CAS 149-30-4
:2-Mercaptobenzotiazol
- 1,3-Benzothiazole-2-thiol
- 1,3-Benzothiazole-2-thione
- 1,3-benzothiazole-2(3H)-thione
- 2(3H)-Benzothiazolethione
- 2,3-Dihydro-1,3-benzothiazole-2-thione
- 2,3-Dihydrobenzothiazole-2-thione
- 2-Benzothiazolethiol
- 2-Benzothiazolinethione
- 2-Benzothiazolthiol
- 2-Benzothiazolyl mercaptan
- 2-Mbt
- 2-Mercapthobenzothiazole Technical
- 2-Mercapto benzothiazole
- 2-Mercapto-1H-benzothiazole
- 2-Mercaptobenzo[d]thiazole
- 2-Mercaptobenzthiazole
- 2-Sulfanylbenzothiazole
- Accel M
- Accelerant M
- Accelerator M
- Accelerator Mbt
- Accelerator Mbt(M)
- Aero 407
- Aero Promoter 412
- Benz-1,3-thiazolidine-2-thione
- Benzo[d]thiazole-2-thiol
- Benzothiazol-2-thiol
- Benzothiazole, 2-Mercapto-
- Benzothiazole-2-thiol
- Benzothiazole-2-thione
- Benzothiazolethiol
- Benzotiazol-2-Tiol
- Captax
- Captax MBT
- Dermacid
- Dt 402
- Ekagom G
- Kaptaks
- Kaptax
- M
- M 2 (rust inhibitor)
- MBT
- MBT (vulcanization accelerator)
- Mbt 80
- Mbt-2
- Mebetizol
- Mebetizole
- Mebithizol
- Mercaptobenzothiazole
- Mercaptobenzthiazole
- Mertax
- Nocceler M
- Nocceler M-P
- Nonflex NB
- Nsc 2041
- Nuodeb 84
- Oricel M
- Perkacit MBT
- Pneumax MBT
- Rhenogran MBT
- Rhenogran MBT 80
- Rotax
- Royal MBT
- Rubator MBT
- Rubber Accelerator M
- Rubber Accelerator MBT
- Rubber Pharmaceutical intermediate Refined(M)
- Sanceler M
- Sanceler M-G
- Soxinol M
- Sulfur Accelerator M
- Thiotax
- Vulkacit M
- Vulkacit Mercapto
- Vulkacit Mercapto MG/C
- Vulkacit Mercapto/C
- Vulkacit Mercapto/MG
- Vulkafil ZN 94TT01
- Wobezit M
- Ver más sinónimos
2-Mercaptobenzothiazole
CAS:Fórmula:C7H5NS2Pureza:>99.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:167.242-Mercaptobenzothiazole, 97%
CAS: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:C7H5NS2Pureza:97%Forma y color:White to Pale yellow to yellow, PowderPeso molecular:167.242-Mercaptobenzothiazole
CAS:Fórmula:C7H5NS2Pureza:≥ 98.0%Forma y color:Light-yellow to yellow powder or crystalsPeso molecular:167.252-Mercaptobenzothiazole
CAS:Producto controladoFórmula:C7H5NS2Forma y color:NeatPeso molecular:167.25(1)2-Mercaptobenzothiazole
CAS:Fórmula:C7H5NS2Pureza:>97.0%(T)(HPLC)Forma y color:White to Green to Brown powder to crystalPeso molecular:167.242-Mercaptobenzothiazole
CAS:2-Mercaptobenzothiazole (Captax) is an organosulfur compound. 2-Mercaptobenzothiazole is used in rubber vulcanization.Fórmula:C7H5NS2Pureza:98.87%Forma y color:Reacts With Acids And Acid Fumes This Produces Toxic And Irritating Fumes (Sulfur Oxides Nitrogen Solid CrystallinePeso molecular:167.251,3-Benzothiazole-2-thiol
CAS:1,3-Benzothiazole-2-thiolPureza:99%Forma y color:Pale Yellow SolidPeso molecular:167.25g/mol2-Benzothiazolethiol
CAS:Producto controladoApplications 2-Benzothiazolethiol is an intermediate used to synthesize benzothiazole derivatives as cyclooxygenase inhibitors. It is also used to prepare pyridinone derivatives as potent non-nucleoside human immunodeficiency virus type 1 specific reverse transcriptase inhibitors.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Paramashivappa, R., et al.: Bioorg. Med. Chem. Lett., 13, 657 (2003); Dolle, V., et al.: J. Med. Chem., 38, 4679 (1995)Fórmula:C7H5NS2Forma y color:NeatPeso molecular:167.25(1)2-Mercaptobenzothiazole
CAS:2-Mercaptobenzothiazole (MBT) is an organosulfur compound that has been shown to have a variety of biological and chemical properties. MBT has been shown to possess potent antibacterial activity against both Gram-positive and Gram-negative bacteria. It has also been shown to be effective in wastewater treatment as a coagulant, sequestering agent, and flocculant. The optical sensor for MBT is based on the Langmuir adsorption isotherm and the optimum concentration of MBT is around 1 mM. The toxicological studies of MBT in animals have shown that it does not produce any adverse effects at doses up to 5000 mg/kg body weight. This may be due to its low solubility in water or its rapid metabolism by liver enzymes. The reaction mechanism of MBT with potassium dichromate involves a nucleophilic attack on the chromium atom, followed by displacement by sulfuric acid generated from hydrogen sulfFórmula:C7H5NS2Pureza:Min. 99 Area-%Forma y color:PowderPeso molecular:167.25 g/mol










