N-(4-((4-Nitrophenyl)diazenyl)phenyl)acrylamide CAS 150375-01-2

Purity 97%+In StockPharmaceutical Standards
CAS No.150375-01-2
Molecular FormulaC15H12N4O3
Molecular Weight296.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-((4-Nitrophenyl)diazenyl)phenyl)acrylamide CAS 150375-01-2 chemical structure

Description

CATO manufactures N-(4-((4-Nitrophenyl)diazenyl)phenyl)acrylamide 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.

CATO supplies N-(4-((4-Nitrophenyl)diazenyl)phenyl)acrylamide (CAS 150375-01-2), a certified reference material (molecular formula C15H12N4O3, MW 296.28 g/mol) for analytical method development and quality control.

The molecular framework of N-(4-((4-Nitrophenyl)diazenyl)phenyl)acrylamide (C15H12N4O3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H12N4O3
Molecular Weight296.28 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Nitrogen Atoms4

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