http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105601542-B

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C273-1863
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C273-189
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C273-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C275-16
filingDate 2016-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105601542-B
titleOfInvention A kind of method that nitration mixture crystallizes N carbamylglutamic acids
abstract The invention discloses a kind of method that nitration mixture crystallizes N carbamylglutamic acids, two kinds are sequentially added into N carbamylglutamic acid reaction solutions or two or more acid is acidified;The solution of gained is stood overnight at 04 DEG C, crystallized;Suction filtration, gained solid is dried, and obtains N carbamylglutamic acid crude products.The acid is two or more in the inorganic acids such as concentrated hydrochloric acid, concentrated nitric acid, the concentrated sulfuric acid, concentrated phosphoric acid.The method for the nitration mixture crystallization N carbamylglutamic acids that the present invention is provided has advantages below compared with single sour acidization tool:Using the method for nitration mixture acidification reaction liquid can avoid it is single acid acidifying when caused common-ion effect, separated out so as to avoid sodium salt with product, be effectively improved product N carbamylglutamic acids crystallization purity.The product primary crystallization purity of the present invention is up to 98.3%.
priorityDate 2016-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 34.