4-Iodo-3-(4-nitrophenyl)-1H-pyrazole CAS 1339261-01-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1339261-01-6
Molecular FormulaC9H6IN3O2
Molecular Weight315.07 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Iodo-3-(4-nitrophenyl)-1H-pyrazole CAS 1339261-01-6 chemical structure

Description

CATO manufactures 4-Iodo-3-(4-nitrophenyl)-1H-pyrazole 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.

4-Iodo-3-(4-nitrophenyl)-1H-pyrazole (CAS 1339261-01-6), molecular formula C9H6IN3O2 and molecular weight 315.07 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-Iodo-3-(4-nitrophenyl)-1H-pyrazole (C9H6IN3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. 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).

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 FormulaC9H6IN3O2
Molecular Weight315.07 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms3

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