PRODUCTS

N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE

N-Cyclohexyl-2-benzothiazole sulfenamide is suitable for the use of black rubber.
N-Cyclohexyl-2-benzothiazole sulfenamide is mainly used for tires, rubber shoes, rubber hose, tape, cable, general industrial products.
N-Cyclohexyl-2-benzothiazole sulfenamide is an excellent after-effect promoter, suitable for natural rubber and synthetic rubber, and can improve the physical and mechanical properties of rubber products.

CAS Number: 95-33-0
EC Number: 202-411-2
MDL Number: MFCD00022872
Molecular Formula: C13H16N2S2
Molecular Weight: 264.41 g/mol

SYNONYMS:
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, NSC 4809, Nocceler CZ, Accelerator CZ, Accicure HBS, N-Cyclohexyl-2-benzothiazolylsulfenamide, Accelerator CZ, N-cyclohexyl-2-benzothiazole Sulfenamide, CBS, 2-(cyclohexylaminothio)benzothiazole, accicurehbs, benzothiazyl-2-cyclohexylsulfenamide, conaca, conach, conacs, curax, cyclohexyl-2-benzothiazolesulfenamide, delacs, ekagomcbs, n-cyclohexyl-2-benzenethiazolesulfenamid, n-cyclohexyl-2-benzothiazolesulfenamid, n-cyclohexyl-2-benzothiazylsulfenamide, noccelercz, pennaccbs, rhodifax16, royalcbts, sancelercm-po, N-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine, Acelerator CZ, Rubber Accelerator CBS, Rubber Accelerator CZ, ACCELERATOR CBS (CZ), ACCELERATOR CBS, CBS, accelerator cz, n-cyclohexylbenzothiazole-2-sulfenamide, curax, DURAX, conaca, conach, conacs, delacs, sulfenax, N-Cyclohexyl-2-benzothiazole sulfonamide, 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, AKROCHEM CBTS, ACCELERATOR, CBTS, 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, DB-057577, N-CYCLOHEXYLBENZOTHIAZYL-SULPHENAMIDE, CS-0040170, NS00006793, 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, 95-33-0, N-Cyclohexyl-2-benzothiazolesulfenamide, Thiohexam, N-Cyclohexyl-2-benzothiazolylsulfenamide, Sulfenax, 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-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine, N-Cyclohexyl-2-benzothiazosulfenamide, N-Cyclohexyl-2-benzothiazole sulfenamide, Cyclohexyl benzothiazolesulfenamide, 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, N-Cyclohexyl-2-benzothiazolesulfenamide, N-[(1,3-Benzothiazol-2-yl)sulfanyl]cyclohexanamine, 2-Benzothiazolesulfenamide, N-cyclohexyl-, 95-33-0, 2-Benzothiazolesulfenamide, N-cyclohexyl-, 4-27-00-01867, 2-(Cyclohexylaminothio)benzothiazole, 2-Benzothiazolesulfenic acid N-cyclohexylamide, Accel CZ, Accelerator CZ, Accicure HBS, Banac CBS, BENZOTHIAZOLE-2-SULFENAMIDE, N-CYCLOHEXYL, Benzothiazyl-2-cyclohexylsulfenamide, Conac A, Conac S, CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE, Delac S, Ekagom CBS, N-ciclohexilbenzotiazol-2-sulfenamida, N-CYCLOHEXYL-2-BENZOTHIAZOLYL