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US 5,312,827 AGranted
Nitrosamine-free-3-isothiazolones and process
AssigneeRohm and Haas Company
InventorsHorst O. Bayer, Barry C. Lange, Ramesh B. Petigara
Life of this patent
Estimating the term…
Abstract
Nitrosamine-free 3-isothiazolone biocidal compositions suitable for applications where substantial human or animal contact is anticipated, their method of use and process of preparation are disclosed.
Claims12
A stabilized 3-isothiazolone composition substantially free of nitrosamine impurities or precursors thereof which comprises:
- (a) a biologically effective amount of 5-chloro-2-methyl-3-isothiazolone and, optionally, one or more other biologically active 3-isothiazolone(s) of the formula ##STR12## wherein R and R.sup.1 are independently selected from hydrogen, halogen or an alkyl group of 1 to 4 carbon atoms;
- Y is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 5 or 6 carbon atoms, an aralkyl group of up to 8 carbon atoms, or an aryl or substituted aryl group of 6 carbon atoms;
- (b) a ring-stabilizing amount of a soluble metal nitrate salt;
- and
- (c) sufficient water to dissolve (a) and (b);
- said composition containing less than 100 ppm of by-product compounds containing an amine moiety capable of being nitrosated or a nitrosamine compound derived therefrom per 150,000 parts of (a).
3 more elements
A stabilized aqueous 3-isothiazolone solution substantially free of nitrosamine impurities or precursors thereof which comprise water and a mixture of:
- (a) a biologically effective amount of a biologically active mixture comprising essentially 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one and containing less than 25 parts per million by weight of by-product nitrosamine impurities or precursors thereof, and
- (b) a ring-stabilizing amount of a water-soluble metal nitrate salt.
Dependencies are inferred from the claim text.