N-CYCLOHEXYL-2-BENZOTHIAZOLESULFENAMIDE
N-Cyclohexyl-2-benzothiazolesulfenamide, often referred to as CBS or CBS accelerator, is an organic compound widely used in the rubber industry as a vulcanization accelerator.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the cross-linking of rubber molecules, thereby improving elasticity and durability.
The use of N-Cyclohexyl-2-benzothiazolesulfenamide in rubber formulations helps in reducing curing times during manufacturing.
CAS Number: 95-33-0
EC Number: 202-411-2
Molecular Formula: C13H16N2S2
Molecular Weight: 264.4 g/mol
Synonyms: N-cyclohexyl-2-benzothiazolesulfenamide, N-cyclohexyl-2-benzothiazyl sulfenamide,N-cyclohexyl-2-benzothiazylsulfenamide,thiohexam,95-33-0,N-Cyclohexyl-2-benzothiazolesulfenamide,Thiohexam,Sulfenax,N-Cyclohexyl-2-benzothiazolylsulfenamide,Accelerator CZ,Vulkacit CZ,Santocure,Curax,Durax,Sulfenamide Ts,Santocure Powder,Sulfenax TsB,Vulkacite CZ,Sulfenax CB,Santocure Pellets,Vulcafor CBS,Conac A,Conac S,Delac S,Ekagom CBS,Royal CBTS,Rhodifax 16,Sulfenax CB 30,Vulcafor hbs,Soxinol cz,Vulkacit c,Sulfenax cb/k,Vulkacit cz/c,Vulkacit cz/k,Nocceler CZ,Accicure HBS,N-Cyclohexyl-2-benzothiazylsulfenamide,Pennac CBS,Sanceler CM-PO,2-(Cyclohexylaminothio)benzothiazole,2,Benzothiazolesulfenamide, N-cyclohexyl-,Benzothiazyl-2-cyclohexylsulfenamide,N-Cyclohexylbenzothiazole-2-sulfenamide,N-Cyclohexyl-2-benzothiazosulfenamide,N-Cyclohexyl-2-benzothiazole sulfenamide,Cyclohexyl benzothiazolesulfenamide,N-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine,Santocure vulcanization accelerator,CBTS,N-Cyclohexylbenzothiazole-2-sulphenamide,2-Benzenethiazolesulfenamide, N-cyclohexyl-,UCA53G94EV,DTXSID5020360,NSC-4809,S-(Benzo[d]thiazol-2-yl)-N-cyclohexylthiohydroxylamine,NCGC00159502-02,N-(1,3-benzothiazol-2-ylthio)cyclohexanamine,Conac H,DTXCID50360,NSC 4809; Nocceler CZ; Accelerator CZ; Accicure HBS,Sufenax cb,CAS-95-33-0,SMR001798878,CCRIS 4910,HSDB 2868,NSC 4809,EINECS 202-411-2,UNII-UCA53G94EV,BRN 0192376,AI3-16782,Vulkacit cz/eg,Perkacit CBS,Akrochem CBTS,Ekaland CBS,Sanceler CM-G,Banac CBS,Vulkacit CZ/EG-C,CBS, N-Cyclohexyl-2-benzothiazolesulfenamide,EC 202-411-2,SCHEMBL80270,4-27-00-01867 (Beilstein Handbook Reference),MLS004773968,MLS006010082,CHEMBL1591074,DEQZTKGFXNUBJL-UHFFFAOYSA-,NSC4809,Cyclohexylbenzothiazyl sulphenamide,Cyclohexylbenzothiazolylsulphenamide,Cyclohexyl benzothiazole sulfenamide,N-Cyclohexylbenzothiazoylsulfenamide,N-Cyclohexylbenzothiazyl sulphenamide,Tox21_111721,Tox21_202436,Tox21_302924,MFCD00022872,AKOS003658709,N-Cyclohexyl-2-benzthiazyl sulfenamide,N-Cyclohexyl-2-benzthiazyl sulfonamide,DB14200,HY-W020755,WLN: T56 BN DSJ CSM- AL6TJ,N-Cyclohexyl-2-benzothiazolylsulfonamide,N-Cyclohexyl-2-benzothiazyl sulphenamide,NCGC00159502-03,NCGC00159502-04,NCGC00256366-01,NCGC00259985-01,AS-15575,N-CYCLOHEXYLBENZOTHIAZYL-SULPHENAMIDE,CS-0040170,FT-0631486,E80913,EN300-7402242,2-(CYCLOHEXYLAMINOTHIO)BENZOTHIAZOLE [HSDB],Q4445828,W-100165,BRD-K64191834-001-03-1,S-(1,3-Benzothiazol-2-yl)-N-cyclohexylthiohydroxylamine,S-(1,3-Benzothiazol-2-yl)-N-cyclohexylthiohydroxylamine #,[(3aS,4R,9S,10aS)-2-amino-5,10,10-trihydroxy-6-imino-9-sulfooxy-3a,4,8,9-tetrahydro-1H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid,InChI=1/C13H16N2S2/c1-2-6-10(7-3-1)15-17-13-14-11-8-4-5-9-12(11)16-13/h4-5,8-10,15H,1-3,6-7H2, N,N’-bis-(1,4-dimethyl-pentyl)-p-phenylenediamine; N-Cyclohexylbenzothiazyl