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1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane

    • Product Name 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane
    • Alias 1-chloromethyl-2,2,3,3-tetrafluorocyclobutane
    • Einecs 615-026-7
    • 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

    277039

    Chemical Name 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane
    Cas Number 138495-42-8
    Molecular Formula C5H5ClF4
    Molecular Weight 178.54
    Appearance Colorless liquid
    Boiling Point N/A
    Melting Point N/A
    Density N/A
    Flash Point N/A
    Solubility In Water N/A
    Refractive Index N/A

    As an accredited 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane is packaged in a 100g amber glass bottle with tamper-evident sealed cap and safety labeling.
    Shipping **Shipping Description:** 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane should be shipped as a hazardous material in accordance with local, national, and international regulations. It must be packed in tightly sealed, compatible containers under cool and well-ventilated conditions, clearly labeled, and protected from heat, moisture, and physical damage during transit.
    Storage 1-Chloromethyl-2,2,3,3-tetrafluorocyclobutane should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Protect from direct sunlight, moisture, and physical damage. Use appropriate personal protective equipment (PPE) when handling, and ensure proper labeling and secure storage to minimize accidental exposure or spills.
    Application of 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane

    Applications of 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane in Industrial Manufacturing

    1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane serves as a specialized intermediate in high-performance fluoropolymer synthesis and advanced chemical industries. This molecule offers unique reactivity and fluorine content, making it valuable in complex downstream processes where stringent compositional control and material purity are essential. Below, we detail its integration across industrial applications based on direct manufacturing and customer technical requirements.

    1. Fluorinated Elastomer Monomer Production

    This material acts as a key building block during production of specific fluorinated elastomers for chemical-resistant seals and gaskets. It provides high fluorine content and specialized cyclobutane structure, supporting tailored polymer backbones. Plants typically introduce this intermediate at the pre-polymerization mixing stage where real-time composition monitoring ensures batch-to-batch consistency. Producers rely on controlled dosing and traceability, especially for automotive, aerospace, and semiconductor fabrication seals where performance and regulatory conformity are critical.

    Industry compliance standards

    • ASTM D1418 (Standard Practice for Rubber and Rubber Latices—Nomenclature)
    • IATF 16949 (Automotive Quality Management)
    • RoHS Directive (2011/65/EU and amendments)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 2–15 mol% as a co-monomer, adjusted according to the required fluorine content and target polymer properties such as compression set and low temperature flexibility.

    Downstream process integration

    • Charged during monomer pre-blend preparation before emulsion or solution polymerization in closed reaction vessels.
    • Monitored for residual chlorinated side groups post-polymerization during quality release.

    Final product types

    • O-rings and valve seals for automotive drivetrains and fuel systems
    • High-integrity gaskets for chemical process equipment
    • Semiconductor manufacturing cleanroom seals
    • Specialty hoses resistant to aggressive solvents

    2. Synthesis of Specialty Agrochemical Intermediates

    1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane enables synthesis of modern fluorinated agrochemical intermediates through selective catalytic substitution and coupling reactions. Agrochemical manufacturers employ this compound where target molecules must deliver specific vapor pressure, persistence, and environmental compatibility. It enters the synthesis path in reaction with amines or aryl nucleophiles to build up key fluorinated ring systems for new-generation crop protection active ingredients.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Good Manufacturing Practice (GMP) for Agrochemicals (ISO 9001:2015)
    • OECD Guideline 105 (Water Solubility)
    • EU Plant Protection Product Regulation (EC) 1107/2009

    Typical usage ratio

    • Used at 1–8% molar basis in stepwise intermediates, depending on final product formulation and activity level requirements of the agrochemical active.

    Downstream process integration

    • Reacted at the nucleophilic substitution step to introduce the cyclobutane scaffold into the target molecule.
    • Undergoes purity assessment post-reaction via LC-MS and GC methods.

