(4S)-2-((1H-Indol-3-yl)methyl)-4-amino-2-hydroxypentanedioic acid CAS 126414-90-2

Purity 97%+In StockPharmaceutical Standards
CAS No.126414-90-2
Molecular FormulaC14H16N2O5
Molecular Weight292.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4S)-2-((1H-Indol-3-yl)methyl)-4-amino-2-hydroxypentanedioic acid CAS 126414-90-2 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 (4S)-2-((1H-Indol-3-yl)methyl)-4-amino-2-hydroxypentanedioic acid (CAS 126414-90-2), a certified reference material (molecular formula C14H16N2O5, MW 292.29 g/mol) for analytical method development and quality control.

The molecular framework of (4S)-2-((1H-Indol-3-yl)methyl)-4-amino-2-hydroxypentanedioic acid (C14H16N2O5) is characterized by a nitrogen-containing heterocyclic scaffold, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures (4S)-2-((1H-Indol-3-yl)methyl)-4-amino-2-hydroxypentanedioic acid 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 FormulaC14H16N2O5
Molecular Weight292.29 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms2

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