Methyl 3-hydroxy-5-(phenylthio)thiophene-2-carboxylate CAS 104386-71-2

Purity 97%+In StockPharmaceutical Standards
CAS No.104386-71-2
Molecular FormulaC12H10O3S2
Molecular Weight266.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-hydroxy-5-(phenylthio)thiophene-2-carboxylate CAS 104386-71-2 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 Methyl 3-hydroxy-5-(phenylthio)thiophene-2-carboxylate.

Methyl 3-hydroxy-5-(phenylthio)thiophene-2-carboxylate (CAS 104386-71-2), molecular formula C12H10O3S2 and molecular weight 266.34 g/mol, is a CATO reference standard with documented purity and traceability.

Methyl 3-hydroxy-5-(phenylthio)thiophene-2-carboxylate (C12H10O3S2) 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 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 FormulaC12H10O3S2
Molecular Weight266.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Sulfur Atoms2

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Why CATO?