http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103965373-B

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K23-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-08
filingDate 2014-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103965373-B
titleOfInvention (2-hydroxyl-3-dehydrogenation fir oxygen base) propyl group chitooligosaccharide-and preparation method thereof
abstract Prepare the technique of three main process through comprising the preparation of dehydrogenation fir base glycidyl ether, water-soluble chitosan-oligosaccharide preparation and (2-hydroxyl-3-dehydrogenation fir oxygen base) propyl group chitooligosaccharide-, obtaining a kind of is nonionogenic tenside (2-hydroxyl-3-dehydrogenation fir oxygen base) the propyl group chitooligosaccharide-of raw material based on rosin and chitosan.Its process is as follows: dehydroabietinol and epoxy chloropropane obtain after dehydrogenation fir base glycidyl ether through addition and ring-closure reaction, react through the chitooligosaccharide-that the molecular weight that oxidative degradation generates is 500 ~ 50000 with chitosan, the final average graft(ing) degree generating glucosamine unit reaches nonionogenic tenside (2-hydroxyl-3-dehydrogenation fir oxygen base) the propyl group chitooligosaccharide-of 5 ~ 300% again.
priorityDate 2014-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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