3-Methyl-5-phenyl-1H-indole-2-carboxylic acid CAS 191868-97-0

Purity 97%+In StockPharmaceutical Standards
CAS No.191868-97-0
Molecular FormulaC16H13NO2
Molecular Weight251.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Methyl-5-phenyl-1H-indole-2-carboxylic acid CAS 191868-97-0 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-Methyl-5-phenyl-1H-indole-2-carboxylic acid.

3-Methyl-5-phenyl-1H-indole-2-carboxylic acid (CAS 191868-97-0) is a high-purity analytical reference standard with the molecular formula C16H13NO2 and a molecular weight of 251.28 g/mol.

3-Methyl-5-phenyl-1H-indole-2-carboxylic acid (C16H13NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 3-Methyl-5-phenyl-1H-indole-2-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 FormulaC16H13NO2
Molecular Weight251.28 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2011
Nitrogen Atoms1

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