N-3-(2-Phenylethyl)-β-alaninamide Hydrochloride CAS 120034-99-3

Purity 97%+In StockPharmaceutical Standards
CAS No.120034-99-3
Molecular FormulaC11H16N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-3-(2-Phenylethyl)-β-alaninamide Hydrochloride CAS 120034-99-3 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 N-3-(2-Phenylethyl)-β-alaninamide Hydrochloride.

CATO supplies N-3-(2-Phenylethyl)-β-alaninamide Hydrochloride (CAS 120034-99-3), a certified reference material (molecular formula C11H16N2OHCl, MW 228.72 g/mol) for analytical method development and quality control.

N-3-(2-Phenylethyl)-β-alaninamide Hydrochloride (C11H16N2OHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC11H16N2O HCl
Molecular Weight228.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms2

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