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2-Butene-1,4-Diyl Bis(Bromoacetate)

    • Product Name 2-Butene-1,4-Diyl Bis(Bromoacetate)
    • Alias 1,4-Bis(bromoacetoxy)-2-butene
    • Einecs 629-621-6
    • 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

    170835

    Chemicalname 2-Butene-1,4-diyl bis(bromoacetate)
    Casnumber 104129-90-8
    Molecularformula C8H10Br2O4
    Molecularweight 345.97
    Appearance Colorless to pale yellow liquid
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically ≥95%
    Storagetemperature 2-8°C (Refrigerated)
    Smiles C(COC(=O)CBr)=C(COC(=O)CBr)

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

    Packing & Storage
    Packing Amber glass bottle, 25g, tightly sealed with a screw cap, labeled with chemical name, formula, hazard symbols, and handling instructions.
    Shipping 2-Butene-1,4-Diyl Bis(Bromoacetate) is shipped in tightly sealed containers, protected from light and moisture. It is transported under controlled conditions, typically as a hazardous material, adhering to relevant regulations. Proper labeling and documentation ensure safe handling, with protection against physical damage during transit to prevent leaks or contamination.
    Storage 2-Butene-1,4-Diyl Bis(Bromoacetate) should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Use secondary containment to prevent spills and ensure storage at room temperature or as specified by the manufacturer’s guidelines. Handle with appropriate personal protective equipment.
    Application of 2-Butene-1,4-Diyl Bis(Bromoacetate)

    Applications of 2-Butene-1,4-Diyl Bis(Bromoacetate) in Industrial Manufacturing

    2-Butene-1,4-Diyl Bis(Bromoacetate) serves as a key specialty intermediate in various niche sectors requiring controlled bromoacetate functionality. As an original manufacturer, we support customers in high-value end-markets with strict compliance and tailored technical cooperation from formulation to scale-up. Below, we outline real-world applications based on established downstream industrial practices, each reflecting unique regulatory demands, formulation techniques, and integrative production workflows our partners utilize in large-scale operations.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Intermediates

    This material enables the introduction of bifunctional bromoacetate groups in the multi-step synthesis of certain anti-cancer drug intermediates. Customers rely on its reactivity profile to facilitate highly selective alkylation reactions, meeting global traceability and documentation demands throughout the API supply chain.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA Current Good Manufacturing Practice)
    • EU GMP Volume 4, Part II
    • Pharmacopoeia monograph references: USP, Ph. Eur. (for downstream actives)

    Typical usage ratio

    • 0.8–1.2 molar equivalents based on primary substrate, with real-time HPLC monitoring guiding addition to minimize residuals

    Downstream process integration

    • Introduced during intermediate stage alkylation step in solvent-controlled glass-lined reactors under inert atmosphere, followed by aqueous quench and chromatographic purification

    Final product types

    • Oncology drug intermediates for targeted small molecule therapies
    • Protected or activated intermediates used in cytostatic agent synthesis

    2. Advanced Monomer Manufacturing for Specialty Polymers

    Polymer engineers employ this molecule as a reactive building block to introduce pendant ester functionalities or controlled crosslinking points within resins designed for electronics or specialty coatings. This function enables precision tuning of molecular architecture unavailable with simpler mono-bromoacetates.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (site certification)
    • RoHS Directive 2011/65/EU (where applicable, for electronics)
    • REACH Regulation (EU) No 1907/2006 registration and SDS compliance
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 1–10% by weight relative to base monomer batch; higher loadings for copolymerization, adjusted for glass transition targets and final crosslink density

    Downstream process integration

    • Metered addition during pre-polymer synthesis or directly into bulk polymerization (radical or step-growth), followed by post-cure to set network architecture

    Final product types

    • Photolithography resists for semiconductor fabrication
    • UV-curable coatings with engineered bromo functionalities
    • Functionalized specialty polyesters and copolymer membranes

    3. Crosslinking Reagent for Biomedical Hydrogels

    Biomedical device producers use controlled amounts of dibromoacetate derivatives as crosslinkers to modulate gelation kinetics or introduce degradable linkages for cell encapsulation matrices. This material's bifunctional structure promotes uniform hydrogel networks essential for precise mechanical properties and drug-release profiles.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management
    • 21 CFR Part 820 (US FDA QSR for medical devices)
    • USP Class VI Biological Reactivity Test standards

    Typical usage ratio

    • 0.1–0.5% w/w of polymer precursor phase; ratio determined by desired crosslink density and swelling characteristics measured by ASTM F1926-12

    Downstream process integration

    • Added in the pre-gelation aqueous formulation phase, followed by controlled temperature-initiated crosslinking, and subsequent washing to meet extractable limits

    Final product types

    • Hydrogel wound dressings and soft tissue scaffolds
    • Injectable biodegradable hydrogel matrices for drug delivery

    4. Surface Functionalization Agent for Bioanalytical Microarrays

    Producers of bioanalytical devices integrate this bifunctional bromoacetate to covalently anchor probe molecules onto activated glass or polymer substrates, improving immobilization efficiency for DNA, protein, or antibody microarrays. Control over linker density and uniformity directly impacts assay reproducibility and background signal reduction.

