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Trans-1,2-Dibromocyclohexane

    • Product Name Trans-1,2-Dibromocyclohexane
    • Alias trans-1,2-Dibromocyclohexane
    • Einecs 221-072-9
    • 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

    753038

    Iupac Name trans-1,2-Dibromocyclohexane
    Molecular Formula C6H10Br2
    Molar Mass 241.95 g/mol
    Appearance Colorless to pale yellow solid
    Melting Point 113-115°C
    Boiling Point 253°C
    Density 1.98 g/cm³
    Solubility In Water Insoluble
    Cas Number 299-83-2
    Refractive Index 1.570 (predicted)
    Structure Type Chair conformation (major), trans stereochemistry
    Odor Characteristic, bromine-like

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

    Packing & Storage
    Packing Trans-1,2-Dibromocyclohexane is packaged in a 100 g amber glass bottle, clearly labeled with chemical name, hazard warnings, and purity.
    Shipping Trans-1,2-Dibromocyclohexane is shipped in tightly sealed containers, compliant with hazardous material regulations. It must be protected from heat, moisture, and incompatible substances. Labeling should include the chemical name, hazard warnings, and emergency instructions. Transportation follows UN guidelines, with proper documentation and safety data sheets accompanying each shipment to ensure safe handling and delivery.
    Storage Trans-1,2-Dibromocyclohexane should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect the chemical from direct sunlight and moisture. Use a chemical storage cabinet designed for hazardous substances, and ensure proper spill containment measures are in place.
    Application of Trans-1,2-Dibromocyclohexane

    Applications of Trans-1,2-Dibromocyclohexane in Industrial Manufacturing

    As a specialized manufacturer of trans-1,2-dibromocyclohexane, we support its use in chemical synthesis processes that demand high standards of quality, consistency, and formulation control. The material plays a crucial role in targeted downstream sectors, each with explicit compliance requirements, unique processing conditions, and specific end product classes. The following application segments reflect its real-world industrial deployment, guided by regulatory, technical, and operational detail.

    1. Agrochemical Intermediate Synthesis

    Our material sees primary demand in agrochemical manufacturing, specifically as an intermediate in the synthesis of selective herbicides and insecticides. Chemical engineers incorporate it during key step reactions owing to its stable dibromo structure, which facilitates ring functionalization for active ingredient development. Careful monitoring of addition rates ensures reaction specificity aligned with crop protection standards, while isolation procedures maintain high purity necessary for regulatory submission batches.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management for Agricultural Chemicals
    • EU Regulation (EC) No 1107/2009 – Approval of Plant Protection Products
    • US EPA guidelines for technical active ingredient impurities

    Typical usage ratio

    • Employed at 3.0–8.0% molar equivalent as a reactant, with concentrations adjusted based on desired halogen incorporation and specific synthetic routes; process chemists determine percentage with respect to limiting reagents.

    Downstream process integration

    • Integrated during the bromination/reduction sequence for cyclohexane modification; charged to batch reactors post solvent charging and pre-neutralization quench step to yield advanced intermediates.

    Final product types

    • Herbicide technical concentrates (e.g., cyclohexyl-based weed control agents)
    • Insecticide formulation actives for soil and foliar application
    • Precursor intermediates for fungicidal compounds

    2. Specialty Flame Retardant Synthesis

    Flame retardant compound manufacturers implement trans-1,2-dibromocyclohexane into ring-structured bromine-donating agents, which support safety compliance for consumer electronics and automotive plastics. Engineers control the incorporation phase in pilot and full-scale extrusion, utilizing its unique reactivity profile to generate brominated oligomers and end-capping agents, achieving regulated flame-resistance ratings for target substrates.

    Industry compliance standards

    • UL 94 – Standard for Safety of Flammability of Plastic Materials (Underwriters Laboratories)
    • RoHS Directive (2011/65/EU) – Restriction of Hazardous Substances
    • EN 45545-2:2013 – Railway applications fire protection
    • ISO/IEC 17025:2017 Laboratory Testing Accreditation

    Typical usage ratio

    • Routinely dosed at 5–15% by weight in brominated flame retardant formulations; proportion selected to balance fire performance index with mechanical property retention and meet substrate-dependent test criteria.

