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1,2-Dichlorooctafluorocyclohex-1-Ene

    • Product Name 1,2-Dichlorooctafluorocyclohex-1-Ene
    • Alias FC-1112
    • Einecs 206-039-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    480807

    Cas Number 2160-21-4
    Molecular Formula C6Cl2F8
    Molecular Weight 324.96 g/mol
    Iupac Name 1,2-dichloro-1,2,3,4,5,6,7,8-octafluorocyclohex-1-ene
    Appearance Colorless liquid
    Boiling Point 80-85°C (at 760 mmHg)
    Density 1.79 g/cm3 (at 25°C)
    Refractive Index 1.312 (approximate)
    Melting Point -38°C (approximate)
    Solubility In Water Insoluble
    Vapor Pressure 135 mmHg at 25°C

    As an accredited 1,2-Dichlorooctafluorocyclohex-1-Ene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2-Dichlorooctafluorocyclohex-1-Ene, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and safety labeling.
    Shipping 1,2-Dichlorooctafluorocyclohex-1-ene should be shipped in tightly sealed, compatible containers under cool, dry conditions. Handle as a hazardous material—avoid heat, incompatible substances, and physical damage. Comply with relevant regulations for toxic and environmentally hazardous chemicals, using appropriate labeling and documentation during transportation. Use safety measures to prevent leaks or spills.
    Storage 1,2-Dichlorooctafluorocyclohex-1-ene should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Keep the chemical in tightly closed, properly labeled containers made of compatible materials. Protect from moisture and direct sunlight. Use secondary containment to prevent spills and ensure emergency procedures and safety data sheets are readily accessible.
    Application of 1,2-Dichlorooctafluorocyclohex-1-Ene

    Applications of 1,2-Dichlorooctafluorocyclohex-1-Ene in Industrial Manufacturing

    As a committed upstream manufacturer, we focus on providing high-purity 1,2-Dichlorooctafluorocyclohex-1-Ene for specialized downstream sectors that depend on fluorinated intermediates for advanced fluorine chemistry. The following application scenarios reflect reputable and direct industrial uses of this raw material along well-established value chains.

    1. Specialty Fluoropolymer Monomer Synthesis

    Large-scale producers employ this compound as a key fluorinated intermediate for synthesizing novel monomers used in the manufacturing of advanced fluoropolymers. Its high degree of fluorination and reactive double bond facilitate the introduction of cyclic fluorinated units in custom copolymer backbones. These specialty fluoropolymers target demanding applications with extreme chemical resistance and dielectrical properties, especially in electronic insulation and chemical processing containment.

    Industry compliance standards

    • ASTM D2116 for fluoropolymer resin specifications
    • ISO 10993-5 for biocompatibility (if used for medical device polymers)
    • RoHS Directive (2011/65/EU) for restricted hazardous substances in electronics
    • REACH (EC 1907/2006) registration and safety evaluation

    Typical usage ratio

    • 3–12% of total monomer content, with exact loading based on target backbone rigidity and fluorine incorporation; adjusted per required barrier or dielectric threshold

    Downstream process integration

    • Charged directly to monomer batch reactor during copolymerization step, reacting under controlled pressure and temperature to ensure correct molar incorporation

    Final product types

    • High-performance fluoropolymer resins for wire and cable insulation
    • Fluorinated coatings for pump interiors and corrosion protection
    • Specialty films for chemical barrier applications
    • Membrane materials with enhanced chemical inertness

    2. Electronic Grade Dielectric Fluid Precursor

    Producers of high-voltage equipment and precision electronics use this material as a fluorinated starting unit in the synthesis of custom dielectric fluids. The compound's unique structure provides a pathway to engineered molecules with extremely low conductivity and high breakdown voltage, which become essential for specialized dielectric immersion fluids and cooling media in power electronics and data centers.

