1329509-49-0

1329509-49-0 structure

Name: 2-Methyl-3-isothiazolone-d3 Hydrochloride
Chemical Name: 2-(2H3)Methyl-1,2-thiazol-3(2H)-one hydrochloride (1:1)
CAS Number: 1329509-49-0
Molecular Formula: C₄H₃D₃ClNOS
Molecular Weight: 154.633
Catalog: analytical chemistry Standard Forensic and veterinary standards
Create Date: 2018-06-03 12:31:04
Modify Date: 2024-01-03 11:42:40
Methylisothiazolinone-d3 (hydrochloride) is the deuterium labeled Methylisothiazolinone (hydrochloride). Methylisothiazolinone hydrochloride is the constituent of the biocide Kathon CG. Methylisothiazolinone hydrochloride is an isothiazolone derivative widely used as a preservative. Methylisothiazolinone hydrochloride is also a moderate sensitizer and reacts with GSH.

Name	2-(2H3)Methyl-1,2-thiazol-3(2H)-one hydrochloride (1:1)
Synonyms	3(2H)-Isothiazolone, 2-(methyl-d3)-, hydrochloride (1:1) 2-(2H3)Methyl-1,2-thiazol-3(2H)-one hydrochloride (1:1)

Description	Methylisothiazolinone-d3 (hydrochloride) is the deuterium labeled Methylisothiazolinone (hydrochloride). Methylisothiazolinone hydrochloride is the constituent of the biocide Kathon CG. Methylisothiazolinone hydrochloride is an isothiazolone derivative widely used as a preservative. Methylisothiazolinone hydrochloride is also a moderate sensitizer and reacts with GSH.
Related Catalog	Research Areas >> Infection Signaling Pathways >> Anti-infection >> Bacterial
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-223. [2]. Rubén Alvarez-Sánchez, et al. Covalent Binding of the 13C-labeled Skin Sensitizers 5-chloro-2-methylisothiazol-3-one (MCI) and 2-methylisothiazol-3-one (MI) to a Model Peptide and Glutathione. Bioorg Med Chem Lett. 2004 Jan 19;14(2):365-8. [3]. Aynur O Aptula, et al. From Experiment to Theory: Molecular Orbital Parameters to Interpret the Skin Sensitization Potential of 5-chloro-2-methylisothiazol-3-one and 2-methylisothiazol-3-one. Chem Res Toxicol. 2005 Feb;18(2):324-9.