PHenyl 3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-glucopyranoside CAS 120498-97-7

Purity 97%+In StockPharmaceutical Standards
CAS No.120498-97-7
Molecular FormulaC26H25NO10
Molecular Weight511.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

PHenyl 3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-glucopyranoside CAS 120498-97-7 chemical structure

Description

PHenyl 3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-glucopyranoside (C26H25NO10) contains a nitrogen-containing heterocyclic scaffold, an amide 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).

PHenyl 3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-glucopyranoside (CAS 120498-97-7), molecular formula C26H25NO10 and molecular weight 511.48 g/mol, is a CATO reference standard with documented purity and traceability.

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 PHenyl 3,4,6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-glucopyranoside 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 FormulaC26H25NO10
Molecular Weight511.48 g/mol
AppearancePale yellow to yellow crystalline powder
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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms1

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