-1 numuneleri için orta derecede iyi yüzey alanl (70-134 m2 g – 1) nano ölçekte bimodal gözenek büyüklüü dalmlarn ortaya koymaktadr. ablonsuz protonlanm MPTA-1 numuneleri, mesopöz çerçevede pozitif yüklü azot atomlar tar ve bu, sulu anyonlardan yüksek anyon deitirme verimlerinde yanstlr. MPTA-1’in yüksek anyon deiim verimlilii, çeitli atk su kaynaklarnda önemli miktarlarda bulunabilen CrO42-, MnO4-, AsO33-, NO3- ve PO43- gibi kirletici anyonlarn uzaklatrlmasndaki potansiyel uygulamasn kefetmemiz için bizi motive etti. .

Si (111) üzerindeki Trialillamin (TAA), (C3H5) 3N’nin yüzey kimyas, UHV koullar altnda adsorpsiyon ve yerinde karakterizasyon ile incelenmitir. Yüksek Çözünürlüklü Elektron Enerji Kayb Spektroskopisi (HREELS), yüzeydeki titreim modlarnn spektrumunu verir ve X-n Fotoelektron Spektroskopisi (XPS), kimyasal balanma ve yakn yüzey bölgesinde farkl adsorbatlarn ksmi konsantrasyonunu verir. Üçüncül amin TAA, ayrma olmadan RT’de phizorbs eder. Parçalanan fazn art arda tavlanma aamalar, 400 ° C’de aminin ayrmasna neden olur. Daha yüksek scaklklarda alil gruplar ksmen deifre edilir ve kalan ksm, 600 ° C’de tamamen ayrr; burada hidrojen, yüzeyden ayrlr ve azot ve karbon, Si substrat içinde yaylmaya balar. TAA’nn stlm bir Si substrat üzerinde adsorpsiyonu için çok benzer bir davran gözlenir. 500-800 ° C scaklk aralnda Triethylgallium (TEG) ile birlikte emilim, Si yüzeyindeki reaksiyonda önemli deiikliklere neden olmaz. ncelenen tüm scaklk aralnda kodlamadan sonra yüzeyde ihmal edilebilir bir Ga miktar tespit edilir. Bir GaN faznn büyümesi, ne Si (111) ne de Al203 (0001) substratlarda gözlenmedi.

Lityum metal, en yüksek özgül kapasitesi (3860 mA h g – 1) ve düük potansiyeli nedeniyle düük nesil Coulombic verimi ve lityum dendrit oluumu nedeniyle yeni nesil arj edilebilir pil için umut verici bir anot adaydr. Burada, elektrolitte bir katk maddesi olarak kükürt içeren polimerler kullanlarak organosülfidler / organopolisülfitler ve inorganik lityum tuzlarnn birlikte biriktirilmesi yoluyla kendiliinden oluturulmu bir esnek hibrit kat-elektrolit interfaz tabakas bildirilmektedir. Organosülfitler / organopolisülfitler, mekanik esnekliini ve tokluunu arttrmak için kat-elektrolit faz içi tabakasnda “plastikletirici” olarak ilev görür. Oluan salam kat-elektrolit interphase katmanlar, dendritsiz lityum biriktirmesini salar ve Coulombic verimliliini önemli ölçüde iyiletirir (2 mA cm current 2 akm younluunda 400 döngü üzerinde% 99). Bu stratejiye dayanan bir lityum-kükürt batarya uzun çevrim ömrü (1000 döngü) ve iyi kapasite tutma sergiler. Bu çalma, lityum metal anotlarla ilikili sorunlar çözmek için stabil kat-elektrolit faz aras tabakasn etkili bir ekilde üretmek için bir yol ortaya koymaktadr.

Alkalin ortamndaki heksasiyanoferrat (III) tarafndan triallaminin oksidasyonunun kinetii incelenmitir. Hz, Fe (CN) 6 (3-) ‘nin konsantrasyonundan bamsz iken, [triallilamin] ve [OH-] siparileri srasyla neredeyse birlik ve 0.33’tür. Reaksiyonun hz, eklenen Fe (CN) 6 (4-) iyonlar tarafndan geciktirilmez. yonik kuvvet, deien katyonlar ve eklenen tuzlarn anyonlar, çözücü bileimi ve scakln reaksiyon hz üzerindeki etkileri rapor edilmitir. Uygun bir mekanizma önerilmitir.

Trialillamin esas olarak organik sentez ve reçine düzenleyicide uygulanr, ayrca yüksek emici ve iyon deitirme reçinesinin ara balarnda da kullanlabilir. Baz raporlara göre, polyester aktivatörü ve bütadien polimerizasyonunun uyandrma ajan üretiminde kullanlabilir.

