N-(3-Chloro-2-methylphenyl)-2-hydroxybenzamide CAS 75300-64-0

Purity 97%+In StockPharmaceutical Standards
CAS No.75300-64-0
Molecular FormulaC14H12ClNO2
Molecular Weight261.70 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Chloro-2-methylphenyl)-2-hydroxybenzamide CAS 75300-64-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 261.70 g/mol gives N-(3-Chloro-2-methylphenyl)-2-hydroxybenzamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-(3-Chloro-2-methylphenyl)-2-hydroxybenzamide (CAS 75300-64-0), a certified reference material (molecular formula C14H12ClNO2, MW 261.70 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, N-(3-Chloro-2-methylphenyl)-2-hydroxybenzamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 261.70 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

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 FormulaC14H12ClNO2
Molecular Weight261.70 g/mol
AppearancePale yellow to 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1978
Halogen ContentCl-containing
Nitrogen Atoms1

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