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Methyl 2-(Bromomethyl)Acrylate

    • Product Name Methyl 2-(Bromomethyl)Acrylate
    • Alias MBMA
    • Einecs 'EINECS 258-041-3'
    • 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

    630815

    Product Name Methyl 2-(Bromomethyl)Acrylate
    Cas Number 5881-45-4
    Molecular Formula C5H7BrO2
    Molecular Weight 179.01 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 68-70°C at 14 mmHg
    Density 1.498 g/mL at 25°C
    Purity Typically >= 97%
    Refractive Index 1.478 (lit.)
    Flash Point 89°C
    Solubility Soluble in most organic solvents
    Storage Temperature 2-8°C (refrigerated)
    Smiles COC(=O)C=CBrC

    As an accredited Methyl 2-(Bromomethyl)Acrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical, Methyl 2-(Bromomethyl)Acrylate (25g), is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Shipping Methyl 2-(Bromomethyl)acrylate should be shipped in tightly sealed, chemical-resistant containers under dry, cool conditions. It is classified as hazardous, requiring labeling and transport according to relevant shipping regulations (e.g., DOT, IATA, IMDG). Appropriate documentation, secondary containment, and safety precautions must be ensured during shipping to prevent leaks or accidental exposure.
    Storage Methyl 2-(Bromomethyl)acrylate should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from heat, sparks, and sources of ignition. Keep it away from incompatible substances such as strong oxidizers and bases. Store under inert atmosphere (e.g., nitrogen) if possible, and protect from moisture. Ensure proper chemical labeling and access control in accordance with safety regulations.
    Application of Methyl 2-(Bromomethyl)Acrylate

    Applications of Methyl 2-(Bromomethyl)Acrylate in Industrial Manufacturing

    Methyl 2-(Bromomethyl)acrylate enables targeted functionalization in multiple chemical manufacturing sectors, serving as a reactive intermediate for precision synthesis. The following segments illustrate real downstream transformations and their process-specific requirements.

    1. Pharmaceutical Intermediates Synthesis

    Pharmaceutical manufacturers employ Methyl 2-(Bromomethyl)acrylate for constructing active pharmaceutical ingredient (API) cores via nucleophilic substitution and Michael addition pathways. Investment in this intermediate supports batch-to-batch consistency in custom syntheses of β-substituted acrylates, which are building blocks for antiviral, anticancer, and central nervous system (CNS) compounds. Site-specific bromomethylation allows rapid linkage with heterocyclic amines or oxygen nucleophiles, demanding material traceability under GMP and regulatory scrutiny.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guide for Active Pharmaceutical Ingredients
    • EU GMP Volume 4 Part II (APIs)
    • 21 CFR Part 210/211 (US FDA cGMP)
    • USP/NF and EP monograph requirements, as applicable for downstream APIs

    Typical usage ratio

    • Intermediate charge levels from 0.9 to 2.2 molar equivalents per targeted nucleophile
    • Range adjusted by desired substitution degree and pathway selectivity

    Downstream process integration

    • Entered after initial building block assembly, following protection/deprotection cycles
    • Introduced before condensation or cyclization steps
    • Purity monitoring at intermediate release using HPLC and NMR

    Final product types

    • Small-molecule active pharmaceutical ingredients (APIs) such as anti-inflammatory and antiviral drugs
    • Pharmaceutical intermediates for custom synthesis
    • Fine chemical precursors for regulated manufacturing

    2. Agrochemical Active Ingredient Production

    Agrochemical formulators utilize this compound to introduce functional acrylate groups within pesticide, herbicide, or insecticide actives via base-catalyzed alkylation and transesterification reactions. The molecule’s bromine leaving group enhances coupling efficiency with aromatic and aliphatic nucleophiles, supporting the development of new-generation crop protection agents with targeted bioactivity. Analytical support aligns manufactured lots with strict residue and purity criteria.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines on pesticide specifications
    • EPA FIFRA regulations (United States)
    • REACH Registration, Evaluation, Authorisation, and Restriction of Chemicals (EU)
    • ISO 9001:2015 Quality Management for production traceability

