N,5-Dimethyl-3-phenylisoxazole-4-carboxamide CAS 60986-88-1

Purity 97%+In StockPharmaceutical Standards
CAS No.60986-88-1
Molecular FormulaC12H12N2O2
Molecular Weight216.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N,5-Dimethyl-3-phenylisoxazole-4-carboxamide CAS 60986-88-1 chemical structure

Description

N,5-Dimethyl-3-phenylisoxazole-4-carboxamide (CAS 60986-88-1), molecular formula C12H12N2O2 and molecular weight 216.24 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of N,5-Dimethyl-3-phenylisoxazole-4-carboxamide (C12H12N2O2) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 N,5-Dimethyl-3-phenylisoxazole-4-carboxamide 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 FormulaC12H12N2O2
Molecular Weight216.24 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Nitrogen Atoms2

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Why CATO?