SULFENAMIDE, N-Cyclohexyl-2-benzothiazolylsulfenamide, N-Cyclohexyl-2-benzothiazolylsulphenamide, N-Cyclohexyl-2-benzothiazylsulfenamide, N-Cyclohexylbenzothiazol-2-sulfenamid, N-Cyclohexylbenzothiazole-2-sulfenamide, N-cyclohexylbenzothiazole-2-sulphenamide, N-Cyclohexylbenzothiazolesulfenamide, Nocceler CZ, Nocceler CZ-G, Nocceler CZ-P, NSC 4809, Pennac CBS, Rhenogran CBS, Rhodifax 16, Royal CBTS, Sanceler CM, Sanceler CM-G, Sanceler CM-PO, Sanceler CZ-P, Santocure, Santocure CBS, Soxinol CZ, Sulfenamide Ts, SULFENAMIDE, N-CYCLOHEXYL-2-BENZOTHIAZYL-, Sulfenax, Sulfenax CB, Sulfenax CB 30, Sulfenax CB/K, Thiohexam, Vulcafor CBS, Vulcafor HBS, Vulkacit C, Vulkacit CZ, Vulkacit CZ/C, Vulkacit CZ/CV, Vulkacit CZ/EG, Vulkacit CZ/EG-C, Vulkacit CZ/K, Vulkafil ZN 94TT02, 2-Benzenethiazolesulfenamide, N-cyclohexyl-, BRN 0192376, Conac H, Cyclohexyl benzothiazolesulfenamide, EINECS 202-411-2, Santocure Pellets, Santocure Powder, Santocure vulcanization accelerator, Sulfenax TsB, Vulkacite CZ, UNII-UCA53G94EV, 108251-59-8, 156014-54-9, 51540-81-9, 929698-33-9, Acelerator CZ, CBS, CBTS, Cyclohexylbenzothazyl Sulphenamide, Curax, Durax, N-Cyclohexyl-2-benzothiazyl Sulphenaminde, N-Cycloyhexylbenzothiazyl Sulphenamide, Santocure, Sulfenax CBS, Sulfenamide, N-Cyclohexyl-2-benzothiazolesulphenamide, N-Cyclohexyl-2-benzothiazyl sulfenamide, Thiohexam, N-Cyclohexyl-2-benzothiazylsulfenamide, N-Cyclohexyl-2-benzothiazolesulfenamide, 2-(Cyclohexylaminothio)benzothiazole, Benzothiazyl-2-cyclohexylsulfenamide, N-(1,3-Benzothiazol-2-ylsulfanyl)cyclohexanamine, CBS, accelerator cz, n-cyclohexylbenzothiazole-2-sulfenamide, HIP4, curax, DURAX, conaca, conach, conacs, delacs, Rubber accelerator CBS, N-cyclohexylbenzothiazole-2-sulfenamide, Accelerator CZ, 2-(cyclohexylaminothio)benzothiazole, n-cyclohexyl-2-benzothiazylsulfenamide, n-cyclohexyl-2-benzothiazolesulphenamide, n-cyclohexylbenzothiazyl sulfenamide, N-Cyclohexyl-2-benzothiazolylsulfenamide, Accelerator CZ, N-cyclohexyl-2-benzothiazole Sulfenamide, CBS, 2-(cyclohexylaminothio)benzothiazole, accicurehbs, benzothiazyl-2-cyclohexylsulfenamide, conaca, conach, conacs, curax, cyclohexyl-2-benzothiazolesulfenamide, delacs, ekagomcbs, n-cyclohexyl-2-benzenethiazolesulfenamid, n-cyclohexyl-2-benzothiazolesulfenamid, n-cyclohexyl-2-benzothiazylsulfenamide, noccelercz, pennaccbs, rhodifax16, royalcbts, sancelercm-po, N-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine, Acelerator CZ, Rubber Accelerator CBS, Rubber Accelerator CZ, ACCELERATOR CBS (CZ), ACCELERATOR CBS, CBS, N-Cyclohexyl-2-benzothiazolylsulfenamide, N-cyclohexylbenzothiazole-2-sulfenamide, Accelerator CBS, Accelerator CZ (CBS), Santocure, Curax, Durax, conaca, conach, conacs, delacs

N-Cyclohexyl-2-benzothiazole sulfenamide is soluble in benzene, dichloromethane, carbon tetrachloride, acetic ether, acetone.
N-Cyclohexyl-2-benzothiazole sulfenamide is slightly soluble in gasoline and ethanol.
N-Cyclohexyl-2-benzothiazole sulfenamide is insoluble in water.

