1-chloro-2-iodo-5-methyl-3-nitrobenzene CAS 861367-57-9

Purity 97%+In StockPharmaceutical Standards
CAS No.861367-57-9
Molecular FormulaC7H5ClINO2
Molecular Weight297.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-chloro-2-iodo-5-methyl-3-nitrobenzene CAS 861367-57-9 chemical structure

Description

1-chloro-2-iodo-5-methyl-3-nitrobenzene (C7H5ClINO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/iodine substitution, an aromatic ring system. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 1-chloro-2-iodo-5-methyl-3-nitrobenzene (CAS 861367-57-9), a certified reference material (molecular formula C7H5ClINO2, MW 297.48 g/mol) for analytical method development and quality control.

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.

CATO manufactures 1-chloro-2-iodo-5-methyl-3-nitrobenzene 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 FormulaC7H5ClINO2
Molecular Weight297.48 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl/I-containing
Nitrogen Atoms1

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