Cyclohexane-1,2,4,5-tetrayl tetraacetate CAS 92298-57-2

Purity 97%+In StockPharmaceutical Standards
CAS No.92298-57-2
Molecular FormulaC14H20O8
Molecular Weight316.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Cyclohexane-1,2,4,5-tetrayl tetraacetate CAS 92298-57-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 316.30 g/mol gives Cyclohexane-1,2,4,5-tetrayl tetraacetate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Cyclohexane-1,2,4,5-tetrayl tetraacetate (CAS 92298-57-2), a certified reference material (molecular formula C14H20O8, MW 316.30 g/mol) for analytical method development and quality control.

Cyclohexane-1,2,4,5-tetrayl tetraacetate (C14H20O8) 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).

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.

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 FormulaC14H20O8
Molecular Weight316.30 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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.)1983

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