tert-Butyl (5-formyl-1-methyl-1H-pyrazol-4-yl)carbamate CAS 796845-65-3

Purity 97%+In StockPharmaceutical Standards
CAS No.796845-65-3
Molecular FormulaC10H15N3O3
Molecular Weight225.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (5-formyl-1-methyl-1H-pyrazol-4-yl)carbamate CAS 796845-65-3 chemical structure

Description

The molecular framework of tert-Butyl (5-formyl-1-methyl-1H-pyrazol-4-yl)carbamate (C10H15N3O3) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

tert-Butyl (5-formyl-1-methyl-1H-pyrazol-4-yl)carbamate (CAS 796845-65-3) is a high-purity analytical reference standard with the molecular formula C10H15N3O3 and a molecular weight of 225.24 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.

CATO manufactures tert-Butyl (5-formyl-1-methyl-1H-pyrazol-4-yl)carbamate 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.

Physical & Chemical Properties

Molecular FormulaC10H15N3O3
Molecular Weight225.24 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.)1986
Nitrogen Atoms3

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