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HS Code |
393775 |
| Product Name | 1-Chloro-2-Iodobenzene |
| Molecular Formula | C6H4ClI |
| Molecular Weight | 238.46 g/mol |
| Cas Number | 615-41-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 245-247 °C |
| Melting Point | 6-7 °C |
| Density | 1.844 g/cm³ at 25 °C |
| Refractive Index | 1.656 |
| Purity | Typically ≥98% |
| Synonyms | 2-Chloroiodobenzene |
| Smiles | ClC1=CC=CC=C1I |
| Inchi | InChI=1S/C6H4ClI/c7-5-3-1-2-4-6(5)8 |
| Solubility | Insoluble in water; soluble in organic solvents |
| Flash Point | 110 °C |
As an accredited 1-Chloro-2-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, with tamper-evident cap and hazard labeling for 1-Chloro-2-Iodobenzene, including safety warnings. |
| Shipping | 1-Chloro-2-iodobenzene is shipped in tightly sealed, chemical-resistant containers, compliant with hazardous materials regulations. The package bears proper labeling for flammable organic compounds and halogenated substances. It is transported under cool, dry conditions, protected from sunlight and incompatible materials, and handled by trained personnel following all relevant safety guidelines and legal requirements. |
| Storage | 1-Chloro-2-iodobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature and avoid exposure to moisture. Properly label the container and keep it away from heat sources, sparks, and open flames. Use secondary containment to prevent spills or leaks. |
Applications of 1-Chloro-2-Iodobenzene in Industrial Manufacturing1-Chloro-2-Iodobenzene serves as a critical intermediate in the production of specialty chemicals and high-value compounds across pharmaceutical, agrochemical, and material science sectors. As a manufacturer, we ensure the product’s quality allows for consistent downstream transformation in multiple complex manufacturing environments. 1. Pharmaceutical Intermediate SynthesisPharmaceutical process engineers apply 1-Chloro-2-Iodobenzene in the synthesis of active pharmaceutical ingredient (API) precursors, especially for molecules containing diaryl or heterocyclic motifs. It enters cross-coupling reactions (Suzuki, Ullmann, or Buchwald–Hartwig) due to the ortho-halogen functionality, supporting site-specific aromatic substitutions. Regulatory documentation mandates full traceability and impurity control at each batch, aligning with strict multinational guidelines applicable to regulated markets. Industry compliance standards
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2. Agrochemical Active SynthesisR&D and manufacturing facilities for crop protection chemicals deploy 1-Chloro-2-Iodobenzene in multi-step synthesis of select pyridine and triazole derivatives. The halogen positioning supports regioselective coupling, critical in structural optimization of fungicides and selective herbicides. Product stewardship and batch traceability are essential due to regulatory restrictions on halogenated byproducts and waste streams. Industry compliance standards
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3. Advanced Material and Liquid Crystal PrecursorElectronics and specialty materials manufacturers utilize 1-Chloro-2-Iodobenzene as a starting material for designer biphenyl or polyaromatic compounds. These compounds enable optical, electronic, or display functions in advanced polymers, especially liquid crystal display (LCD) and organic semiconductor R&D. Consistent halogen purity and absence of elemental contamination is required to achieve target anisotropy and electro-optical properties for downstream integration. Industry compliance standards
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4. Dye and Pigment Intermediate ProductionSpecialty pigment and dye facilities employ 1-Chloro-2-Iodobenzene for synthesizing halogenated aromatic intermediates, which serve as key chromophore backbones for high-end colorants. Batch-to-batch QC ensures spectral purity, while process operators control inclusion in sequences such as Sandmeyer-type transformations, which lead to unique color properties not achievable by less reactive halogenated benzenes. Industry compliance standards
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