http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109668988-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N30-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N30-74
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-74
filingDate 2019-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109668988-B
titleOfInvention Method for analyzing and determining 2- (dibromomethyl) -4-fluorobenzonitrile in trelagliptin succinate
abstract The invention provides a method for analyzing and determining genotoxic impurity 2- (dibromomethyl) -4-fluorobenzonitrile in trelagliptin succinate by using an HPLC method. The built high-efficiency liquid phase analysis method can accurately determine the potential genotoxic impurity 2- (dibromomethyl) -4-fluorobenzonitrile in the trelagliptin succinate by adopting octadecylsilane chemically bonded silica as a stationary phase, a phosphoric acid aqueous solution and an acetonitrile solution as mobile phases and adopting a gradient elution mode. The HPLC-UV method is simple to operate, short in analysis time, high in accuracy and good in repeatability, the sensitivity can reach 1.6ppm, a reliable detection method is provided for the quality standard of trelagliptin succinate, a guarantee is provided for the healthy medication of patients, and the method belongs to the technical field of medicines.
priorityDate 2019-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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