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(E)-1,4-Dibromobut-2-Ene

    • Product Name (E)-1,4-Dibromobut-2-Ene
    • Alias trans-1,4-Dibromo-2-butene
    • Einecs 210-808-5
    • 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
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    Specifications

    HS Code

    233318

    Iupac Name (E)-1,4-Dibromobut-2-ene
    Molecular Formula C4H6Br2
    Molar Mass 213.90 g/mol
    Appearance Colorless to pale yellow liquid
    Density 2.09 g/cm³
    Boiling Point 170-172 °C
    Melting Point -36 °C
    Solubility In Water Insoluble
    Structure BrCH2CH=CHCH2Br (trans-configuration)
    Cas Number 638-37-1

    As an accredited (E)-1,4-Dibromobut-2-Ene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 g of (E)-1,4-Dibromobut-2-ene is supplied in an amber glass bottle with a secure, chemically-resistant screw cap and hazard labeling.
    Shipping (E)-1,4-Dibromobut-2-ene is shipped in tightly sealed containers, protected from light, heat, and moisture. Due to its hazardous nature, it is transported according to international regulations for dangerous goods, typically under UN 2810 (Toxic liquid, organic, n.o.s.), with appropriate hazard labeling, documentation, and handling precautions to ensure safety.
    Storage (E)-1,4-Dibromobut-2-ene 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 protected from direct sunlight. Store in a suitable, chemically-resistant container, and ensure proper labeling. Handle with care, using appropriate personal protective equipment to avoid inhalation and skin contact.
    Application of (E)-1,4-Dibromobut-2-Ene

    Applications of (E)-1,4-Dibromobut-2-Ene in Industrial Manufacturing

    (E)-1,4-Dibromobut-2-ene is a key intermediate in specialized organic synthesis. As a direct manufacturer, we focus on high-purity supply for demanding downstream sectors, including pharmaceutical actives, specialty agrochemicals, polymer crosslinking, and advanced materials synthesis. Below are actual industrial application scenarios with detailed technical context.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ (E)-1,4-dibromobut-2-ene for the construction of carbon frameworks in API precursors via alkylation and cross-coupling reactions. Its symmetrical electrophilic groups enable selective transformations critical for active molecule complexity, especially in the production of heterocyclic or halogenated drug intermediates. Compliance focuses on stringent impurity control and GMP traceability, requiring controlled reaction stoichiometry and validated purification steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF guidelines for starting materials
    • Ph. Eur. monographs (where applicable)
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Applied at 1.0–1.5 molecular equivalents per target carbon center
    • Stoichiometry adjusted based on target yield and process step
    • Excess minimized due to regulatory control on residual bromide
    • Typical concentration: 0.5–2.0% w/w in reaction charge

    Downstream process integration

    • Charged in early to mid-stage API intermediate synthesis
    • Introduced to alkylation or Suzuki-type cross-coupling reactors
    • Unreacted raw material removed via solvent extraction and chromatography
    • Traceability documented from batch intake to purification output

    Final product types

    • Specialty alkylated pharmaceutical intermediates
    • Piperazine, pyridine, and pyrimidine derivatives
    • Halogenated heterocyclic building blocks
    • Precursor compounds for anti-infectives and oncology APIs

    2. Agrochemical Active Ingredient Manufacturing

    Agrochemical producers utilize (E)-1,4-dibromobut-2-ene as a halogenated linker for synthesizing dual-function molecular scaffolds. Its even-chain geometry facilitates the construction of new-mode-of-action herbicide and insecticide actives, particularly those incorporating double-bonded C4 fragments and controlled bromination for metabolic stability in field applications. Quality control ensures minimal residual organic halides in accordance with crop safety standards.

    Industry compliance standards

    • FAO/WHO specifications for technical grade pesticide ingredients
    • ISO 9001:2015 certified production
    • EPA regulations for inert ingredients in agricultural products
    • REACH registration (Europe) for industrial chemical use

    Typical usage ratio

    • Generally 1.0–1.2 equivalents per target ring closure or alkylation step
    • Adjusted depending on impurity profile of final active
    • Dilution in solvent phase typically 0.8–1.5% w/v
    • Residual content in technical concentrate: <0.05% w/w

    Downstream process integration

    • Reacted in controlled addition to Grignard or Michael-type syntheses
    • Incorporated at early-stage condensation or as terminal modification
    • Purified via phase separation, filtration, and recrystallization
    • Residuals monitored using GC-MS at each batch stage

    Final product types

    • Halogenated herbicide actives
    • Synthetic pyrethroid insecticides
    • Novel antifeedant or growth regulator active ingredients
    • Dual-action pesticide technical concentrates

    3. Polymer Crosslinking Agent Production

    Specialty polymer and elastomer makers use (E)-1,4-dibromobut-2-ene as a bifunctional crosslinking agent, particularly to introduce defined unsaturation and halogen resistance. Its linear diene configuration ensures uniform crosslink spacing in electron-beam-cured and brominated copolymer products. Batch processing emphasizes residual monomer limits due to mechanical property control and regulatory demands for automotive and electrical-grade polymers.

