1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene CAS 172606-28-9

Purity 97%+In StockPharmaceutical Standards
CAS No.172606-28-9
Molecular FormulaC22H22N8
Molecular Weight398.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene CAS 172606-28-9 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene.

CATO supplies 1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene (CAS 172606-28-9), a certified reference material (molecular formula C22H22N8, MW 398.46 g/mol) for analytical method development and quality control.

The molecular framework of 1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene (C22H22N8) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 1,2,4,5-Tetrakis((1H-pyrazol-1-yl)methyl)benzene 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 FormulaC22H22N8
Molecular Weight398.46 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.)2006
Nitrogen Atoms8

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