3-Iodo-4-nitro-1H-indazole-6-carboxylic acid CAS 885521-14-2

Purity 97%+In StockPharmaceutical Standards
CAS No.885521-14-2
Molecular FormulaC8H4IN3O4
Molecular Weight333.04 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Iodo-4-nitro-1H-indazole-6-carboxylic acid CAS 885521-14-2 chemical structure

Description

CATO supplies 3-Iodo-4-nitro-1H-indazole-6-carboxylic acid (CAS 885521-14-2), a certified reference material (molecular formula C8H4IN3O4, MW 333.04 g/mol) for analytical method development and quality control.

Structurally, 3-Iodo-4-nitro-1H-indazole-6-carboxylic acid (C8H4IN3O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 333.04 g/mol, it falls into the moderately-high-molecular-weight range. 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).

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.

As a certified reference material (CRM), 3-Iodo-4-nitro-1H-indazole-6-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC8H4IN3O4
Molecular Weight333.04 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 methanol, ethanol, DMSO
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.)1987
Halogen ContentI-containing
Nitrogen Atoms3

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