Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside CAS 108032-93-5

Purity 97%+In StockPharmaceutical Standards
CAS No.108032-93-5
Molecular FormulaC20H24O9S
Molecular Weight440.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside CAS 108032-93-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 440.46 g/mol gives Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside (CAS 108032-93-5), a certified reference material (molecular formula C20H24O9S, MW 440.46 g/mol) for analytical method development and quality control.

Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside (C20H24O9S) contains a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage. 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.

As a certified reference material (CRM), Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside 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 FormulaC20H24O9S
Molecular Weight440.46 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Sulfur Atoms1

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