(S)-3-Amino-4-(naphthalen-2-yl)butanoic acid hydrochloride CAS 331847-01-9

Purity 97%+In StockPharmaceutical Standards
CAS No.331847-01-9
Molecular FormulaC14H15NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-3-Amino-4-(naphthalen-2-yl)butanoic acid hydrochloride CAS 331847-01-9 chemical structure

Description

CATO supplies (S)-3-Amino-4-(naphthalen-2-yl)butanoic acid hydrochloride (CAS 331847-01-9), a certified reference material (molecular formula C14H15NO2HCl, MW 265.74 g/mol) for analytical method development and quality control.

(S)-3-Amino-4-(naphthalen-2-yl)butanoic acid hydrochloride (C14H15NO2HCl) 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, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 (S)-3-Amino-4-(naphthalen-2-yl)butanoic acid hydrochloride 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 FormulaC14H15NO2 HCl
Molecular Weight265.74 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1

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