N-BUTYLAMINE

N-BUTYLAMINE

N-BUTYLAMINE

CAS NO: 109-73-9

METATAGS;Butylamine;N-BUTYLAMINE;1-Butanamine;butan-1-amine;1-Aminobutane;109-739;1Butylamine;Butylamin;Butylaminen;femanumber3130.
;Monobutilamina;Monobutylamine;n-Butilamina;N-Butylamin;n-C4H9NH2Monobutylamine;N-Butylamin;Mono-n-butylamine;1-Aminobutan;Norvalamine;1-Amino-butaan;Monobutilamina;Butanamine;n-Butilamina;n-Butylamin [German];n-Butilamina [Italian];1-Aminobutan [German];butyl amine;FEMA Number 3130;n-butyl amine;Monobutilamina [Romanian];1-Amino-butaan [Dutch];UNII-N2QV60B4WR;NSC 8029;FEMA No. 3130;CCRIS 4756;HSDB 515;1-Butanaminen-butilamina;EINECS 203699-2;UN1125;nC4H9NH2;AI324197;CHEBI:43799;
HQABUPZFAYXKJWUHFFFAOYSAN;MFCD00011690;LYT;Aminobutane;Butylarnine;Monobutylamime;Norralamine;n-butyiamine;n-butyl-amine;butane-1-amine;1 amino-butan;n-butan-1-amine;normal-butyl amine;Butylamine, 99%;Pharmaceutical Intermediates;Anilines, Aromatic Amines and Nitro Compounds;Alkylamines;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes;Amines;Building Blocks;C2 to C5;Chemical Synthesis;Nitrogen Compounds;Organic Building

