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HS Code |
346166 |
| Cas Number | 460-36-2 |
| Molecular Formula | C2Cl2F2 |
| Molar Mass | 133.93 g/mol |
| Appearance | Colorless gas |
| Boiling Point | 6.3°C |
| Melting Point | -130°C |
| Density | 1.42 g/cm³ (at 0°C, liquid) |
| Solubility In Water | Negligible |
| Vapor Pressure | 2.07 bar (at 20°C) |
| Refractive Index | 1.319 (at 20°C, liquid) |
| Odor | Sweet, ether-like |
| Stability | Stable under recommended storage conditions |
As an accredited 1,2-Dichloro-1,2-Difluoroethylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A sturdy 500 mL amber glass bottle with a secure screw cap, labeled “1,2-Dichloro-1,2-Difluoroethylene, 99%.” |
| Shipping | 1,2-Dichloro-1,2-difluoroethylene is shipped as a compressed, liquefied gas in high-pressure, sealed cylinders. It is classified as a hazardous material (UN 1957, Class 2.1, Flammable Gas) and must be transported according to international regulations, ensuring proper labeling, documentation, and handling to prevent leaks, fire, or exposure during transit. |
| Storage | 1,2-Dichloro-1,2-difluoroethylene should be stored in tightly closed, clearly labeled containers in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and incompatible materials such as strong oxidizers. It should be kept away from sources of ignition, and storage areas should be equipped to contain leaks or spills. Proper safety signage and access restrictions are recommended. |
Applications of 1,2-Dichloro-1,2-Difluoroethylene in Industrial Manufacturing1,2-Dichloro-1,2-Difluoroethylene serves a defined role as an intermediate and specialty monomer in several advanced chemical sectors. The below sections give specific, real-world application groupings, each with detailed processing considerations. 1. Fluoropolymer and Fluoroelastomer ManufacturingProducers of fluorinated polymers use 1,2-dichloro-1,2-difluoroethylene as a functional comonomer during emulsion or suspension polymerization processes. The compound's dual halogenation supports targeted modification of polymer chain architecture to drive chemical and thermal resistance in finished products. Dosing occurs during the monomer feed stage, requiring rigorous ratio control to achieve specific end-use mechanical properties. Final fluoroelastomer grades meet regulatory requirements for applications involving high-temperature gaskets, hoses, and linings exposed to aggressive chemicals and fuels. Industry compliance standards
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2. Specialty Solvent SynthesisChemical plants synthesize targeted low-permittivity solvents by chlorination or fluorination pathways that employ 1,2-dichloro-1,2-difluoroethylene as a controlled feedstock. Its defined reactivity profile allows for formation of designer molecules with unique properties for microelectronics cleaning or precision degreasing. The starting material's purity and reaction progress are strictly controlled under batch or continuous conditions, and all solvent products undergo detailed residual halogen analysis to align with electronics industry requirements. Industry compliance standards
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3. Refrigerant Intermediate for Hydrofluoroolefin (HFO) ProductionKey refrigerant manufacturers utilize 1,2-dichloro-1,2-difluoroethylene as a precursor in catalytic rearrangement and hydrodechlorination steps to synthesize next-generation HFOs. The controlled introduction during these multistep syntheses ensures high atom economy and conversion to desired low-global warming potential refrigerants, matching the latest climate directives. These intermediates demand specialized handling to prevent hydrolysis and minimize side reactions, directly contributing to certified low-emission refrigerant blends via closed-loop purification. Industry compliance standards
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4. Precursors for Pharmaceutical Fluorinated Building BlocksPharmaceutical synthesis groups employ 1,2-dichloro-1,2-difluoroethylene to prepare advanced intermediates for fluorine-containing active pharmaceutical ingredients (APIs). Its defined reactivity under cross-coupling and addition protocols enables chemoselective introduction of fluorinated motifs. This allows for modulation of metabolic stability and target binding in modern small molecule drugs. Strict process analytical checks ensure that no chlorinated or fluorinated impurities pass into the final pharma-grade building blocks. Industry compliance standards
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