    Final product types

    • Fluorinated pesticide intermediates
    • Active ingredients for herbicides with selective crop safety
    • Precursor molecules for insect-resistant coatings
    • Building blocks for advanced plant growth regulators

    3. Refrigerant Gas Blending and Development

    Manufacturers incorporate this compound to develop next-generation refrigerant gases and heat transfer fluids that demand non-flammability and low global warming potential (GWP). The raw material provides a precise cyclobutane and fluorine backbone, allowing researchers and engineers to fine-tune vapor pressure, stability, and environmental behavior of refrigerant blends. It supports production of new molecules intended to replace legacy CFC and HFC refrigerants under industry transition programs.

    Industry compliance standards

    • ASHRAE Standard 34 (Designation and Safety Classification of Refrigerants)
    • ISO 817 (Refrigerants—Designation and Safety Classification)
    • Kigali Amendment to the Montreal Protocol
    • EN 378-1:2016 (Refrigerating Systems and Heat Pumps—Safety and Environmental Requirements)

    Typical usage ratio

    • Used as a blending precursor at 3–12% mass for pilot refrigerant R&D; process scale-up varies based on thermodynamic targets and blend reactivity testing.

    Downstream process integration

    • Introduced pre-distillation in mixing reactors to synthesize new refrigerant candidates by catalytic transformation and halogen exchange.
    • Analyzed post-blending for purity, decomposition products, and pressure-temperature properties.

    Final product types

    • Test blends for low-GWP commercial refrigeration
    • Pilot refrigerants for residential and automotive AC systems
    • Heat pump working fluids for industrial applications
    • Specialty coolant blends for electronics thermal management

    4. Pharmaceutical Fluorinated Cyclobutane Scaffold Synthesis

    1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane finds use in synthesis of advanced pharmaceutical intermediates, especially for drug candidates incorporating a rigid, fluorinated cyclobutane ring. Pharmaceutical processors utilize the raw material in strictly controlled environments for stepwise synthesis where regiochemistry and enantiopurity are monitored. Its unique structure helps medicinal chemists optimize pharmacokinetics and metabolic stability of clinical and pre-clinical compounds.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary)
    • Ph. Eur. (European Pharmacopoeia)
    • 21 CFR Part 211 (US FDA Current Good Manufacturing Practice)

    Typical usage ratio

    • Applied at 0.5–6 molar equivalents in multi-step organic synthesis, adjusted based on the complexity and target functionalization of the intermediate or final active ingredient.

    Downstream process integration

    • Introduced into Grignard reaction or Suzuki coupling phase to construct bicyclic fluorinated frameworks.
    • Maintains traceability and purity validation at each synthetic step.

    Final product types

    • Fluorinated API scaffolds for oncology research
    • Pharmaceutical intermediates for CNS therapeutics
    • Building blocks for anti-viral and anti-bacterial drug development
    • Reference compounds for pharmaceutical analysis
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    Certification & Compliance
    More Introduction

    1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane: Advancing Specialty Chemistry

    As a manufacturer who has spent years refining production methods for fluorinated cyclic compounds, I can tell you that 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane stands out as a specialty building block in modern synthesis. The model often referenced by its CAS number reflects our commitment to consistent quality at high purity, and we’ve seen this compound open new doors for our partners in pharmaceuticals, agrochemicals, electronics, and advanced materials. We focus on supplying this product to meet specific purity requirements, with tightly controlled water content and minimal trace impurities. We monitor the synthesis from the first halogenation reaction all the way to final distillation, using analytical standards that match the rigorous specifications demanded by leading labs and manufacturers worldwide.

    Origins and Process Consistency

    Our process begins with selecting high-quality cyclobutane precursors and ultra-pure fluorine sources. We employ sealed, corrosion-resistant reactors under anhydrous conditions and carefully monitor temperatures and pressures throughout the halogenation and chloromethylation steps. This approach leads to consistent batch-to-batch quality and minimizes the risk of byproducts that could compromise downstream synthesis. Analytical testing covers GC, NMR, and trace contaminant screening, because in fluoro-organic chemistry, even low ppm levels of uncontrolled byproducts can trigger side reactions further down the line. From firsthand experience, problems from poor purification often get noticed too late, causing wasted effort on re-runs and troubleshooting. Reliable outcomes come from rigorous controls at the plant.

