Nafamostat Impurity 35 CAS 130200-58-7

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.130200-58-7
Molecular FormulaC11H7NO
Molecular Weight169.18 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Nafamostat Impurity 35 CAS 130200-58-7 chemical structure

Description

As a certified reference material (CRM), Nafamostat Impurity 35 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies Nafamostat Impurity 35 (CAS 130200-58-7), a pharmacopoeial impurity reference standard (molecular formula C11H7NO, MW 169.18 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C11H7NO, Nafamostat Impurity 35 contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 169.18 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

Physical & Chemical Properties

Molecular FormulaC11H7NO
Molecular Weight169.18 g/mol
Purity>95%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Nitrogen Atoms1

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