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Volumn 56, Issue 2, 2011, Pages 191-199
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Identification, synthesis and quantification of process-related impurities in auraptene
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Author keywords
Auraptene; Identification; Impurity; Quantification; Synthesis
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Indexed keywords
4 METHYLAURAPTENE;
6,7 DIHYDROXY 3,7 DIMETHYL 2 OCTEN UMBELLIFERONE;
6,7 EPOXY 3,7 DIMETHYL 2 OCTEN UMBELLIFERONE;
AURAPTENE;
PROTON;
SODIUM ION;
UMBELLIFERONE;
UMBELLIFERONE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CONTROLLED STUDY;
DRUG IDENTIFICATION;
DRUG IMPURITY;
DRUG SYNTHESIS;
INFRARED SPECTROSCOPY;
MOLECULAR WEIGHT;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PRIORITY JOURNAL;
QUADRUPOLE MASS SPECTROMETRY;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
VALIDATION STUDY;
CHEMISTRY, PHARMACEUTICAL;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CHROMATOGRAPHY, REVERSE-PHASE;
COUMARINS;
DRUG COMPOUNDING;
DRUG CONTAMINATION;
GUIDELINES AS TOPIC;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR STRUCTURE;
QUALITY CONTROL;
REPRODUCIBILITY OF RESULTS;
SPECTROPHOTOMETRY, INFRARED;
TANDEM MASS SPECTROMETRY;
TECHNOLOGY, PHARMACEUTICAL;
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EID: 79960058643
PISSN: 07317085
EISSN: 1873264X
Source Type: Journal
DOI: 10.1016/j.jpba.2011.05.011 Document Type: Article |
Times cited : (4)
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References (9)
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