Bis(3,4,6-trichloro-2-((isopentyloxy)carbonyl)phenyl) oxalate CAS 71527-73-6

Purity 97%+In StockPharmaceutical Standards
CAS No.71527-73-6
Molecular FormulaC26H24Cl6O8
Molecular Weight677.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Bis(3,4,6-trichloro-2-((isopentyloxy)carbonyl)phenyl) oxalate CAS 71527-73-6 chemical structure

Description

The molecular framework of Bis(3,4,6-trichloro-2-((isopentyloxy)carbonyl)phenyl) oxalate (C26H24Cl6O8) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, a polycyclic aromatic 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies Bis(3,4,6-trichloro-2-((isopentyloxy)carbonyl)phenyl) oxalate (CAS 71527-73-6), a certified reference material (molecular formula C26H24Cl6O8, MW 677.18 g/mol) for analytical method development and quality control.

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), Bis(3,4,6-trichloro-2-((isopentyloxy)carbonyl)phenyl) oxalate 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 FormulaC26H24Cl6O8
Molecular Weight677.18 g/mol
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentCl-containing

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