    Typical usage ratio

    • Usage at 1.0 to 1.4 molar equivalents, based on targeted active group loading
    • Batch correction by stoichiometric yield and side reaction minimization

    Downstream process integration

    • Charged into multi-step synthesis after precursor halogenation or esterification
    • Paired with selective nucleophiles for diversification of core structures
    • Intermediate isolated or purified prior to final formulation

    Final product types

    • Herbicide active ingredient compounds
    • Insecticidal and fungicidal intermediates
    • Protective crop spray concentrates

    3. Specialty Monomer Manufacturing for Advanced Polymers

    Advanced polymer producers incorporate Methyl 2-(Bromomethyl)acrylate as a functional monomer to introduce pendant bromomethyl groups into acrylic copolymers and specialty resins. Its compatibility with radical and anionic polymerization systems supports chain extension, crosslinking, and subsequent functionalization like quaternization or thiol-ene modifications. Strict process control and impurity profiling ensure the monomer integrates without defect generation.

    Industry compliance standards

    • ISO 9001:2015 for polymer plant quality systems
    • ASTM D2567 for acrylate monomers in industrial resins
    • REACH Annex XVII (Monomer purity limits in EU polymers)
    • Food Contact Notification (FCN) requirements for select packaging polymers

    Typical usage ratio

    • Feedstock at 0.1% to 8% by weight in copolymerization blends
    • Ratio varies with desired bromomethylation density and end-use performance

    Downstream process integration

    • Pre-mixed with acrylate or methacrylate monomer solutions before polymerization
    • Added during monomer charge to reactor under inert atmosphere
    • Post-polymerization analysis to check grafting efficiency and residual monomer

    Final product types

    • Ionomer and specialty acrylic resins for coatings and adhesives
    • Functionalized block and graft copolymers
    • Membrane and separator films for electrochemical devices

    4. Fine Chemical Synthesis for Organic Laboratory Reagents

    Producers of laboratory-scale chemicals and catalog reagents apply this raw material as an electrophilic component in the preparation of diversified acrylate derivatives. Its strong bromomethyl group enables construction of molecular probes, reactive intermediates for method development, and standards for chromatographic calibration. Precision weighing, lot documentation, and impurity mapping guarantee compliance with analytical supplier regulations.

    Industry compliance standards

    • ACS Reagent Chemicals certification guidelines
    • ISO/IEC 17025 standards for reference material production
    • Good Laboratory Practice (GLP) as per OECD and national regulations
    • Internal COA release requirements for chemical suppliers

    Typical usage ratio

    • Applied at 0.05 to 1.2 equivalents, strictly monitored depending on pathway
    • Adjusted for scale of preparative vs. analytical syntheses

    Downstream process integration

    • Dissolved in anhydrous solvents for controlled addition to organics
    • Introduced during method validation or chemical standards synthesis
    • Purity analysis using GC-MS and NMR platforms

    Final product types

    • Analytical reference standards
    • Specialty organic building blocks for research
    • Screening compound libraries for pharmaceutical and materials R&D
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    Certification & Compliance
    More Introduction

    Methyl 2-(Bromomethyl)Acrylate: From Our Plant to Your Lab

    Delivering Consistency and Reliability with Methyl 2-(Bromomethyl)Acrylate

    Watching the drum lids unscrew and the faint, sharp aroma rise as we fill each container, our team knows the value of a well-made intermediate. We work with Methyl 2-(Bromomethyl)Acrylate at every stage, from the first drop of raw material to the last batch testing report. This compound—C5H7BrO2, a light yellow liquid—serves chemists building out more complex molecules in crop science, pharmaceuticals, and specialty materials.

    You see its practical character in our approach to processing. Each run draws on high-purity reagents and careful reaction monitoring. With a molecular weight of 195.01, our product typically arrives with a purity above 98%. The boiling point and density remain in-house standards we verify with each lot. We fill each drum for shipment only after confirming regulatory compliance and shelf stability in dark storage, because no one wants a degraded allylic ester arriving at their facility.