    Industry compliance standards

    • ISO 13485:2016 for diagnostic device component production
    • EN ISO 18385:2016 Minimizing risk of human DNA contamination
    • MIL-STD-883 (for microelectronic substrate qualification)

    Typical usage ratio

    • 0.5–3.0% by volume in functionalizing bath, proportional to substrate active site density determined by surface spectroscopy

    Downstream process integration

    • Applied during surface activation step after plasma cleaning, followed by thermal curing and blocking steps to finalize substrate preparation

    Final product types

    • Fluorescence-based gene expression microarrays
    • Protein and antibody capture chips for multiplexed diagnostics

    5. Alkylating Intermediate for Agrochemical Synthesis

    Agrochemical synthesis groups select this dibromo ester for precise alkylation in the manufacture of certain active pesticide intermediates, where other alkylating agents lack the required selectivity or leave persistent residues. Process engineers value its contribution to generating target structural motifs under mild conditions, minimizing environmental byproducts during downstream processing.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025 for analytical laboratories (residue monitoring)
    • REACH pre-registration for agro precursor handling
    • Local environmental release limits (e.g., EU Directive 2010/75/EU)

    Typical usage ratio

    • Discrete 0.3–0.9 molar equivalents, adjusted to active site stoichiometry; monitored by GC-MS during reaction progress

    Downstream process integration

    • Charged into alkylation step after in situ deprotonation of nucleophilic precursor, followed by solvent swap and successive work-up, including phase separation and crystallization

    Final product types

    • Active intermediate precursors for herbicides, fungicides, and insecticides
    • Stabilized protected building blocks for later formulation steps
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    Certification & Compliance
    More Introduction

    2-Butene-1,4-Diyl Bis(Bromoacetate): On the Shop Floor and in the Lab

    Real-World Insights Into a Specialized Intermediate

    We have spent years producing 2-Butene-1,4-Diyl Bis(Bromoacetate), watching it transform from a niche lab chemical to a staple in the synthesis toolkit for custom molecule builders. The industry asks a lot from manufacturers and intermediate producers now; every batch faces sharp eyes for purity, consistency, and specific isomer ratios. This particular compound, with the formula C10H12Br2O4, delivers a rare combination: a reactive double bond and two well-placed bromoacetate groups attached to opposite ends of the butene backbone. The 1,4-di-substitution means the molecule gives chemists a straight, symmetrical starting material for controlled addition or coupling reactions—putting the hard work into building more advanced specialty chemicals, fine pharmaceuticals, and active ingredients.

    Why We Focus on Model Consistency: From Raw Material to Final Product

    Every manufacturer has a story about that one shipment that nearly missed the mark because an upstream supplier pulled a fast one on a diol spec. With our 2-Butene-1,4-Diyl Bis(Bromoacetate), we learned early that you don’t cut corners. Only well-characterized 1,4-butanediol, pure acetic acid, and properly handled bromination agents enter the reactor. At scale, it means batches remain stable and each drum, every lot, matches the standards a custom pharmaceutical customer would expect. Moisture control takes daily attention. Exposing the intermediate to variable heat or oxygen can generate either colored impurities or side reactions, so the system design has to account for rapid quenching and inert atmosphere handling. Over time, we’ve tightened up these small details so the end user, the chemical researcher or production chemist, can trust the bottle in their hand without worrying about off-notes, by-products or unexplained test results.

    Technical Specifications That Matter on the Ground

    It is easy to read specs from a web page or datasheet, but the practical aspects come from working the production line itself. This intermediate appears as a colorless to pale yellow liquid with a characteristic, somewhat acrid odor during handling. We set our purity levels above 98% by GC, and bromine content gets closely monitored to avoid overbromination or trace halogen leftovers that might complicate a downstream reaction. Handling density (approximately 1.67 g/cm³ at room temperature) and boiling point (around 312°C, but it decomposes before reaching this) shape both packaging and shipping protocol. Our packaging team uses amber glass and protected drums to shield the material from stray light or humidity. These might sound like small touches, though for customers scaling to multikilogram lots, it keeps performance predictable.

