(7-Carboxyheptyl)triphenylphosphonium bromide CAS 52956-93-1

Purity 97%+In StockPharmaceutical Standards
CAS No.52956-93-1
Molecular FormulaC26H30O2P
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(7-Carboxyheptyl)triphenylphosphonium bromide CAS 52956-93-1 chemical structure

Description

Based on its molecular formula C26H30O2PBr, (7-Carboxyheptyl)triphenylphosphonium bromide contains a steroid core, organophosphorus functionality, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 485.40 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

(7-Carboxyheptyl)triphenylphosphonium bromide (CAS 52956-93-1), molecular formula C26H30O2PBr and molecular weight 485.40 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 (7-Carboxyheptyl)triphenylphosphonium bromide 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 FormulaC26H30O2P Br
Molecular Weight485.40 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)11.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Halogen ContentBr-containing

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