http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012530160-A

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G65-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G65-2609
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G65-2612
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G65-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K8-81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F290-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G65-06
filingDate 2010-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2012530160-A
titleOfInvention Terminally unsaturated glycidol-based macromonomers, polymers obtained therefrom, preparation and use
abstract The present invention relates to a process for the production of the macromonomer, the starting compounds H 2 C = CR 1 -C 6 H 4-s (R 4) s -R 3 -OH or H 2 C = CR 2 -CO- NH-R 3 - OH, wherein R 1 and R 2 are each H or a linear or branched alkyl group having 1 to 4 carbon atoms, and R 3 can contain one or more hydroxy groups A linear or branched alkylene, aralkylene group having 1 carbon atom, and the R 4 group is independently a linear or branched alkyl, aralkyl, alkoxy or aralkoxy group having 1-20 carbon atoms. , S is 0-4) after partial deprotonation, reacting at least one hydroxy functional oxirane compound with the opening of the oxirane ring in the presence of a free radical polymerization inhibitor, the molar ratio of n ( Originating Compound): n (oxirane compound) is 1: 100 to 1: 1. The invention further relates to the macromonomers obtained by this process, the polymers and coatings obtained therefrom, their use in plastics and cosmetics. [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016510081-A
priorityDate 2009-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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