    Downstream process integration

    • Fed into polymerization or compounding steps as a reactive flame-retardant monomer or additive; introduced alongside crosslinkers and stabilizers before melt blending or reactive extrusion phases.

    Final product types

    • Thermoplastic and thermoset flame retardant masterbatches
    • Insulation panels for electronics
    • Molded automotive components requiring enhanced fire safety
    • Textile backcoatings for public transport seating

    3. Pharmaceutical Building Block Manufacturing

    Within the pharmaceutical sector, process scientists utilize trans-1,2-dibromocyclohexane as a halogenated precursor for constructing cyclic amines and alkyl bromide side chains during active pharmaceutical ingredient (API) synthesis. The controlled introduction of bromine enables subsequent functional group transformations under GMP-compliant conditions, supporting batch reproducibility and minimizing byproduct profiles in chiral or racemic drug scaffolds.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Monographs for intermediates
    • US FDA 21 CFR Part 210/211 for Drug Manufacturing Controls
    • ISO 13485:2016 for Medical Device-Related APIs (where applicable)

    Typical usage ratio

    • Introduced at 1.5–6.0% molar proportion with respect to the cyclohexane core, adjusted by scale-up chemists based on API route selectivity and step yield optimization studies.

    Downstream process integration

    • Appears in early-stage batch reactor synthesis following raw material qualification; undergoes halogen exchange or nucleophilic substitution, leading to pharmaceutically valuable intermediates under closed-system, validated conditions.

    Final product types

    • Advanced intermediates for antihypertensive and CNS drug molecules
    • API scaffolds incorporating cyclohexyl or bromo side chains
    • Key intermediates for contract pharma synthesis and route optimization projects

    4. Industrial Polymer Modification

    Manufacturers of specialty polymers and performance resins rely on trans-1,2-dibromocyclohexane as a reactive modifier to impart halogen compatibility, enhance material durability, and adjust dielectric properties. The compound is precisely metered during the chain extension or crosslinking stages, supporting applications where strict mechanical and flammability parameters intersect, such as in wire coatings and elastomeric seals.

    Industry compliance standards

    • ASTM D2863 – Oxygen Index for Polymer Flammability
    • ISO 9001:2015 for Quality Management in Polymer Manufacturing
    • UL 1581 – Reference Standard for Electrical Wires, Cables, and Flexible Cords
    • REACH Regulation (EC) No 1907/2006 Registration

    Typical usage ratio

    • Dosed at 2–7% by weight during initial compounding, with final level defined by electrical insulation requirements, component geometry, and in-process property validation.

    Downstream process integration

    • Added prior to or during bulk polymerization or reactive blending, co-introduced with fillers, flame retardants, or plasticizers; in some systems, introduced via solution agitation to ensure uniform dispersion before extrusion.

    Final product types

    • Low-smoke wire jacketing compounds
    • Elastomeric gaskets for industrial fluid handling
    • High-clarity, flame-retardant engineering plastics
    • Specialty resin blends for sensitive electronic applications

    5. Fine Chemical Synthesis for Analytical Standards

    Producers of certified reference materials and analytical standards include trans-1,2-dibromocyclohexane for calibration of chromatographic instruments and mass spectrometry validation methods. It is utilized as a matrix spiking standard or as a reactant in producing trace-level chemical entities supporting laboratory quality control and regulatory submissions.

    Industry compliance standards

    • ISO 17034:2016 – General Requirements for Reference Material Producers
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO/IEC 17025:2017 – Testing and Calibration Laboratories
    • US EPA Method 8270D for Semi-Volatile Organic Compounds Analysis

    Typical usage ratio

    • Weigh-in is strictly based on required calibration concentration, typically 0.01–0.5% w/v for solution standards; actual mass is determined according to method detection limit, analyte class, and reference certificate batch size.

