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Cis-1-Bromo-2-Ethoxyethylene

    • Product Name Cis-1-Bromo-2-Ethoxyethylene
    • Alias (E)-1-Bromo-2-ethoxyethene
    • Einecs 221-216-6
    • 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
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    Specifications

    HS Code

    734592

    Chemical Name Cis-1-Bromo-2-Ethoxyethylene
    Molecular Formula C4H7BrO
    Molecular Weight 151.01 g/mol
    Cas Number 72241-76-4
    Appearance Colorless to pale yellow liquid
    Boiling Point Estimated ~140-145 °C
    Density Approximately 1.5 g/cm3
    Refractive Index n20/D ~1.490
    Solubility In Water Low
    Flash Point Estimated >40 °C
    Smiles BrC=C(OCC)H
    Isomerism Cis-isomer (Z-configuration)
    Stability Stable under recommended storage conditions
    Hazard Statements Irritant

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

    Packing & Storage
    Packing Cis-1-Bromo-2-Ethoxyethylene is packaged in a tightly sealed 100 mL amber glass bottle with secure labeling and hazard warnings.
    Shipping Cis-1-Bromo-2-Ethoxyethylene is shipped in tightly sealed, appropriately labeled containers, compliant with local and international regulations. The chemical should be protected from light, moisture, and heat during transit. It is classified as hazardous; therefore, handling and shipping require suitable cushioning and containment to prevent leaks or accidental exposure.
    Storage **Cis-1-Bromo-2-Ethoxyethylene** should be stored in a cool, dry, and well-ventilated area, tightly sealed in a suitable, chemical-resistant container. Protect from direct sunlight, moisture, heat, and ignition sources. Store separately from strong oxidizers and incompatible materials. Properly label the container and follow all applicable safety and environmental regulations for storage and handling of hazardous chemicals.
    Application of Cis-1-Bromo-2-Ethoxyethylene

    Applications of Cis-1-Bromo-2-Ethoxyethylene in Industrial Manufacturing

    Cis-1-Bromo-2-Ethoxyethylene serves as a specialty intermediate in advanced manufacturing environments. Our direct production supports precise downstream needs in high-value chemical syntheses and formulations. Below we detail main application sectors and relevant process know-how derived from our experience supplying global customers.

    1. Synthesis of Pharmaceutical Intermediates

    This compound plays a vital role as a vinylation or halogenation agent in multi-step pharmaceutical ingredient production. Its functional groups permit selective reactions, such as coupling and substitution, in heterocycle synthesis. Integrated mainly during the early or mid-stage of API precursor chains, it allows enhanced process yields and controlled impurity profiles. Typical examples include its use in the construction of substituted pyridine or pyrimidine structures for cardiovascular and neurological therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 U.S. FDA cGMP
    • European Pharmacopoeia (Ph. Eur.) directives
    • China GMP (2020 revision)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to nucleophilic starting material, adjusted based on target yield and side product minimization requirements

    Downstream process integration

    • Charged to reaction vessels after initial substrate activation steps; undergoes controlled reaction under anhydrous or inert gas conditions
    • Followed by isolation, purification, and direct further transformation into advanced pharmaceutical intermediates
    • Subject to in-process QC checks for residual bromide and unreacted vinyl ether

    Final product types

    • Pyridine- and pyrimidine-based API intermediates
    • Fluoroalkylated small molecules
    • Custom synthesis blocks for medicinal chemistry pipelines

    2. Agrochemical Active Ingredient Synthesis

    Producers of advanced crop protection agents employ this chemical for constructing complex vinyl ether motifs in new fungicide, herbicide, or insecticide actives. It incorporates into reaction paths generating select alkylated or halogenated aromatic rings, essential for high bioactivity. Users carefully monitor dosage and order-of-addition to maximize conversion and protect sensitive chiral centers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Specifications for Pesticide Active Ingredients
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • REACH (EC) No 1907/2006 registration for manufacture and import

    Typical usage ratio

    • 10–25 wt% of the stepwise reaction charge, dependent on molecular design and selectivity targets

    Downstream process integration

    • Introduced after preliminary ring assembly; enters vinylation or etherification subprocess
    • Requires closed system with exhaust scrubbing due to bromine emissions; introduces stage gate analysis for product content
    • Output feeds directly into formulation for technical concentrate or further derivatization

    Final product types

    • Halogenated aromatic agrochemicals
    • Vinyl ether-based insecticide and fungicide actives
    • Tank-mix formulation intermediates

    3. Electronic Material Additive Manufacturing

    The ethoxy and bromo functional groups facilitate highly selective modifications in the synthesis of specialty precursors for electronic photoresists and dielectric coatings. Materials engineers integrate this intermediate into process flows for generating proprietary monomers and oligomers, later polymerized into light-sensitive or insulating films critical for semiconductor patterning and PCB fabrication.

