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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 | 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. |
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 SynthesisPharmaceutical 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
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2. Agrochemical Active Ingredient ManufacturingAgrochemical 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
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3. Polymer Crosslinking Agent ProductionSpecialty 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
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4. Advanced Materials and Organic Electronics SynthesisProducers 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
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(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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.