    Experience With Sensitive Chemistry: Why this Building Block Earns Its Place

    Choosing 2-Butene-1,4-Diyl Bis(Bromoacetate) over run-of-the-mill dihalides or diesters comes from its unique structure. In our workshops, customers use this intermediate in multistep syntheses—often as a linker or bridgehead species—where both electronic structure and spatial arrangement matter. Unlike simple dibromoalkanes, which can introduce unwanted flexibility or side reactions, the butene backbone locks in geometry. Click chemistry, macrocycle assembly, and fluorophore functionalization all use this core. In some advanced material synthesis projects, the symmetrical substitution enables rigid cross-linking that holds up under conditions that would break more flexible intermediates. Efficiency in these syntheses often rises, and purification gets easier, because side products do not bunch up around an asymmetric carbon or an odd stereocenter.

    Handling and Storage on the Manufacturing Floor

    A chemical like this demands careful storage. Draw from our own barrel room and see climate control running day and night, keeping temperature shifts at bay. Without active management, batches attract moisture and break down—releasing acetic acid fumes. Leaks, vapor exposure, and bromide release push us to maintain robust venting and spill protocols. Our teams always use proper PPE and ventilated hoods; for customers, we recommend similar caution. What works for developers at the bench rarely scales without good labels, tight monitoring, and practical know-how on how the product behaves across seasons. In our facility, we regularly rotate inventory to keep fresh stock moving through and backward trace batches to audit purity and historical handling.

    What Sets 2-Butene-1,4-Diyl Bis(Bromoacetate) Apart From Related Compounds

    The differences between our 2-Butene-1,4-Diyl Bis(Bromoacetate) and more common bifunctional alkylating agents become clear in scale-up and advanced R&D. Classic dibromoalkanes or glycols equipped with bromides tend to offer higher reactivity, but they lack selectivity and structure. Our experience shows they introduce unpredictable by-products or low yields when customers attempt complex cyclizations or coupling reactions. In contrast, the butene bridge in our material provides a slightly more rigid scaffold. In one collaborative project with a peptide manufacturer, the rigid backbone boosted the selectivity of the bridging reaction, leading to higher target purity and less column chromatography during cleanup.

    Replace the central double bond with a fully saturated chain, like 1,4-dibromobutane diacetate, and the molecule loses its utility in certain click or step-growth polymerizations. The double bond offers unique points of attack for Diels–Alder or Michael additions and enables tandem reactions where saturated species would stall. For others focused on stimuli-responsive materials, that unsaturation permits later-stage derivatization—photochemical cross-linking or redox-based switching are a few real-world uses we've supported with technical guidance and fresh samples.

    Meeting Challenges in Scale-Up and Compliance

    Major pharmaceutical and specialty chemical firms come to established manufacturers for more than just raw materials; they expect batch-to-batch reliability and prompt troubleshooting support. On our side, compliance isn’t an afterthought—it’s woven into every stage. Regulatory documentation and ISO-certified lot tracing reassure stakeholders, but the practical benefits come from the dialogue between our QC chemists and customers. When a user in a regulated industry reported microtrace by-products above their detection threshold, we gathered both historical batch data and process details from their scaling run. By tightening reactor temperature windows and optimizing the workup protocol, together we dropped impurity levels below the threshold and documented corrective actions for all future lots.

    Adapting processes for new formulation requirements or substance notifications in global markets stretches in-house teams. In some geographies, transportation and environmental classifications restrict storage or shipment modes. Our compliance officers double-check SDS updates for current regulatory needs, and our logistics staff tackles the documentation so that product moves with no customs surprises or downtime in the customer’s supply line.

    Feedback From the Field: Continual Process Refinement

    Years of direct customer engagement means hearing both praise and the challenges users face. For one synthetic dye producer, rapid color change in the final product traced back to trace oxidation in the supplied intermediate. With targeted process improvements—deeper degassing and better inert gas blankets on every drum—we resolved the oxidative side reactions. Users working in medical device coatings and innovative hydrogels shaped another round of refinements. After pushbacks on the solubility in certain mixed organic solvents, our R&D piloted purification tweaks, optimizing for downstream compatibility while holding tight to the same purity benchmarks.

    Feedback loops never close; technical support calls and trial samples keep us revising packaging, analytic tests, and formulation guides for new market applications. What might seem like a simple shift—adjusting fill volumes or swapping cap materials—sometimes makes the difference between a smooth production run and ruined product. We handle these adaptations with both flexibility and commitment because every successful application strengthens trust in our technical capacity and builds long-term partnerships.