    Industry compliance standards

    • ASTM D2000 for rubber materials in automotive applications
    • UL 94 for flammability of plastic materials
    • RoHS (Restriction of Hazardous Substances) for halogen content
    • ISO 14001 for environmental management in production

    Typical usage ratio

    • 0.2–0.8 phr (parts per hundred rubber) for vulcanization or crosslinking
    • Can reach 1.2 phr in high-performance cable insulation
    • Ratio determined by mechanical testing (tensile, elongation)
    • Excess agent removed via devolatilization and vacuum treatment

    Downstream process integration

    • Mixed with base elastomer in internal mixer or extruder
    • Crosslinking triggered thermally or via radiation cure
    • Unreacted dibromobutene extracted by solvent washing
    • Batch monitoring for gel content and crosslink density

    Final product types

    • Automotive rubber seals and gaskets
    • Halogen-resistant cable sheathing
    • High-performance elastomeric membranes
    • Electron-beam-cured specialty polymers

    4. Advanced Materials and Organic Electronics Synthesis

    Producers of advanced materials and organic semiconductors use (E)-1,4-dibromobut-2-ene for the precise introduction of halogenated vinyl units into custom molecular backbones. Its use allows tuning of charge transport and film-forming characteristics in the synthesis of semiconducting polymers and OLED precursors. Stringent electronic-grade QC targets water, metal, and organobromine impurity limits per device reliability requirements.

    Industry compliance standards

    • JEDEC J-STD-033 for moisture sensitivity in electronic compounds
    • IPC-4101 for base materials in printed circuit applications
    • IEC 61249-2-21 for halogen-free base materials
    • IATF 16949 for automotive electronics

    Typical usage ratio

    • Incorporated at 0.3–0.7 molar equivalents per oligomer or polymer repeat unit
    • Adjusted for target molecular weight and conductivity
    • Residuals controlled down to <50 ppm depending on product class
    • Usually in toluene or DMF at 1–3% (w/v)

    Downstream process integration

    • Fed to C–C coupling reactors or vinyl polymerization modules
    • Phase-transfer catalysts often required for full conversion
    • Product isolated by precipitation and repeated washing
    • Final product tested for purity by LC and microanalysis

    Final product types

    • Semiconducting polymer films for electronic devices
    • OLED intermediate compounds
    • Precursor materials for organic thin-film transistors
    • Halogenated monomers for specialty copolymers
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    Certification & Compliance
    More Introduction

    (E)-1,4-Dibromobut-2-Ene: A Closer Look at This Versatile Intermediate

    Introduction to (E)-1,4-Dibromobut-2-Ene

    (E)-1,4-Dibromobut-2-ene stands out among specialty brominated intermediates. Our experience with this molecule goes back decades, and its importance for advanced synthesis has never been clearer. This compound, also known by its CAS number 6974-77-2, contains a four-carbon backbone with an (E)-alkene sandwiched between terminal bromines. The geometric configuration offers both stability and predictable reactivity — a combination that synthetic chemists appreciate when building more complex molecular architectures.

    Over the years, we've observed how the uniform placement of bromine atoms at the 1 and 4 positions creates a reliable starting point for a wide range of organic transformations. Almost every batch we produce finds its way into innovation pipelines, from pharmaceutical intermediates to new materials for electronics and coatings.

    The Chemistry Behind (E)-1,4-Dibromobut-2-Ene

    From a manufacturing standpoint, producing (E)-1,4-dibromobut-2-ene involves carefully controlled bromination procedures. The challenge always centers around maintaining the precise E-stereochemistry during synthesis. Years of refining our process have taught us that attention to purification steps pays dividends in both yield and reliability.

    The double bond at the 2-position introduces reactivity that sets this molecule apart from related alternatives like 1,4-dibromobutane or 1,2-dibromoethene. We find that customers leveraging the unique (E)-configuration can dial in selectivity during coupling, alkylation, and elimination reactions, letting them avoid unwanted side products and streamline downstream purification routines.

