tert-Butyl (S)-2-hydroxy-3-phenylpropanoate CAS 7622-23-3

Purity 97%+In StockPharmaceutical Standards
CAS No.7622-23-3
Molecular FormulaC13H18O3
Molecular Weight222.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (S)-2-hydroxy-3-phenylpropanoate CAS 7622-23-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including tert-Butyl (S)-2-hydroxy-3-phenylpropanoate.

tert-Butyl (S)-2-hydroxy-3-phenylpropanoate (CAS 7622-23-3), molecular formula C13H18O3 and molecular weight 222.28 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of tert-Butyl (S)-2-hydroxy-3-phenylpropanoate (C13H18O3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 tert-Butyl (S)-2-hydroxy-3-phenylpropanoate 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 FormulaC13H18O3
Molecular Weight222.28 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959

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