4'-Hydroxy-2-methyl-[1,1'-biphenyl]-3-carboxylic acid CAS 1261993-26-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1261993-26-3
Molecular FormulaC14H12O3
Molecular Weight228.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4'-Hydroxy-2-methyl-[1,1'-biphenyl]-3-carboxylic acid CAS 1261993-26-3 chemical structure

Description

Based on its molecular formula C14H12O3, 4'-Hydroxy-2-methyl-[1,1'-biphenyl]-3-carboxylic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 228.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

4'-Hydroxy-2-methyl-[1,1'-biphenyl]-3-carboxylic acid (CAS 1261993-26-3), molecular formula C14H12O3 and molecular weight 228.24 g/mol, is a CATO reference standard with documented purity and traceability.

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 4'-Hydroxy-2-methyl-[1,1'-biphenyl]-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 FormulaC14H12O3
Molecular Weight228.24 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990

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