The good storage stability period of N-Cyclohexyl-2-benzothiazole sulfenamide is half year.
Easy to cake, but N-Cyclohexyl-2-benzothiazole sulfenamide will not affect the normal use.
At its core, N-Cyclohexyl-2-benzothiazole sulfenamide is a sulfenamide derivative, characterized by its chemical formula C13H16N2S2 and CAS number 95-33-0.

This molecular structure of N-Cyclohexyl-2-benzothiazole sulfenamide is key to its functionality.
N-Cyclohexyl-2-benzothiazole sulfenamide features a benzothiazole ring connected to a cyclohexyl group via a sulfur-nitrogen bond (sulfenamide linkage).

This specific arrangement allows N-Cyclohexyl-2-benzothiazole sulfenamide to act as a source of active sulfur species when subjected to heat during the vulcanization process.
The molecular weight of N-Cyclohexyl-2-benzothiazole sulfenamide is approximately 264.41 g/mol.

N-Cyclohexyl-2-benzothiazole sulfenamide's melting point typically falls in the range of 97-103°C, indicating a stable solid form under ambient conditions.
N-Cyclohexyl-2-benzothiazole sulfenamide is a sulfenamide accelerator for use in the production of vulcanized rubbers, sealants and a wide range of other applications.

N-Cyclohexyl-2-benzothiazole sulfenamide is provided as a grey-white powder or granule and has a high curing rate with excellent scorching properties.
N-Cyclohexyl-2-benzothiazole sulfenamide is a rubber cure accelerator.

N-Cyclohexyl-2-benzothiazole sulfenamide is a rubber accelerator chemical.
N-Cyclohexyl-2-benzothiazole sulfenamide is high-quality industrial-grade granule that offer excellent purity levels ranging from 80-99%.
N-Cyclohexyl-2-benzothiazole sulfenamide is round in shape and have a normal smell.

Sensitivity to N-Cyclohexyl-2-benzothiazole sulfenamide may be identified with a clinical patch test.
Derived from benzothiazole, a heterocyclic aromatic compound, N-Cyclohexyl-2-benzothiazole sulfenamide manifests as a white, odorless crystalline powder.

N-Cyclohexyl-2-benzothiazole sulfenamide is a sulfenamide accelerator for use in the production of vulcanized rubbers, sealants and a wide range of other applications.
N-Cyclohexyl-2-benzothiazole sulfenamide is provided as a gray-white powder or granule and has a high curing rate with excellent scorching properties.

N-Cyclohexyl-2-benzothiazole sulfenamide is an organosulfur compound belonging to the sulfenamide class of chemicals.
N-Cyclohexyl-2-benzothiazole sulfenamide typically appears as an off-white, pale yellow, beige or grey-white solid powder or granules with very slight odor.
N-Cyclohexyl-2-benzothiazole sulfenamide is practically insoluble in water and soluble to only a limited extent in some organic solvents.

USES and APPLICATIONS of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
N-Cyclohexyl-2-benzothiazole sulfenamide is used to promote common aftereffect on sexual one.
Furnace applicable to the use of black plastic material, N-Cyclohexyl-2-benzothiazole sulfenamide, both anti-burning performance and excellent short curing time two major advantages.

N-Cyclohexyl-2-benzothiazole sulfenamide is used enable for natural rubber, recycled rubber, vinyl synthetic rubber, especially for the SBR.
N-Cyclohexyl-2-benzothiazole sulfenamide may be used alone, but also with promoting agent D, DT, TT, TS and others use.
Because of a bitter, N-Cyclohexyl-2-benzothiazole sulfenamide can not be used for food-related products.

Photochromic minor, N-Cyclohexyl-2-benzothiazole sulfenamide does not emit cream vulcanizate excellent anti-aging properties.
N-Cyclohexyl-2-benzothiazole sulfenamide is used tires, shoes, hose and belt, cable, general industrial products.
One of the most significant chemical properties of N-Cyclohexyl-2-benzothiazole sulfenamide is its delayed-action mechanism.

This is a direct result of the sulfenamide bond, which is relatively stable at lower temperatures but readily cleaves at elevated vulcanization temperatures.
This controlled decomposition releases active sulfur donors, which then initiate and accelerate the cross-linking of polymer chains in rubber compounds.

