3-Methyl-4-nitro-1-propyl-1H-pyrazole-5-carboxamide CAS 89239-75-8

Purity 97%+In StockPharmaceutical Standards
CAS No.89239-75-8
Molecular FormulaC8H12N4O3
Molecular Weight212.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Methyl-4-nitro-1-propyl-1H-pyrazole-5-carboxamide CAS 89239-75-8 chemical structure

Description

3-Methyl-4-nitro-1-propyl-1H-pyrazole-5-carboxamide (C8H12N4O3) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

3-Methyl-4-nitro-1-propyl-1H-pyrazole-5-carboxamide (CAS 89239-75-8) is a high-purity analytical reference standard with the molecular formula C8H12N4O3 and a molecular weight of 212.21 g/mol.

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), 3-Methyl-4-nitro-1-propyl-1H-pyrazole-5-carboxamide 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 FormulaC8H12N4O3
Molecular Weight212.21 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms4

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