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Methyl 3,3-Dimethylpent-4-Enoate

    • Product Name Methyl 3,3-Dimethylpent-4-Enoate
    • Alias methyl-3,3-dimethylpent-4-enoate
    • Einecs Einecs 258-449-1
    • 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

    908751

    Chemical Name Methyl 3,3-Dimethylpent-4-enoate
    Molecular Formula C8H14O2
    Molecular Weight 142.20 g/mol
    Cas Number 28782-14-1
    Appearance Colorless liquid
    Boiling Point 164-166°C
    Density 0.874 g/cm³
    Refractive Index 1.422
    Smiles CC(C)(C)CC=CC(=O)OC
    Iupac Name methyl 3,3-dimethylpent-4-enoate

    As an accredited Methyl 3,3-Dimethylpent-4-Enoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of Methyl 3,3-Dimethylpent-4-enoate is supplied in an amber glass bottle with a secure, tamper-evident screw cap.
    Shipping Methyl 3,3-Dimethylpent-4-enoate should be shipped in tightly sealed, chemical-resistant containers, protected from moisture and direct sunlight. Transport in accordance with local, national, and international regulations for chemicals. Ensure proper labeling and documentation. Handle with care to prevent leaks or spills, and store the product in a cool, dry place during transit.
    Storage **Methyl 3,3-Dimethylpent-4-enoate** should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible chemicals such as oxidizers. Keep the container tightly closed and protected from direct sunlight. Store under inert atmosphere if possible. Use proper chemical storage containers, label appropriately, and ensure access is limited to trained personnel.
    Application of Methyl 3,3-Dimethylpent-4-Enoate

    Applications of Methyl 3,3-Dimethylpent-4-enoate in Industrial Manufacturing

    Methyl 3,3-dimethylpent-4-enoate serves as a specialty intermediate supporting multiple value chains in high-end industrial manufacturing. Its unique structural features allow tailored incorporation into synthesis routes for agrochemicals, pharmaceutical APIs, fine fragrances, specialty polymers, and advanced materials, facilitating demanding formulations and targeted downstream transformations.

    1. Agrochemical Intermediate Synthesis

    Our material provides a reactive synthon for selective ester transformations in herbicide and insecticide precursor manufacturing. Its methyl ester functionality enables precise amidation, hydrolysis, or alkylation under controlled conditions, fitting seamlessly into existing agrochemical synthesis blocks. Manufacturers leverage this chemistry to construct branched-chain motifs critical for selective crop protection compounds. During process scale-up, careful adjustment to reagent concentration and temperature profiles ensures stringent control over product purity and traceability.

    Industry compliance standards

    • GB/T 38262-2019 (China Agrochemical Industry Standard)
    • ISO 9001:2015 quality management for agrochemical production
    • REACH Annex III for European registration
    • US EPA 40 CFR Part 169 recordkeeping for pesticide ingredients

    Typical usage ratio

    • 5–20% w/w in base solution; adjust within formulation to match stoichiometric needs for specific agrochemical actives and batch size

    Downstream process integration

    • Charged pre-neutralization in protected vessel
    • Alkali-catalyzed amidation or hydrolysis for precursor conversion
    • Inline monitoring via GC or HPLC to track conversion, minimize by-products
    • Direct transfer to formulation blending for technical grade pesticide or pre-formulation ingredient isolation

    Final product types

    • Selective herbicide intermediates
    • Insecticide technical concentrates
    • Seed treatment additives
    • Plant growth regulator base compounds

    2. Pharmaceutical API Synthesis

    This ester enters pharmaceutical manufacturing as a foundation for advanced building blocks in the synthesis of APIs containing branched aliphatic backbones. Process chemists use its carbon skeleton to construct chiral intermediates by enantioselective hydrogenation or functional group interconversion. As a raw ingredient for cGMP-compliant multi-step syntheses, its high chemical purity and defined impurity profile preserve batch-to-batch consistency throughout the kilo lab up to full-scale API plant operation.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP/NF monographs (where specific API applies)
    • European Pharmacopoeia (Ph. Eur.) 10th Edition process quality
    • FDA 21 CFR Parts 210/211 for finished pharmaceuticals

    Typical usage ratio

    • Determined by molar equivalence in stepwise API synthesis; typically 10–50% of initial batch charge depending on route and scale

    Downstream process integration

    • Loaded in reaction vessels for Grignard, reductive amination, or selective hydrogenation steps
    • Monitored using in-process controls (IPC) and validated analytical assays
    • Solvent extractions and phase separations post-reaction
    • Input for chiral separation columns and further downstream derivatization