    Industry compliance standards

    • JEITA (Japan Electronics and Information Technology Industries Association) photoresist material standards
    • RoHS Directive 2011/65/EU compliance for electronics chemicals
    • SEMI C93 for Electronic Grade Materials
    • ISO 14001 Environmental Management for chemical processes

    Typical usage ratio

    • 5–15 mol% relative to comonomer or oligomer feed, adjusted based on desired polymer composition and photoreactivity

    Downstream process integration

    • Added in monomer synthesis step, often via controlled anionic or radical polymerization
    • Finalized resin passed to spin-coating or printing for thin film application
    • Batch-tested for bromo impurity profile and glass transition temperature effects

    Final product types

    • Photoresist monomers and polymers for semiconductor lithography
    • Insulating dielectric coatings for microelectronics
    • Solder mask precursor components

    4. Organic Synthesis Building Block for Fine Chemicals

    R&D labs and contract manufacturers leverage this compound for targeted synthesis of fine organic molecules with vinyl ether or bromoalkene functionalities. Its chemical nature supports advanced transformations, such as cross-coupling or substitution, for library development in specialty fragrance, flavor, and dye industries. Downstream users integrate it according to precise stoichiometric demand for building unique chemical backbones.

    Industry compliance standards

    • ISO 9001:2015 certified laboratory and production sites
    • Responsible Care Chemical Distribution Institute (CDI) guidelines
    • Specific customer protocol for purity and heavy metal screening
    • REACH registered substance dossier for European market

    Typical usage ratio

    • Varies from 0.5 to 1.5 equivalents per reaction, further adjusted based on conversion efficiency and side-product monitoring

    Downstream process integration

    • Fed directly into microreactors or batch synthesis vessels for stepwise transformations
    • Utilized in both nucleophilic substitution and vinylation techniques
    • Rigid QA on intermediate storage and transfer to maintain chemical integrity

    Final product types

    • Functionalized fine chemicals for fragrance and flavor synthesis
    • Dye and pigment intermediates
    • Custom reagents for contract synthetic services
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    Certification & Compliance
    More Introduction

    Cis-1-Bromo-2-Ethoxyethylene: A Chemist’s Perspective on a Unique Intermediate

    Introduction: Why Cis-1-Bromo-2-Ethoxyethylene Matters

    In a chemical environment dominated by incremental advances, real tools for synthesis stand out. Cis-1-Bromo-2-Ethoxyethylene (Model: C2H3BrOC2H5) steps into this gap for anyone exploring advanced organic transformations or looking for unique functional handles in fine chemical production. Our journey with this compound started in the development labs—striving to make more flexible routes toward heterocycles, specialty pharmaceuticals, and agricultural ingredients. Problems around selectivity and mild reactivity started these conversations. Too many vinyl bromides stall out during coupling reactions, or their trans/cis ratios spark headaches. Cis-1-Bromo-2-Ethoxyethylene takes on these issues directly by prioritizing geometric consistency and a well-tuned electron environment for downstream chemistry.

    Model and Specifications: Experience from the Factory Floor

    Manufacturing this molecule in-house brings several realities into play. We synthesize Cis-1-Bromo-2-Ethoxyethylene in batches where geometric integrity counts—nobody wants a mixed bag of isomers during scale up. After repeated runs, we found a sweet spot using carefully selected catalysts and solvent systems. Product purity reaches above 98% by GC analysis. With this, color sits clear to pale yellow, offering visual confirmation of clean handling. Our team bottles product under nitrogen, minimizing any hydrolysis risk, especially since bromovinyl ethers react readily with water over time. Material is shipped in amber glass and always kept cool during storage, reducing unwanted shifts or degradation. Attention to these details came from years listening to feedback from pilot plant chemists and R&D scientists who value repeatability over vague claims.

    Usage: Direct Applications, Not Hype

    Practical chemists lean into this compound for specific transformations. The cis-bromovinyl ether structure allows more predictable behavior during cross-coupling, halogen-exchange, or cyclization steps. We’ve seen especially strong value in Suzuki and Stille couplings, where the cis geometry gives distinct product distributions—something customers aiming for tight control in pharmaceuticals or crop protection products notice right away. The ethoxy group further stabilizes intermediates along several reaction chains. Our internal team has put Cis-1-Bromo-2-Ethoxyethylene through dozens of test reactions, often using it to build substituted pyridines, furans, or fused bicyclic structures that demand both regio- and stereochemical control from the start.