BlocksAminob(Related);BUTYLAMINE,N;Butylamine,>=99%;Butylamine,9.5%;2amino2methylpropan;-1AMINOBUTANE;DSSTox_CID_1904;AC1L1Q1U;DSSTox_RID_76395;
N2QV60B4WR;NCIOpen2_009229;DSSTox_GSID_21904;WLN: Z4;KSC175M4L;CHEMBL13968;Butylamine, puriss.,99.0%;DTXSID1021904;1-Butylamine, 99% 100ml;3858-78-4 (hydrochloride);CTK0H5645;KS-00000UWE;NSC8029;MolPort-001-788-476;BB_SC-6761;ACMC-209948;NSC-8029;ZINC1586365;Tox21_301131;ANW-16086;BBL027788;
LS-485;STL308736;AKOS000118810;Butylamine, purum, >=98.0% (GC);Butylamine, purum, >=99.0% (GC);DB03659;MCULE-4233278050;RP18328;RTR-002082;TRA0026534;UN 1125;Butylamine, analytical reference material;Butylamine, puriss., >=99.5% (GC);NCGC00248302-01;NCGC00255030-01;AJ-27547;AN-22572;BT000102;CAS-109-73-9;KB-48519;LP113871;OR034464;TR-002082;B0707;FT-0623326;n-Butylamine [UN1125] [Flammable liquid];n-Butylamine [UN1125] [Flammable liquid];4454-EP2281563A1;4454-EP2287141A1;4454-EP2289510A1;4454-EP2289887A2;4454-EP2289888A2;4454-EP2289894A2;4454-EP2298746A1;4454-EP2305629A1;4454-EP2308838A1;4454-EP2308867A2;4454-EP2308870A2;4454-EP2311804A2;12339-EP2270010A1;12339-EP2272517A1;12339-EP2289509A2;12339-EP2292619A1;12339-EP2295418A1;12339-EP2298742A1;12339-EP2298761A1;12339-EP2305250A1;12339-EP2305642A2;12339-EP2308812A2;12339-EP2314298A1;12339-EP2314593A1;12339-EP2316974A1;12339-EP2377849A2;56744-EP2298305A1;56744-EP2298769A1;56744-EP2308878A2;I05-0345;J-002322;InChI=1/C4H11N/c1-2-3-4-5/h2-5H2,1H;F2190-0358;42939-72-0;50929-03-8;85404-21-3;N-BUTYLAMINE (SEE ALSO: SEC-BUTYLAMINE (CAS 13952-84-6) &TERT-BUTYLAMINE (CAS 75-64-9));n-butylamine [Wiki];109-73-9 [RN];1-Amino-butaan [Dutch];1-Aminobutan [German];1-aminobutane;1-AMINO-BUTANE;1-Butanamin [German] [ACD/IUPAC Name];1-Butanamine [ACD/Index Name] [ACD/IUPAC Name];1-Butanamine [French] [ACD/Index Name] [ACD/IUPAC Name];1-butylamine;Butan-1-amin [German];butan-1-amine;butyl amine;Butylamine [ISO] [Wiki];n-Butilamina [Italian];n-Butylamin [German];1-Amino-butaan;1-Amino-butaan [Dutch];1-Aminobutan;1-Aminobutan [German];1-aminobutane; 1-butanamine; n-butylamine;1-Butanamine, 9CI;203-699-2 [EINECS];3858-78-4 [RN;42939-72-0 [RN];50929-03-8 [RN];605269 [Beilstein];776285-22-4 [RN];85404-21-3 [RN];aminobutane;butanamine;butilamina [Portuguese];butyl-amine;BUTYLAMINE, N;butylammoniu;EINECS 203-699-2;FEMA 3130;InChI=1/C4H11N/c1-2-3-4-5/h2-5H2,1H;LYT;Monobutilamina [Romanian];monobutylamine;N2QV60B4WR;n-Butilamina [Italian];n-Butyl amine;n-Butylamin [German];n-Butyl-d9-amine;n-C4H9NH2;Norralamine;Norvalamine;UN 1125;UNII:N2QV60B4WR;UNII-N2QV60B4WR;WLN: Z4;BA;MNBA;AMINE C4;n-C4H9NH2;Butylamin;FEMA 3130;BUTYLAMINE;Butanamine;Norvalamine;Norralamine;Butylamine;1-AMINOBUTANE;1-BUTANAMINE;BUTYLAMINE;1-BUTYLAMINE;
MONO-N-BUTYLAMINE;MONOBUTYLAMINE;N-BUTYLAMINE;NORRALAMINE;NORVALAMINE;TUTANE;N-Nitrosomethyl-n-butylamine;1-Butanamine; 1-Butanamine; n-Butylamine; 1-Butylamine; Butanamine; Mono-n-butylamine; Monobutylamine; Norvalamine; 1-Aminobutane; n-C4H9NH2; N-Butylamin; 1-Amino-butaan; 1-Aminobutan; n-Butilamina; Monobutilamina; UN 1125; Norralamine; NSC 8029; NMBA; MBNA; butylamine, N-Methyl-N-nitroso-; butanamine, N-Methyl-N-nitroso-; Methylbutylnitrosamine; Methyl-n-butylnitrosamine; N-Methyl-N-nitrosobutylamine; N-Nitroso-n-butylmethylamine; Nitrosomethyl-n-butylamine;Butylamine;Tri-n-butylamine;1- aminobutane;butan-1-amine;butanamine;1-butanamine;mono-butyl amine;N-butyl amine;butyl-amine;butylamine;1-butylamine;norvalamine;1-Butanamine, N-butyl-N-nitroso-; Dibutylamine, N-nitroso-; Dibutylnitrosoamine; N-Nitrosodi-N-butylamine; N-Nitrosodibutylamine; Nitrosodibutylamine; N-Nitrosobutylamine; N-di-n-Butylnitrosoamine; Butylamine, N-nitrosodi-; Di-N-butylnitrosamin; Di-N-butylnitrosoamine; DBN; DBNA; N-Butyl-N-nitroso-1-butamine; N-Butyl-N-nitroso-1-butaneamine; N,N-Di-n-butylnitrosamine; N,N-Dibutylnitrosoamine; Nitrosodi-N-butylamine; NDBA; Dibutylnitrosamine; Di-n-butylnitrosamine; Rcra waste number U172; N-Butyl-N-nitroso-1-butanamine; 1,1-Dibutyl-2-oxohydrazine; N-butyl-N-nitrosobutanamine;1-Amino-butaan;1-Aminobutan;1-Aminobutane;1 Butylamine;Butanamine;Butylamine;Mono-n-butylamine;Monobutilamina;Monobutylamine;N-Butylamin;NSC8029;Norralamine;Norvalamine;UN 1125;n-Butilamina;n-Butylamine;n-C4H9NH2;1R)-1-[4-(3-METHOXYPHENYL)PHENYL]BUTYLAMINE 2-AMINO-3,3-DIMETHYLBUTANE (1R)-1-[4,5-DIFLUORO-2-(TRIFLUOROMETHYL)PHENYL]BUTYLAMINE 1-(3,4-DIMETHYLPHENOXY)-2-BUTANAMINE 1-(2-ETHYLBUTOXY)-2-BUTANAMINE Salbutamol Loperamide AMIKACIN Butylamine Isobutyl chloride 2-Bromo-2-methylpropane Albuterol sulfate ISOBUTANE Tributylamine N-BUTANE sec-Butylamine DOBUTAMINE HYDROCHLORIDE Loperamide hydrochloride;Butylamine;n-Butylamine;Mono-n-butylamine;Monobutylamine;Norvalamine;1-Aminobutane;1-Butylamine;n-C4H9NH2;Butylamine, n;N-Butylamin;1-Amino-butaan;1-Aminobutan;1-Butanaminen-butilamina;n-Butilamina;Monobutilamina;UN 1125;Aminobutane;Norralamine;Tutane;Butanamine;1-Butanamine; n-Butylamine; 1-Butylamine; Butanamine; Mono-n-butylamine; Monobutylamine; Norvalamine; 1-Aminobutane; n-C4H9NH2; N-Butylamin; 1-Amino-butaan; 1-Aminobutan; n-Butilamina; Monobutilamina; UN 1125; Norralamine; NSC 8029;1-Aminobutane, Butylamine;TERMIUM Plus;n-Butylamine;1-Aminobutane;Butylamine;N-butylamine;1-aminobutane;1-butylamine;1-Butanamine;N-BÜTL AMN; N-BUTIL AMINE; N-BÜTIL AMINE;N-BÜTIL AMINE;
N-BUTIL AMIN; N-BÜTL AMN; N-BUTL AMIN; N- BÜTIL AMN; NBUTILAMINE;NBÜTLAMNE;NBÜTLAMN;NBUTILAMIN;N-BÜTL AMN FYATLARI;N-BÜTL AMN TEDARKÇLER; N-BÜTL AMN KULLANIMI; N-BÜTL AMN ÜRETM;n-butylamine prices;n-butylamine suppliers;n-nutylamine manufacture;n-butylamine uses; -butly amin;n-butyl amin; n-butyl amine; n-nutyl amin.

