4-Hydroxy-8-thioxocyclohepta[c][1,2]oxathiol-3(8H)-one CAS 89550-93-6

Purity 97%+In StockPharmaceutical Standards
CAS No.89550-93-6
Molecular FormulaC8H4O3S2
Molecular Weight212.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Hydroxy-8-thioxocyclohepta[c][1,2]oxathiol-3(8H)-one CAS 89550-93-6 chemical structure

Description

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 4-Hydroxy-8-thioxocyclohepta[c][1,2]oxathiol-3(8H)-one is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 212.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

4-Hydroxy-8-thioxocyclohepta[c][1,2]oxathiol-3(8H)-one (CAS 89550-93-6), molecular formula C8H4O3S2 and molecular weight 212.25 g/mol, is a CATO reference standard with documented purity and traceability.

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.

CATO manufactures 4-Hydroxy-8-thioxocyclohepta[c][1,2]oxathiol-3(8H)-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H4O3S2
Molecular Weight212.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Sulfur Atoms2

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