CAS 95-31-8

N-(1,1-Dimethylethyl)-2-benzothiazolesulfenamide

Description:

N-(1,1-Dimethylethyl)-2-benzothiazolesulfenamide, commonly known as dibenzothiazyl disulfide, is an organic compound characterized by its sulfenamide functional group attached to a benzothiazole ring. This compound typically appears as a white to light yellow crystalline solid and is known for its role as a rubber accelerator, particularly in the vulcanization process of rubber. It exhibits good thermal stability and is soluble in organic solvents, but less so in water. The presence of the dimethyl group enhances its steric hindrance, which can influence its reactivity and interaction with other compounds. Additionally, it is recognized for its antioxidant properties, making it useful in various industrial applications. Safety data indicates that it should be handled with care, as it may cause skin and eye irritation. Overall, N-(1,1-Dimethylethyl)-2-benzothiazolesulfenamide is significant in the field of polymer chemistry and materials science.

Formula: C₁₁H₁₄N₂S₂

InChI: InChI=1S/C11H14N2S2/c1-11(2,3)13-15-10-12-8-6-4-5-7-9(8)14-10/h4-7,13H,1-3H3

InChI key: InChIKey=IUJLOAKJZQBENM-UHFFFAOYSA-N

SMILES: S(NC(C)(C)C)C1=NC=2C(S1)=CC=CC2

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-benzothiazolesulfenamide
• 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-benzothiazolesulfenamide, 97%

CAS: 95-31-8

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₁H₁₄N₂S₂

Purity: 97%

Color and Shape: White to pale cream, Powder or pellets

Molecular weight: 238.38

Ref: 02-L13356

N-Tert-Butyl-2-Benzothiazolesulfenamide

CAS: 95-31-8

N-Tert-Butyl-2-Benzothiazolesulfenamide

Formula: C₁₁H₁₄N₂S₂

Purity: 99%

Color and Shape: Solid

Molecular weight: 238.37

Ref: 54-OR1014487

N-tert-Butyl-2-benzothiazolesulfenamide

CAS: 95-31-8

N-tert-Butyl-2-benzothiazolesulfenamide

Formula: C₁₁H₁₄N₂S₂

Purity: 97%

Molecular weight: 238.37

Ref: IN-DG23241

N-tert-Butyl-2-benzothiazolesulfenamide

CAS: 95-31-8

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.

Formula: C₁₁H₁₄N₂S₂

Purity: Min. 95%

Molecular weight: 238.37 g/mol

Ref: 3D-FB33606

S-(Benzo[d]thiazol-2-yl)-N-(tert-butyl)thiohydroxylamine

CAS: 95-31-8

Formula: C₁₁H₁₄N₂S₂

Purity: 90%

Molecular weight: 238.37

Ref: 10-F242865

S-(Benzo[d]thiazol-2-yl)-N-(tert-butyl)thiohydroxylamine

CAS: 95-31-8

Formula: C₁₁H₁₄N₂S₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 238.3723

Ref: IN-DA003U67