Ethylene Terephthalate Cyclic Dimer CAS 24388-68-9

Purity 97%+In StockPharmaceutical Standards
CAS No.24388-68-9
Molecular FormulaC20H16O8
Molecular Weight384.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethylene Terephthalate Cyclic Dimer CAS 24388-68-9 chemical structure

Description

The occurrence of Ethylene Terephthalate Cyclic Dimer is closely related to a flavonoid core, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Ethylene Terephthalate Cyclic Dimer (CAS 24388-68-9), a certified reference material (molecular formula C20H16O8, MW 384.34 g/mol) for analytical method development and quality control.

The molecular framework of Ethylene Terephthalate Cyclic Dimer (C20H16O8) is characterized by a flavonoid core, a hydroxyl group, an ether linkage. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Ethylene Terephthalate Cyclic Dimer 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 FormulaC20H16O8
Molecular Weight384.34 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, 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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963

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