    Downstream process integration

    • Prepared in solvent mixtures for spiking into quality control matrixes or used as a derivatization reagent during the preparation of ultra-pure chemical standards; handled under cleanroom or Class 1000 environmental conditions.

    Final product types

    • Certified calibration standards for GC-MS, HPLC, LC-MS
    • Trace-level quality control solutions for environmental, industrial, and pharmaceutical laboratories
    • Proficiency testing sample kits for laboratory accreditation bodies
    Free Quote

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    Certification & Compliance
    More Introduction

    Trans-1,2-Dibromocyclohexane: Reliable Consistency from a Ground-Level Manufacturer

    In-Depth Look at Trans-1,2-Dibromocyclohexane

    Having spent years on the production floor and in research facilities, I’ve seen how the right isomer can change the direction of a synthesis. Trans-1,2-Dibromocyclohexane stands out as a high-purity intermediate where molecular geometry and precise stereochemistry make all the difference. Each batch reflects the realities of chemical manufacturing rather than the demands of presentation-driven metrics displayed by third parties. Unlike the bland generalities of offsite brokers, our viewpoint reflects first-hand encounter with this molecule in both small-scale pilot runs and scaled industrial campaigns.

    Trans-1,2-Dibromocyclohexane carries the trans configuration across the cyclohexane ring, which imparts its own predictable behaviors in organic synthesis. In this business, cycloalkane bromides can all carry similar labels, but the exact isomer has a real impact. Cis and trans isomers do not swap places in the flask, and in our plant, that matters when planning out resources and equipment. Staight from our line, the trans-isomer’s melting point, physical phase, and in-process handling differ from those of its cis twin, influencing drying methods, downstream blending, and purification. The time between synthesis and packaging gets calculated down to hours, not days, because precise handling affects not only purity but also how the crystalline product behaves later.

    Why This Isomer, Why This Way?

    We’ve run the process with both forms, and the trans isomer brings more than just textbook value. In halogenated cyclohexanes, only the trans-form meets the targeting for many syntheses, especially in multi-step organic routes building pharmaceuticals, agrochemicals, or specialty polymers. From our direct experience, this comes down to the stereochemistry enabling further functionalization, either through elimination, substitution, or ring contraction. Downstream clients, and our own R&D chemists, rely on chromatographic reproducibility, meaning we avoid the cross-contamination and isomeric confusion that muddies outcomes in contract-manufactured lots.

    We don’t sweep the plant floor for adjectives, but every batch gets run through GC analysis to prove what we say. The trans-isomer, as it leaves our drying hoods, won’t give you the same thermodynamic properties as cis-1,2-dibromocyclohexane. We see repeat orders from regular customers who learned this difference after wasted time running reactivity trials with mixed or low-purity material. One customer in the polymer sector told me their yield jumped noticeably once they shifted from a generic cyclohexane dibromide to our trans-isomer, as traced contaminants no longer gummed up their reaction filtration. This isn’t marketing: it’s a real outcome of careful batch management.

    Product Handling, Storage, and Quality Control

    Within our plant, controlling every aspect of production means we understand this molecule beyond its formula. Each drum gets a lot number. Each sample comes off the main reactor’s finished goods conveyor, not a warehouse shelf months after production. We maintain a short storage timeline because lingering exposure, humidity, or variations in warehouse temperature can affect crystalline structure or, in more extreme cases, purity. Moisture ingress remains the biggest enemy, not because the molecule hydrolyzes easily, but because physical clumping leads to batch variability in downstream applications.

    We keep close relationships with the custom synthesis industry. Researchers sometimes request unusually tight purity limits, not because it looks impressive on paper but due to sensitivity in catalysts or chiral auxiliaries. No plant inspector ever needed to remind us that a little leftover bromide or an inch too much solvent residue in the drum leads to headaches down the line. That kind of feedback comes directly from those of us who also spend time trouble-shooting reactions when things go wrong.

    Quality teams don’t just rely on third-party spot checks. Our chemists sample each output batch, monitor crystal habit, pack, and ship, and maintain a repository of historic samples for backdating in the event of a customer question. GC, NMR, and elemental analyses run side by side, and comparison checks against the previous month’s output stay routine. We approach specification drift as a costly nuisance, not an abstract risk.

