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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G59-5073
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-72
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-72
filingDate 1969-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1972-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edfc32b106b3377b175823763235d54b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce573a0784ac3c3e592d130a2ee423af
publicationDate 1972-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3697539-A
titleOfInvention Bis-(1-{65 -aminopropyl-hydantoinyl-3)-alkanes
abstract New bis-(1- gamma -aminopropyl-hydantoinyl-3)-alkanes, for example 1,6-bis-(1''-( gamma -aminopropyl)-5'',5''dimethylhydantoinyl-3'')-hexane or Beta , Beta ''-bis-(1-(3''aminopropyl)-5,5-dimethyl-hydantoinyl-3)-diethyl ether, and their use as curing agents in curable moulding, coating and adhesive compositions which contain a polyepoxide compound, for example a liquid polyglycidyl ether of bisphenol A. Curing can be carried out at relatively low temperatures, for example at 40* C. The new type of curing agent bridges, in respect of its gradation of reactivity, a gap between aliphatic polyamines and cycloaliphatic polyamines. The new curing agents furthermore have the advantage relative to the aromatic polyamines of being non-toxic.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4691021-A
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priorityDate 1968-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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