4-Hydroxy-3-(1-hydroxypentyl)benzoic acid CAS 17243-33-3

Purity 97%+In StockPharmaceutical Standards
CAS No.17243-33-3
Molecular FormulaC12H16O4
Molecular Weight224.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Hydroxy-3-(1-hydroxypentyl)benzoic acid CAS 17243-33-3 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 4-Hydroxy-3-(1-hydroxypentyl)benzoic acid.

CATO supplies 4-Hydroxy-3-(1-hydroxypentyl)benzoic acid (CAS 17243-33-3), a certified reference material (molecular formula C12H16O4, MW 224.25 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H16O4, 4-Hydroxy-3-(1-hydroxypentyl)benzoic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 224.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC12H16O4
Molecular Weight224.25 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961

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