    Processing this molecule requires ordinary precautions: well-ventilated workspace, protection from moisture, and glassware free of acidic residues. In practice, few reagents offer as much versatility along with the predictability of stereochemical outcome. Compared to bromoacetaldehyde derivatives, Cis-1-Bromo-2-Ethoxyethylene brings lower toxicity, improved storage, and less reactivity toward air and water. The ethoxy functionality allows broader compatibility with organometallic reagents, while the bromine atom remains active under a variety of coupling and substitution conditions.

    Differences: A Day at the Bench Reveals the Details

    A lot of vinyl bromides float around in catalogs. In the hands of a synthetic chemist, differences between them show up quickly. Working with the cis-isomer rather than a trans- or mixed geometrical isomer translates to more predictable addition or substitution. When we test competitive products, we see that their mixtures often lead to extra work in purification or need for chiral separation—adding costs and time downstream. Chemists designing syntheses welcome our strict control since fewer side products accumulate, and the yield stays steady batch-to-batch.

    Trans-1-Bromo-2-Ethoxyethylene, by contrast, tends to behave differently, especially in pericyclic reactions where geometric constraints become controlling. We routinely supply technical data that details why the cis isomer supports better stereocontrol, reflecting direct analytical observation and process data from our own reactors. In every release, we check for minor by-products—a matter of habit after watching how impurities can impact a whole pilot plant run.

    Other bromoethoxy compounds occasionally serve as intermediates, yet most lack the balance of reactivity and selectivity this molecule brings. For example, bromoethyl ethers generally escape easy coupling or elimination conditions. The vinyl linkage in Cis-1-Bromo-2-Ethoxyethylene cuts these problems, opening easier entry to substituted aromatic rings and functionalized alkenes through standard transition metal catalysis—meaning less need for workaround chemistry.

    From Sourcing to Scale: Lessons Learned Manufacturing in an Evolving Industry

    We have built our production process through a combination of statistical process control and old-fashioned trouble-shooting. Sourcing raw materials pushes us into partnerships with suppliers who keep hydrocarbon contamination low, since even small impurities disturb catalyst performance. Introducing any new lot, we double check material balances at each stage, verify the value stream to minimize yield losses, and always track byproduct formation. Each of these steps arose from hard experience—too many early runs where careless solvent selection or unchecked pH destabilized the bromo-ethoxy backbone before isolation even started.

    This in-house manufacturing base means security for our clients. Multi-ton runs depend on resourcefulness. Years ago, we shifted to closed-loop recycling of organics to limit waste. After feedback from customers needing higher optical purity for pharmaceutical work, we adopted in-line gas chromatography, letting us actively monitor geometric ratios during distillation, not just at final QC. Factor in climate-controlled storage for our drums and you end up with a consistent product, each and every time.

    Supporting the Synthetic Community: Conversations That Shape Product Direction

    Our connection to end-users—the researchers building molecules that end up in medicines, pest controls, and advanced materials—directs how we invest in production and distribution. Some years, requests center on larger volumes for pilot scale. Other years, it’s the need for higher-purity, with technical back-and-forth on solvents and customer IP. These conversations keep us grounded; nothing replaces a phone call with a process chemist troubleshooting an unexplained precipitate, or the back-and-forth with a team troubleshooting a yield dip. Out of this, we developed a technical data package for Cis-1-Bromo-2-Ethoxyethylene that compiles NMR, GC-MS, and elemental analysis data, plus batch certificates with every shipment. This comes from daily attention to reproducibility—nothing feels as bad as finding your product contributes a byproduct that never showed up on the first GC trace.

    Feedback from research groups using the material inside university or industrial innovation labs has led us to invest in new packaging and reduction of permeation issues—vinyl bromides aren’t the friendliest to plastics, and a glass bottle makes the difference over time. Each improvement has roots in actual user stories. No one in a manufacturing plant can afford to chase ghosts caused by marginal material.

    Product Lifecycle: From Development to End-Use

    Stepping back, it’s clear Cis-1-Bromo-2-Ethoxyethylene forms a building block on which more value gets constructed. In our own R&D, we’ve leveraged this intermediate for alkynylation, arylation, and heteroatom additions—reactions often hampered by mixed isomer feeds or minor decomposition. In comparison, our partners using commodity vinyl bromides see higher losses. Our in-house data draws clear lines—less byproduct, more direct path, fewer purification headaches. The product rarely lingers on the shelf since it plugs directly into diverse pipelines, including medicinal chemistry, blending, functional material creation, or crop chemistry.

