Methyl 3-(6-methoxynicotinoyl)benzoate CAS 898786-05-5

Purity 97%+In StockPharmaceutical Standards
CAS No.898786-05-5
Molecular FormulaC15H13NO4
Molecular Weight271.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(6-methoxynicotinoyl)benzoate CAS 898786-05-5 chemical structure

Description

CATO manufactures Methyl 3-(6-methoxynicotinoyl)benzoate 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 Methyl 3-(6-methoxynicotinoyl)benzoate (CAS 898786-05-5), a certified reference material (molecular formula C15H13NO4, MW 271.27 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 3-(6-methoxynicotinoyl)benzoate (C15H13NO4) is characterized by a flavonoid core, 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. 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.

Physical & Chemical Properties

Molecular FormulaC15H13NO4
Molecular Weight271.27 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 methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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