6,8-Dimethyl-[1,2,4]triazolo[4,3-b]pyridazine CAS 18591-75-8

Purity 97%+In StockPharmaceutical Standards
CAS No.18591-75-8
Molecular FormulaC7H8N4
Molecular Weight148.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,8-Dimethyl-[1,2,4]triazolo[4,3-b]pyridazine CAS 18591-75-8 chemical structure

Description

The occurrence of 6,8-Dimethyl-[1,2,4]triazolo[4,3-b]pyridazine is closely related to a nitrile group, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 6,8-Dimethyl-[1,2,4]triazolo[4,3-b]pyridazine (CAS 18591-75-8), a certified reference material (molecular formula C7H8N4, MW 148.17 g/mol) for analytical method development and quality control.

The molecular framework of 6,8-Dimethyl-[1,2,4]triazolo[4,3-b]pyridazine (C7H8N4) is characterized by a nitrile group, an aromatic ring system. 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.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC7H8N4
Molecular Weight148.17 g/mol
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962
Nitrogen Atoms4

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