N-BUTYLAMINE

N-Butylamine (n-Butylamine, BuA) is a primary aliphatic amine. Its pyrolysis mechanism has been investigated.[1] BuA can be synthesized from butyronitrile via Co/SiO2 (silicon dioxide) assisted hydrogenation.[2][3] A decrease in fluorescence intensity was observed on adding BuA to a solution of colloidal CdSe nanoparticles (NPs).[4]A clear colorless liquid with an ammonia-like odor. Flash point 10°F. Less dense (6.2 lb / gal) than water. Vapors heavier than air. Produces toxic oxides of nitrogen during combustion.

N-Butylamine belongs to the class of monoalkylamines. Butylamine is produced from Butanol. N-Butylamine is a versatile intermediate with a variety of applications. Butylamine is used to produce agricultural chemicals (e.g. benomyl), rubber chemicals (e.g. di-n-butylthiourea), nylon plasticers (e.g. n-butylbenzenesulphonamide), alkyl alkanol amines (Butyldiethanolamine) as well as fuel and oil additives.

Butylamine (CAS 109-73-9) has many isomerides. To make its name clear and unique, we use n-Butylamine as recommend by Wikipedia. n-Butylamine is an organic amine compound with the formula CH3CH2CH2CH2NH2(C4H11N). This colorless liquid is one of the four isomeric amines of butane, the others being sec-butylamine(CAS 33966-50-6) , tert-butylamine(CAS 75-64-9) and isobutylamine(CAS 78-81-9 ). At standard temperature and pressure, n-butylamine is a liquid having the fishy, ammonia-like odor common to amines. The liquid acquires a yellow color upon storage in air. It is soluble in all organic solvents. Like other simple aliphatic amines, n-butylamine is a weak base with a pKa of 10.59 in its protonated form.
1-Aminobutane is the intermediate for the herbicide butralin. It is mainly used to synthesize medicine, dyestuff, and pesticide.

PROPERTIES OF N-BUTYLAMINE

Molecular Weight: 73.14 g/mole

Form Liquid
Color Clear
Odor: Amine like.
Taste: Not available.
Melting point:-49 °C(lit.)
Boiling point:78 °C(lit.)
Density 0.74 g/mL at 25 °C(lit.)
vapor density 2.5 (vs air)
vapor pressure 68 mm Hg ( 20 °C)
refractive index n20/D 1.401(lit.)
Flash point:30 °F
storage temp. 2-8°C
solubility water: miscible
Stability:Stable. Incompatible with oxidizing agents, aluminium, copper, copper alloys, acids. Highly flammable.

APPLICATION/USES OF N-BUTYLAMINE

Butylamine (n-Butylamine) may be used as a template to generate hierarchical monolithic zeolites. N-Butylamine may also be used as a dispersion medium for fluorinated graphene sheets (F-GSs) to generate butylamine modified F-GSs.
1-Butanamine is used in the preparation of 5-HT6 receptor antagonists affecting the concentrations of dopamine and norephinephrine. May be used in the treatment of the neurological degenerative disease, Alzheimer’s.

n-Butylamine is an important intermediate in the manufacture of pesticides (such as thiocarbazides), pharmaceuticals, and emulsifiers. It is also a precursor for the manufacture of N,N’-dibutylthiourea, a rubber vulcanization accelerator, and n-butylbenzenesulfonamide, a plasticizer of nylon.
N-Butylamine was used in the synthesis of Fengabine.

