Methyl 2-amino-3-(2-hydroxyphenyl)propanoate hydrochloride CAS 194795-20-5

Purity 97%+In StockPharmaceutical Standards
CAS No.194795-20-5
Molecular FormulaC10H13NO3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-amino-3-(2-hydroxyphenyl)propanoate hydrochloride CAS 194795-20-5 chemical structure

Description

As a certified reference material (CRM), Methyl 2-amino-3-(2-hydroxyphenyl)propanoate hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies Methyl 2-amino-3-(2-hydroxyphenyl)propanoate hydrochloride (CAS 194795-20-5), a certified reference material (molecular formula C10H13NO3HCl, MW 231.68 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 2-amino-3-(2-hydroxyphenyl)propanoate hydrochloride (C10H13NO3HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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. 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.

Physical & Chemical Properties

Molecular FormulaC10H13NO3 HCl
Molecular Weight231.68 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2012
Halogen ContentCl-containing
Nitrogen Atoms1

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