CAS 95-31-8

N-(1,1-Dimetiletil)-2-benzotiazolsulfenamida

Descripción:

N-(1,1-Dimetiletil)-2-benzotiazolsulfenamida, comúnmente conocido como disulfuro de dibenzotiazilo, es un compuesto orgánico caracterizado por su grupo funcional sulfenamida unido a un anillo de benzotiazol. Este compuesto típicamente aparece como un sólido cristalino blanco a amarillo claro y es conocido por su papel como acelerador de caucho, particularmente en el proceso de vulcanización del caucho. Exhibe buena estabilidad térmica y es soluble en disolventes orgánicos, pero menos en agua. La presencia del grupo dimetilo mejora su impedancia estérica, lo que puede influir en su reactividad e interacción con otros compuestos. Además, se reconoce por sus propiedades antioxidantes, lo que lo hace útil en diversas aplicaciones industriales. Los datos de seguridad indican que debe manejarse con cuidado, ya que puede causar irritación en la piel y los ojos. En general, N-(1,1-Dimetiletil)-2-benzotiazolsulfenamida es significativo en el campo de la química de polímeros y la ciencia de materiales.

Fórmula: 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

Clave InChI: InChIKey=IUJLOAKJZQBENM-UHFFFAOYSA-N

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

Sinónimos:

• 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

Fórmula: C₁₁H₁₄N₂S₂

Pureza: 97%

Forma y color: White to pale cream, Powder or pellets

Peso molecular: 238.38

Ref: 02-L13356

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

CAS: 95-31-8

Fórmula: C₁₁H₁₄N₂S₂

Pureza: 97%

Forma y color: Solid

Peso molecular: 238.3723

Ref: IN-DA003U67

N-Tert-Butyl-2-Benzothiazolesulfenamide

CAS: 95-31-8

N-Tert-Butyl-2-Benzothiazolesulfenamide

Pureza: 99%

Peso molecular: 238.37g/mol

Ref: 54-OR1014487

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.

Fórmula: C₁₁H₁₄N₂S₂

Pureza: Min. 95%

Peso molecular: 238.37 g/mol

Ref: 3D-FB33606

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

CAS: 95-31-8

Fórmula: C₁₁H₁₄N₂S₂

Pureza: 99%;RG

Peso molecular: 238.37

Ref: 10-F242865