Methyl (S)-2-amino-3-(2,5,7-tri-tert-butyl-1H-indol-3-yl)propanoate CAS 1638744-52-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1638744-52-1
Molecular FormulaC24H38N2O2
Molecular Weight386.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (S)-2-amino-3-(2,5,7-tri-tert-butyl-1H-indol-3-yl)propanoate CAS 1638744-52-1 chemical structure

Description

CATO supplies Methyl (S)-2-amino-3-(2,5,7-tri-tert-butyl-1H-indol-3-yl)propanoate (CAS 1638744-52-1), a certified reference material (molecular formula C24H38N2O2, MW 386.57 g/mol) for analytical method development and quality control.

The molecular framework of Methyl (S)-2-amino-3-(2,5,7-tri-tert-butyl-1H-indol-3-yl)propanoate (C24H38N2O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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).

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 Methyl (S)-2-amino-3-(2,5,7-tri-tert-butyl-1H-indol-3-yl)propanoate 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 FormulaC24H38N2O2
Molecular Weight386.57 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 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms2

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