sulfenamide; CBTS, CBS; Cyclohexylbenzothiazyl sulfenamide; N-Cyclohexyl-2-benzothiazyl sulfenamide; Santocure; N,N’-bis(1,4-dimethylpentyl) 1,4-benzenediamine; N,N-di(1,4-dimethylpentyl)-p-phenylenediamine; eastozone 33; eastozone; tenamene; santoflex 77; Vulkanox 4030, 2-(Cyclohexylaminothio)benzothiazole;Accelerator CZ;AccicureHBS;Banac CBS;Benzothiazyl-2-cyclohexylsulfenamide;CBS;CBS (accelerator);CBTS;Conac A;Conac S;Delac S;Ekagom CBS;N-Cyclohexyl-2-benzothiazolesulfenamide;N-Cyclohexyl-2-benzothiazolylsulphenamide;N-Cyclohexyl-2-benzothiazylsulfenamide;N-Cyclohexylbenzothiazole-2-sulphenamide;NSC 4809;Nocceler CZ-G;Nocceler CZ-P;Pennac CBS;Rhodifax 16;Accel CZ;2-Benzothiazolesulfenic acid N-cyclohexylamide;Sanceler CM;Royal CBTS;Sanceler CM-G;Santocure;Santocure CBS;Sulfenamide Ts;Sulfenax;SulfenaxCB;Sulfenax CB 30;Vulkacit C;Vulkacit CZ/C;Vulkacit CZ/EG;Vulkacit CZ/EG-C;
N-Cyclohexyl-2-benzothiazolesulfenamide is a crystalline compound with a pale yellow to light brown color.
N-Cyclohexyl-2-benzothiazolesulfenamide is widely recognized as a key accelerator in the vulcanization process of rubber.
N-Cyclohexyl-2-benzothiazolesulfenamide plays a pivotal role in enhancing the mechanical properties of rubber products.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the cross-linking of rubber molecules, thereby improving elasticity and durability.
N-Cyclohexyl-2-benzothiazolesulfenamide is sparingly soluble in water but dissolves readily in organic solvents like acetone and benzene.
N-Cyclohexyl-2-benzothiazolesulfenamide has a distinct chemical structure characterized by a benzothiazole ring with a cyclohexylamine group.
The use of N-Cyclohexyl-2-benzothiazolesulfenamide in rubber formulations helps in reducing curing times during manufacturing.
N-Cyclohexyl-2-benzothiazolesulfenamide facilitates the formation of sulfur cross-links within rubber, crucial for its strength and resilience.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed across various industries, including automotive, aerospace, and consumer goods.
Rubber compounds containing N-Cyclohexyl-2-benzothiazolesulfenamide exhibit excellent heat aging properties.
N-Cyclohexyl-2-benzothiazolesulfenamide is known for its compatibility with both natural and synthetic rubbers.
N-Cyclohexyl-2-benzothiazolesulfenamide enhances the tensile strength and tear resistance of vulcanized rubber products.
The chemical stability of N-Cyclohexyl-2-benzothiazolesulfenamide ensures consistent performance under diverse environmental conditions.
Manufacturers rely on N-Cyclohexyl-2-benzothiazolesulfenamide to achieve uniform quality and reliability in rubber manufacturing.
N-Cyclohexyl-2-benzothiazolesulfenamide, often referred to as CBS or CBS accelerator, is an organic compound widely used in the rubber industry as a vulcanization accelerator
N-Cyclohexyl-2-benzothiazolesulfenamide is a rubber cure accelerator.
N-Cyclohexyl-2-benzothiazolesulfenamide is also a known allergen and dermatological sensitizer.
Sensitivity to N-Cyclohexyl-2-benzothiazolesulfenamide may be identified with a clinical patch test.
