N-(6-Chloropyridazin-3-yl)-2-(3-pentadecylphenoxy)butanamide CAS 850195-52-7

Purity 97%+In StockPharmaceutical Standards
CAS No.850195-52-7
Molecular FormulaC29H44ClN3O2
Molecular Weight502.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(6-Chloropyridazin-3-yl)-2-(3-pentadecylphenoxy)butanamide CAS 850195-52-7 chemical structure

Description

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 supplies N-(6-Chloropyridazin-3-yl)-2-(3-pentadecylphenoxy)butanamide (CAS 850195-52-7), a certified reference material (molecular formula C29H44ClN3O2, MW 502.13 g/mol) for analytical method development and quality control.

The molecular framework of N-(6-Chloropyridazin-3-yl)-2-(3-pentadecylphenoxy)butanamide (C29H44ClN3O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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. 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 manufactures N-(6-Chloropyridazin-3-yl)-2-(3-pentadecylphenoxy)butanamide 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 FormulaC29H44ClN3O2
Molecular Weight502.13 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms3

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