CAS 95-31-8

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

Descrizione:

N-(1,1-Dimetiletil)-2-benzotiazolsulfenamide, comunemente noto come disolfuro di dibenzotiazile, è un composto organico caratterizzato dal suo gruppo funzionale sulfenamide attaccato a un anello di benzotiazolo. Questo composto appare tipicamente come un solido cristallino bianco a giallo chiaro ed è noto per il suo ruolo come acceleratore della gomma, in particolare nel processo di vulcanizzazione della gomma. Mostra una buona stabilità termica ed è solubile in solventi organici, ma meno in acqua. La presenza del gruppo dimetile aumenta il suo ingombro sterico, il che può influenzare la sua reattività e interazione con altri composti. Inoltre, è riconosciuto per le sue proprietà antiossidanti, rendendolo utile in varie applicazioni industriali. I dati di sicurezza indicano che deve essere maneggiato con cura, poiché può causare irritazione della pelle e degli occhi. In generale, N-(1,1-Dimetiletil)-2-benzotiazolsulfenamide è significativo nel campo della chimica dei polimeri e della scienza dei materiali.

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

Sinonimi:

• 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

Purezza: 97%

Colore e forma: White to pale cream, Powder or pellets

Peso molecolare: 238.38

Ref: 02-L13356

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

CAS: 95-31-8

Formula: C₁₁H₁₄N₂S₂

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 238.3723

Ref: IN-DA003U67

N-Tert-Butyl-2-Benzothiazolesulfenamide

CAS: 95-31-8

N-Tert-Butyl-2-Benzothiazolesulfenamide

Purezza: 99%

Peso molecolare: 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.

Formula: C₁₁H₁₄N₂S₂

Purezza: Min. 95%

Peso molecolare: 238.37 g/mol

Ref: 3D-FB33606

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

CAS: 95-31-8

Formula: C₁₁H₁₄N₂S₂

Purezza: 99%;RG

Peso molecolare: 238.37

Ref: 10-F242865