    Structural and Physical Characteristics

    This cyclobutane derivative combines a four-membered ring with two pairs of geminal fluorines and a functionalized chloromethyl group. This backbone creates a unique blend of reactivity and stability, contrasting sharply with more common chloroalkyl or fluorinated alkanes. The sterics and electronics of the ring and the strong inductive effects of the fluorines yield a compound whose reactivity profile sets it apart from linear or branched analogues. Compounds like trifluoromethylcyclobutanes, for instance, display lower reactivity and different solubility—attributes which change the course of reactions in fields from surface modification to pharmaceutical intermediates.

    The melting and boiling points, along with solubility parameters, track with the high degree of fluorination. From the bottles we deliver to customers in specialty glass ampoules or corrosion-resistant containers, you can expect colorless, mobile liquid at ambient conditions, ideal for both scale-up and analytical work. Purity above 99 percent is maintained, with water content under a few hundred ppm to prevent hydrolysis.

    Applications in Synthesis

    Over the last decade, our clients have put 1-Chloromethyl-2,2,3,3-Tetrafluorocyclobutane to surprising and beneficial uses. Fluorinated cyclobutanes have found homes in agrochemical R&D as unique core motifs for crop protection agents and seed coatings. In pharmaceuticals, they’re useful for introducing fluorine atoms in metabolically stable regions of drug candidates, enhancing bioavailability and controlling molecular conformation. Medicinal chemists exploit the molecule’s ring strain and electron-withdrawing attributes to design scaffolds that resist oxidative degradation, leading to longer duration of action for some active ingredients.

    On the materials science side, the high fluorine content and rigid backbone make this molecule a candidate for performance coatings, membranes, and specialized polymer feedstocks. It brings distinct advantages compared to less fluorinated cyclics by increasing hydrophobicity and lowering surface energy. We’ve also seen demand from the electronics sector, where its structure imparts insulation properties and chemical resistance, especially in the manufacture of specialty resins and dielectrics that must survive harsh process conditions and exposure to solvents or oxidizing agents.

    Distinguishing Features Compared to Other Cyclobutanes

    Most standard cyclobutanes or partially fluorinated analogues fall short in several ways if your process needs maximum chemical stability combined with targeted reactivity. Adding two fluorine pairs at the 2,2,3,3-positions isn’t just a minor molecular tweak. Those fluorines alter the electron density across the whole ring, suppressing unwanted side reactions and opening the door to regioselective modifications. Chloroalkyl cyclobutanes that lack fluorine tend to hydrolyze or undergo nucleophilic substitution too quickly, especially in basic environments.

    From years spent troubleshooting batch inconsistencies for clients testing different supplies of cyclobutanes, we noticed that most off-shelf chlorocyclobutanes either ingrain excess color from oxidation or show halide impurities. Such weaknesses get amplified when scaling reactions, sometimes requiring customers to rework protection schemes or purification stages. In contrast, our fully fluorinated cyclobutane demonstrates robust shelf-life. No off-colors, no secondary halide bleed-through, and every lot comes in certified containers to block atmospheric contamination.

    Supported Claims and Real-World Performance

    As any chemist who has run pilot or commercial campaigns using fluorinated building blocks knows, trace contaminants make or break yields and selectivity in key transformations. We verify real-world performance by offering samples for initial pilot reactions and solicit feedback from industrial partners running kilogram-to-tonne scale reactions. For some clients, the main advantage comes in Suzuki or Negishi cross-couplings, where cleaner profiles prevent poisoning of expensive catalyst beds. For others, downstream hydrofunctionalization or ring-opening becomes more predictable with the enhanced stability profile conferred by the fully fluorinated backbone.

