N-Cyclohexyl-2-benzothiazolesulfenamide (CAS 95-33-0)
QUICK LINKS
N-Cyclohexyl-2-benzothiazolesulfenamide (CBS) 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, it 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.
N-Cyclohexyl-2-benzothiazolesulfenamide (CAS 95-33-0) References
- Benzothiazolamines as tire-derived molecular markers: sorptive behavior in street runoff and application to source apportioning. | Kumata, H., et al. 2002. Environ Sci Technol. 36: 702-8. PMID: 11878386
- Distribution of polycyclic aromatic hydrocarbons (PAHs) in rivers and estuaries in Malaysia: a widespread input of petrogenic PAHs. | Zakaria, MP., et al. 2002. Environ Sci Technol. 36: 1907-18. PMID: 12026970
- Two-generation reproductive toxicity study of the rubber accelerator N,N-dicyclohexyl-2-benzothiazolesulfenamide in rats. | Ema, M., et al. 2008. Reprod Toxicol. 25: 21-38. PMID: 18078738
- Stress-induced stabilization of crystals in shape memory natural rubber. | Heuwers, B., et al. 2013. Macromol Rapid Commun. 34: 180-4. PMID: 23124898
- Rubber: new allergens and preventive measures. | Crepy, MN. 2016. Eur J Dermatol. 26: 523-530. PMID: 28007673
- Impact of additives of commercial rubber compounds on the microbial and enzymatic degradation of poly(cis-1,4-isoprene). | Altenhoff, AL., et al. 2019. Biodegradation. 30: 13-26. PMID: 30324341
- Shoe dermatitis in India. | Bajaj, AK., et al. 1988. Contact Dermatitis. 19: 372-5. PMID: 3233958
- Molecular Damage Detection in an Elastomer Nanocomposite with a Coumarin Dimer Mechanophore. | Zhang, Y., et al. 2021. Macromol Rapid Commun. 42: e2000359. PMID: 32761960
- The Influence of Local Strain Distribution on the Effective Electrical Resistance of Carbon Black Filled Natural Rubber. | Harea, E., et al. 2021. Polymers (Basel). 13: PMID: 34372015
- Contact dermatitis to hair cosmetics: Current diagnostic recommendations. | Thomas, ZM., et al. 2021. J Dtsch Dermatol Ges. 19: 1729-1734. PMID: 34427043
- Hypervalent Iodine-Mediated Synthesis of Sulfinimidate Esters from Sulfenamides. | Lu, X., et al. 2023. Org Lett. 25: 2151-2156. PMID: 36946517
- Redox-Neutral Synthesis of Sulfilimines through the S-Alkylation of Sulfenamides. | Huang, G., et al. 2023. Org Lett. 25: 3173-3178. PMID: 37102689
- Effect of oral Sulfenamide TS administration on prenatal development in rats. | Sitarek, K., et al. 1996. Teratog Carcinog Mutagen. 16: 1-6. PMID: 8792528
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-Cyclohexyl-2-benzothiazolesulfenamide, 5 g | sc-357392B | 5 g | $21.00 | |||
N-Cyclohexyl-2-benzothiazolesulfenamide, 25 g | sc-357392 | 25 g | $41.00 | |||
N-Cyclohexyl-2-benzothiazolesulfenamide, 100 g | sc-357392A | 100 g | $120.00 | |||
N-Cyclohexyl-2-benzothiazolesulfenamide, 500 g | sc-357392C | 500 g | $267.00 |