70264-24-3

Usage

Appearance

White crystalline powder

Odor

Slightly sweet

Usage

Preservative in personal care products (shampoos, lotions, cosmetics)

Properties

Antimicrobial, inhibits growth of bacteria and fungi

Purpose

Extends shelf life of products

Potential Issues

Toxicity concerns, possible allergic reactions in some individuals

Upstream product

• 6345-19-3 3,5,5-trimethyl-2,4-imidazolidinedione 
• 77-71-4 5,5-dimethyl-imidazolidine-2,4-dione 
• 128070-44-0 1-Benzylsulfanyl-3,5,5-trimethyl-imidazolidine-2,4-dione 

Downstream Products

• 128070-51-9 1-Benzenesulfinyl-3,5,5-trimethyl-imidazolidine-2,4-dione 
• 128070-43-9 3,5,5-Trimethyl-1-phenylsulfanyl-imidazolidine-2,4-dione 
• 6345-19-3 3,5,5-trimethyl-2,4-imidazolidinedione 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF ORGANIC BROMIDES

The present invention provides a process for the preparation of organic bromides, by a radical bromodecarboxylation of carboxylic acids with a bromoisocyanurate.

N3-(ARYLTHIO-, ARALKYLTHIO- AND ALKYLTHIO)-5,5-DIMETHYLHYDANTOINS: SULFENYL GROUP TRANSFER REACTIONS AND THEIR PROPERTIES

Sulfenyl-transfer reactions toward a variety of nucleophiles were successfully carried out using N3-sulfenyl-substituted 5,5-dimethylhydantoins (2a-c).During the course of the synthesis of 2 by the reaction of N1-bromo-5,5-dimethylhydantoin (1c) with disulfides, the sulfenyl groups were found to be at the position of N3 although the bromine was at N1 in the starting monobromohydantoin (1c).Some mechanistic speculations were considered for the formation of 2 from 1c.