    Industry compliance standards

    • IEC 60243 testing for breakdown voltage in solid- and liquid-dielectrics
    • UL 94 flammability testing for fluid end products
    • RoHS/REACH regulations regarding use and waste management
    • IEC 61099 for synthetic organic ester fluids in transformers

    Typical usage ratio

    • Serves as an upstream building block (10–30% of total synthetic route intermediates); final composition varies after fluorination and post-processing into finished dielectric fluid

    Downstream process integration

    • Undergoes chemical transformation (hydrogenation, telomerization) before final blending; intermediate is introduced in multi-step synthetic schemes within dedicated fluorination production lines

    Final product types

    • Dielectric coolant fluids for power semiconductors and transformers
    • Immersion cooling media for data center electronic racks
    • Precision dielectric fluids used in sensitive magnetic and optical measurement apparatus

    3. Pharmaceutical Agrochemical Intermediate

    Major agrochemical and pharmaceutical manufacturers select this compound for constructing fluorinated heterocycles that impart metabolic stability and improved bioactivity in active ingredient molecules. The raw material’s rigid, perfluorinated ring facilitates downstream halogen-exchange and cyclization routes, supporting the creation of new molecules targeting pest control and advanced pharma formulations.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines (21 CFR 210/211 for API precursors)
    • Food and Agriculture Organization (FAO) specifications for pesticide ingredients
    • IUPAC recommendations for agricultural active ingredient definitions
    • OECD guidelines for chemical testing and environmental safety

    Typical usage ratio

    • Employed as a key intermediate (1–8% molar equivalent in multi-stage syntheses, adjusted for targeted substitution pattern and final product yield optimization)

    Downstream process integration

    • Introduced during the fluorination or cyclization stage of complex molecule construction, via controlled halogen exchange or ring expansion pathways

    Final product types

    • Agrochemical actives with enhanced persistence (e.g., insecticides, fungicides containing cyclohexene cores)
    • Synergist components for veterinary pharmaceuticals
    • Pharma intermediate blocks for advanced fluorinated APIs

    4. Lithographic Etchant Precursor in Semiconductor Fabrication

    Top-tier semiconductor etchant manufacturers leverage this material in the custom synthesis of perfluorinated etchants used for plasma processing and photolithography in advanced chip production. Its high purity and defined halogen structure grant reliable performance when producing etchant gases for microconductors and fine-featured wafer processes, contributing to cleaner profiles and critical plasma conditioning.

    Industry compliance standards

    • SEMI S2/S8 safety standards for semiconductor process chemicals
    • IATF 16949 quality system for electronics supply chains
    • REACH registration as per EC guidelines for use in Europe
    • CEPA (Canadian Environmental Protection Act) for environmental stewardship in effluent and emissions

    Typical usage ratio

    • Deployed as a precursor at 5–18% input on a molar basis versus total etchant feedstock; precise ratio individualized based on conductor material (Si, GaN, etc.) and feature size

    Downstream process integration

    • Fed into gas-phase halogenation or plasma-generation unit during etchant blending, either by in-situ conversion or separate synthesis line ahead of storage and shipment

    Final product types

    • Custom perfluorocyclohexene etchant gases for advanced microfab etch processes
    • High-purity plasma etchant blends for sub-10nm lithographic feature etching
    • Finishing and cleaning agents for precision wafer processing

    5. Surface Modification Agent in Advanced Coatings

    Manufacturers of high-durability surface coatings and repellency additives turn to this fluorinated compound as a specialized modifier for introducing fluorinated functional groups to polymer matrices. It enables production of next-generation coatings with excellent water, oil, and chemical repellency, thanks to its multi-halogenated structure, supporting demand in textile finishes, protective films, and anti-corrosion treatments for industrial environments.