N-Cyclohexyl-2-benzothiazolesulfenamide is a Standardized Chemical Allergen.
The physiologic effect of N-Cyclohexyl-2-benzothiazolesulfenamide is by means of Increased Histamine Release, and Cell-mediated Immunity.
This is a chemical used as a rubber accelerator and can be found in rubber products.
Further research may identify additional product or industrial usages of N-Cyclohexyl-2-benzothiazolesulfenamide.
N-Cyclohexyl-2-benzothiazolesulfenamide holds a prominent position in the realm of organic compounds, finding extensive utilization in rubber vulcanization and as an accelerator in the rubber industry.
Derived from benzothiazole, a heterocyclic aromatic compound, N-Cyclohexyl-2-benzothiazolesulfenamide manifests as a white, odorless crystalline powder.
The function of N-Cyclohexyl-2-benzothiazolesulfenamide lies in its ability to expedite the vulcanization process of rubber compounds.
Acting as an activator, N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the cross-linking of rubber molecules, leading to the production of a robust and enduring rubber product.
Moreover, N-Cyclohexyl-2-benzothiazolesulfenamide heightens the reactivity between rubber molecules and sulfur, facilitating a more uniform and comprehensive vulcanization process.
Applications of N-Cyclohexyl-2-benzothiazolesulfenamide:
N-Cyclohexyl-2-benzothiazolesulfenamide is extensively used as an accelerator in the production of rubber goods.
N-Cyclohexyl-2-benzothiazolesulfenamide is a key component in the manufacturing of automotive tires to improve their performance and durability.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the vulcanization process of rubber, enhancing its elasticity and strength.
N-Cyclohexyl-2-benzothiazolesulfenamide is crucial in the production of conveyor belts for industrial applications, ensuring robustness and wear resistance.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the formulation of seals and gaskets to maintain tight seals in various mechanical systems.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of rubber hoses for automotive and industrial applications, ensuring flexibility and durability.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in footwear, including shoes and boots, to improve their resilience.
N-Cyclohexyl-2-benzothiazolesulfenamide is utilized in the production of rubber components for machinery and equipment, enhancing their mechanical properties.
N-Cyclohexyl-2-benzothiazolesulfenamide plays a role in the manufacturing of rubberized fabrics used in rainwear and protective clothing.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber compounds used in the construction of sporting goods such as balls and mats for their durability.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the production of rubber coatings and linings for tanks and containers to prevent corrosion.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of industrial rubber rollers for their resistance to wear and tear.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the vulcanization of rubber used in marine applications, including boat fenders and dock bumpers.
N-Cyclohexyl-2-benzothiazolesulfenamide is crucial in the production of agricultural rubber products such as hoses and belts for their resilience.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the manufacturing of rubber components for electrical insulation due to its dielectric properties.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber compounds used in medical devices and equipment for its biocompatibility.
N-Cyclohexyl-2-benzothiazolesulfenamide enhances the performance of rubber seals and gaskets used in food processing equipment.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in aerospace applications for its reliability under extreme conditions.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of rubber vibration isolators and dampeners for machinery and equipment.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the formulation of rubber components used in building construction for its durability.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber compounds used in mining applications, including conveyor belts and hoses.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of rubber components for automotive suspension systems to improve performance.
N-Cyclohexyl-2-benzothiazolesulfenamide is utilized in the manufacturing of rubber seals and O-rings for automotive and mechanical systems.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in household appliances such as washing machine seals.
N-Cyclohexyl-2-benzothiazolesulfenamide is essential across various industries where rubber products require enhanced mechanical properties and performance.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of rubber flooring and mats for gyms and playgrounds due to its impact resistance.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber components in the automotive industry, such as engine mounts and suspension bushings, for vibration damping.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the vulcanization process of rubber used in the production of railway track pads and ties for durability.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the manufacturing of inflatable products like air mattresses and balloons for their strength and elasticity.
N-Cyclohexyl-2-benzothiazolesulfenamide is utilized in the formulation of rubber diaphragms and membranes used in pumps and valves for chemical resistance.
N-Cyclohexyl-2-benzothiazolesulfenamide plays a role in the production of rubber components for industrial machinery, ensuring reliability and longevity.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the production of rubber sheets and liners for agricultural applications, including irrigation systems and silage pits.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in the production of insulation materials for electrical cables and wiring harnesses.
