Diethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate CAS 58381-22-9

Purity 97%+In StockPharmaceutical Standards
CAS No.58381-22-9
Molecular FormulaC9H11N3O6
Molecular Weight257.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Diethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate CAS 58381-22-9 chemical structure

Description

CATO manufactures Diethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Diethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate (CAS 58381-22-9) is a high-purity analytical reference standard with the molecular formula C9H11N3O6 and a molecular weight of 257.20 g/mol.

Based on its molecular formula C9H11N3O6, Diethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 257.20 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC9H11N3O6
Molecular Weight257.20 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Nitrogen Atoms3

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