H-α-Me-Phe-OH CAS 23239-35-2

Purity >95%In StockPharmaceutical Standards
CAS No.23239-35-2
Molecular FormulaC10H13NO2
Molecular Weight179.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

H-α-Me-Phe-OH CAS 23239-35-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 179.22 g/mol gives H-α-Me-Phe-OH distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

H-α-Me-Phe-OH (CAS 23239-35-2) is a high-purity analytical reference standard with the molecular formula C10H13NO2 and a molecular weight of 179.22 g/mol.

H-α-Me-Phe-OH (C10H13NO2) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 H-α-Me-Phe-OH 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 FormulaC10H13NO2
Molecular Weight179.22 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity>95%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Nitrogen Atoms1

Recommended Standards

Why CATO?