    Differences From Other Cyclohexyl Bromides

    While general distributors group all cyclohexane-based bromides together, only those who handle the actual chemistry get to see the differences first-hand. Trans-1,2-Dibromocyclohexane, prepared in our facility through controlled bromination and phase purification, bears real differences from the cis isomer and other positional analogs such as 1,3- or 1,4-dibromocyclohexane. The isomer sets the reactivity. Stereochemical rigidity in the trans molecule benefits steps like nucleophilic displacement or dehydrohalogenation, where the ring inversion barrier physically blocks side reactions found with the more flexible cis form.

    Our colleagues in the resin precursors sector notice that trans-1,2-dibromocyclohexane grants sharper transition points when deployed as a curing agent or as a precursor for flame retardants. The cis isomer, lying closer in energy and more subject to ring flipping, tends to give softer blend points when processed on hot rollers or in extruded lines. That distinction only appears after years spent loading reactors and pulling off samples at 2:00 a.m. with a production deadline looming.

    We hear from research users that high-purity trans material opens up easier access to well-defined products in stereospecific syntheses. For example, certain macrolactone assembly routes benefit from the rigidity of this trans-dibromide intermediate, as unwanted ring openings go down and product isolation proves simpler at the bench.

    We don’t just describe these outcomes abstractly. Our own R&D group has explored several test reactions, including Suzuki-type couplings and elimination-driven syntheses of cyclohexene derivatives, that would appear routine for those relying on library-standard material. The trans isomer avoids complications of syn-addition, meaning predictable, high-yielding conversion rates with proper workup and no guesswork when writing up standard operating procedures.

    Usage in Laboratory and Industrial Environments

    We sell most drums to downstream plants looking to streamline multi-step synthesis, but bench chemists and pilot lines also pull from our stock due to known batch quality. For these applications, our product enters processes such as mono-dehalogenation, catalytic hydrogenations, or ring contractions aimed at forming substituted cyclohexenes, cyclohexanones, and related compounds. Our plant’s familiarity with the practicalities of packing, thermal control, and cleanliness impacts the result for those looking to maintain traceability and batch reproducibility.

    In the case of flame retardants and crosslinkable resins, the trans-isomer’s handling properties—powder flow, resistance to cold caking, and retained whiteness—mean easier integration in production lines. Handling conditions make a real difference: packaging gets loaded onto shipping pallets only after headspace analysis, not just a visual check for leaks. We offer technical advice for safely storing material—tight drum closures, shaded areas away from sources of water vapor, and routine inspection of seals. Smart handling, in our experience, preserves not only customer satisfaction but also the reputation of the product in competitive sectors.

    Knowing the Sourcing: Keeping Production In-House

    Sourcing directly from the plant, not a faceless warehouse, means end users can count on single-site traceability and concrete answers if batch inconsistencies happen. We don’t just forward freight tickets from third-party sources. Each delivery comes out of an integrated synthesis line, starting with raw materials we select, purified bromine delivered through our measured dosing lines, and cyclohexane sourced from longstanding suppliers with closed-cycle purity controls.

    The real strength of in-house manufacturing lies in seeing failures up front. If a batch of bromine sits too long in the delivery tank, or humidity creeps into the feed, that gets discovered here where it can be corrected, not weeks later halfway around the world. Chemists and technicians stand behind the product. When something goes wrong, we fix it; we don’t make up excuses or pass the blame. Regular on-site reviews don’t just satisfy compliance, they teach the team what subtle changes in color or bulk density mean for final product handling.

    Small differences in preparation can cause problems that only surface in use—clumping during blending, inconsistent dispersal in compounding, small but recurring issues around reactivity windows. Taking on the responsibility of production, we’ve learned first-hand to adapt and optimize—small changes to agitation rates, timing for quench and extraction steps, drying curves—because customer experience comes back to the producer, not a third-party registry.

