Ethyl 5-amino-4-iodo-1-methyl-1H-pyrazole-3-carboxylate CAS 1379360-46-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1379360-46-9
Molecular FormulaC7H10IN3O2
Molecular Weight295.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-amino-4-iodo-1-methyl-1H-pyrazole-3-carboxylate CAS 1379360-46-9 chemical structure

Description

Ethyl 5-amino-4-iodo-1-methyl-1H-pyrazole-3-carboxylate (CAS 1379360-46-9), molecular formula C7H10IN3O2 and molecular weight 295.08 g/mol, is a CATO reference standard with documented purity and traceability.

Ethyl 5-amino-4-iodo-1-methyl-1H-pyrazole-3-carboxylate (C7H10IN3O2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 Ethyl 5-amino-4-iodo-1-methyl-1H-pyrazole-3-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 FormulaC7H10IN3O2
Molecular Weight295.08 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms3

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