http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101914035-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_34ceee3826a2a29252c70138f1789607
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-26
filingDate 2010-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d70b4b473617d0358e94f66d388f7e95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4368f77ed30d162af08c01028dd14e76
publicationDate 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101914035-B
titleOfInvention Method for preparing oxytetracycline hydrochloride
abstract The invention provides a method for preparing oxytetracycline hydrochloride. In the method, oxytetracycline is used as an initiative raw material, hydrochloric acid and methanol are used as co-solvents, and active carbon is used for decolorizing. A finished product is obtained by salt formation under the action of dry HCL, dynamical stirring, cooling and crystallization, crushing and screening of a wet product and airflow drying. The oxytetracycline hydrochloride prepared by the preparation method accords with the standards of Chinese Pharmacopoeia, United States Pharmacopeia, British Pharmacopoeia and European Pharmacopoeia, the methanol residue is superior to ICH requirement, and the yield reaches over 95.5 percent.
priorityDate 2010-08-27-04:00^^<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: 32.