Methyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylate CAS 130613-19-3

Purity 97%+In StockPharmaceutical Standards
CAS No.130613-19-3
Molecular FormulaC11H7Cl2NO3
Molecular Weight272.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylate CAS 130613-19-3 chemical structure

Description

CATO supplies Methyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylate (CAS 130613-19-3), a certified reference material (molecular formula C11H7Cl2NO3, MW 272.08 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylate (C11H7Cl2NO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H7Cl2NO3
Molecular Weight272.08 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentCl-containing
Nitrogen Atoms1

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