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1-Bromo-2-(Bromodifluoromethyl)Cyclohexane

    • Product Name 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane
    • Alias BCDMCH
    • Einecs 831-841-7
    • 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

    891031

    Cas Number 2179828-75-5
    Molecular Formula C7H10Br2F2
    Molecular Weight 295.97 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point No data available
    Density No data available
    Refractive Index No data available
    Melting Point No data available
    Smiles C1CCC(C(C1)Br)C(F)(F)Br
    Inchi InChI=1S/C7H10Br2F2/c8-6-4-2-1-3-5(6)7(9,10)11/h5-6H,1-4H2
    Purity Typically ≥97% (check supplier for specifics)
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Hazard Statements Harmful if swallowed or in contact with skin; causes skin and eye irritation

    As an accredited 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tightly sealed with a screw cap, labeled clearly; contains 25 grams of 1-Bromo-2-(Bromodifluoromethyl)cyclohexane, hazard symbols displayed.
    Shipping 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane is shipped as a hazardous chemical, typically in sealed, chemically resistant containers. It requires secure packaging, clear labeling, and compliance with international transport regulations (IATA, IMDG, DOT). Shipping includes material safety data sheets, and handling should be by trained personnel, avoiding heat, moisture, and incompatible substances.
    Storage **1-Bromo-2-(bromodifluoromethyl)cyclohexane** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from direct sunlight and moisture. Store under inert atmosphere if possible, and handle using proper chemical safety protocols, including gloves and eye protection.
    Application of 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane

    Applications of 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane in Industrial Manufacturing

    We supply high-purity 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane to leading manufacturers engaged in advanced specialty synthesis. Our technical support addresses the stringent demands and exacting process controls of downstream sectors. Below are primary industrial scenarios where this fluorinated bromine cycloalkane derivative is directly integrated into production, with specific focus on compliance, formulation, industrial procedures, and resulting goods.

    1. Pharmaceutical Intermediate Synthesis for API Manufacturing

    Pharmaceutical companies use this compound in multi-step syntheses to introduce difluoromethyl and bromine groups when building advanced heterocyclic scaffolds, widely used as intermediates for selective kinase inhibitors and other small molecule drugs. Such applications often require batch production under strict cGMP conditions, leveraging this material’s unique regioselectivity in cyclohexane ring modification for targeted substitution patterns not achievable with alternative reagents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals (FDA)
    • Chinese Pharmacopoeia, European Pharmacopoeia (for relevant intermediate sections)

    Typical usage ratio

    • Used at 0.3–2.5 molar equivalents relative to starting material, depending on substitution yield and batch size adjustments; process chemists optimize ratio based on targeted conversion and minimization of by-products.

    Downstream process integration

    • Charged during functionalization steps after base cyclohexane core preparation, typically following initial protection/deprotection reactions. Directly participates in nucleophilic substitution or halogen-exchange reactions carried out in halogenated or polar aprotic solvents under controlled temperature and inert atmosphere.

    Final product types

    • API intermediates for kinase inhibitors
    • Antiviral drug building blocks
    • Custom intermediates for oncology pipeline compounds

    2. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers introduce this compound at key points in proprietary synthesis routes to modify cycloalkane fragments in fungicides and herbicides. Its difluoromethylated, brominated structure is critical to altering bioactivity profiles, providing sources for further coupling or cross-coupling reactions in crop protection R&D. Production lines utilize it in campaign-style manufacturing, followed by stringent purification to meet field toxicity and residue standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Specifications for Plant Protection Products (agrochemical active ingredient quality and purity)
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market (Europe)

    Typical usage ratio

    • Incorporated at 1.0–2.0 equivalents per functional group to be brominated, varied according to required degree of substitution and end-use formulation specifications.

    Downstream process integration

    • Integrated at halogenation or fluorination stages within the multi-step synthesis sequence, with process chemists introducing it at late-stage modification steps after initial ring formation, often followed by chromatographic purification, concentration, and crystallization before formulation.

