6-(2-Methoxyphenyl)-2-(2-methylbenzyl)pyridazin-3(2H)-one CAS 922864-32-2

Purity 97%+In StockPharmaceutical Standards
CAS No.922864-32-2
Molecular FormulaC19H18N2O2
Molecular Weight306.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(2-Methoxyphenyl)-2-(2-methylbenzyl)pyridazin-3(2H)-one CAS 922864-32-2 chemical structure

Description

As a certified reference material (CRM), 6-(2-Methoxyphenyl)-2-(2-methylbenzyl)pyridazin-3(2H)-one 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.

CATO supplies 6-(2-Methoxyphenyl)-2-(2-methylbenzyl)pyridazin-3(2H)-one (CAS 922864-32-2), a certified reference material (molecular formula C19H18N2O2, MW 306.36 g/mol) for analytical method development and quality control.

Structurally, 6-(2-Methoxyphenyl)-2-(2-methylbenzyl)pyridazin-3(2H)-one (C19H18N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 306.36 g/mol, it falls into the moderately-high-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC19H18N2O2
Molecular Weight306.36 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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