    Key Features: Why Chemists Keep Coming Back to Our Methyl 2-(Bromomethyl)Acrylate

    Fewer side products mean less trouble during scale-up work. When we watch orders come from research labs and downstream manufacturing, we recognize why customers rely on the predictable reactivity of this bromoacrylate. That bromomethyl group doesn’t linger unreacted like a sluggish leaving group in a multi-step process. The acrylate moiety, with its electron-withdrawing capacity, lets colleagues achieve selective alkylation, olefination, or cyclization.

    Unlike some other bromoalkyl acrylates, this compound resists gumming up lines due to unwanted polymerization or contamination. We use inhibitors and nitrogen blankets during filling for this reason. It doesn’t behave as erratically as bromoacetate analogs, often notorious for their moisture sensitivity and pronounced volatility—a concern for scale-up facilities that can’t tolerate evaporative loss or ventilation headaches.

    Our process was informed by practical failures and setbacks as much as it was engineered from textbooks. After early struggles with product discoloration, we rewired our purification sequence—adding a careful wash and distillation method to pull down color bodies and stabilizers without stripping out reactive groups. That adjustment let us raise our typical shelf life and enable tighter batch-to-batch consistency, which remains a frequent sticking point for researchers working to file regulatory data packages.

    Applications from Synthesis to Scale: Direct Input from Downstream Users

    Methyl 2-(Bromomethyl)Acrylate leaves our buildings destined for hands-on chemistry, not for warehouse stasis. Most users pick it as an intermediate in complex molecule construction, whether for small pilot work or commercial syntheses. Every kilo heading out gets used for introducing a versatile bromo function or acrylate group into pharmaceuticals—including proprietary synthetic routes for anti-infectives and cardiovascular agents. Others use it in advanced agrochemical synthesis, where the bromoacrylate skeleton streamlines development of specific pesticides and herbicides.

    We learned early to avoid using catch-all terms like “multi-purpose” when customers demand specifics. Buyers using it as an alkylating agent for heterocycle synthesis told us clear downstream examples have more value than generic claims. One customer supplied feedback after several months of use, noting that competing material could not be incorporated directly into their one-pot preclinical route. Our product’s stability made the difference.

    Scale-up teams especially care about containment and reactivity of the methyl ester. Experience taught us to keep each shipment in corrosion-safe containers, with a batch-specific COA so every project owner knows what they’re handling—especially under the heat and varied pH of process development trials. We maintain tight control over water content and acidity to minimize side reactions, because nothing halts a multi-week campaign like product decomposition or corrosive off-gassing mid-assembly.

    Comparing Methyl 2-(Bromomethyl)Acrylate to Similar Intermediates

    On paper, this product lines up with other bromoalkyl acrylates or bromoacetates. In practice, practical distinctions reveal themselves the moment we start a batch or our partners fill a reactor. Compared to Methyl 2-Bromoacetate, Methyl 2-(Bromomethyl)Acrylate displays greater selectivity in substitution reactions. The bromomethyl at the β-position offers unique reactivity not present in standard haloacetates, making it less prone to unwanted hydrolysis and easier to control under both acidic and basic conditions.

    Some labs previously used Methyl 3-Bromopropionate, only to find the acrylate version brought higher reactivity and more straightforward purification. The electron-withdrawing double bond in our product allows more precise introduction of functionalities, especially in the synthesis of molecules containing aromatic or heteroaromatic motifs. The controlled reactivity means less downstream purification, which our manufacturing partners say saves hours and precious raw solvent per campaign.

    With some β-bromo-α,β-unsaturated esters, customers see batch variability or high tendency toward by-product formation. We cracked down on this by adopting moisture monitoring, in-line filtration, and stainless-steel handling. We reinforced our packaging protocols and instituted double-sealing for every shipment leaving our warehouse, cutting losses from decomposition in older packaging. This predictable quality didn’t emerge overnight—we learned from failed arrivals, customer returns, and shared our analytical fingerprints with trusted downstream users to demonstrate improvements.