    Learning from Problems: Quality and Transparency

    No chemical plant runs forever without hitting snags, but the reality is that the sooner you act, the fewer headaches build downstream. A blocked filtration setup led us years ago to tighten up in-house pre-purification routines, so that sticky impurity layers wouldn’t end up in customer reactors. Batch color drift in a summer run led us to invest in better cooling and climate control on the plant floor. When clumping in a shipped drum led to complaints, we altered the crystallization step and built extra checks into the final drying and sieving process. No one learns as much about a raw material’s performance as the people making it day after day.

    We put emphasis on open documentation—batch sheets, full analytical certificates, and historic GC prints. Nothing gets shipped out without at least a three-step approval process, overseen by chemists who know the work involved firsthand. For us, traceability and transparency aren’t just printed words, but operating principles. No plant veteran enjoys a late-night call from a frustrated technical director running a delayed process, and so we head off surprises by keeping early warning signals in our own hands.

    Customers notice the distinction between a drum delivered from the original source and one repackaged through intermediaries. We’ve found that directly addressing batch-to-batch consistency minimizes plant-side rework, saves time in process scheduling, and bolsters confidence for technical users in time-sensitive environments. Our commitment runs deeper than compliance and aims to deliver actual time and cost savings on the ground.

    Technical Support Born from Real-World Experience

    Our staff go beyond shipping out boxes. If a partner company runs into snags with crystallization, solubility, or unforeseen reactivity, they connect directly with our chemists and technical teams. Working on the same equipment and reactions, we’ve collected enough odd real-life issues to know how to cross troubleshooting off the list quickly. Whether that means confirming impurity drift, adjusting moisture handling upstream, or working out replacement batches for unexpected down-time, we walk through solutions together.

    As a producer, direct access to source analytics and process records shortens the feedback cycle for customers. We don’t recite technical brochures or transfer calls through layers of sales staff; those working with us get access to the plant’s own quality team, not a disconnected hotline. In the rare cases someone uncovers a process anomaly—a point-of-use crystallization issue, or inconsistent reactivity in a synthetic trial—our plant has the notebooks and batch records needed to hand.

    Future Trends and Continual Improvement

    Staying on top of the game means always evaluating new catalyst options, reactor setups, and sustainability measures. We regularly test greener purification approaches, explore more closed-cycle solvent recovery, and invest in minimizing byproduct formation. The science behind trans-1,2-dibromocyclohexane hasn't changed in decades, but the know-how and care put into making it continues to evolve with demand.

    Sustainability goals on site go beyond following regulations. We shred and recycle all packaging not sent out, recapture bromine residues, and keep waste streams monitored by in-house staff familiar with day-to-day output levels. Efficiency in resource handling and energy use keeps us competitive in price and future-proofed against new environmental benchmarks. Efficiency pays off—not only by reducing overhead but by keeping the product in line with expectations for low-residue, high-purity output.

    Every process tweak gets logged for internal review—plant veterans and junior chemists alike contribute improvements. We learn by doing, and shared experiences travel across teams for future adjustments. This continuous cycle pays off in the real world, where each improvement in process reliability reflects in the end usage for bench chemists, pilot-line process developers, and large-volume industrial users alike.

    The Real Value of the Producer’s Approach

    The chemical sector brims with listings, but the people on the inside—those who run the reactors and tweak the drying lines—know that not all sources provide peace of mind. We don’t throw around claims lightly. The experience of hands-on manufacture makes each drum a guarantee of not only chemical identity, but also the care, attention, and accountability behind its creation. Our approach with trans-1,2-dibromocyclohexane remains built on experience, conversation, and a willingness to adapt alongside our users.

    For technical users who care about outcome, not just a certificate, product origin means much more than a paperwork trail. It means reliable performance, faster troubleshooting, and stronger support from the team that built the batch. In our plant, each drum shipped provides a reminder of the difference that hands-on manufacturing makes for users running real processes under pressure.

    The difference between a product drawn from a source like ours and one lost in multi-tiered supply chains shows up not only in technical sheets, but in smoother syntheses, reliable blending, and fewer phone calls about unexpected results. We trust in good chemistry because we run the lines ourselves, every day.