N-Cyclohexyl-2-benzothiazolesulfenamide enhances the performance of rubber seals and gaskets used in HVAC systems for their sealing effectiveness.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber compounds used in the construction of bridges and infrastructure for weather resistance and durability.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the vulcanization of rubber used in the production of footwear components such as soles and heels.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the formulation of rubber parts for bicycles and motorcycles, including tires and inner tubes.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the production of rubber gloves and protective clothing for its barrier properties against chemicals and contaminants.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber compounds used in the production of marine equipment such as seals and gaskets for saltwater resistance.
N-Cyclohexyl-2-benzothiazolesulfenamide is crucial in the formulation of rubber components used in the aerospace industry, including seals and insulation.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in the production of seals and gaskets for automotive engines and transmissions.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the manufacturing of rubber pads and buffers for construction equipment to absorb shock and vibration.
N-Cyclohexyl-2-benzothiazolesulfenamide is employed in the production of rubber components for consumer electronics, including keypads and seals for water resistance.
N-Cyclohexyl-2-benzothiazolesulfenamide is added to rubber formulations for medical devices such as surgical gloves and tubing for biocompatibility.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in the production of industrial belts and hoses for conveying fluids and materials.
N-Cyclohexyl-2-benzothiazolesulfenamide is used in the formulation of rubber components for recreational vehicles and trailers, including tires and suspension parts.
N-Cyclohexyl-2-benzothiazolesulfenamide plays a role in the production of rubber seals and gaskets used in oil and gas exploration and drilling equipment.
N-Cyclohexyl-2-benzothiazolesulfenamide enhances the performance of rubber components used in the manufacture of household appliances such as washing machines and dishwashers.
N-Cyclohexyl-2-benzothiazolesulfenamide accelerates the curing of rubber used in the production of protective gear and apparel for sports and outdoor activities.
N-Cyclohexyl-2-benzothiazolesulfenamide is indispensable in a wide range of industries where rubber products are essential for performance, safety, and reliability.
N-Cyclohexyl-2-benzothiazolesulfenamide formulations are carefully optimized to meet specific requirements for different rubber applications.
N-Cyclohexyl-2-benzothiazolesulfenamide acts as a sulfur donor during vulcanization, contributing to enhanced heat resistance of rubber.
N-Cyclohexyl-2-benzothiazolesulfenamide is integral in the production of tires, seals, gaskets, and industrial rubber components.
The chemical properties of N-Cyclohexyl-2-benzothiazolesulfenamide make it suitable for high-performance rubber products.
N-Cyclohexyl-2-benzothiazolesulfenamide undergoes controlled chemical reactions during vulcanization, leading to robust rubber networks.
N-Cyclohexyl-2-benzothiazolesulfenamide formulations are tailored to improve the processing and performance of rubber goods.
The use of N-Cyclohexyl-2-benzothiazolesulfenamide in rubber compounding ensures superior mechanical properties and longevity.
N-Cyclohexyl-2-benzothiazolesulfenamide is essential in achieving consistent curing characteristics in rubber manufacturing processes.
N-Cyclohexyl-2-benzothiazolesulfenamide is handled and stored with care due to its reactivity and potential health hazards.
The versatile applications of N-Cyclohexyl-2-benzothiazolesulfenamide extend to various sectors requiring durable rubber materials.
N-Cyclohexyl-2-benzothiazolesulfenamide is indispensable in modern rubber technology for its role in enhancing product performance and longevity.
Uses of N-Cyclohexyl-2-benzothiazolesulfenamide:
N-Cyclohexyl-2-benzothiazolesulfenamide is used as Intermediate in organic synthesis.
N-Cyclohexyl-2-benzothiazolesulfenamide is used as Accelerator in natural and styrene-butadienethiazyl sulfenamide rubber.
N-Cyclohexyl-2-benzothiazolesulfenamide is useful for the production of sulfur-modified chloroprene rubber.
N-Cyclohexyl-2-benzothiazolesulfenamide is a sulfenamide accelerator for use in the production of vulcanized rubbers, sealants and a wide range of other applications.
N-Cyclohexyl-2-benzothiazolesulfenamide is provided as a grey-white powder or granule and has a high curing rate with excellent scorching properties.
Vulcanization Accelerator:
N-Cyclohexyl-2-benzothiazolesulfenamide is primarily used as an accelerator in the vulcanization process of rubber, which improves the speed and efficiency of the cross-linking reaction between sulfur and rubber.
This process enhances the elasticity, strength, and durability of rubber products.
Rubber Industry:
N-Cyclohexyl-2-benzothiazolesulfenamideis extensively used in the manufacture of tires, belts, hoses, and other rubber goods due to its ability to provide a delayed action in vulcanization, which allows for better processing safety and improved product properties.
