Ethyl 5-amino-1-(4-butylphenyl)-1H-pyrazole-4-carboxylate CAS 1416340-07-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1416340-07-2
Molecular FormulaC16H21N3O2
Molecular Weight287.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-amino-1-(4-butylphenyl)-1H-pyrazole-4-carboxylate CAS 1416340-07-2 chemical structure

Description

As a certified reference material (CRM), Ethyl 5-amino-1-(4-butylphenyl)-1H-pyrazole-4-carboxylate 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.

CATO supplies Ethyl 5-amino-1-(4-butylphenyl)-1H-pyrazole-4-carboxylate (CAS 1416340-07-2), a certified reference material (molecular formula C16H21N3O2, MW 287.36 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, Ethyl 5-amino-1-(4-butylphenyl)-1H-pyrazole-4-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 287.36 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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

Physical & Chemical Properties

Molecular FormulaC16H21N3O2
Molecular Weight287.36 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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