    Industry compliance standards

    • ISO 15711:2003 for industrial coatings—measurement of water and chemical resistance
    • OEKO-TEX Standard 100 Annex 6 (for limited use of fluorinated agents in textiles)
    • EU REACH Annex XVII on fluorinated substances in consumer products
    • ASTM D6577 for coating resistance to environmental attack

    Typical usage ratio

    • Typically 0.5–3% by weight in coatings formulations; adjusted according to target repellency metrics and substrate compatibility

    Downstream process integration

    • Introduced during the polymer pre-blend or reactor functionalization step for backbone modification, followed by post-treatments to ensure long-term migration stability

    Final product types

    • Anti-corrosive industrial coatings for metal structures
    • Textile finish treatments for water and oil repellency
    • Self-cleaning architectural surface membranes
    • Protective films for chemical process equipment
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    Certification & Compliance
    More Introduction

    1,2-Dichlorooctafluorocyclohex-1-Ene: Our Experience With a Demanding Compound

    Introducing a Consistent Performer in the Fluorochemical Arena

    As a chemical manufacturer committed to specialty fluorinated products, our journey with 1,2-dichlorooctafluorocyclohex-1-ene has taught us much about the persistence and care that complex molecules demand. Unlike many of the linear or branched fluorocarbons, cycloalkene structures like this one pose their own particular set of challenges and advantages. Over the years, hands-on refinement of our synthetic processes has allowed us to dependably deliver C8F8Cl2 compounds to demanding industries.

    Model and Specifications as Developed in Our Facility

    We know from experience that reliable outcomes trace back to every detail in the plant, from reagent purity to reactor pressure cycles. The 1,2-dichlorooctafluorocyclohex-1-ene we manufacture holds a molecular formula of C6Cl2F8, fitting the cyclohexene backbone with two chlorine atoms and eight fluorines. Rigorous analytical controls ensure only high-purity product leaves our line—GC/MS assays and 19F NMR lend us keen insight into molecular integrity, turning production into a blend of science and discipline rather than conjecture.

    Customers who seek 1,2-dichlorooctafluorocyclohex-1-ene often report difficulties sourcing consistent quality elsewhere. By running targeted distillation and vacuum handling, we supply this compound as a clear, low-viscosity liquid. We minimize metallic surface exposure in handling, since halogenated cycloalkenes can experience slow decomposition if they dwell on reactive surfaces or high-energy environments. Secure packaging, typically in PTFE-lined drums, ensures shelf life without compromise.

    What Sets This Molecule Apart in Industrial Application

    Working directly with those formulating for electronics, surface treatment, pharmaceutical intermediates, or specialized solvents, we have seen the unique reactivity of this compound offer solutions which linear perfluorocarbons or even many perfluoroalkenes cannot provide. The chlorine atoms in the 1,2-positions create accessibility for subsequent functionalization by nucleophiles, a feature highly valued in complex organic synthesis. Structural ring strain is lower compared to some smaller cycles, reducing unwanted side reactions that complicate downstream chemistry.

    For applications in the manufacture of high-performance lubricants, this compound forms a backbone resistant to aggressive oxidation and thermal breakdown, all while providing sites for well-defined chemical modification. In specialty coatings, its fluorinated surface influences repellency and durability far better than partially fluorinated blends. This distinct set of advantages arises from a combination of cycloalkene resilience and controlled site-activation.

    Comparison to Other Fluorochemicals Based on Real-World Outcomes

    Manufacturers often contrast 1,2-dichlorooctafluorocyclohex-1-ene with its saturated analogs or with fluoroalkenes lacking halogen substitution. Fully perfluorinated cycloalkanes, for example, exhibit superb chemical inertness but lack the ability to undergo selective derivatization. In contrast, the dichloro substituents on our product offer synthetic chemists an anchor for controlled couplings. Those needing perfluoromatic compounds configured for tough conditions but also for controlled downstream reactivity opt to leverage this dichloro fluorocycloalkene rather than more inert, unreactive analogues.

    In our early years, some clients insisted on using perfluorocyclohexene for similar projects, only to return after facing bottlenecks during later-stage modification. The dichloro version offered a clear difference—increased control over site-specific substitution, resulting in cleaner, more scalable synthesis of target compounds. This has been especially true for those in the fluoropolymer sector, where controlled integration of such motifs builds out new classes of functionally active materials.

    Another frequently cited reference point is hexafluorocyclohexene. We have firsthand comparisons where differentiation at the two halogen sites allows for sequential reactions, opening access to new molecules that would otherwise require cumbersome pathways. This not only enables technical advancements but often makes a real difference in process cost, reaction step economy, and overall yield.

