n-(2-Aminoethyl)-1-methyl-1h-pyrazole-5-carboxamide CAS 442870-29-3

Purity 97%+In StockPharmaceutical Standards
CAS No.442870-29-3
Molecular FormulaC7H12N4O
Molecular Weight168.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(2-Aminoethyl)-1-methyl-1h-pyrazole-5-carboxamide CAS 442870-29-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 168.20 g/mol gives n-(2-Aminoethyl)-1-methyl-1h-pyrazole-5-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

n-(2-Aminoethyl)-1-methyl-1h-pyrazole-5-carboxamide (CAS 442870-29-3) is a high-purity analytical reference standard with the molecular formula C7H12N4O and a molecular weight of 168.20 g/mol.

Based on its molecular formula C7H12N4O, n-(2-Aminoethyl)-1-methyl-1h-pyrazole-5-carboxamide contains an amide group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 168.20 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), n-(2-Aminoethyl)-1-methyl-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 FormulaC7H12N4O
Molecular Weight168.20 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms4

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