Catalysts
Chemicals and Pharmaceuticals
Electronics industry
Paints, coatings & resins
PU catalysts

N-BÜTLAMN

N-Butilamin (n-Butilamin, BuA), primer bir alifatik amindir. Piroliz mekanizmas aratrlmtr. [1] BuA, Co / Si02 (silikon dioksit) destekli hidrojenasyon yoluyla butirnitrilden sentezlenebilir. [2] [3] BuA kolloidal CdSe nanopartiküllerinin (NP) bir solüsyonuna eklenmesiyle flüoresan younluunda bir azalma gözlenmitir [4] Amonyak benzeri bir kokuya sahip berrakta renksiz bir sv. Parlama noktas 10 ° F. Suya göre daha az youn (6.2 lb / gal). Buhar havadan daha ar. Yanma esnasnda zehirli oksit azotu üretir.

N-Butilamin, monoalkilamin snfna aittir. Butilamin, Butanol’dan üretilir. N-Butylamine, çeitli uygulamalara sahip çok yönlü bir ara maddedir. Bütilamin, tarm kimyasallar (örnein benomil), kauçuk kimyasallar (örnein di-n-bütiltioüre), naylon plastikletiriciler (örnein n-bütilbenzensülfonamid), alkil alkanol aminler (Butildiyetanolamin) ve ayrca yakt ve ya ilave maddeleri üretmek için kullanlr.

Butilamin (CAS 109-73-9) birçok izomeridi vardr. Adn açk ve benzersiz klmak için, Wikipedia tarafndan tavsiye edilen ekilde n-Butilamin kullanyoruz. n-Butilamin CH3CH2CH2CH2NH2 (C4H11N) formülüne sahip organik bir amin bileiidir. Bu renksiz sv bütann dört izomerik aminlerinden biridir, dierleri sec-bütilamin (CAS 33966-50-6), tert-bütilamin (CAS 75-64-9) ve izobutilamin (CAS 78-81-9) ‘dur. Standart scaklk ve basnçta, n-bütilamin, aminlere benzer, amonyak benzeri bir kokuya sahip olan bir svdr. Sv, havada saklandktan sonra sar bir renk alr. Tüm organik çözücüler içinde çözünür. Dier basit alifatik aminler gibi, n-bütilamin, protonlanm formda 10.59 pKa olan zayf bir bazdr.
1-Aminobutan, herbisit butralin’in ara maddesidir. Temel olarak ilaç, boya maddeleri ve böcek ilac sentezlemek için kullanlr.

N-BÜTLAMN ÖZELLKLER

Moleküler Arlk: 73.14 g / mole

Sv Formu
Renksiz
Koku: Aminler gibi.
Tat: Mevcut deil.
Erime noktas: -49 ° C (aydnlk)
Kaynama noktas: 78 ° C (aydnlk)
Younluk 0.74 g / mL, 25 ° C’de (aydnlk)
buhar younluu 2,5 (vs hava)
buhar basnc 68 mm Hg (20 ° C)
krlma indisi n20 / D 1.401 (lit.)
Parlama noktas: 30 ° F
saklama scakl. 2-8 ° C
çözünürlük su: karabilir
Kararllk: Kararl. Oksitleyici maddeler, alüminyum, bakr, bakr alamlar, asitlerle uyumaz. Son derece yanc.

N-BÜTLAMN UYGULAMA / KULLANIMI

Butilamin (n-Butilamin) hiyerarik monolitik zeolitler oluturmak için bir kalp olarak kullanlabilir. N-Butilamin ayrca, butilamin deitirilmi F-GS’ler üretmek üzere florlanm grafen tabakalar (F-GS’ler) için bir dalm arac olarak da kullanlabilir.
1-Butanamin, dopamin ve norefinefrin konsantrasyonlarn etkileyen 5-HT6 reseptör antagonistlerinin hazrlanmasnda kullanlr. Alzheimer nörolojik dejeneratif hastaln tedavisinde kullanlabilir.

n-Bütilamin pestisitlerin (tiyokarbazidler gibi), farmasötik maddeler ve emülsiyon yapclarn üretiminde önemli bir aracdr. Ayn zamanda, bir kauçuk vulkanizasyon hzlandrcs olan N, N’-dibutiltioüre ve naylonun bir plastikletiricisi olan n-butilbenzensülfonamid üretiminin öncüsüdür.
Fengabin sentezinde N-Butilamin kullanld.

Katalizörler
Kimyasallar ve laçlar
Elektronik endüstrisi
Boyalar, kaplamalar ve reçineler
PU katalizörleri