    Focus on Reliability, Not Just Technical Data

    Producing this compound consistently involves a long learning curve. Literatures and technical datasheets rarely delve into the headaches we deal with day after day. Regular testing of starting raw materials and continual investment in reactor lining materials have proven essential. We rely on feedback from both process and quality teams, making incremental improvements each quarter. Sometimes, unexpected viscosity changes in the reaction mixture hint at trace impurities; reacting quickly helps avoid off-specification batches or downstream customer issues. These are operational realities not captured in standard references.

    Maintaining a trusted supply chain marks a turning point. Users often recount frustration with receiving off-color, partially degraded, or container-contaminated product from less established outfits. Our lab and shipping staff dedicate themselves to ensuring each drum looks pristine and conforms to tight tolerance bands, since even a trace impurity—undetectable in non-specialized labs—can derail a downstream reaction or instrument. It’s this level of care that draws repeat customers, not just the basic product specifications or broad market descriptors.

    Safety and Environmental Stewardship in Daily Operations

    Nobody working at a chemical manufacturing plant overlooks the hazards built into halogenated organics. Over time, we have developed cleaner, more contained processes to reduce both occupational exposure and environmental footprint from waste streams. Specifics matter—a closed-loop condensation setup, investment in advanced scrubber systems, and routine maintenance make a far larger difference than one-off efforts. Careful containerization prevents leaks, while documented, traceable batch records keep accountability front and center.

    Fluorochemicals pose distinctive challenges during disposal or accidental release. By working closely with local regulatory agencies and recycling wherever feasible, we minimize both immediate and legacy impact. We see environmental compliance not as a burden, but as a natural part of staying in business in a world that is justifiably skeptical of complex fluorinated compounds. This flows from hands-on experience dealing with solvent recovery, neutralization of byproducts, and employee health tracking over long years in the segment.

    Challenges Unique to 1,2-Dichlorooctafluorocyclohex-1-Ene Manufacturing

    Among the compounds we produce, this dichloro-fluorocyclohexene stands out for its exacting production demands. For example, fluorination must remain precise, since side reactions can easily produce over-chlorinated or partially defluorinated impurities. Every deviation hits final product purity hard, so real-time monitoring and frequent, robust intermediate analysis are non-negotiable. Batch failures, though rare, spark post-mortem reviews led by technical leads who have guided this process since its inception here. Troubleshooting leans not only on instrumentation, but also on lived experience and “chemical intuition” developed over decades.

    Sourcing fluorine gas and maintaining reactor materials that resist both extremes of temperature and chemical attack force us to keep up with new material science research. PTFE lining, rigorous cleaning protocols, and protective handling gear all come standard; these are investments, not options. Skimping on these, as some past competitors discovered, leads only to degraded quality and unnecessary risks.

    Use Cases and Solutions We’ve Observed Over the Years

    While this molecule has academic curiosity, its real value surfaces in direct industrial application. We’ve watched our 1,2-dichlorooctafluorocyclohex-1-ene find use as a controlled intermediate for fluorinated pharmaceuticals, where its particular arrangement of labile chlorines streamlines industrial-scale coupling reactions. Major advances in photoresist coatings and specialty plastics incorporate this motif because it combines chemical durability with modifiable chemistry.

    One partner in the electronics sector approached us with yield issues attributed to trace impurities in their old supply chain. After switching to our material, their defect rates dropped, since a consistently high-purity backbone removed the unpredictable behavior seen in photolithography steps. In the field of advanced lubricants, the unique stability and rheology imparted by this cyclohexene derive specifically from the balance between rigid core and functional handles—insights borne out by direct field trials, not only in formulation labs.

    We’ve seen research teams accelerate R&D cycles when they access this compound without fighting batch inconsistencies. Some found new synthetic approaches previously blocked by purity or impurity spectrum constraints. This highlights the simple truth: investment in manufacturing discipline isn’t only about prestige, but about unlocking new science and commercial opportunity across supply chains.