This delayed reaction is crucial for preventing premature vulcanization, often referred to as 'scorching,' during the mixing and processing stages.
This property makes N-Cyclohexyl-2-benzothiazole sulfenamide an excellent choice for complex molding operations where extended flow times are necessary, ensuring the integrity of the rubber material before curing commences.

Furthermore, once activated, N-Cyclohexyl-2-benzothiazole sulfenamide exhibits a fast curing rate.
This attribute is highly valued in the industrial rubber sector, as N-Cyclohexyl-2-benzothiazole sulfenamide allows for reduced curing times, thereby increasing production efficiency and throughput.

The synergy between delayed action and fast cure rate makes N-Cyclohexyl-2-benzothiazole sulfenamide a highly versatile accelerator, suitable for a wide range of elastomers, including natural rubber, styrene-butadiene rubber (SBR), and butadiene rubber (BR).
The benefits derived from these chemical properties are substantial.

In applications like tire manufacturing, the consistent and controlled cross-linking facilitated by N-Cyclohexyl-2-benzothiazole sulfenamide leads to improved tread wear resistance, better overall durability, and enhanced safety.
For rubber hoses and cables, N-Cyclohexyl-2-benzothiazole sulfenamide ensures the development of robust mechanical properties, including tensile strength and flexibility, vital for their demanding applications.

The efficiency gains from faster curing cycles also translate into cost savings for manufacturers.
When considering the purchase of this chemical auxiliary, N-Cyclohexyl-2-benzothiazole sulfenamide's chemical properties dictate its performance, making a deep understanding essential.

The most frequent occupational categories of N-Cyclohexyl-2-benzothiazole sulfenamide are metal industry, homemakers, health services and laboratories, and building industries.
N-Cyclohexyl-2-benzothiazole sulfenamide is useful for the production of sulfur-modified chloroprene rubber.

N-Cyclohexyl-2-benzothiazole sulfenamide is one of the important kinds of sulfenamide vulcanization accelerator, have an anti-incipient scorch and the big advantage of curing process rate fast two concurrently in natural rubber, butadiene-styrene rubber, butadiene rubber, isoprene rubber.

N-Cyclohexyl-2-benzothiazole sulfenamide is particularly suited for the furnace black sizing material that alkalescence is higher, variable colour and pollution are slight, and volume of production and the consumption of the most external CBS account for the 50% of thiazoles sulfuration chemicals total amount.

N-Cyclohexyl-2-benzothiazole sulfenamide is designed to be stored at room temperature and are suitable for a wide range of industrial applications.
N-Cyclohexyl-2-benzothiazole sulfenamide is widely recognized for its superior quality and performance.

N-Cyclohexyl-2-benzothiazole sulfenamide is a highly active aftereffect accelerator with excellent scorch resistance, safe processing and short vulcanization time.
N-Cyclohexyl-2-benzothiazole sulfenamide is often used with TMTD or other alkaline accelerators such as Tyuram and dithiocarbamates to increase its activity.

N-Cyclohexyl-2-benzothiazole sulfenamide is mainly used in the manufacture of tires, hoses, shoes, cables and other industrial rubber products.
N-Cyclohexyl-2-benzothiazole sulfenamide is useful for the production of sulfur-modified chloroprene rubber.
Rubber vulcanization accelerator CZ, the scientific name N-Cyclohexyl-2-benzothiazole sulfenamide, is a highly active after-effect semi-overspeed accelerator, excellent coke resistance, processing safety, short vulcanization time.

N-Cyclohexyl-2-benzothiazole sulfenamide can be used as vulcanization accelerator alone or in combination with other accelerators such as D, DT, TT and TS.
N-Cyclohexyl-2-benzothiazole sulfenamide is used for the preparation of tires, rubber belts, cables, rubber pipes and other general industrial supplies.

N-Cyclohexyl-2-benzothiazole sulfenamide is an excellent after-effect promoter, suitable for natural rubber and synthetic rubber and rubber products such as tires.
One of the commonly used aftereffect promoters.

