1-Methyl-3,4-dihydronaphthalene-2-carboxylic acid CAS 6279-88-5

Purity 97%+In StockPharmaceutical Standards
CAS No.6279-88-5
Molecular FormulaC12H12O2
Molecular Weight188.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-3,4-dihydronaphthalene-2-carboxylic acid CAS 6279-88-5 chemical structure

Description

The molecular framework of 1-Methyl-3,4-dihydronaphthalene-2-carboxylic acid (C12H12O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. 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).

1-Methyl-3,4-dihydronaphthalene-2-carboxylic acid (CAS 6279-88-5) is a high-purity analytical reference standard with the molecular formula C12H12O2 and a molecular weight of 188.22 g/mol.

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 1-Methyl-3,4-dihydronaphthalene-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 FormulaC12H12O2
Molecular Weight188.22 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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