4-bromo-3-methyl-1-phenyl-1H-pyrazol-5-amine hydrobromide CAS 1955515-61-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1955515-61-3
Molecular FormulaC10H10BrN3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-bromo-3-methyl-1-phenyl-1H-pyrazol-5-amine hydrobromide CAS 1955515-61-3 chemical structure

Description

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 supplies 4-bromo-3-methyl-1-phenyl-1H-pyrazol-5-amine hydrobromide (CAS 1955515-61-3), a certified reference material (molecular formula C10H10BrN3HBr, MW 333.03 g/mol) for analytical method development and quality control.

Structurally, 4-bromo-3-methyl-1-phenyl-1H-pyrazol-5-amine hydrobromide (C10H10BrN3HBr) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 333.03 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC10H10BrN3 HBr
Molecular Weight333.03 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentBr-containing
Nitrogen Atoms3

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