n-(1-(2,5-Difluorophenyl)ethyl)-1-methyl-1h-pyrazol-3-amine CAS 1178664-94-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1178664-94-2
Molecular FormulaC12H13F2N3
Molecular Weight237.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(1-(2,5-Difluorophenyl)ethyl)-1-methyl-1h-pyrazol-3-amine CAS 1178664-94-2 chemical structure

Description

Structurally, n-(1-(2,5-Difluorophenyl)ethyl)-1-methyl-1h-pyrazol-3-amine (C12H13F2N3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 237.25 g/mol, it falls into the medium-molecular-weight range. 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 supplies n-(1-(2,5-Difluorophenyl)ethyl)-1-methyl-1h-pyrazol-3-amine (CAS 1178664-94-2), a certified reference material (molecular formula C12H13F2N3, MW 237.25 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), n-(1-(2,5-Difluorophenyl)ethyl)-1-methyl-1h-pyrazol-3-amine 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.

Physical & Chemical Properties

Molecular FormulaC12H13F2N3
Molecular Weight237.25 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3

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