6-Iodo-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid CAS 40107-06-0

Purity 97%+In StockPharmaceutical Standards
CAS No.40107-06-0
Molecular FormulaC10H6INO3
Molecular Weight315.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Iodo-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid CAS 40107-06-0 chemical structure

Description

6-Iodo-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid (CAS 40107-06-0), molecular formula C10H6INO3 and molecular weight 315.06 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 6-Iodo-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid (C10H6INO3) 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 315.06 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), 6-Iodo-4-oxo-1,4-dihydro-3-quinoline-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 FormulaC10H6INO3
Molecular Weight315.06 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.)1968
Halogen ContentI-containing
Nitrogen Atoms1

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