methyl 2-[(2S)-2-amino-3-phenylpropanamido]acetate hydrochloride CAS 7625-59-4

Purity 97%+In StockPharmaceutical Standards
CAS No.7625-59-4
Molecular FormulaC12H16N2O3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

methyl 2-[(2S)-2-amino-3-phenylpropanamido]acetate hydrochloride CAS 7625-59-4 chemical structure

Description

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

methyl 2-[(2S)-2-amino-3-phenylpropanamido]acetate hydrochloride (CAS 7625-59-4) is a high-purity analytical reference standard with the molecular formula C12H16N2O3HCl and a molecular weight of 272.73 g/mol.

Structurally, methyl 2-[(2S)-2-amino-3-phenylpropanamido]acetate hydrochloride (C12H16N2O3HCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 272.73 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC12H16N2O3 HCl
Molecular Weight272.73 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-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 DMSO, DMF, methanol
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Halogen ContentCl-containing
Nitrogen Atoms2

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