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HS Code |
192954 |
| Name | 2-Chloro-3-Fluorotoluene |
| Cas Number | 204939-85-5 |
| Molecular Formula | C7H6ClF |
| Molecular Weight | 144.58 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 162-164 °C |
| Melting Point | -14 °C |
| Density | 1.25 g/cm3 |
| Refractive Index | 1.525 |
| Flash Point | 52 °C |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | CC1=C(C(=CC=C1)Cl)F |
| Purity | Typically ≥98% |
| Synonyms | 2-Chloro-3-fluoromethylbenzene |
| Storage Conditions | Store at room temperature, in a tightly closed container |
As an accredited 2-Chloro-3-Fluorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 2-Chloro-3-Fluorotoluene, tightly sealed, labeled with hazard warnings and chemical details. |
| Shipping | 2-Chloro-3-Fluorotoluene is typically shipped in sealed, chemical-resistant containers to prevent leaks or contamination. It should be packaged and labeled in accordance with local and international hazardous material transport regulations. The product must be handled with care, kept away from heat and ignition sources, and transported by approved carriers. |
| Storage | 2-Chloro-3-fluorotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and ensure proper chemical labeling. Avoid unnecessary handling; use spark-proof tools and explosion-proof equipment where necessary. |
Applications of 2-Chloro-3-Fluorotoluene in Industrial ManufacturingAs the primary manufacturer of 2-Chloro-3-Fluorotoluene, we supply this high-purity intermediate to specialized customers operating in several advanced chemical sectors. Our material supports process innovation and product reliability in downstream formulations, with controlled specifications to address individual requirements across regulated industries. Below, we outline the principal end-use scenarios documented in our commercial practice, including the defining technical and regulatory elements critical to B2B partners’ compliance, production, and quality management. 1. Pharmaceutical Intermediates: Synthesis of Fluorinated Active IngredientsMajor pharmaceutical companies use this compound in small-molecule synthesis, particularly where selective aryl halides are required as core scaffolds for cardiovascular or CNS APIs. Process chemists introduce it during early-stage Grignard or Suzuki coupling reactions to yield advanced building blocks, allowing precise placement of functional groups in patent-protected molecules. Its inclusion in regulated pharma manufacturing has set specific expectations for contaminant control, documentation, and downstream traceability. Industry compliance standards
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2. Agrochemical Synthesis: Advanced Herbicide and Fungicide IntermediatesAgrochemical manufacturers employ our compound as an aryl halide starting material for the construction of advanced pesticide molecules. It integrates into bromination or amination routes to achieve selective fluorinated aromatic rings indispensable in the synthesis of modern herbicides and fungicides. Precision in halogen balance and impurity suppression is strictly monitored as part of global regulatory alignment and field safety data requirements. Industry compliance standards
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3. Liquid Crystal Display (LCD) Material IntermediatesProducers of advanced liquid crystal materials integrate this specialty halogenated aromatic in the design of high-contrast LCD mixtures for consumer electronics. The aromatic ring’s substitution pattern confers controlled dielectric and optical properties required for thin-film transistor LCD performance. High-purity requirements and stringent process audits form core elements in qualifying our material for embedded electronics supply chains. Industry compliance standards
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4. Advanced Dyes and Pigment ManufacturingIndustrial dye-makers rely on the reactivity of this compound to construct specialty fluorinated aryl moieties for high-performance pigment intermediates. Through Regio-selective halogen exchange or coupling protocols, the compound enters into pigment backbone construction, delivering unique hues and improved lightfastness. Regulatory adherence, particularly concerning halogen content and impurity levels, remains central during both pigment and downstream textile or plastics certification. Industry compliance standards
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5. Aromatic Polymer Building BlocksProducers of specialty polymers incorporate this fluorinated aromatic intermediate into the backbone of high-performance materials such as polyarylene ethers and sulfone polymers. Its unique halogen substitution pattern introduces steric and electronic effects sought in polymers with enhanced chemical resistance and glass transition temperature. Careful control of raw material handling and compliance with polymer additive specificities is strictly required by downstream technical users. Industry compliance standards
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