N-Cyclohexyl-2-benzothiazole sulfenamide is a good delayed action accelerator, suitable for natural and synthetic rubber and tire rubber products, able to improve the physical and mechanical properties of rubber products.
N-Cyclohexyl-2-benzothiazole sulfenamide is regulated for use in articles in contact with food as specified under.

N-Cyclohexyl-2-benzothiazole sulfenamide holds a prominent position in the realm of organic compounds, finding extensive utilization in rubber vulcanization and as an accelerator in the rubber industry.
The function of N-Cyclohexyl-2-benzothiazole sulfenamide lies in its ability to expedite the vulcanization process of rubber compounds.

Acting as an activator, N-Cyclohexyl-2-benzothiazole sulfenamide accelerates the cross-linking of rubber molecules, leading to the production of a robust and enduring rubber product.
Moreover, N-Cyclohexyl-2-benzothiazole sulfenamide heightens the reactivity between rubber molecules and sulfur, facilitating a more uniform and comprehensive vulcanization process.

N-Cyclohexyl-2-benzothiazole sulfenamide is used accelerator in natural and styrene-butadienethiazyl sulfenamide.
N-Cyclohexyl-2-benzothiazole sulfenamide is used adhesives and cements, Antifreeze, Condoms and diaphragms, Culling oils, Detergents, Swimwear, Disinfectants, repellents, fungicides, Gloves, Grease, Leather shoes (insoles, adhesives, linings)

N-Cyclohexyl-2-benzothiazole sulfenamide is used Medical devices, Photographic film emulsion, Rubber, Rubber eyelash curlers, Rubber in elasticized undergarments and clothing, Rubber sheets and pillows, Shampoo.
N-Cyclohexyl-2-benzothiazole sulfenamide is used Soaps, Sponge makeup applicators, Veterinarian products like tick and flea powders and sprays.

In industry, N-Cyclohexyl-2-benzothiazole sulfenamide is best known as a vulcanization accelerator (CBS) for rubber — meaning it helps accelerate the chemical cross-linking (vulcanization) of elastomers such as natural rubber, styrene-butadiene rubber, and other synthetic rubbers.
N-Cyclohexyl-2-benzothiazole sulfenamide enhances the speed of cure and improves processing safety by reducing premature scorch.

ALTERNATIVE PARENTSN of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
*Benzenoids
*Thiazoles
*Heteroaromatic compounds
*Sulfenyl compounds
*Organosulfenic acid amides
*Azacyclic compounds
*Organopnictogen compounds
*Organonitrogen compounds
*Hydrocarbon derivatives

SUBSTITUENTS of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
*1,3-benzothiazole
*Benzenoid
*Heteroaromatic compound
*Thiazole
*Azole
*Azacycle
*Sulfenyl compound
*Organosulfenic acid amide
*Organic nitrogen compound
*Organopnictogen compound
*Hydrocarbon derivative
*Organosulfur compound
*Organonitrogen compound
*Aromatic heteropolycyclic compound

A DEEP DIVE INTO N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE'S CHEMICAL PROPERTIES AND BENEFITS
The world of chemical engineering and material science constantly seeks compounds that can enhance product performance and streamline manufacturing processes.
N-Cyclohexyl-2-benzothiazole sulfenamide, commonly known as CBS, stands out as a critical chemical auxiliary in the rubber industry.

CHEMICAL PROPERTIES of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
N-Cyclohexyl-2-benzothiazole sulfenamide is milky white or beige powder.
N-Cyclohexyl-2-benzothiazole sulfenamide is soluble in benzene, dichloromethane, carbon tetrachloride, ethyl acetate, acetone, slightly soluble in ethanol and gasoline, insoluble in water.

PRODUCTION METHODS of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
The synthetic method of N-Cyclohexyl-2-benzothiazole sulfenamide mainly has sodium hypochlorite oxidization, Oxygen Catalytic Oxidation method, electrolytic oxidation, chlorine oxidation process, hydrogen peroxide oxidation method etc. at present, oxidizing process has raw material and is easy to get, the advantages such as equipment requirements is the highest.

