4-(6-Chloro-pyridazin-3-ylmethyl)-1-isopropyl-azepane CAS 1361114-45-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1361114-45-5
Molecular FormulaC14H22ClN3
Molecular Weight267.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(6-Chloro-pyridazin-3-ylmethyl)-1-isopropyl-azepane CAS 1361114-45-5 chemical structure

Description

CATO supplies 4-(6-Chloro-pyridazin-3-ylmethyl)-1-isopropyl-azepane (CAS 1361114-45-5), a certified reference material (molecular formula C14H22ClN3, MW 267.80 g/mol) for analytical method development and quality control.

The molecular framework of 4-(6-Chloro-pyridazin-3-ylmethyl)-1-isopropyl-azepane (C14H22ClN3) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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.

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 4-(6-Chloro-pyridazin-3-ylmethyl)-1-isopropyl-azepane 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 FormulaC14H22ClN3
Molecular Weight267.80 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms3

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