(1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate CAS 33989-10-5

Purity 97%+In StockPharmaceutical Standards
CAS No.33989-10-5
Molecular FormulaC48H38CuN2P2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate CAS 33989-10-5 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a phosphonate group, a hydroxyl group, an ether linkage, (1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 830.34 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies (1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate (CAS 33989-10-5), a certified reference material (molecular formula C48H38CuN2P2NO3, MW 830.34 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.

CATO manufactures (1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate 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 FormulaC48H38CuN2P2 NO3
Molecular Weight830.34 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)31.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1966
Nitrogen Atoms3

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