2,5-Furandione, polymer with 4,4'-(1-methylethylidene)bis[cyclohexanol] and 1,2-propanediol CAS 50821-50-6

Purity 97%+In StockPharmaceutical Standards
CAS No.50821-50-6
Molecular FormulaC15H28O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,5-Furandione, polymer with 4,4'-(1-methylethylidene)bis[cyclohexanol] and 1,2-propanediol CAS 50821-50-6 chemical structure

Description

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.

2,5-Furandione, polymer with 4,4'-(1-methylethylidene)bis[cyclohexanol] and 1,2-propanediol (CAS 50821-50-6), molecular formula C15H28O2C4H2O3C3H8O2 and molecular weight 414.54 g/mol, is a CATO reference standard with documented purity and traceability.

2,5-Furandione, polymer with 4,4'-(1-methylethylidene)bis[cyclohexanol] and 1,2-propanediol (C15H28O2C4H2O3C3H8O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. 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).

CATO manufactures 2,5-Furandione, polymer with 4,4'-(1-methylethylidene)bis[cyclohexanol] and 1,2-propanediol 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 FormulaC15H28O2 C4H2O3 C3H8O2
Molecular Weight414.54 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971

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