{1-phenyl-1h,4h,5h,6h-cyclopenta[c]pyrazol-3-yl}methanamine hydrochloride CAS 1193389-93-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1193389-93-3
Molecular FormulaC13H15N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

{1-phenyl-1h,4h,5h,6h-cyclopenta[c]pyrazol-3-yl}methanamine hydrochloride CAS 1193389-93-3 chemical structure

Description

Structurally, {1-phenyl-1h,4h,5h,6h-cyclopenta[c]pyrazol-3-yl}methanamine hydrochloride (C13H15N3HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine 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 249.74 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies {1-phenyl-1h,4h,5h,6h-cyclopenta[c]pyrazol-3-yl}methanamine hydrochloride (CAS 1193389-93-3), a certified reference material (molecular formula C13H15N3HCl, MW 249.74 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.

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 FormulaC13H15N3 HCl
Molecular Weight249.74 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 ContentCl-containing
Nitrogen Atoms3

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