Isopentyl 3-amino-1H-1,2,4-triazole-5-carboxylate CAS 91163-35-8

Purity 97%+In StockPharmaceutical Standards
CAS No.91163-35-8
Molecular FormulaC8H14N4O2
Molecular Weight198.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Isopentyl 3-amino-1H-1,2,4-triazole-5-carboxylate CAS 91163-35-8 chemical structure

Description

Based on its molecular formula C8H14N4O2, Isopentyl 3-amino-1H-1,2,4-triazole-5-carboxylate 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 198.22 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

CATO supplies Isopentyl 3-amino-1H-1,2,4-triazole-5-carboxylate (CAS 91163-35-8), a certified reference material (molecular formula C8H14N4O2, MW 198.22 g/mol) for analytical method development and quality control.

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

CATO manufactures Isopentyl 3-amino-1H-1,2,4-triazole-5-carboxylate 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 FormulaC8H14N4O2
Molecular Weight198.22 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 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1983
Nitrogen Atoms4

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