Benefits of N-Cyclohexyl-2-benzothiazolesulfenamide:
Benefits in Rubber Manufacturing:
Improved Processing Safety:
N-Cyclohexyl-2-benzothiazolesulfenamide provides a delayed action in vulcanization, allowing for safer handling and processing of rubber compounds.
Enhanced Product Properties:
The use of N-Cyclohexyl-2-benzothiazolesulfenamide results in rubber products with superior mechanical properties, including better resistance to wear and tear, which is critical for high-performance applications.
Manufacturing Methods
N-Cyclohexyl-2-benzothiazolesulfenamide is derived from the reaction of accelerator M (2-thiol benzothiazole) with cyclohexylamin added dropwise under stirring to obtain a crude product.
The solid material is separated, washed with water to neutrality, and dried below 75°C to obtain a finished product.
Raw material consumption (kg/t) accelerator M (95%) 745 cyclohexylamine (95%) 500
Handling and Storage of N-Cyclohexyl-2-benzothiazolesulfenamide:
Precautions for safe handling:
Avoid inhalation of vapour or mist.
Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510):
8A: Combustible, corrosive hazardous materials
Stability and Reactivity of N-Cyclohexyl-2-benzothiazolesulfenamide:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.
Disposal considerations:
Waste treatment methods:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of N-Cyclohexyl-2-benzothiazolesulfenamide.
Contaminated packaging:
Dispose of as unused product
First Aid Measures of N-Cyclohexyl-2-benzothiazolesulfenamide:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:
If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.
In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.
If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.
Firefighting Measures of N-Cyclohexyl-2-benzothiazolesulfenamide:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas
Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental Release Measures of N-Cyclohexyl-2-benzothiazolesulfenamide:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.
Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.
Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.
Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.
Exposure Controls/Personal Protection of N-Cyclohexyl-2-benzothiazolesulfenamide:
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove removal technique (without touching glove’s outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
N-Cyclohexyl-2-benzothiazolesulfenamide should not be construed as offering an approval for any specific use scenario.
Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.
If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.
Identifiers of Cyclohexyl benzothiazole sulfenamide:
Chemical Formula: C13H16N2S2
CAS Number: 95-33-0
Molecular Weight: 264.41 g/mol
EC Number: 202-411-2
SMILES Notation: C1CCC(CC1)NC2=NC3=CC=CC=C3S2
InChI: InChI=1S/C13H16N2S2/c16-15(11-6-2-1-3-7-11)13-14-12-9-5-4-8-10(12)17-13/h4-5,8-9,11H,1-3,6-7H2
InChI Key: KTCGVRHCKWSZIQ-UHFFFAOYSA-N
Properties of N-Cyclohexyl-2-benzothiazolesulfenamide:
Molecular Weight: 264.4 g/mol
XLogP3-AA: 4.4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 3
Exact Mass: 264.07549087 g/mol
Monoisotopic Mass: 264.07549087 g/mol
Topological Polar Surface Area: 78.5Ų
Heavy Atom Count: 17
Complexity: 244
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Molecular Formula: C13H16N2S2
Average mass: 264.409 Da
Monoisotopic mass: 264.075500 Da
ChemSpider ID: 6962
Melting point: 93-100°C
Boiling point: 410.4±28.0 °C(Predicted)
Density: 1.31~1.34g/cm3
vapor pressure: 0Pa at 25℃
refractive index: 1.5700 (estimate)
storage temp.: Keep in dark place,Sealed in dry,Room Temperature
solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetatae (Slightly)
form: Solid
pka: 0.59±0.10(Predicted)
color: Pale Yellow to Light Beige
Water Solubility: Insoluble
InChIKey: DEQZTKGFXNUBJL-UHFFFAOYSA-N
LogP: 5 at 25℃
Name, Cyclohexyl benzothiazole sulfenamide
EINECS, 202-411-2
CAS No., 95-33-0, Density, 1.26 g/cm3
PSA, 78.46000, LogP, 4.61660
Solubility, Insoluble in water, Melting Point, 93-100 °C
Formula, C13H16N2S2, Boiling Point, 410.4 °C at 760 mmHg
Molecular Weight, 264.415, Flash Point, 202 °C
PSA: 78.5
XLogP3: 5.32
Appearance: DryPowder; OtherSolid; PelletsLargeCrystals
Density: 1.27 g/cm3
Melting Point: 93-100 °C
Boiling Point: 410.4±28.0 °C at 760 mmHg
Flash Point: 202.0±24.0 °C
Refractive Index: 1.665
Water Solubility: INSOL IN WATER; SOL IN BENZENE