Ethyl 6-oxo-6-(3-thienyl)hexanoate CAS 333355-34-3

Purity 97%+In StockPharmaceutical Standards
CAS No.333355-34-3
Molecular FormulaC12H16O3S
Molecular Weight240.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 6-oxo-6-(3-thienyl)hexanoate CAS 333355-34-3 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 Ethyl 6-oxo-6-(3-thienyl)hexanoate.

CATO supplies Ethyl 6-oxo-6-(3-thienyl)hexanoate (CAS 333355-34-3), a certified reference material (molecular formula C12H16O3S, MW 240.32 g/mol) for analytical method development and quality control.

Ethyl 6-oxo-6-(3-thienyl)hexanoate (C12H16O3S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC12H16O3S
Molecular Weight240.32 g/mol
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.)2025
Sulfur Atoms1

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