    Final product types

    • Chiral pharmaceutical intermediates
    • Generic API key intermediates
    • Branched-chain drug substances (pre-PAR submission)
    • Precursor compounds for cardiovascular and CNS actives

    3. Fragrance and Aroma Molecule Production

    Perfume and flavor manufacturers apply this compound in base-note synthesis to introduce unique branched aliphatic characters. Its tailored reactivity supports Diels-Alder adducts or lactonization routes, producing complex aroma ingredients for fine and functional fragrances. Careful control of reaction time and catalysis parameters permits the custom formation of macrocyclic musk compounds, enhancing olfactive depth in designer formulas while adhering to industry allergen and safety directives.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9235:2013 (Aromatics—Nomenclature)
    • FEMA GRAS status for US food and fragrance ingredients

    Typical usage ratio

    • 0.5–8% on weight of total formulation; adjustments based on targeted flavor or fragrance intensity and base formula dilution

    Downstream process integration

    • Batched for Diels-Alder or ring-closing metathesis reactions
    • Custom fractional distillation to isolate aroma grades
    • Co-processing with natural essential oils or synthetic modifiers
    • Quality release through sensory panel and GC-MS purity profiles

    Final product types

    • Macrocyclic musk aroma compounds
    • Novel lactone odorants
    • Custom base notes for Eau de Parfum
    • Food flavorings for beverages and confectionery

    4. Specialty Polymer Synthesis

    Polymer manufacturers employ this methyl ester to introduce pendant groups and controlled branching into acrylic and specialty polyester resins. Its unsaturated chain supports copolymerization under free-radical or anionic mechanisms, conferring flexibility and heat resistance to final plastic materials. Blending at prescribed levels allows precise modification of molecular weight distribution for low-VOC coatings and advanced elastomeric adhesives. Detailed process mapping ensures alignment with environmental and end-use regulatory requirements in demanding application environments.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • US EPA TSCA compliance for new chemical substances
    • ISO 14001:2015 (Environmental Management Systems)
    • GB/T 19495.3 for synthetic resin products in China

    Typical usage ratio

    • 3–12% of monomer feedstock; balanced according to targeted copolymer properties and final application performance requirements

    Downstream process integration

    • Continuous addition to polymerization reactors as branch-point modifier
    • Initial pre-blend with main monomers to ensure uniformity
    • Inline viscosity monitoring and molecular weight analysis
    • Final purification and pelletization for plastics processing

    Final product types

    • Heat-resistant acrylic polymers
    • Low-VOC industrial coatings
    • Specialty elastomeric adhesives
    • Branched polyester engineering resins (for automotive and electronics)

    5. Advanced Materials Science Research and Development

    R&D groups in high-performance materials exploit the molecular structure of this ester for custom molecule design, particularly in surface functionalization and new composite matrix development. As a model substrate for organocatalytic and photochemical transformations, it allows academic and industrial labs to open new reaction pathways for materials innovation. Digital batch records and secure impurity profiling support reproducible experiments and technology transfer to pilot plant processes, upholding the demands of intellectual property protection and scientific publication standards.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) guidelines
    • ISO 17025:2017 General requirements for the competence of testing and calibration laboratories
    • Institutional health and safety protocols (local standards)
    • Material transfer and research compliance forms (where relevant)

    Typical usage ratio

    • Variable; typically 1–20 mmol scale for pre-formulation experiments, with scaling based on observed reactivity, yield, and downstream compatibility

    Downstream process integration

    • Dispensed by precision syringe in controlled microreactor or batch setup
    • Combined with catalytic reagents for functional group exploration
    • Sequential process mapping using analytical LC/MS and NMR
    • Integration into pilot batches for further property verification

    Final product types

    • Novel monomer units for prototype polymers
    • Surface-active agents for advanced composites
    • Material property modifiers for research applications
    • Functional model compounds for publication and patent development
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    Certification & Compliance
    More Introduction

    Methyl 3,3-Dimethylpent-4-enoate: A Closer Look from the Manufacturer’s Bench

    Understanding Methyl 3,3-Dimethylpent-4-enoate

    Years of hands-on experience in the lab and plant floor have shaped a certain respect for clear-cut molecules that wear many hats. Methyl 3,3-dimethylpent-4-enoate falls into that group — a niche compound that steps up for demanding synthesis settings where bulk commodity esters simply fall short. With its distinct structure, this ester brings a blend of reactivity and selectivity that stands out across every technical batch we run.