    Final product types

    • Cyclohexyl-based fungicide actives
    • Difluoromethylated herbicide precursors
    • Specialty agrochemical intermediate concentrates

    3. Specialty Fluorochemical Synthesis for Material Science

    Producers of advanced fluoropolymers and specialty fluorochemicals incorporate this material in custom monomer synthesis, especially for performance films, coatings, and specialty elastomers. The presence of both difluoromethyl and bromine functionalities enables precise control over surface energy and thermal properties in the resulting polymer structures. Use aligns with rigorous material purity and traceability protocols governing electronic and high-performance plastic sectors.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer synthesis
    • REACH Regulation (EC) No 1907/2006 for registration and traceability
    • ASTM D5630 for fluorinated polymer purity

    Typical usage ratio

    • Added at 0.05–0.12 wt% in monomer preparation, with adjustments based on target chain length or specific surface property modification goals.

    Downstream process integration

    • Fed into a condensation or free radical polymerization reactor, introduced after charge of main backbone monomers. Its incorporation occurs prior to polymerization, undergoing in situ functionalization.

    Final product types

    • Low surface energy fluoropolymer pellets
    • Specialty elastomer compounds
    • Fluorinated coating intermediates

    4. Advanced Electronic Chemical Precursors

    Producers of microelectronic and semiconductor process chemicals use this molecule as a precursor in the production of difluorinated cyclohexane derivatives essential for next-generation photoresist formulations and dielectric materials. Recipients demand tightly controlled impurity profiles and batch traceability, with this intermediate supporting the synthesis of highly pure structures crucial in advanced lithography and etching applications.

    Industry compliance standards

    • SEMI C64 Specification for Electronic Grade Chemicals
    • ISO 14644-1 Cleanroom Standards for production environment
    • IEC 62474 Material Declaration for the Electrical and Electronic Industry

    Typical usage ratio

    • Charged at 0.02–0.10 wt%, with batch engineers adjusting ratios to fine-tune resist sensitivity, depending on product line and node size requirements.

    Downstream process integration

    • Dosed directly into reaction vessels during critical step-growth or cyclization reactions leading to the formation of photosensitive or insulating molecular frameworks, with immediate QC verification for trace metal content and halogen distribution.

    Final product types

    • Cyclohexyl difluorinated photoresist additives
    • Specialty dielectric material bases
    • Electronic wet process chemical intermediates
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    Certification & Compliance
    More Introduction

    1-Bromo-2-(Bromodifluoromethyl)Cyclohexane: Direct Insights from Our Plant

    Behind the Molecule: Putting Our Experience into Practice

    Every year, more engineers and laboratory professionals look for strong-performing intermediates in fluorinated chemistry. 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane has kept a special place in our portfolio as industries demand compounds with tailored reactivity and reliable performance. Our team spends much of its time working closely with end users—from pharmaceutical research labs to agrochemical formulation plants—so we see firsthand the challenges they face sourcing reliable specialty chemicals, and we understand how one molecule’s performance can shift an entire project.

    Our facility scales up 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane batches under strict monitoring, driven by process controls and regular quality checks. We focus on delivering consistent purity and traceability, which matters to customers who rely on reproducible results. With new markets opening up for fluorinated building blocks, expectations for supply quality run higher than ever. Several experienced chemists on our team helped pioneer the process optimizations that now keep impurities low and lot variation minimal.

    On-Spec Product: Character, Form, and Manufacturing Process

    To serve the research and development community, we typically supply this molecule as a colorless liquid with a slightly sweet odor, packaged under an inert atmosphere. Years of honing process parameters allow us to supply typical assay values around 97–99%, but we often run further analysis—including GC-MS and NMR—to verify consistency batch after batch. Moisture and residue management form the backbone of our handling protocol: we keep these levels low through nitrogen blanketing and scrupulous equipment cleaning. Minimizing byproducts starts with attention to every step: we build in points for in-process adjustments and sample frequently before a batch ever reaches the drum or ampoule.

    Don’t underestimate the impact of small differences in the synthetic route. We’ve tested several variations over the years, with feedback from bench chemists shaping each change. This particular process starts with high-purity cyclohexane as the base, introducing both bromo- and bromodifluoromethyl groups. Control of temperature ramps, timing, and feed order delivers cleaner separations and helps limit formation of side isomers. Careful tuning at this stage means scientists can expect less clean-up and fewer analytical headaches later.

