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filingDate 1994-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56f46ea92c653a4256d4a9d122397083
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publicationDate 1995-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07179309-A
titleOfInvention Method for producing 3-isothiazolone composition
abstract (57) [Summary] [Purpose] Stabilized biocidal water-soluble 3-substantially free of nitrosamine impurities and nitrosamine precursors Providing an isothiazolone composition. [Structure] An intermediate amide obtained by amidating a mixture of dimethyl-3,3'-dithiodipropionate and methyl 3-mercaptan propionate (nucleophilic scavenger) is cyclized with a chlorinating agent. 3-isothiazolone is formed and metal nitrate is further added as a stabilizer to give the desired 5-chloro-2-methyl-4-isothiazoline- A method for producing a 3-isothiazolone composition containing 3-one as an active ingredient. Effects: Nitrosamine impurities and nitrosamine precursors can be 110 ppm or less of the 3-isothiazolone composition.
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