    Market shifts sometimes push attention away from such tailored intermediates, focusing on bulk solvents or commodity monomers. Process chemists, though, know value comes from consistency and reliability. Each year, we’re approached to adapt the specifications—higher or lower bromine content, new solvents for delivery, adjusted packaging volumes. Instead of fixed templates, we listen to lab-scale stories and adjust as required. In the past, requests for higher-purity led us to pilot new column packing materials that improved separation by a full percentage point, translating directly into less downstream purification.

    Commitment to Stewardship: Risk, Safety, and Environmental Responsibility

    We recognize that stewardship extends beyond just keeping the process safe—although continuous training makes sure everybody on the floor treats bromine compounds with the respect they deserve. Vinyl bromides, handled incorrectly, can release toxic vapors or react unpredictably with strong bases or nucleophiles. Regular audits and investment in scrubber systems mitigate these risks long before the material leaves our plant.

    Waste minimization remains a strong focus. We recover as much solvent as technically possible during distillation, and all spent wash streams pass through treatment—neutralizing acidity and safely breaking down bromo-organics before disposal. Each kilo of raw material is tracked from receipt through final shipment, paired with a batch record noting every process touch. By sharing waste profiles and exposure recommendations with downstream users, our customers step into their own safety reviews well-prepared—nobody likes surprises when new materials hit the bench.

    Transparency and Trust: Anchoring in Science Over Marketing

    A trust relationship between manufacturer and chemist grows from openness. We share characterization spectra and process notes alongside samples and bulk shipments, because real-world buyers don’t want marketing—they want testable facts. Our own analytical chemists keep detailed logs comparing batch fingerprints against industry references. Over time, these comparisons guide us toward process improvement and root cause analysis; if we spot a drift in impurity profile linked to upstream solvent changes, we communicate with the customer, adjust, and verify. No voice gets lost in the discussion.

    Working directly from process knowledge grants us a wider view than traders or catalog resellers. We see where raw material fluctuations or changing market regulations forecast possible disruptions, and our forecasting includes detailed risk analysis—never just maximizing batch number at the expense of predictability. Our data isn’t theoretical—it’s built up through years of measuring, adapting, and listening. Customers, in turn, draw on this bank of experience rather than just reading off a standard specification sheet.

    Future Trends: Meeting New Challenges with Proven Groundwork

    As specialty chemicals markets shift toward more complex, customized molecules, reliable intermediates like Cis-1-Bromo-2-Ethoxyethylene attract growing attention. The continued expansion of green chemistry pushes us, too, towards ever-safer processes. We anchor our development on well-characterized intermediates. Each new regulatory change, whether a local emission standard or ROW import limitation, prompts upgrades in containment, documentation, and traceability. Already, we’ve updated our processing lines with in-line sensors enabling real-time bromine tracking, preempting non-compliance issues and minimizing resource use.

    One emerging need is for ever-sharper control of minor isomers and byproducts. For us, continuous investment in in-process analytics backs our commitment to deliver not just ‘close enough’ but precise, reproducible quality. Our teams frequently re-examine legacy production runs and benchmark against the latest academic literature, not just to stay competitive, but to add confidence for innovators who want intermediates they can rely on without re-developing purification protocols.

    Collaboration with downstream users drives how we evolve—whether that means a pharmaceutical company requesting non-standard concentration solutions for a unique reaction flow, or new packaging innovations to tackle static discharge risks in winter shipping. As feedback loops closer to the lab bench and R&D pilot plants feed back into manufacturing, everyone gains in efficiency and safety.

    Conclusion: More Than an Intermediate—A Partner in Synthesis

    Cis-1-Bromo-2-Ethoxyethylene represents the coming together of small details—geometric selectivity, manageable reactivity, robust supply chain controls, and a culture anchored in technical dialogue. For every batch produced, we bring not just technical know-how but a library of collaborations, feedback, and hard-earned insight. With each shipment, our team stands by the product, tracking it from formulation to its inclusion in the next medical candidate, agricultural innovation, or novel material. The journey for this molecule starts long before a purchase order ever arrives, rooted in manufacturing discipline and curiosity for pushing what’s possible in organic synthesis.

    Looking ahead, new methodologies and regulatory environments promise even more opportunities. At every stage, being an actual manufacturer means carrying responsibility to the community—from safety to sustainability, and from technical clarity to honest, fact-based guidance. Any chemist reaching for Cis-1-Bromo-2-Ethoxyethylene in their next breakthrough can know it carries the backing of a factory team that solves problems, answers questions, and adapts to each new challenge side by side with the field.