(1,2-Phenylenebis(methylene))bis(triphenylphosphonium) CAS 47861-42-7

Purity 97%+In StockPharmaceutical Standards
CAS No.47861-42-7
Molecular FormulaC44H38P2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1,2-Phenylenebis(methylene))bis(triphenylphosphonium) CAS 47861-42-7 chemical structure

Description

The occurrence of (1,2-Phenylenebis(methylene))bis(triphenylphosphonium) is closely related to organophosphorus functionality, chlorine substitution, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(1,2-Phenylenebis(methylene))bis(triphenylphosphonium) (CAS 47861-42-7), molecular formula C44H38P2Cl and molecular weight 664.19 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to organophosphorus functionality, chlorine substitution, a polycyclic aromatic system, (1,2-Phenylenebis(methylene))bis(triphenylphosphonium) is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 664.19 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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), (1,2-Phenylenebis(methylene))bis(triphenylphosphonium) 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 FormulaC44H38P2 2*Cl
Molecular Weight664.19 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)25.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1970
Halogen ContentCl-containing

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Why CATO?