Product yield is high, and technique is simple and widely used by institute both at home and abroad.
This method is to carry out condensation with 2-benzothiazolyl mercaptan (hereinafter referred to as M) in the presence of an oxidizer with cyclohexylamine to generate N-Cyclohexyl-2-benzothiazole sulfenamide.

WHERE IS N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE FOUND?
N-Cyclohexyl-2-benzothiazole sulfenamide is a rubber accelerator.
N-Cyclohexyl-2-benzothiazole sulfenamide is found in the rubber industry.
N-Cyclohexyl-2-benzothiazole sulfenamide is a cross-linking agent that is used in the production of polymeric matrices.

N-Cyclohexyl-2-benzothiazole sulfenamide is a multi-walled carbon molecule with an aromatic hydrocarbon cross-linker.
N-Cyclohexyl-2-benzothiazole sulfenamide reacts with fatty acids to form cationic surfactants, which can be used as antimicrobial agents.

The reaction mechanism for this type of chemical reaction has been studied under constant pressure conditions and N-Cyclohexyl-2-benzothiazole sulfenamide was found that sulfur transfer occurs in the first step, followed by activation energies for the second and third steps.
The diameter of N-Cyclohexyl-2-benzothiazole sulfenamide depends on the degree of polymerization (DP).

PRODUCTION METHOD of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
N-Cyclohexyl-2-benzothiazole sulfenamide is obtained by the reaction of accelerator M (2-thiolyl benzothiazole) with cyclohexylamine.
The accelerator M is mixed with cyclohexylamine aqueous solution, and the crude product is oxidized by adding sodium hypochlorite dropwise under stirring to separate the solid material, washed with water to neutral, and dried below 75°C to obtain the finished product, N-Cyclohexyl-2-benzothiazole sulfenamide.

PHYSICAL and CHEMICAL PROPERTIES of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
CAS Number: 95-33-0
Purity: 99%
MDL Number: MFCD00022872
Molecular Formula: C13H16N2S2
Molecular Weight: 264.41 g/mol
Melting Point: 93-100°C
Boiling Point: 410.4°C
Flash Point: 202°C
EINECS Number: 202-411-2
Density: 1.31-1.34 g/cm3

Appearance: White to light gray and red-gray to brown crystals or powder
Drying Loss: 0.40% Max
Ash: 0.40% Max
Solubility: Soluble in benzene, ethanol, and acetone. Insoluble in water.
pKa: 0.59±0.10 (Predicted)
Vapor Pressure: 6.04E-07 mmHg at 25°C
Refractive Index: n20D ~1.67 (Predicted)
Storage Condition: Keep in a dark place, sealed in dry, at room temperature
InChI: 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

InChI Key: DEQZTKGFXNUBJL-UHFFFAOYSA-N
Molecular Formula: C13H16N2S2
Molecular Weight: 296.408 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: 78.5 Å²
Heavy Atom Count: 17

Formal Charge: 0
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
Chemical Information:
CAS Number: 95-33-0
Other Names: N-Cyclohexyl-2-benzothiazole sulfonamide
EINECS Number: 202-411-2
Purity: 99.7%
Type: Sulfenamides Rubber Accelerator
Physical Properties:
Physical State (20°C): Solid
Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)

Identification and References:
Reaxys Registry Number: 192376
PubChem Substance ID: 87565678
MDL Number: MFCD00022872
Appearance: Pale yellow to light beige powder
Physical State: Solid
Solubility: Soluble in benzene, ethanol, and acetone; insoluble in water
Storage: Keep in a dark place, sealed in dry conditions, at room temperature
Melting Point: 93-100 °C (94-102 °C in another source)

Boiling Point: 410.4 °C at 760 mmHg
Density: 1.26 g/cm³ (Specific Gravity: 1.29 in another source)
Refractive Index: n20D ~1.67 (Predicted), 1.5700 (estimate in another source)
CAS Registry Number: 95-33-0
Molecular Formula: C13H16N2S2
Molecular Weight: 264.41 g/mol (264.415 g/mol in another source)
MDL Number: MFCD00022872
CBNumber: CB9360750
EINECS Number: 202-411-2