Depolama ve tama

Ürünü kapal, serin ve kuru bir ortamda ambalajlayn ve saklayn, güçlü oksidanlarla temastan kaçnn, açk ateten uzak tutun. Geçerlilik süresi: Üç yl. Ulam: Tehlikeli mallar.

Üretim ve reaksiyonlar

Her üç alillamin, mono-, di- ve triallylamin, allil klorürün amonyakla muamele edilmesi ve ardndan damtlmas ile üretilir. Saf numuneler allil izotiyosiyanatn hidrolizi ile hazrlanabilir. Tipik bir amin gibi davranr.Polimerizasyon, homopolimeri (polialilamin) veya kopolimerleri hazrlamak için kullanlabilir. Polimerler, ters ozmozda kullanm için ümit vaat eden membranlardr.

Dier allilaminler

levselletirilmi alillaminler, geni farmasötik uygulamalara sahiptir. Farmasötik olarak önemli allilaminler arasnda flunarizin ve naftifin bulunur. Flunarizin, migrenlerin rahatlamasna yardmc olurken, naftifin, sporcu aya, sporcu kants ve saçkran gibi enfeksiyonlara neden olan yaygn mantarlarla savamak için hareket eder.

A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. The TRIALLYLAMINE molecule contains a total of 24 bond(s). There are 9 non-H bond(s), 3 multiple bond(s), 6 rotatable bond(s), 3 double bond(s) and 1 tertiary amine(s) (aliphatic).

Triallylamine can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

The gas phase thermal decomposition of triallylamine was studied in the temperature range 531 to 620 K. The major products observed in the reaction were propylene and 3-picoline. The first order rate constants for depletion of triallylamine, obtained using the internal standard technique, are found to be independent of pressure and conversion, and fit the Arrheniusrelationship equation imageThe reaction appears to be homogeneous, as a 15-fold change in thc surface-to-volume ratio of the vessel left the rate constants unchanged. The Arrhenius parameters are consistent with a molecular elimination reaction involving a six-center transition state, yielding propylene and N-allyl-prop-2-enaldimine. It is proposed that the latter product undergoes a 1,5-hydrogen transfer, followed by a ring closure reaction to yield dihydropicoline, which in turn reacts forming 3-picoline via a self-initiated decomposition reaction.

Colorless alicyclic polyimides (ALPIs) were synthesized from an alicyclic dianhydride, bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride (BCDA) and an aromatic diamine, 3,4′-oxydianiline (3,4′-ODA). For comparison, a series of crosslinkable ALPI membranes with different content of crosslinkable reagents were prepared. The crosslinkable PI reacts with the crosslinkers and forms covalent bond to create the crosslink structure between PI backbones by free radical reaction. Almost of the crosslinkable PIs exhibit excellent dimensional stability and higher transparency because of the crosslink structure and non-conjugate alicyclic chain. All of the crosslink ALPIs could be coated into flexible and tough films. They had a UV-Vis cut-off at 297 nm and a transmittance of higher than 80% in near ultraviolet region. These PIs show low coefficient of thermal expansion ranging from 57.36 to 47.53 ppm/°C, the glass transition temperature in the range of 336.2-333.0 °C, the decomposition temperature in the range of 433.7-440.0 °C. The crosslinkable ALPIs show excellent optical properties with the excited wavelength ranging from 340 to 328 nm and stronger emission intensity than linear PI, the haze lower than 0.7, the refractive index about 1.6 and the abbe numbers over 165.

Allylamine is a colorless or yellowish volatile liquid that is highly flammable and moderately reactive with oxidizing materials (HSDB 2003). It is completely soluble in water with a pKa of 9.7 and has a very sharp ammonia-like odor that is irritating to mucous membranes (Budavari et al. 1996; HSDB 2003; Boor and Hysmith 1987).2 Industrially, it is used in the vulcanization of rubber and in the synthesis of commercial products, including mercurial diuretics, sedatives, and antiseptics (Benya and Harbison 1994). Allylamine is manufactured by the amination of alkyl halides (e.g., allyl chloride and ammonia) and is also a natural constituent of foodstuffs (Budavari et al. 1996; HSDB 2003).In addition to being a severe respiratory, eye, and skin irritant, allylamine is cardiotoxic when administered at high doses orally, by inhalation, or by injection. It has been used to induce cardiac and vascular lesions in laboratory animals to model human cardiovascular disease. Allylamine cardiotoxicity is proposed to be related to its metabolism to acrolein and hydrogen peroxide in cardiac and vascular tissues (Boor and Hysmith 1987; Ramos et al. 1988). Allylamine lethal inhalation toxicity has been examined in rats and mice and its nonlethal inhalation toxicity in single- and multiple-exposure studies using monkeys, rats, mice, and rabbits. Studies with human volunteers and exposures in the workplace have yielded limited information about the irritant and toxic effects of short-term inhalation exposure. The allylamine odor threshold s 2 pKa is the negative log of the acid dissociation constant.

