1-Hydroxy-N-methyl-2-naphthalenecarboxamide CAS 62353-81-5

Purity 97%+In StockPharmaceutical Standards
CAS No.62353-81-5
Molecular FormulaC12H11NO2
Molecular Weight201.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Hydroxy-N-methyl-2-naphthalenecarboxamide CAS 62353-81-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 1-Hydroxy-N-methyl-2-naphthalenecarboxamide.

1-Hydroxy-N-methyl-2-naphthalenecarboxamide (CAS 62353-81-5), molecular formula C12H11NO2 and molecular weight 201.22 g/mol, is a CATO reference standard with documented purity and traceability.

1-Hydroxy-N-methyl-2-naphthalenecarboxamide (C12H11NO2) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 1-Hydroxy-N-methyl-2-naphthalenecarboxamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H11NO2
Molecular Weight201.22 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Nitrogen Atoms1

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