    Where Demand Comes From: Real-World Uses that Push the Boundaries

    Applications keep growing as our partners push further into advanced organic synthesis. The unique combination of two bromine atoms—one in a direct ring position, the other on a difluoromethyl side group—gives synthetic chemists a versatile scaffold. The molecule serves as a handy intermediate in constructing heterocyclic rings and fluorinated chains, both hot topics in drug design and crop protection. Fluorinated fragments are recognized for increasing metabolic stability in medicinal compounds. That extra resilience against oxidative breakdown can transform a promising molecule into a market-viable candidate.

    Teams developing agrochemicals see an added edge from the presence of both difluoromethyl and bromo groups. These features let chemists fine-tune reactivity and introduce new substitutions into complex targets. In the past decade, we’ve noticed more demand for this building block in seed treatment and post-emergent herbicide research, where companies search for low-application-rate actives. With international patent filings on fluorinated pesticides expanding, this precursor has caught the eye of several innovation groups at major companies.

    What Sets Us Apart: Beyond Simple Delivery

    Consistent supply sometimes means working behind the scenes to iron out problems other manufacturers shy away from. Shipping times, packaging failures, shelf-life concerns—every detail makes a difference to end users with tight timelines. We ship the compound in certified steel or PTFE-lined glass, using sealed ampoules for research-scale, or air-free drums for bulk. Our packaging team steps up storage duration with dunnage that locks out moisture and temperature swings.

    Down in the plant, we’ve been able to avoid batch variability that can complicate synthesis by building in robust analytic checkpoints. Random sampling from finished lots, cross-referenced with retained samples, lets us give customers confidence in each lot’s traceability. Regulatory trends toward higher transparency have led us to keep digital logs of every parameter and analytic printout—no room for surprises or “black box” shipments.

    How 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane Differs from Other Cyclohexane Derivatives

    Over the years, our customers have used a range of brominated cyclohexanes and related fluorinated intermediates. The 1-Bromo-2-(Bromodifluoromethyl) configuration stands out for two main reasons: reactivity balance and substitution flexibility. Including a difluoromethyl group changes electronic properties, creating options for selective derivatization not seen with plain dibromocyclohexanes. The presence of bromine at two points on the molecule—one directly on the ring, the other on a substituent—opens doors for orthogonal modification. Chemists working on stepwise functionalisations have found this feature invaluable, as it gives control over reaction order.

    Similar cyclohexane compounds that replace one or more fluorines with hydrogens lack that crucial electron-withdrawing effect, which can impact reactivity in nucleophilic substitution or metalation reactions. From a manufacturing angle, more complex analogs with added trifluoromethyl or multiple brominated methyls complicate purification and often drive costs higher. We’ve tested routes to comparable compounds, but the difference in aqueous and solvent stability—with the difluoromethyl group providing a sweet spot between reactivity and shelf stability—gives 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane an edge.

    From a safety and handling perspective, the molecule’s vapor pressure and decomposition pathway allow safer long-term storage than some heavier halogenated intermediates. 1,2-dibromocyclohexane, for example, tends to offer less versatility in downstream modification and sometimes raises more regulatory red flags for emissions controls. We maintain records tracking workplace exposure thresholds and have worked with several international customers to provide supporting paperwork for occupational health audits.

    Technical Specification—A Story of Continual Refinement

    Unlike off-the-shelf commodity chemicals, our process for this specialty intermediate places equal value on both certificate-backed purity and ease of use in the customer’s synthetic route. Most laboratory batches run at or above a purity threshold of 98%, with our internal analyses covering chromatographic purity, residual metals (sometimes overlooked in non-pharma supply), water content, and byproduct profiles. We use both classical and electronic documentation of analytic runs, tying every lot number to a traceable dataset available for inspection. Consistency keeps development timelines on track: our customers don’t waste days troubleshooting unexpected byproducts or polishing up low-yield steps caused by trace contaminants.