Low-molecular-weight poly(allylamine) is prepared via free-radical polymerization, and the resulting polymer is impregnated into mesocellular silica foams at different amine loadings. The resulting poly(allylamine)-silica composites are demonstrated as effective adsorbents for the extraction of carbon dioxide from dilute (simulated flue gas) and ultradilute (simulated ambient air) gas streams. The composite adsorbents are shown to have comparable adsorption capacities to more-conventional poly(ethyleneimine)-silica adsorbents. Potential advantages of poly(allylamine)-derived adsorbents are discussed. Triallylamine uses and applications include: unsaturated polyester resin comonomer; crosslinking comonomer; production of some rubbers, ion exchange resins, organic chemicals

Cycloaddition reactions of 2,5-bis(trifluoromethyl)-1,3,4-oxadiazole and ethyl 5-(trifluoromethyl)-1,3,4-oxadiazole-2-carboxylate with triallylamine were studied. The investigated reactions yielded products of further intramolecular cycloaddition – cage compounds of octahydro-2,7-methanofuro[3,2-c]pyridine series. The synthesized compounds had strongly basic properties and formed stable salts.

Anilines react with triallylamine in dioxane at 180 °C in the presence of a catalytic amount of ruthenium chloride and triphenylphosphine together with tin(II) chloride dihydrate to afford the corresponding 2-ethyl-3-methylquinolines in good yields.

Allyl- is the prefix for the univalent organic group, -CH2=CHCH2. Allyl alcohol is an example, CH2=CHCH2OH, clear, pungent liquid, boiling at 96 C; soluble in water. It is prepared from allyl chloride by hydrolysis. Allyl compound, an alkene hydrocarbon, has a vinyl group, CH2=CH-, attached to a methylene -CH2. Because of the highly reactive solid bond, allyl can undergo free radical addition to solid bond which readily combine with themselves or other monomers to form homopolymers or co-polymers which are used in the production of coatings, adhesives and elastomers. In addition to free radical addition, allyl compounds can participate in a wide variety of reactions including electrophilic additions, allylic substitution and oxidation. Allyl, an unsaturated bond, imparts a characteristic odor in some compounds. An example is allyl isothiocyanate which is the main ingredient of black mustards. (white mustard consists principally of p-hydroxybenzyl isothiocyanate). Allyl isothiocyanate is called mustard oil. Allyl esters are involved in fragrance, flavor, or odor.Triallylamine is used as an intermediate for the manufacture of rubber chemicals, ion exchange resins, polymerization initiators, quaternary ammonium salts, cross-linking agents

Crosslinked polymer beads containing regions of acid and basic groups are preferred structures for the efficient operation of a thermally regenerable ion-exchange process. This study is designed to examine the question of grafting between the acidic and basic regions in the resins. Two approaches were used. First, trapped macroradicals from acrylamide were prepared and then either acrylic acid or triallylamine added. Secondly, the grafting of triallylamine hydrochloride to an autoxidized polyisopropylstyrene sample containing hydroperoxide groups was attempted. However, no grafting of triallylamine hydrochloride occurred even though the hydroperoxide groups, in the presence of cobalt naphthenate, initiated rapid and quantitative grafting of acrylic acid.

Several nitrogen precursors without nitrogen hydrogen bonds were tested to dope ZnSe in a MOVPE process. Bisditrimethylsilylamidozinc (ZnBTM), trimethylsilylazide (TMSiN) and triallylamine (TAN) were used to grow ZnSe:N with ditertiarybutylselenide (DTBSe), diisopropylselenide (DIPSe) and dimethylzinc-triethylamine (DMZn?TEN) at growth temperatures between 340 and 420°C. The samples were analysed by photoluminescence (PL), current-voltage (I?V), capacitance-voltage (C?V) and Hall measurements. The dependence of nitrogen incorporation and electrical activation on growth temperature, VI/II ratio and dopant flow were investigated. In the PL spectra of the layers grown with TMSiN an intense bound-exciton emission, correlated to Zn vacancies is observed, besides the IN1 emission line for high dopant flows. The samples grown with ZnBTM and TAN as precursors exhibit a broadening of the excitonic emissions and a shift towards the energetic position of the IN1 emission line for increasing nitrogen incorporation in the layers. The intensity of the excitonic emissions in comparison to the donor-acceptor pair emissions remains dominating. Although Hall measurements of several samples doped with ZnBTM and TAN indicate p-type conductivity, the analysis of the C?V and I?V measurements shows the n-type or semi-insulating character of the samples.

