Methyl 4-iodo-1H-pyrazole-3-carboxylate CAS 136944-79-1

Purity 97%+In StockPharmaceutical Standards
CAS No.136944-79-1
Molecular FormulaC5H5IN2O2
Molecular Weight252.01 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-iodo-1H-pyrazole-3-carboxylate CAS 136944-79-1 chemical structure

Description

Methyl 4-iodo-1H-pyrazole-3-carboxylate (CAS 136944-79-1) is a high-purity analytical reference standard with the molecular formula C5H5IN2O2 and a molecular weight of 252.01 g/mol.

Owing to an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, Methyl 4-iodo-1H-pyrazole-3-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 252.01 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 Methyl 4-iodo-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 FormulaC5H5IN2O2
Molecular Weight252.01 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
CAS Registry Year (est.)1996
Halogen ContentI-containing
Nitrogen Atoms2

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