http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102639474-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-12
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C25-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-12
filingDate 2010-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5711bf98477ebb285db0ef26e3da4b89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b12a49fcde5a970d1e26724491aa005
publicationDate 2014-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102639474-B
titleOfInvention Preparation of high assay decabromodiphenylalkane product with low occluded free bromine content
abstract A high assay decabromodiphenylalkane product in which the alkylene group contains in the range of about 1-10 carbon atoms and has an occluded free bromine content of <500 ppm is prepared. The process comprises brominating, in a liquid phase reaction mixture, at least one a, -diphenylalkane having an alkylene group of 1-10 carbon atoms, with a limited excess of bromine, in the presence of an aluminum, aluminum halide or a ferric halide catalyst in which the original halogen atoms of such halides are chlorine atoms, bromine atoms, or both. The limited excess of bromine is such that the maximum excess amount of bromine used in conducting the reaction is about 20 mole % relative to the stoichiometric amount required to convert the amount of a, -diphenylalkane used to decabromodiphenylalkane.; Crude high assay decabromodiphenylalkane product is prepared without use of heat treatment, oven ageing, or grinding or other forms of pulverization.
priorityDate 2009-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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