A new mesoporous polymer, mesoporous poly-triallylamine (MPTA-1), has been synthesized by a simple and facile in situ radical polymerization of triallylamine through organic-organic self-assembly of anionic or anionic/non-ionic mixed surfactant systems. Powder XRD and TEM image analysis suggests the presence of disordered wormhole-like mesopores in these samples. N2 sorption analyses reveal bimodal pore size distributions on the nanoscale with moderately good surface areas (70-134 m2 g-1) for these MPTA-1 samples. Template-free protonated MPTA-1 samples carry positively charged nitrogen atoms in the mesoporous framework, which is reflected in its high anion exchange efficiencies from aqueous solutions. High anion exchange efficiency of MPTA-1 has motivated us to explore its potential application in the removal of pollutant anions such as CrO42-, MnO4-, AsO33-, NO3- and PO43-, which can be present in significant quantities in various wastewater sources.

The surface chemistry of Triallylamine (TAA), (C3H5)3N on Si(111) has been studied by adsorption under UHV conditions and in-situ characterization. High Resolution Electron Energy Loss Spectroscopy (HREELS) yields the spectrum of vibration modes at the surface, and X-ray Photoelectron Spectroscopy (XPS) yields the chemical bonding and the partial concentration of the different adsorbates in the near surface region. The tertiary amine TAA physisorbs at RT without dissociation. Successive annealing steps of the physisorbed phase induce the dissociation of the amine at 400 °C. At higher temperatures the allyl groups are partially desorbed and the rest fully dissociated at 600 °C, where the hydrogen leaves the surface and the nitrogen and carbon start to diffuse into the Si substrate. A very similar behaviour is observed for the adsorption of TAA on a heated Si substrate. The coadsorption with Triethylgallium (TEG) in the temperature range 500-800 °C does not induce significant changes in the reaction at the Si surface. A negligible quantity of Ga is detected at the surface after codeposition in the whole investigated temperature range. The growth of a GaN phase has not been observed, neither on Si(111) nor on Al2O3(0001) substrates.

Lithium metal is a promising anode candidate for the next-generation rechargeable battery due to its highest specific capacity (3860?mA?h?g-1) and lowest potential, but low Coulombic efficiency and formation of lithium dendrites hinder its practical application. Here, we report a self-formed flexible hybrid solid-electrolyte interphase layer through co-deposition of organosulfides/organopolysulfides and inorganic lithium salts using sulfur-containing polymers as an additive in the electrolyte. The organosulfides/organopolysulfides serve as “plasticizer” in the solid-electrolyte interphase layer to improve its mechanical flexibility and toughness. The as-formed robust solid-electrolyte interphase layers enable dendrite-free lithium deposition and significantly improve Coulombic efficiency (99% over 400 cycles at a current density of 2?mA?cm-2). A lithium-sulfur battery based on this strategy exhibits long cycling life (1000 cycles) and good capacity retention. This study reveals an avenue to effectively fabricate stable solid-electrolyte interphase layer for solving the issues associated with lithium metal anodes.

Kinetics of the oxidation of triallylamine by hexacyanoferrate(III) in alkaline medium have been studied. The rate is independent of the concentration of Fe(CN)6(3-), while the orders in [triallylamine] and [OH-] are nearly unity and 0.33 respectively. The rate of the reaction is not retarded by added Fe(CN)6(4-) ions. The effects of ionic strength, varying cations and anions of added salts, solvent composition and temperature on the reaction rate are reported. A suitable mechanism has been proposed.

Physical properties

Chemical Formula:

C9H15N

Flash Point: 103 ° F (NTP, 1992)

Melting Point: -94 ° F (NTP, 1992)

Specific Gravity: 0.809 at 68 ° F (NTP, 1992)

Boiling Point: 311 to 313 ° F at 760 mm Hg (NTP, 1992)

Molecular Weight: 137.23 (NTP, 1992)

Water Solubility: 2.5 mg/mL (NTP, 1992)

Application

Triallylamine is mainly applied in organic synthesis and resin modifier, also can be used in the crosslinking of high absorbent and the intermediates of ion exchange resin. According to some reports, it can be used in producing polyester activator and the evocating agent of butadiene polymerization.

Storage and transportation

Pack and preserve the product in a sealed, cool and dry condition, avoid contacting strong oxidants, keep away from open fire.The term of validity: Three years. Transportation: Dangerous goods.

Production and reactions

All three allylamines, mono-, di-, and triallylamine, are produced by the treating allyl chloride with ammonia followed by distillation. Pure samples can be prepared by hydrolysis of allyl isothiocyanate. It behaves as a typical amine.Polymerization can be used to prepare the homopolymer (polyallylamine) or copolymers. The polymers are promising membranes for use in reverse osmosis.

Other allylamines

Functionalized allylamines have extensive pharmaceutical applications. Pharmaceutically important allylamines include flunarizine and naftifine. Flunarizine aids in the relief of migraines while naftifine acts to fight common fungus causing infections such as athlete’s foot, jock itch, and ringworm.