http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03206085-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fb78b459e21bb4fd52850a12cab27387
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C10M135-36
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N25-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D5-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K8-49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-46
filingDate 1990-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ad41f530dc6972d369a198662642a50
publicationDate 1991-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03206085-A
titleOfInvention Use of carbonyl stabilizer for 3-isothiazolone
abstract A microbicidal composition is disclosed comprising a) at least one 3-isothiazolone of the formula (I) <CHEM> wherein Y is (C1-C18)alkyl or (C3-C12)cycloalkyl each optionally substituted with one or more of hydroxy, halo, cyano, alkylamino, dialkylamine, arylamino, carboxy, carbalkoxy, alkoxy, aryloxy, alkylthio, arylthio, haloalkoxy, cycloalkylamino, carbamoxy, or isothiazolonyl; an unsubstituted or halo-substituted (C2-C8) alkenyl or alkynyl; a (C7-C10)aralkyl optionally substituted with one or more of halogen, (C1-C4)alkyl or (C1-C4)alkoxy; and an aryl optionally substituted with one or more of halogen, nitro, (C1-C4)alkyl, (C1-C4)alkyl-acylamino, carb(C1-C4)alkoxy or sulfamyl; and R and R<1> is each independently H, halogen or (C1-C4) alkyl; and b) a carbonyl compound comprising (C2-C6) aldehydes, (C7-C10) aromatic aldehydes or acids, (C2-C4) dialdehydes, (C1-C12) acids, (C2-C8) diacids, triacids or tetracids, (C3-C10) alpha , beta unsaturated carbonyls, (C1-C6) haloamides of the formula <CHEM> where R3 = phenyl or (C1-C4)alkyl-substituted phenyl, R2 = (C1-C7)alkyl, (C1-C7)alkoxylalkyl, or (C1-C7)carbalkoxyalkyl, X1, X2, X3 = H or halogen wherein at least one X is halogen; or furfural, dibutylene furfural and maleimides of the formula <CHEM> where R sec is H, (C1-C4) alkyl or aryl; provided that when (b) comprises an aldehyde or dialdehyde the ratio (b):(a) is less than 10:1. The carbonyl compound acts as a stabiliser for the 3-isothiazolone.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009096997-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010229158-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009041014-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020246452-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20220006129-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008146436-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4615068-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012509330-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2008146436-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007161729-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4639265-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010260870-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114173563-A
priorityDate 1989-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6488
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Total number of triples: 41.