    Flow chemistry advances have reinforced our ability to scale production. In the last few years, we overhauled our reactor train, incorporating real-time feedback systems on pressure, temperature, and mixing. Small changes in agitation or reagent feed order can make outsized differences in yield—something our veteran process engineers learned through trial, error, and close communication with customers experiencing batch-to-batch differences. Early on, we documented better selectivity and color consistency by holding the introduction of bromine at a tightly controlled pH range. These tweaks mean our product stands up to the harsh scrutiny of both pilot plant and high-throughput production facilities.

    Documented Use Cases and Feedback

    We see persistent demand from medicinal chemistry teams, not only for lead generation but for scale-up runs to support preclinical studies. Researchers at pharmaceutical companies want structures with both bromine and difluoromethyl groups because these fragments improve the property profile of actives—leading to better oral bioavailability and target affinity. Often, scientists use this intermediate to introduce chain extensions, heteroatoms, or ring fusions in a late-stage modification, saving precious synthetic steps downstream.

    In several agrochemical projects, our product has featured as a bridge to more complex fluorinated scaffolds. Customers reported higher conversion rates and more predictable coupling yields compared to starting from less substituted cyclohexanes. They value the possibility of swapping out the difluoromethyl group or using selective activation of one of the bromines to guide their downstream synthesis, knowing that competing pathways remain manageable due to careful manufacturing design that prioritizes isomeric purity.

    Market and Regulatory Perspectives

    Global demand has pushed us to refine our downstream logistics. International shipments now face stricter oversight, especially for brominated and fluorinated organics bound for regulated markets. We stay proactive on evolving requirements—toxicological testing, impurity profiling, shipping hazard classification, and transparency for registration purposes. While rules change, we keep a clear channel open with industry partners, sharing validated data to help everyone stay on schedule with compliance filings.

    We’ve heard from pharmaceutical and crop science customers that audit trails and transparent lot histories have become non-negotiable. Gone are the days where a vendor could ship without full analytic support. Our investment in electronic batch records, accessible audit paths, and accessible support (with technical staff who know the molecule inside-out) has supported customers through numerous international launches and regulatory reviews.

    Challenges in the Field: What Still Needs Work

    Producing high-reactivity halogenated intermediates calls for constant vigilance. Even small environmental lapses can affect yield and color. Trace metals, undetected moisture, or residual solvents can trip up project timelines. Companies relying on low-purity versions often end up with reproducibility problems or product recalls. To head off these issues, we’ve thrown resources into staff training, material control, and better in-line analytical equipment.

    Supply chain breakdowns remain a risk. Raw material procurement—especially specialty fluorinating agents—sometimes faces bottlenecks or logistical delays. We keep multiple sourcing options open and maintain buffer stocks. By acting quickly when disruptions threaten, we’ve helped customers avoid the costly delays that ripple through a research cycle.

    Pushing the Industry Forward: Future Directions

    As greener chemistry trends expand, we re-examine how we minimize waste in each production run. Effluent treatment, minimizing use of hazardous solvents, and energy-efficient syntheses occupy our R&D groups daily. We don’t claim to have solved sustainability for halogenated specialty chemicals, but we regularly partner with academics and technology providers to test better methods. Switching to greener reagents and embracing continuous process intensification has begun to shrink the overall waste profile.

    We also invest in collaborative research—feeding real-world user experience back into product development. Many fine chemical producers see specialty intermediates like this simply as a line item. We take each new use case as a chance to re-evaluate specs and process stability, ensuring our partners never feel shortchanged by silent changes or uncommunicated risks. By putting chemical and process expertise on the front line, we build solutions that suit realistic laboratory and plant conditions.

    Summary: Experience Matters in Specialty Chemicals

    Working hands-on with 1-Bromo-2-(Bromodifluoromethyl)Cyclohexane for years has shown us each molecule’s journey extends well beyond our reactor walls. Careful synthesis, steadfast analytic controls, and responsive logistics bring confidence to professional chemists in the field. It’s not only about purity or specification sheets; it’s about trust built on direct experience and staying responsive to the evolving needs of those who rely on precise chemical tools. The value of an intermediate like this lies in the deep expertise and attention baked into every step, from raw material to delivered drum or vial.