    Chemists with strict time lines regularly ask about material differences. What keeps our product distinct from basic methyl bromoacetate is direct: the acrylate system provides a reactive yet controllable site for further modifications. You gain options if you want to use cross-coupling, nucleophilic substitution, or even tandem catalyzed reactions. Our internal labs have run head-to-head pilot experiments alongside competitors’ batches and stored samples—measuring not only yield but also ease of handling across different climate zones and exposure durations.

    On-Site Insights: How Our Team Tackles Real-World Problems

    No intermediate is ever “easy” until it’s stable enough to survive storage, shipment, and the pace of an industrial lab. We see ongoing requests for technical support directly from bench chemists—those troubleshooting a blown reaction, or validating the ingredient list for a regulatory filing. Our technical group reports patterns year after year: some partners see residue or “ghost peaks” in their analytical testing, which we traced back to mishandling by other suppliers. We fixed this with hands-on training for warehouse and logistics teams. Product that shows up clean, with every impurity threshold listed and batch-by-batch GC and NMR spectra handed over, means our partners stop wasting time double-checking or resubmitting their own paperwork.

    Every year, we review and tweak our logistics pipeline. High-purity intermediates get compromised quickly with improper storage—humidity, temperature swings, or contamination can spike impurity levels. After several hot summers led to quality complaints, we switched all inventory to climate-controlled units and rejected the cost-cutting urge to use standard drums. This commitment has paid off with repeat business from R&D teams and multi-year procurement contracts, who saw the improved stability translate directly into smoother scale-up campaigns.

    It took time for us to earn direct input from end-users. Many large buyers stick with catalog suppliers out of habit, only switching when a delay, failing certification batch, or persistent off-odor sends them hunting for a manufacturer willing to listen. We put our chemical engineering team on early morning troubleshooting calls, coordinated side-by-side pilot synthesis runs with partner labs, and even used our own test batches to help users adapt to process problems mid-project. Chemical manufacturing is never about shipping a drum and walking away. It’s about keeping the line moving—helping others get their next molecule off the ground.

    Supporting Diverse Synthesis: Product Usability and Performance

    Some customers focus on cost per kilo. Others want documentation to support regulatory filings. Out of all the performance characteristics, stability has become the core demand from our recurring partners in pharmaceuticals and crop protection research. In one specialty material project, a partner pursued a polymer additive that needed consistent acrylate incorporation. By supplying documentation on inhibitor levels and every batch chromatogram, we made it possible for their QC team to validate every step, which they told us let them cut days from their timeline.

    Raw materials sometimes arrive at our gates with inconsistent performance, so we began collaborating more closely with key suppliers. We run test reactions in our own application lab: alkylations, nucleophilic additions, and even exploratory cross-coupling trials under varied temperature and solvent conditions. This means customers can rely on data backed up by our own team’s hands-on experience, not just a PDF copied from a generic product sheet.

    Comparisons with similar intermediates sometimes lead back to questions about safety and handling. Our team receives calls about odor, storage, and best disposal protocols. We always advocate direct ventilation, tightly controlled storage below room temperature, and safe disposal in accordance with all local regulations—because a clean, safe lab beats any claims of convenience. The product’s handling properties reflect our day-to-day reality: color, odor, corrosion—all tested and confirmed, so no surprises slow down the next campaign.

    Changes in regulatory expectations, especially regarding trace-level impurities and in-process testing, drove us to modernize our analytics protocols. We invested in new HPLC units and routine mass spect analysis, so our partners receive firm data not just on main content but also trace contaminant profiles. Projects in late-stage development no longer hit roadblocks from last-minute questions about batch quality or missing analytical backup.

