n-((1-Methyl-1h-pyrazol-4-yl)methyl)-1-phenylethan-1-amine CAS 1152861-75-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1152861-75-0
Molecular FormulaC13H17N3
Molecular Weight215.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-((1-Methyl-1h-pyrazol-4-yl)methyl)-1-phenylethan-1-amine CAS 1152861-75-0 chemical structure

Description

The occurrence of n-((1-Methyl-1h-pyrazol-4-yl)methyl)-1-phenylethan-1-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

n-((1-Methyl-1h-pyrazol-4-yl)methyl)-1-phenylethan-1-amine (CAS 1152861-75-0), molecular formula C13H17N3 and molecular weight 215.29 g/mol, is a CATO reference standard with documented purity and traceability.

n-((1-Methyl-1h-pyrazol-4-yl)methyl)-1-phenylethan-1-amine (C13H17N3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC13H17N3
Molecular Weight215.29 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms3

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