Cyclohexane-1,2,3,4,5,6-hexaone octahydrate CAS 7255-28-9

Purity 97%+In StockPharmaceutical Standards
CAS No.7255-28-9
Molecular FormulaC6O6
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Cyclohexane-1,2,3,4,5,6-hexaone octahydrate CAS 7255-28-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 186.08 g/mol gives Cyclohexane-1,2,3,4,5,6-hexaone octahydrate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Cyclohexane-1,2,3,4,5,6-hexaone octahydrate (CAS 7255-28-9), molecular formula C6O6H2O and molecular weight 186.08 g/mol, is a CATO reference standard with documented purity and traceability.

Cyclohexane-1,2,3,4,5,6-hexaone octahydrate (C6O6H2O) contains a carbohydrate-derived structure. 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).

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 Cyclohexane-1,2,3,4,5,6-hexaone octahydrate 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 FormulaC6O6 8*H2O
Molecular Weight186.08 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959

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