2-Ethyl-6-fluoro-1-methyl-1H-indole-3-carboxylic acid CAS 1782835-72-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1782835-72-6
Molecular FormulaC12H12FNO2
Molecular Weight221.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Ethyl-6-fluoro-1-methyl-1H-indole-3-carboxylic acid CAS 1782835-72-6 chemical structure

Description

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 supplies 2-Ethyl-6-fluoro-1-methyl-1H-indole-3-carboxylic acid (CAS 1782835-72-6), a certified reference material (molecular formula C12H12FNO2, MW 221.23 g/mol) for analytical method development and quality control.

The molecular framework of 2-Ethyl-6-fluoro-1-methyl-1H-indole-3-carboxylic acid (C12H12FNO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. 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 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).

CATO manufactures 2-Ethyl-6-fluoro-1-methyl-1H-indole-3-carboxylic 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 FormulaC12H12FNO2
Molecular Weight221.23 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF-containing
Nitrogen Atoms1

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