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Determination of Potential Genotoxic Impurity, 5-Amino-2-Chloropyridine, in Active Pharmaceutical Ingredient Using the HPLC-UV System

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dc.contributor.authorSOYSEVEN, MURAT
dc.contributor.authorKEÇİLİ, RÜSTEM
dc.contributor.authorARLİ, GÖKSEL
dc.contributor.authorGöksel Arlı
dc.contributor.orcid0000-0002-6433-2392
dc.contributor.orcid0000-0002-8377-9042
dc.contributor.orcid0000-0003-0249-7009
dc.contributor.orcid0000-0003-2559-1196
dc.date.accessioned2025-11-13T11:52:19Z
dc.date.issued2020-10-28
dc.identifier.doihttps://doi.org/10.1093/chromsci/bmaa100
dc.identifier.endpage245
dc.identifier.issn0021-9665
dc.identifier.issue3
dc.identifier.openalexW3109126534
dc.identifier.startpage241
dc.identifier.urihttps://hdl.handle.net/11421/8224
dc.identifier.urihttps://doi.org/10.1093/chromsci/bmaa100
dc.identifier.volume59
dc.language.isoen
dc.relation.ispartofJournal of Chromatographic Science
dc.rightsrestrictedAccess
dc.subjectChemistry
dc.subjectChromatography
dc.subjectHigh-performance liquid chromatography
dc.subjectDetection limit
dc.subjectActive ingredient
dc.subjectImpurity
dc.subjectCalibration curve
dc.subjectLinear range
dc.subjectPharmaceutical formulation
dc.subjectOrganic chemistry
dc.subject.sdg6
dc.titleDetermination of Potential Genotoxic Impurity, 5-Amino-2-Chloropyridine, in Active Pharmaceutical Ingredient Using the HPLC-UV System
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5061548919
local.authorid.openalexA5061557042
local.authorid.openalexA5054074736

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