(S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid dihydrate CAS 145224-90-4

Purity 97%+In StockPharmaceutical Standards
CAS No.145224-90-4
Molecular FormulaC11H12N2O3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid dihydrate CAS 145224-90-4 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.

CATO supplies (S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid dihydrate (CAS 145224-90-4), a certified reference material (molecular formula C11H12N2O3H2O, MW 238.24 g/mol) for analytical method development and quality control.

The molecular framework of (S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid dihydrate (C11H12N2O3H2O) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, 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).

As a certified reference material (CRM), (S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid dihydrate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H12N2O3 2*H2O
Molecular Weight238.24 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Nitrogen Atoms2

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