(1H-indol-3-yl)methanamine oxalate CAS 296775-93-4

Purity 97%+In StockPharmaceutical Standards
CAS No.296775-93-4
Molecular FormulaC9H10N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1H-indol-3-yl)methanamine oxalate CAS 296775-93-4 chemical structure

Description

CATO manufactures (1H-indol-3-yl)methanamine oxalate 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.

CATO supplies (1H-indol-3-yl)methanamine oxalate (CAS 296775-93-4), a certified reference material (molecular formula C9H10N2C2H2O4, MW 236.23 g/mol) for analytical method development and quality control.

The molecular framework of (1H-indol-3-yl)methanamine oxalate (C9H10N2C2H2O4) 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 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.

Physical & Chemical Properties

Molecular FormulaC9H10N2 C2H2O4
Molecular Weight236.23 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2

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