N-tert-Butyl-2-benzothiazolesulfenamide

CAS: 95-31-8

Ref. 3D-FB33606

Product Information

• Name: N-tert-Butyl-2-benzothiazolesulfenamide
• Synonyms: 2-(Tert-Butylaminothio)Benzothiazole, 2-Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-, 2-Benzothiazolesulfenamide, N-Tert-Butyl-, 2-[(Tert-Butylamino)Sulfanyl]-1,3-Benzothiazole, 2-[[(1,1-Dimethylethyl)amino]thio]benzothiazole, Accel Bns, Accelbns, Accelerator Ns, Accelerator Tbbs, Accelerator Tbbs(Ns), Acceleratorns, Acelerator NS, Akrochem Bbts, Antioxidant NS, Bbts, Benzothiazolesulfenamide, N-(1,1-Dimethylethyl)-, Benzothiazolyl-2-Tert-Butylsulfenamide, Butyl 2-Benzothiazole Sulfenamide, Butylbenzothiazole Sulfenamide, Conacns,(Dupont), Cure NS, Delac Ns, Luvomaxx TBBS, N-(1,1-Dimethylethyl)-2-Benzothiazolesulfenamid, N-(1,1-Dimethylethyl)-2-Benzothiazolesulfenamide, N-(1,1-Dimethylethyl)-Benzothiazolesulfenamid, N-(1,1-Dimethylethyl)Benzothiazolesulfenamide, N-(1,3-benzothiazol-2-ylsulfanyl)-2-methylpropan-2-amine, N-T-Butyl-2-Benzothioazole Sulfenamide, N-Tert-Butyl-2-Benzothiazolesulphenamide, N-Tertiarybutyl-2-Benzothiazole Sulfennamide, N-tert-Butyl-2-benzothiazolylsulfenamide, N-tert-Butyl-2-benzothiazolylsulphenamide, N-tert-Butylbenzothiazolesulfenamide, NS, NS 80 (vulcanization accelerator), NSC 84176, NSG (heterocycle), Nocceler NS, Nocceler NS-F, Nocceler NS-G, Nocceler NS-P, Ns 80, Perkacit TBBS, Rhenogran TBBS 80, Rubber Accelerator NS, Rubber Accelerator TBBS, Rubenamid T/Gr, Sa-Tb, Sanceler NS, Sanceler NS-F, Sanceler NS-G, Santocure BBTS, Santocure NS, Santocure TBBS, Soxinol NS, Sulfenamide T, Sulfenamide TBBS, Tbbs, Tbbs 80, Vanax NS Rodform, Vulkacit NZ, Vulkacit NZ/C, Vulkacit NZ/EG-C, n-tert-Butyl-2-benzothaiazole sulfonamide
• CAS: 95-31-8

Description

N-tert-Butyl-2-benzothiazolesulfenamide (TBBS) is an efficient and cost effective chemical for the removal of hydroxylated aromatic hydrocarbons from wastewater. It can be used at a concentration of 10 mg/L with a pH range of 3 to 7, and exhibits high resistance to pressure, temperature and pH changes. TBBS reacts with hydroxyl groups in the presence of sodium citrate and zinc diethyldithiocarbamate to form a complex that can be precipitated as particles. The reaction solution has antioxidative properties due to its ability to scavenge free radicals, thus increasing energy efficiency. This compound also has interactions with other chemicals, such as low energy, which may provide additional benefits for the environment.

• Brand: Biosynth

Chemical properties

• Molecular weight: 238.37 g/mol
• Formula: C₁₁H₁₄N₂S₂
• Purity: Min. 95%