16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303 CAS 16713-80-7

Purity 97%+In StockPharmaceutical Standards
CAS No.16713-80-7
Molecular FormulaC14H22O7
Molecular Weight302.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303 CAS 16713-80-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303.

CATO supplies 16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303 (CAS 16713-80-7), a certified reference material (molecular formula C14H22O7, MW 302.32 g/mol) for analytical method development and quality control.

The molecular framework of 16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303 (C14H22O7) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. 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).

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 16713-80-7 alpha-D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-, acetate 4-19-00-06106 (Beilstein Handbook Reference) 3-O-Acetyl-1,2,5,6-di-O-isopropylidene-alpha-D-glucofuranose 1,2:5,6-Bis-O-(1-methylethylidene)-alpha-D-glucofuranose acetate BRN 0033303 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 FormulaC14H22O7
Molecular Weight302.32 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961

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