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N-acetyl-S-1,3-benzothiazol-2-ylcysteine, also known as N-acetylcysteine conjugate, is a chemical compound derived from the combination of N-acetylcysteine (NAC) and 2-mercaptobenzothiazole (MBT). This conjugate is formed as a result of the reaction between NAC and MBT, which is a common reaction in various chemical and industrial processes. N-acetyl-S-1,3-benzothiazol-2-ylcysteine plays a significant role in understanding the detoxification pathways of MBT and its derivatives, as well as in studying the formation and fate of these conjugates in the environment and biological systems. The compound has potential applications in the fields of environmental chemistry, toxicology, and pharmaceutical research, as it can provide insights into the mechanisms of chemical reactions and the detoxification processes in living organisms.

452-45-9

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452-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 452-45:
(5*4)+(4*5)+(3*2)+(2*4)+(1*5)=59
59 % 10 = 9
So 452-45-9 is a valid CAS Registry Number.

452-45-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-acetamido-3-(1,3-benzothiazol-2-ylsulfanyl)propanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:452-45-9 SDS

452-45-9Downstream Products

452-45-9Relevant academic research and scientific papers

Metabolism of 2-thiobenzothiazoles in the rat. Urinary, fecal and biliary metabolites of 2-benzothiazyl sulfenamides

Fukuoka, Masamichi,Satoh, Michio,Tanaka, Akira

, p. 1 - 9 (2007/10/03)

Metabolic fates of 2-benzothiazyl sulfenamides, N-oxydiethylene-2-benzothiazyl sulfenamide and N-cyclohexyl-2-benzothiazyl sulfenamide in rats were studied using tracer technique. These compounds given orally to rats were excreted rapidly in the urine and feces. Five urinary metabolites, 2-mercaptobenzothiazole (MBT), its three conjugates, mercapturate, glucuronide and sulfate, and 2,2'-dibenzothiazyl difulfide (BTDS) were confirmed. Furthermore, BTDS was found as a fecal metabolite. The sulfenamides were partly transformed in the stomach to BTDS, which was predominantly excreted into the feces. In the liver, the sulfenamides were mainly transformed to MBT and its conjugates. The S-glucuronide and S-sulfate conjugates were predominantly excreted into the bile. Mechanisms were discussed concerning the metabolite formation of sulfenamide derivatives in vivo and in vitro. - Keywords: Vulcanization accelerator; 2-Benzothiazyl sulfenamides; Metabolism; N-Oxydiethylene-2-benzothiazyl sulfenamide; Urinary metabolites; Mercapturate; Glucuronide; Sulfate; Disulfide formation; Rat stomach

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