N-Cyclohexyl-2-benzothiazolylsulfenamide
CAS: 95-33-0
Ref. 3D-FC43991
1kg | 633.00 € | ||
2kg | 1,050.00 € | ||
100g | 145.00 € | ||
250g | 261.00 € | ||
500g | 410.00 € |
Product Information
- 2-(Cyclohexylaminothio)benzothiazole Benzothiazyl-2-cyclohexylsulfenamide N-(1,3-Benzothiazol-2-ylsulfanyl)cyclohexanamine
- 2-(Cyclohexylaminothio)benzothiazole
- 2-Benzothiazolesulfenic acid N-cyclohexylamide
- Accel CZ
- Accelerator CBS
- Accelerator CM
- Accelerator CZ
- Accicure HBS
- Banac CBS
- Benzothiazole-2-Sulfenamide, N-Cyclohexyl
- See more synonyms
- Benzothiazyl-2-cyclohexylsulfenamide
- CBS
- CBS (accelerator)
- CZ Vulcanizer
- Cbs 80
- Cbts
- Conac A
- Conac S
- Curax
- Cyclohexyl-2-Benzothiazole Sulfenamide
- Cz 80
- Cz-G
- Delac S
- Durax
- Ekagom CBS
- N-Cyclohexyl-2-Benzothiazolyl Sulfenamide
- N-Cyclohexyl-2-benzothiazolesulfenamide
- N-Cyclohexyl-2-benzothiazolylsulphenamide
- N-Cyclohexyl-2-benzothiazylsulfenamide
- N-Cyclohexylbenzothiazol-2-sulfenamid
- N-Cyclohexylbenzothiazole-2-sulfenamide
- N-Cyclohexylbenzothiazolesulfenamide
- N-ciclohexilbenzotiazol-2-sulfenamida
- N-cyclohexylbenzothiazole-2-sulphenamide
- Nocceler CZ
- Nocceler CZ-G
- Nocceler CZ-P
- Nocceler CZ-R
- Nsc 4809
- Oricel CZ
- Pennac CBS
- Perkacit CBS
- Rhenogran CBS
- Rhenogran CBS 80
- Rhodifax 16
- Royal CBTS
- Sanceler CM
- Sanceler CM-G
- Sanceler CM-PO
- Sanceler CZ-G
- 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
N-Cyclohexyl-2-benzothiazolylsulfenamide is a cross-linking agent that is used in the production of polymeric matrices. It is a multi-walled carbon molecule with an aromatic hydrocarbon cross-linker. N-Cyclohexyl-2-benzothiazolylsulfenamide 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 it was found that sulfur transfer occurs in the first step, followed by activation energies for the second and third steps. The diameter of the product depends on the degree of polymerization (DP).
Chemical properties
Technical inquiry about: 3D-FC43991 N-Cyclohexyl-2-benzothiazolylsulfenamide
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