2-3-4-6-Tetra-O-acetyl-D-galactopyranose CAS 47339-09-3

Purity 97%+In StockPharmaceutical Standards
CAS No.47339-09-3
Molecular FormulaC14H20O10
Molecular Weight348.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-3-4-6-Tetra-O-acetyl-D-galactopyranose CAS 47339-09-3 chemical structure

Description

2-3-4-6-Tetra-O-acetyl-D-galactopyranose (C14H20O10) 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 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 2-3-4-6-Tetra-O-acetyl-D-galactopyranose (CAS 47339-09-3), a certified reference material (molecular formula C14H20O10, MW 348.30 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.

As a certified reference material (CRM), 2-3-4-6-Tetra-O-acetyl-D-galactopyranose 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 FormulaC14H20O10
Molecular Weight348.30 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.)1970

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