Methyl 4-hydroxy-3-(2-hydroxy-1-phenylethyl)-5-(methylcarbamoyl)benzoate CAS 2306054-96-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2306054-96-4
Molecular FormulaC18H19NO5
Molecular Weight329.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-hydroxy-3-(2-hydroxy-1-phenylethyl)-5-(methylcarbamoyl)benzoate CAS 2306054-96-4 chemical structure

Description

CATO supplies Methyl 4-hydroxy-3-(2-hydroxy-1-phenylethyl)-5-(methylcarbamoyl)benzoate (CAS 2306054-96-4), a certified reference material (molecular formula C18H19NO5, MW 329.35 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, Methyl 4-hydroxy-3-(2-hydroxy-1-phenylethyl)-5-(methylcarbamoyl)benzoate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 329.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures Methyl 4-hydroxy-3-(2-hydroxy-1-phenylethyl)-5-(methylcarbamoyl)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.

Physical & Chemical Properties

Molecular FormulaC18H19NO5
Molecular Weight329.35 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.)1999
Nitrogen Atoms1

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