Tosylchloramide sodium trihydrate

• CAT Number: I013381
• CAS Number: 7080-50-4
• Molecular Formula: C₇H₁₃ClNNaO₅S
• Molecular Weight: 281.69
• Purity: ≥95%
• Target: Bacterial
• Solubility: DMSO
• IUPAC Name: sodium;chloro-(4-methylphenyl)sulfonylazanide;trihydrate
• InChI: InChI=1S/C7H7ClNO2S.Na.3H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;;;/h2-5H,1H3;;3*1H2/q-1;+1
• InChIKey: NZYOAGBNMCVQIV-UHFFFAOYSA-N
• SMILES: CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.O.O.[Na+]

Tosylchloramide sodium trihydrate（Cat No.:I013381）, also known as Chloramine T sodium trihydrate, is a commonly used disinfectant agent in laboratories, kitchens, and hospitals. It exhibits strong antimicrobial properties, making it effective against a wide range of pathogens. In addition to its use as a disinfectant, it is also employed as a biocide in air fresheners and deodorants to eliminate unpleasant odors. The broad-spectrum activity and versatility of Tosylchloramide sodium trihydrate make it a valuable tool for maintaining cleanliness and hygiene in various settings.

Reference

[1]. Kloth LC, et al. Bactericidal and cytotoxic effects of chloramine-T on wound pathogens and human fibroblasts in vitro. Adv Skin Wound Care. 2007 Jun;20(6):331-45.[2]. Shim I, et al. Inhalation exposure to chloramine T induces DNA damage and inflammation in lung of Sprague-Dawley rats. J Toxicol Sci. 2013;38(6):937-46.[3]. Kuklina I, et al. Investigation of chloramine-T impact on crayfish Astacus leptodactylus (Esch., 1823) cardiac activity. Environ Sci Pollut Res Int. 2014 Sep;21(17):10262-9. [4]. Martínez MA, et al. Induction of cytochrome P450-dependent mixed function oxidase activities and peroxisome proliferation by chloramine-T in male rat liver. Food Chem Toxicol. 2017 Aug;106(Pt A):86-91.