    Our technical team often works alongside clients during scale-ups, helping them translate laboratory successes to manufacturing runs. In every case, our experience with the isolation, handling, and storage of this liquid brominated compound proves critical for safety and consistency.

    Model and Specifications from the Manufacturer’s Point of View

    Every shipment we release undergoes a battery of analytical tests. GC and NMR spectra provide direct confirmation of the (E)-configuration and rule out isomerization byproducts. As a manufacturer, we apply strict thresholds for purity, often delivering product in excess of 98% (by area). Water content, inorganic salts, and color specifications matter to our customers, so we routinely verify these parameters prior to shipping.

    The characteristic pale yellow to colorless appearance comes from the absence of oxidation byproducts and heavy-metal residues. We take surface safety seriously; proper venting and bromine fume scrubbing during reaction and packaging have proven essential over hundreds of lots. Each drum or container ships sealed under inert gas when customers require additional stability or intend to perform sensitive transformations downstream.

    Our decades of experience tell us that even seemingly minor impurities can affect catalyzed reactions or polymerizations. Collaboration with our analytical and logistics departments ensures that we’re meeting our clients’ needs rather than just fulfilling orders from a sheet of specifications.

    Applications: What Sets This Compound Apart?

    Customers from small lab teams to multinational manufacturers ask us about the differences between this compound and other dibromoalkenes or saturated haloalkanes. (E)-1,4-dibromobut-2-ene brings unique value with its unsaturated core. The alkene enables a host of organic reactions — cycloadditions, substitutions, oxidative couplings, and ring closures become feasible.

    We’ve seen medicinal chemists employ it as a linker in constructing macrocycles, leveraging the rigidity imparted by the double bond to control biological activity. Some customers in materials science build ladder polymers and new resins where the stereochemistry plays a role in thermal stability and mechanical performance.

    Fine chemical manufacturers turn to this intermediate in the scalable production of advanced monomers and pharmaceutical API side chains. The two bromine atoms function as handles for further substitution, allowing rapid transformation using palladium or nickel catalysis. Compared to more common 1,4-dibromobutane (fully saturated) or 1,4-dichlorobut-2-ene (less reactive chlorines), the (E)-dibromo analog speeds up reaction kinetics—cutting process times and reducing energy consumption in plant settings.

    Differences from Other Products

    From behind the scenes at our plant, we see real distinctions between (E)-1,4-dibromobut-2-ene and similar compounds. The position and geometry of the double bond gives this molecule a profile distinct from simple alkane-based dihalides. In reactions with nucleophiles, for example, the reactivity of the allylic position allows for targeted functionalization that is simply not possible with the saturated analogs.

    We often field requests for comparison data, so our lab routinely tests reactivity trends using real-world conditions. The differences become evident in everything from copper-catalyzed coupling yields to selectivity in Grignard additions. The E-configuration also helps users avoid complications from cis isomer contamination, which can lead to byproduct formation or batch-to-batch variability in downstream steps.

    Chemists who have struggled with less reactive substrates appreciate being able to lower activation barriers. Customers tackling new synthetic methodologies, such as cross-couplings aiming to conserve atom economy, often reach out for our insights from pilot-scale manufacturing. Our team brings practical knowledge from handling these differences daily, which can help resolve issues that aren’t always clear from the literature.

    Why Purity and Lot Consistency Matter

    As a direct manufacturer, nothing frustrates us more than seeing a promising process derailed by inconsistent starting materials. In our experience, the purity and isomeric ratio of (E)-1,4-dibromobut-2-ene directly affect catalyst performance, isolation of pharmaceutical targets, and even long-term material shelf life.

    Consistency across shipments is a non-negotiable. We track every raw material intake, lot blending, and reactor parameter using batch records and in-line monitoring. With stricter regulatory oversight in fine chemicals and pharma, our ability to supply stable, well-characterized lots reduces requalification and validation cycles. We often find that open communication with customers about minor specification shifts — even those within published limits — saves considerable troubleshooting time and cost downstream.

    We learned early on that even typical storage conditions can alter product quality if not tightly controlled. Each filled drum receives a unique identifier and traceability documentation, which supports both our clients’ compliance efforts and our own internal quality improvement cycles.

    Handling and Safety Experience

    Brominated alkenes bring specific hazards, so we train every operator on containment and personal protective equipment protocols. Our own teams use closed systems whenever possible and regularly review detection systems around storage tanks. Every spill response and safety improvement adds to our in-house knowledge base; we advise our customers with proven tactics for safe handling, drawn from lessons learned over many campaigns.

