[1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine CAS 1569868-34-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1569868-34-3
Molecular FormulaC24H22N4
Molecular Weight366.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine CAS 1569868-34-3 chemical structure

Description

The occurrence of [1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

[1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine (CAS 1569868-34-3) is a high-purity analytical reference standard with the molecular formula C24H22N4 and a molecular weight of 366.46 g/mol.

[1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine (C24H22N4) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 [1,1':4',1'':4'',1'''-Quaterphenyl]-3,3''',5,5'''-tetraamine 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 FormulaC24H22N4
Molecular Weight366.46 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms4

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