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| | 2-Methylmercaptobenzothiazole Basic information |
| | 2-Methylmercaptobenzothiazole Chemical Properties |
| Melting point | 43-46 °C(lit.) | | Boiling point | 177 °C / 22mmHg | | density | 1.2625 (rough estimate) | | refractive index | 1.5700 (estimate) | | Fp | >230 °F | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Sparingly), Methanol (Slightly, Sonicated) | | form | Solid | | pka | 1.22±0.10(Predicted) | | color | White to Off-White | | Odor | at 0.10 % in dipropylene glycol. fatty woody smoky | | Odor Type | fatty | | InChIKey | UTBVIMLZIRIFFR-UHFFFAOYSA-N | | LogP | 3.150 | | CAS DataBase Reference | 615-22-5(CAS DataBase Reference) | | NIST Chemistry Reference | 2-(Methylthio)benzothiazole(615-22-5) | | EPA Substance Registry System | 2-(Methylthio)benzothiazole (615-22-5) |
| | 2-Methylmercaptobenzothiazole Usage And Synthesis |
| Chemical Properties | colorless to light yellow crystalline powder | | Uses | 2-(Methylthio)benzothiazole was used in trace determination of polar 1H-benzotriazoles and benzothiazoles in drinking and surface water by liquid chromatography-electrospray mass spectrometry. | | Uses | 2-(Methylthio)Benzothiazole could be useful for removing pollutants in drinking water. | | Definition | ChEBI: An organic sulfide that is the methyl thioether of 1,3-benzothiazole-2-thiol. | | General Description | 2-(Methylthio)benzothiazole is the degradation product of 2-(thiocyanomethylthio)benzothiazole, a biocide used in the leather, pulp, paper and water-treatment industries. | | Metabolic pathway | When 2-methylthiobenzothiazole and 35S-labeled
glutathione (GSH) are incubated with rat liver
microsomes, both 35S-labeled S-(2-
benzothiazolyl)glutathione and 2-
mercaptobenzothiazole are isolated from the reaction
mixtures. Glutathione-S-transferase appears to be
involved in the S-(2- benzothiazolyl)glutathione
formation. Although sulfur is exchanged in this
pathway, the net result of this pathway which involves
oxidation of the methylthio group and GSH conjugation
is an apparent S-demethylation of the methylthio
group. Another S-demethylation pathway that does not
involve GSH conjugation also functions in vitro. |
| | 2-Methylmercaptobenzothiazole Preparation Products And Raw materials |
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