    We have worked with environmental, health, and safety teams to minimize fugitive emissions, both in our facility and at customer sites. Brominated intermediates can cause skin and airway irritation; we support downstream users with technical notes and first-hand observations rather than just safety data from the open literature.

    Supporting Sustainable and Efficient Use

    Demand for environmentally responsible brominated intermediates continues to grow. Our synthesis emphasizes atom economy and minimizes halogenated waste streams by reclaiming and recycling process solvents. Customers looking to shrink their EHS footprint appreciate support with recyclable packaging, detailed waste compatibility specifications, and options for custom concentration or dilution.

    Through our supply agreements, we share process optimizations and downstream recycling solutions, using data from our closed-loop solvent recovery and bromide reclamation units. We believe that open sharing in this area lifts the entire supply chain, supporting both profitability and environmental stewardship.

    Insights into Research and Scale-Up

    Synthetic chemists rely on intermediates like (E)-1,4-dibromobut-2-ene for new molecule discovery, but process scale-up can reveal unforeseen challenges. Our plant has supported numerous scale transitions — from grams through kilograms to multi-ton supply. Planning for scale-up requires direct feedback from both bench and plant teams, and our experience helps close gaps between theory and practice.

    We see challenges in heat management, mixing efficiency, and bromine dosing at larger volumes. Sometimes, novel purification approaches pay off handsomely. This direct feedback loop between production and R&D keeps our operations nimble and lets us adapt to new process constraints faster than organizations tied to rigid legacy recipes.

    Troubleshooting during client ramp-ups has fostered a culture of problem-solving. We encourage our partners to visit our facilities or invite our chemists into their own process development labs, sharing what we’ve learned through thousands of batch records and process adjustments.

    Batch Customization and Technical Support

    Our ability to tailor production runs for specific applications comes from years of direct engagement with a spectrum of industries. Some partners require custom packaging under inert atmosphere for moisture-sensitive downstream syntheses; others specify unique concentration ranges to support in-line blending or continuous flow reactions.

    Our technical support begins long before the first shipment. We help customers select batch sizes, packaging types, and even recommend compatible transfer pumps or drum fittings based on our own experience. We pride ourselves on making real-world suggestions that address laboratory realities, not just paper specifications. Oscillating global supply chains, evolving regulations, and application-specific demands have sharpened our sense of urgency and flexibility.

    The Changing Landscape of Brominated Intermediates

    The specialty chemical industry faces upward pressures on pricing for high-purity brominated intermediates. Factors like raw material volatility, regulatory shifts, and tightening waste disposal laws create challenges that demand both technical expertise and relationship building.

    Our history has taught us that process innovation — from improved bromine usage efficiency to real-time byproduct monitoring — pays off by insulating our clients against some of these external shocks. Direct feedback from end-users helps us prioritize investments in debottlenecking and scaling capacity when downstream needs jump unexpectedly or new applications demand rapid onboarding.

    Being a manufacturer means seeing every part of the business — from raw material sourcing and operator training to risk mitigation and customer audits. Our commitment to quality, consistency, and transparency builds trust with research teams and process engineers who rely on us for both day-to-day supply and support during project pivots or market upswings.

    Looking Forward: Innovation and Collaboration

    We see advances in catalysis and green chemistry driving greater use of intermediates like (E)-1,4-dibromobut-2-ene. Our R&D team collaborates with industrial partners as they expand into new drug discovery or materials science programs, innovating alongside them to address supply, safety, and impurity questions. We draw regularly on our field experience to help customers adapt to emerging regulations governing bromine-containing compounds or to streamline production by redesigning key steps in their synthetic routes.

    Each partnership brings new challenges and learning opportunities. Whether working through a tricky scale-up or helping solve lingering issues with polymer functionalization, we rely on our accumulated knowledge to support rapid problem-solving. Our staff includes operators, chemists, and process engineers who have grown with us and now serve as essential resources for both newer hires and customer technical teams.

    Conclusion: The Value of Experience

    Long-term manufacturing of (E)-1,4-dibromobut-2-ene has taught us that success depends on every detail. From understanding the nuances of isomer purity to helping clients solve their process bottlenecks, we invest in both technology and people. Real improvements happen not just at the reaction vessel, but in how we communicate, respond, and innovate for each new requirement.

    Direct producers carry a unique responsibility to deliver both materials and expertise. We view each batch as a promise — not just to deliver the compound itself, but to supply insights and guidance built on real, hands-on experience. Whether supporting a single experiment in a startup lab or full-scale production for a global brand, we value each opportunity to help customers achieve reliable, cost-effective, and innovative outcomes.