    Innovation on the Factory Floor: What We’ve Learned from Years in Production

    Years of manufacturing this compound shaped our approach to both process and people. Every run teaches us something about yield optimization, waste reduction, or downstream bottleneck avoidance. A new batch isn’t measured just by its chemical purity—it’s judged by its track record in the field. Every lost hour or day can spiral into missed launches and reshuffling of entire synthesis plans. Our teams know delays affect real projects, not just spreadsheets.

    Sometimes innovation means stripping back: less emphasis on fancy new tech, more focus on process discipline and steady investment in staff training. New operators shadow experienced hands in both batchwise and continuous mode, learning the nuanced steps that don’t appear in process flow diagrams—like how flow rates or minor temperature deviations can produce outsized changes in color or product consistency. Routine feedback from users led us to install new sensor arrays in product storage zones, since the wrong humidity or temperature can damage months of cumulative work overnight.

    Turnover in chemical manufacturing is inevitable. We address it by maintaining robust written procedures and ongoing mentorship, ensuring that every technician understands not just the how, but the why behind each process step. Periodic collaboration with end-users keeps our focus practical. Many of our best improvements—the double-vacuum sealing after distillation, or the real-time moisture readouts—came directly from user complaints or return data. Nothing matches the pressure of having products fail in a demanding research application; it pushes our plant team to hunt for root causes and implement fixes before the next run leaves the line.

    We track not just basic yield but product loss at every stage, calculating waste and correcting process drift before it eats into reliability. Minor investments—a new chiller, a secondary filtration stage, or updated container linings—often pay back with greater end-user satisfaction. In the rare event of a customer concern, documented resolution and transparent sharing of analytics build trust and prevent recurrence across future lots.

    Trust Rooted in Practice: Lessons from Troubleshooting and Teamwork

    Partnership means sharing responsibility for success and setbacks. Manufacturing Methyl 2-(Bromomethyl)Acrylate taught us to stay engaged with users long after the paperwork clears. When a user flagged unexpected trace impurities in one campaign, our technical manager walked through each batch record, shipment log, and handling report, eventually pinpointing a supplier issue upstream. Full transparency—inclusive of root cause disclosure and corrected supply chain measures—earned us better outcomes and new opportunities for collaboration.

    Some partners run side-by-side evaluations with ours and competitor products. In most cases, our extra attention to storage, shipping, and real-time customer support helps our material perform more reliably—translating to higher batch success rates and less wasted R&D investment. Newer users regularly report that previous intermediates needed double-filtration or even redistillation, while consistent manufacturing keeps workflows predictable and outcomes reproducible.

    Nobody values a “perfect” product in theory—practical results mean more. After switching from off-the-shelf suppliers, one research group tracking process impurities observed our product gave cleaner reaction profiles, leading to less time spent in downstream purification. Another partner commented on the cleaner odor and consistent color, giving their analytical team confidence in batch-to-batch reproducibility.

    Looking Ahead: Responsive Supply and Sustainable Progress

    Long-term supply security and compliance with tightening regulations inform every decision we make. Our move to local sourcing of critical precursors reduced the risk of missed shipments. Building relationships with trusted hauliers and warehouse partners means our product doesn’t linger in transit, picking up impurities or falling victim to mishandling. Chemistry is only as good as logistics, and we invest where reliability meets compliance.

    We remain watchful for new application trends—especially as lab-scale needs build out to pilot and full production. With sustainability and green chemistry on the rise, increasing pressure falls on manufacturers to minimize waste, recycle solvents, and back up product claims with firm analytics. Our future investments will go into cleaner manufacturing, improved recycling protocols, and application R&D to identify even more efficient synthetic routes using Methyl 2-(Bromomethyl)Acrylate.

    Summary of Practical Benefits

    We built our offering around the realities of field chemistry and process development. Direct feedback from users, years of process optimization, and a commitment to stability, quality, and transparency have shaped every drum that leaves our gates. For researchers, production managers, and developers relying on strong performance and responsive support, this compound serves as more than a generic building block—it acts as a cornerstone for reliable, efficient synthesis work in tomorrow’s advanced industries.