    Industry Applications: What Customers Have Achieved With This Intermediate

    Across our customer base, 2-Butene-1,4-Diyl Bis(Bromoacetate) demonstrates its strongest impact as a versatile building block for advanced organic synthesis. Fine chemical firms leverage it in custom coupling reactions—expanding access to new ligands and catalysts that classical dihalides struggle to achieve. Electronic material manufacturers exploit its unique geometry for assembling rigid, conjugated structures, and in the past year alone, we have supplied batches to teams developing functionalized OLED intermediates for next-generation displays.

    Bioconjugation also stands out. In targeted drug delivery, the symmetrical sites of reactivity mean researchers can dial in cross-links or controlled-release mechanisms with high fidelity, skipping several labor-intensive protecting group steps. Medical researchers designing bespoke hydrogels or responsive matrices describe fewer unwanted side reactions with this intermediate, leading to more consistent batches of finished therapeutic products. In each case, customers benefit not just from a chemical, but from the confidence that what we deliver meets the same standards every time: tested, verified, and ready for innovation.

    Quality as a Continuous Practice, Not a Checkbox

    Delivering critical intermediates like 2-Butene-1,4-Diyl Bis(Bromoacetate) goes beyond ticking boxes on a quality chart. Each lot gets tailored attention, both on the line and in the lab, from dry-down under vacuum to advanced spectroscopic verification. Our team checks for low-level impurities using both GC and NMR, giving customers deeper analytic insight if they need it. Sometimes real-world conditions introduce fresh challenges: a heat wave spikes shipment temperatures, a port delay threatens shelf life, or a customer tests under tighter specs for a new regulatory environment. In these cases, our technical team steps up—analyzing samples side by side with customer labs and working through accelerated aging studies to keep performance stable.

    We do not chase ISO labels for the sake of it, but clean rooms, staff training refreshers, and validated SOPs keep our operation aligned with global best practices. Long relationships with reputable raw material suppliers make each upstream molecule traceable and predictable. At every stage, facility managers review safety audits and performance metrics, holding the process accountable to the same benchmarks regardless of customer size or origin.

    Practical Advice for Laboratories and Production Teams

    Customers buying at pilot or commercial scale often ask for handling tips shaped by our direct experience. We strongly advise sealing containers immediately after each draw to prevent water ingress or slow decomposition. For those handling multiple lots, stagger storage so the oldest stock ships first and keep inventory records clean. In terms of waste management, the bromoacetate groups break down under alkaline conditions, so use compatible scavenging procedures in spent batches for easy neutralization. Never ignore local environmental regulations on halogenated waste; our teams can share disposal stories from years on the job to help new users set up safe and compliant routines.

    When repackaging for sampling or lab trials, avoid metal containers that could catalyze decomposition. Many industrial-scale users have transitioned to inert-lined drums or fluoropolymer inner bags, lessons learned from failed early shipments in the early 2000s. Keeping labs and plant floors organized saves much heartache; more than one customer fixed an erratic yield spike with a careful check of transfer lines for residual water or improperly cleaned vessels.

    Outlook: Navigating Tight Markets and Evolving Applications

    As a core intermediate, 2-Butene-1,4-Diyl Bis(Bromoacetate) carves a stable niche with steady, if not explosive, global demand. Recent supply chain shocks strengthened our commitment to dual-sourcing key reagents and keeping a buffer in finished stock. Chemistry, like every industry, goes through cycles, but successful producers survive by innovating—adjusting synthesis pathways to cut process steps or introducing real-time purity analytics to smooth out the bumps. We anticipate further use in precision drug conjugates and smart polymer architectures as research teams grasp the value of symmetry and double-bond reactivity.

    Energy management, emissions control, and safer work environments stay at the center of our operation. Waste solvents get recaptured wherever possible, batch sheets document each input and handling step, and our factory teams join training sessions regularly. We see those investments pay back every day on the production floor, in customer feedback, and in the long-term trust that builds when a fresh drum of 2-Butene-1,4-Diyl Bis(Bromoacetate) performs just as well as the last one.

    Strength Through Knowledge, Not Hype

    Customers, especially in fields with high barriers to entry like pharmaceuticals or advanced materials, want more than a label—they want transparency, competence, and partnership from their suppliers. Manufacturing 2-Butene-1,4-Diyl Bis(Bromoacetate) for years, we have found that responsiveness and a willingness to troubleshoot both technical and logistical hurdles matter more than the flashiest marketing. We regularly open doors to facility tours for longstanding clients, share validation reports, and bring feedback from the shop floor directly to our R&D and executive teams.

    Each drum or bottle shipped signals an investment in the downstream success of our customers. The relationships forged over technical support calls, shared analytics, and collaborative troubleshooting build confidence that runs deeper than any single batch. For everyone involved—from the handlers on the blending line to the scientists at the bench—the goal remains unchanged: precise, predictable performance in every application, and a commitment to improving both product and process, batch after batch.