(S)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic acid CAS 2462-30-8

Purity 97%+In StockPharmaceutical Standards
CAS No.2462-30-8
Molecular FormulaC20H28O
Molecular Weight284.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic acid CAS 2462-30-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 284.44 g/mol gives (S)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (S)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic acid (CAS 2462-30-8), a certified reference material (molecular formula C20H28O, MW 284.44 g/mol) for analytical method development and quality control.

Structurally, (S)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic acid (C20H28O) contains a steroid core, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 284.44 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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)-2-Amino-3-(6-amino-1H-indol-3-yl)propanoic 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 FormulaC20H28O
Molecular Weight284.44 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

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