http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0322610-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D5-4496
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-6407
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-8041
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D5-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-64
filingDate 1988-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2eb247530310248ed2031cc3536900fe
publicationDate 1989-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0322610-A1
titleOfInvention Process for curing cationic lacquer binders, and said binders containing the curing agents for use in the process
abstract The invention relates to a method for crosslinking cationic paint binders, in particular cathodically depositable paints by (poly) -2-hydroxyalkylurea compounds.n n n The 2-hydroxyalkylureas are obtained by reacting organic di- or polyisocyanates with secondary β-hydroxyalkylamines.n n n The claimed crosslinking agents not only allow film formation in the stoving range of approximately 140 ° C., which is particularly favorable for water-based paints, but also a more selective half-blocking due to the more pronounced difference in reactivity of the NCO groups of individual diisocyanates compared to the secondary amino groups compared to hydroxyl groups.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2020377758-A1
priorityDate 1987-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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