Methyl (3s)-3-amino-3-(4-chlorophenyl)propanoate hydrochloride CAS 1217775-76-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1217775-76-2
Molecular FormulaC10H12ClNO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (3s)-3-amino-3-(4-chlorophenyl)propanoate hydrochloride CAS 1217775-76-2 chemical structure

Description

CATO supplies Methyl (3s)-3-amino-3-(4-chlorophenyl)propanoate hydrochloride (CAS 1217775-76-2), a certified reference material (molecular formula C10H12ClNO2HCl, MW 250.12 g/mol) for analytical method development and quality control.

The molecular framework of Methyl (3s)-3-amino-3-(4-chlorophenyl)propanoate hydrochloride (C10H12ClNO2HCl) 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H12ClNO2 HCl
Molecular Weight250.12 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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