http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2550250-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_df1a05610c0c37f74bfca54f1405100c
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-68
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D11-101
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-10
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filingDate 2011-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f196146ac5903774dc3556a13844f33
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8f1beecd9385462f241ad6e2beb0bba
publicationDate 2013-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2550250-A2
titleOfInvention Amine synergists and their use in radiation curing
abstract Compounds of formula (I): wherein Ar represents an, optionally substituted, aryl or heteroaryl group, R represents an, optionally substituted, aryl or heteroaryl group, an optionally substituted straight or branched chain C 1.10 -alkyl, R 1 is H or methyl, X is an extender group, n is 0 or an integer between 1 and 12 inclusive, A is a polyol residue wherein the unsubstituted polyol from which the residue is derived has at least y OH groups, and y is an integer>1, can easily be prepared, and are useful as synergists in radiation curing.
priorityDate 2010-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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