263764-83-6 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)- CAS 263764-83-6

Purity 97%+In StockPharmaceutical Standards
CAS No.263764-83-6
Molecular FormulaC9H12O4
Molecular Weight184.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

263764-83-6
7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)- CAS 263764-83-6 chemical structure

Description

263764-83-6 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)- (C9H12O4) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, 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).

263764-83-6 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)- (CAS 263764-83-6) is a high-purity analytical reference standard with the molecular formula C9H12O4 and a molecular weight of 184.19 g/mol.

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.

As a certified reference material (CRM), 263764-83-6 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)- meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC9H12O4
Molecular Weight184.19 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025

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