    Continuous Improvement for a Demanding Market

    Over the years, market needs rarely remain static. Incoming analytical techniques grow more sophisticated, and expectations for impurity profiling grow tighter. Achieving trace-level control over byproducts means working with local academic partners, investing in mass spectrometry, and setting up redundancy in production so no learning is lost. Adjusting to technical advances on both sides—manufacturing and downstream application—fuels our improvements far more than paperwork mandates ever could.

    Some years back, as the electronics sector introduced advanced node processes, a new class of impurities previously thought trivial began interfering with pattern fidelity. These surfaced as barely-detectable features on chromatograms, often eluding labs with less invested in instrumentation. By dedicating plant capacity to pre-release impurity modeling, we kept up with evolving specs and clients stayed competitive.

    Collaborative research with users also shapes our approach. Problems rarely show up in isolation—sometimes we uncover process bottlenecks in customer lines that trace back to interactions between our molecule and a commonly used stabilizer or solvent impurity. Rather than point fingers, our teams work one-on-one, sharing analytical data and testing alternative batches until root cause resolution emerges. Real partnerships shape both innovation and reputation far more than theoretical “continuous improvement.”

    Realities of Scale and Future Directions

    Scaling up production involves more than reenacting pilot runs. Early trials often missed process dynamics that only emerged at commercial scale—temperature profiles, localized hot spots, and even unexpected pressure drops across filters. Our engineering staff carved out real solutions through repeated redesigns, not quick fixes. We’ve replaced antiquated control systems, invested in process analytical technology, and built-in redundancy for critical utilities so as to never jeopardize consistent quality. Market confidence stems from these investments, not from generic promises of “commitment to quality.”

    Looking ahead, the evolving demands of electronics, medical, and surface treatment industries offer both new challenges and fresh opportunities for materials like 1,2-dichlorooctafluorocyclohex-1-ene. Our teams focus on meeting tighter specifications for residual metals and trace volatile organics, and deploy molecular sieving and advanced guard-bed filtration. Similarly, automation in filling and packaging now ensures fewer handling lapses; it also provides tractable audit trails when customers need documentation at every stage.

    Developments in green chemistry may present new synthesis options in the coming years. We’re tracking catalyst innovations and milder halogen-transfer methods that—if proven at pilot scale—could one day lower energy input and minimize side product formation. Should regulation restrict certain starting materials, our deep familiarity with process variables means we are prepared to respond with practical solutions, not just theoretical compliance. This adaptability defines our track record as a true manufacturer rather than a passive broker.

    Supporting Technical Expertise with Accessible Service

    Few businesses, regardless of field, appreciate the value of technical support that comes from direct manufacturing knowledge. Every batch we ship reflects input from operators and chemists who know the molecular profile inside and out. Routine discussions with users—addressing handling quirks, storage best practices, and downstream adaptations—make a marked difference. Accessibility to our technical and quality leads means issues find solutions, often long before they spiral into costly downtime.

    Some of our most loyal partners began as single-barrel customers, gradually scaling up as they discovered the confidence that comes from unbroken dialogue with the actual manufacturer. In return, we gain invaluable on-the-ground feedback, sharpening our aims for both incremental improvements and quantum-leap enhancements. Manufacturing this molecule doesn’t end with shipment; it stretches into every process we help facilitate and problem we help solve.

    Community, Responsibility, and Enduring Value Through Manufacturing

    Many see specialty fluorochemicals as interchangeable commodities. Our lived experience says otherwise. The array of regulatory, occupational, and operational details transforms these compounds from mere lines on a data sheet into dynamic assets—tools which enable next-generation products, competitive advances, and even environmental solutions. Our investment is ongoing, grounded in practical realities rather than abstraction.

    We learn by doing: adapting processes, supporting users in real-world conditions, and keeping pace with the changing landscape around halogenated and fluorinated organics. Every success story builds on a foundation of scrutiny, personal commitment, and pride in the product that’s been shaped not only by theory, but by daily decision-making and the cumulative effort of a dedicated workforce. This, as much as any technical parameter, shapes the enduring place of 1,2-dichlorooctafluorocyclohex-1-ene in our catalog and, more importantly, in the continued progress of our partners' innovations.