Hexane-1,6-diylbis((3-methylbut-2-en-1-yl)diphenylphosphonium) chloride CAS 81194-93-6

Purity 97%+In StockPharmaceutical Standards
CAS No.81194-93-6
Molecular FormulaC40H50P2
Molecular Weight592.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Hexane-1,6-diylbis((3-methylbut-2-en-1-yl)diphenylphosphonium) chloride CAS 81194-93-6 chemical structure

Description

The molecular framework of Hexane-1,6-diylbis((3-methylbut-2-en-1-yl)diphenylphosphonium) chloride (C40H50P2) is characterized by organophosphorus functionality, a polycyclic aromatic system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies Hexane-1,6-diylbis((3-methylbut-2-en-1-yl)diphenylphosphonium) chloride (CAS 81194-93-6), a certified reference material (molecular formula C40H50P2, MW 592.77 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), Hexane-1,6-diylbis((3-methylbut-2-en-1-yl)diphenylphosphonium) chloride 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 FormulaC40H50P2
Molecular Weight592.77 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980

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