    Our technical service team documents the downstream chemistry to corroborate initial purity claims, ensuring that benchmarks established during method development stand up to scrutiny during process validation. Examples from customers include leveraging the product in the synthesis of fluorinated phenethylamine analogues or in the preparation of high-molecular weight perfluoroalkylated polymers. Certain applications demand even tighter water control, so we invested in on-site vacuum-drying systems and upgraded to argon-backed storage vessels.

    Trends from the Producer’s Perspective

    Trends in specialty fluorochemicals change constantly, yet demand for robust, trackable, and high-purity intermediates remains. The surge in medicinal applications stems from regulatory shifts requiring more detailed impurity profiling and greater material traceability—a challenge we’ve risen to meet by updating lot tracking and purity analytics. Synthetic chemists continue to look for niche building blocks to distinguish their proprietary processes from mass-market competition. With each advance in reaction methodology—photoredox, organocatalysis, C–H functionalization—interest in unique cyclic and fluorinated compounds like this one grows.

    We keep pace by adapting our reactor fleets, retraining operators, and upgrading analytical instrumentation. Clients expect not only the material but also answers to supply chain assurance, precipitation behavior, and stability in long-term storage. Our operators undergo factory-level training to troubleshoot vacuum integrity, inert atmosphere management, and bottle transfer to minimize contact with moisture or air. These hands-on measures directly impact the reliability of each delivery, which gets measured by our ability to maintain customer trust year after year.

    Safety and Handling from a Manufacturer’s Viewpoint

    Unlike experience with more benign hydrocarbons, handlers who work with high-fluorine cyclobutanes need strict protocols. Liquid handling happens under inert gas, with dedicated PPE, and every vessel receives leak testing before use. Batch records get reviewed by process chemists, not just operators. Packaging design stems from past lessons with container stress cracking, so our packaging engineers select only materials proved compatible, after real-world shipping trials. Our internal safety teams run regular drills on chemical exposure and spill response, based on realistic risk assessments, not minimum compliance.

    Our customer onboarding includes transfer techniques and disposal instructions because these details matter in the lab and at production scale. Having supplied material to customers ranging from global innovators to boutique R&D outfits, we’ve documented practical guidance for thermal handling, pressure release, and shelf-life limits backed by accelerated aging studies, not marketing promises.

    Addressing Production and Supply Challenges

    Scalability for this compound has been one of our focus points. Early on, limitations came from sourcing reliable fluorine suppliers and managing byproduct containment. Pressure equipment rating standards and process hazard analysis were non-negotiable topics, especially after lessons learned from scaling up from kilo to multi-ton operations. Our investment in closed-loop emission controls pays off, meeting both our company’s environmental goals and stringent regulatory thresholds.

    We’ve found that close relationships with specialty glass and fluorocarbon polymer suppliers permit rapid turnaround on new vessel designs when production parameters evolve. Any time demand spikes or process improvements arise, engineering teams coordinate in real time with plant operators, so scale-up doesn’t get derailed by an unexpected equipment gap. This hands-on approach means customer projects don’t stall for lack of technical or logistical support.

    Quality Control, Transparency, and Future Outlook

    Consistent quality builds long-term partnerships. We share batch-level analysis, retain control samples, and maintain full traceability of raw materials back to approved suppliers. Sometimes customers ask for extended stability or product compatibility data under new process conditions—requests we fulfill through in-house and third-party verification. Updates to our internal knowledge base draw from actual user outcomes, giving us a feedback loop that isn’t just lip service.

    Long-term, we plan continued upgrades to both process and analytical technology. Fluorinated cyclic compounds will feature more prominently as demands for specialty moieties and more selective reactivity grow. We keep an ear directly to the market—not just to spot trends, but to ensure each batch delivers what stringent R&D and manufacturing customers expect. Manufacturing specialty chemicals is a continuous improvement effort grounded in practical challenges, not just theoretical capabilities. In this field, hands-on experience and process-level insight make the crucial difference that helps our customers innovate with confidence.