InChI: InChI=1S/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
InChIKey: DEQZTKGFXNUBJL-UHFFFAOYSA-N
PSA: 78.46000 Å²
LogP: 4.61660
Flash Point: 202 °C
Transport Information: UN 3077
Classification: Compounds containing sulfur; ureas, amides, cyanurates
Content: Ash Content= 0.50%, Moisture Content= 9.50%

Physical State: Solid (powder or granules)
Color: Pale yellow, beige, off-white or grey-white.
Odor: Slight inherent odor (weak).
Melting Point: ~93–104 °C (varies with purity).
Boiling Point: ~410 °C (predicted).
Density: ~1.31–1.34 g/cm³.
Vapor Pressure: ~0 Pa at 25 °C (negligible).
Water Solubility: Practically insoluble.
Solubility in Organic Solvents: Slightly soluble in chloroform, DMSO, ethyl acetate.

Slightly soluble in ethanol, gasoline.
Soluble in benzene, dichloromethane, acetone (depending on grade).
Refractive Index: ~1.57 (estimate).
Log P (Partition Coefficient): ~5 (indicating high hydrophobicity).
pKₐ: ~0.59 (predicted).
Chemical Formula: C13H16N2S2
Molecular Weight: 264.41 g/mol
Smiles: C1CCC(CC1)NSC2=NC3=CC=CC=C3S2
Long Term Storage: store at 10°C - 25°C, protect from light

CAS:95-33-0
Purity:99%
MDL No:MFCD00022872
Molecular Formula:C13H16N2S2
Molecular Weight:264.41
Melting Point:93-100°C
Boiling Point:410.4ºC
Flash Point:202°C
EINECS:202-411-2

Density:1.31-1.34g/cm3
Appearance:White to Light gray and red gray to gray to brown crystal or powder
Drying loss:0.40%Max
Ash:0.40%Max
Solubility:Soluble in benzene, ethanol, and acetone. Insoluble in water.
pKa:0.59±0.10(Predicted)
Vapor Presure:6.04E-07mmHg at 25°C
refractive index:n20D ~1.67 (Predicted)
Storage condition:Keep in dark place,Sealed in dry,Room Temperature
InChI: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

InChIKey:DEQZTKGFXNUBJL-UHFFFAOYSA-N
Physical State: Solid (powder or granules)
Color: Pale yellow, beige, off-white or grey-white
Odor: Slight inherent odor (weak)
Melting Point: ~93–104 °C (varies with purity)
Boiling Point: ~410 °C (predicted)
Density: ~1.31–1.34 g/cm³
Vapor Pressure: ~0 Pa at 25 °C (negligible)

Water Solubility: Practically insoluble
Solubility in Organic Solvents: Slightly soluble in chloroform, DMSO, ethyl acetate;
slightly soluble in ethanol, gasoline; soluble in benzene, dichloromethane, acetone (depending on grade)
Refractive Index: ~1.57 (estimate)
Log P (Partition Coefficient): ~5 (indicating high hydrophobicity)
pKₐ: ~0.59 (predicted)

Definition of enzyme activity: under the conditions of 37 ℃ and pH 8.0,
the formation of 1 micromolar cystathionine per minute is defined as an enzyme activity unit.
Molecular weight: 56kD (SDS-PAGE).
Isoelectric point: 6.8.
Michaelis constant: 5.8 × 10 -5 M (L-homocysteine).
Optimal pH value: 8.0-8.5.
Optimal temperature: 40 ℃.
pH stability: 6.5-7.5.

FIRST AID MEASURES of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available

ACCIDENTAL RELEASE MEASURES of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.

FIRE FIGHTING MEASURES of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available

EXPOSURE CONTROLS/PERSONAL PROTECTION of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
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.

STABILITY and REACTIVITY of N-CYCLOHEXYL-2-BENZOTHIAZOLE SULFENAMIDE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available