1,2:3,4-Di-O-cyclohexylidene-5-O-methyl-L-chiro-inositol 6848-53-9 CTK8F2865 CAS 6848-53-9

Purity 97%+In StockPharmaceutical Standards
CAS No.6848-53-9
Molecular FormulaC19H30O6
Molecular Weight354.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2:3,4-Di-O-cyclohexylidene-5-O-methyl-L-chiro-inositol 6848-53-9 CTK8F2865 CAS 6848-53-9 chemical structure

Description

The molecular framework of 1,2:3,4-Di-O-cyclohexylidene-5-O-methyl-L-chiro-inositol 6848-53-9 CTK8F2865 (C19H30O6) is characterized by a steroid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

CATO supplies 1,2:3,4-Di-O-cyclohexylidene-5-O-methyl-L-chiro-inositol 6848-53-9 CTK8F2865 (CAS 6848-53-9), a certified reference material (molecular formula C19H30O6, MW 354.44 g/mol) for analytical method development and quality control.

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 FormulaC19H30O6
Molecular Weight354.44 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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