    Packed with a 3,3-dimethyl motif, it lines up a branched carbon backbone next to a reactive pent-4-enoate group. Colleagues in R&D first approached this ester for their search in optimizing routes to tailored intermediates. The model, cataloged internally as M33MD4 for batch tracking, has since proven its worth many times over in our reactors. Each lot rolls out according to strict instrument calibration, ensuring that the NMR spectra match the targets chemists request — typically above 98% purity, checked by both GC and HPLC.

    Where This Molecule Earns Its Keep

    On the shop floor, staff handle thousands of liters across a spectrum of esters. This one gets more special attention, both for the value per kilogram and the impact downstream in complex organic synthesis. Methyl 3,3-dimethylpent-4-enoate holds a strategic advantage in multistep synthesis, particularly for customers building advanced agrochemical scaffolds and pharmaceutical intermediates. The double bond in the pent-4-enoate moiety offers a handsome handle for further transformations: hydroboration, cross-coupling, and selective reduction all benefit from that allylic position.

    Working closely with in-house chemists and visiting technical teams, we see this ester serve in reactions where steric hindrance blocks simpler esters. The gem-dimethyl group at the 3-position helps shield the ester against non-specific enzymes in biocatalysis, improving selectivity during key step modifications. During scale-up trials, we noticed significantly cleaner reaction profiles and easier workups compared to older methyl pentenoate variants.

    Specification and Batch Integrity

    Each customer shipment reflects a combination of analytical vigilance and practical process know-how. We prepare Methyl 3,3-dimethylpent-4-enoate as a clear liquid under inert nitrogen blanketing, keeping residual water under 0.1% based on Karl Fischer titration. This matters for moisture-sensitive transformations, especially for Grignard or LDA-driven couplings where adventitious water can tank a whole batch. Packing lines test every drum for both purity and residual solvents, with ethyl acetate and toluene levels kept well below ICH limits.

    The manufacturing protocol balances throughput and quality. Columns charged for distillation run with precise cut points to prevent product degradation at higher temperatures. At least 90% of the staff in processing have hands-on certification with these operations, not just spreadsheet training. This weeds out subtle operational hiccups that could otherwise slip through. Technicians routinely sample every batch, confirming both spectral fingerprint and chemical stability, which matters when the product travels overseas or sits on a customer’s shelf for an extended time.

    Product Differentiation: Why This Ester Over Others?

    Industrial customers run headlong into the limitations of standard methyl pentenoates. Once you tweak for more complex skeletons, basic linear esters just can’t deliver the degree of regioselectivity or the precise branching needed for target molecules. Our team worked through a dozen process tweaks before hitting the right alkylation sequence to consistently produce the 3,3-dimethyl arrangement.

    That small change in structure leads to marked benefits. In catalytic hydrogenation runs, the gem-dimethyl group blocks unwanted side reduction at the 3-position. Colleagues pulled dozens of reaction logs showing far fewer byproducts — this simplifies purification, cuts solvent use, and trims time at every downstream stage. Academic collaborators using the ester in ring-closing reactions noticed sharper yields and higher chiral selectivity, outcomes verified by independent labs.

    Another benefit comes during scale-up. The branched backbone makes Methyl 3,3-dimethylpent-4-enoate less volatile than lower homologs, improving containment and reducing scrubber loading during high-volume runs. Every operator on site values a product that balances manageable vapor pressure with strong reactivity, especially in equipment maintenance. Less gumming, less fouling, fewer shutdowns.

    Inside the Reactor: Production and Handling Observations

    Throughout the last production cycles, handling Methyl 3,3-dimethylpent-4-enoate has confirmed its physical stability. Material stored under nitrogen in stainless steel or HDPE drums holds up well, showing no color pick-up or acid formation, even after six months’ retention. We validate every warehouse batch monthly through rapid GC checks, so downstream partners start their syntheses confident in product freshness.

    Operators always take precautions with any reactive ester. Open trays or careless venting remain rare in our lines, but plant protocols strictly require splash shields and local exhaust with this ester because its allylic double bond can pick up atmospheric oxidants if left exposed. In the fill lines, manual valves only open under controlled nitrogen sweep, and the product flows directly to blanketed containers. This may seem like belt-and-suspenders, but the years have shown that procedure saves time and money over batch failures and spilled drums.

    Meeting Regulatory and Quality Demands

    Experience has taught us that documentation can never slip in a product with specialty applications. Each shipment comes with both an analytical report from our in-house QC team and confirmation that all raw materials have cleared compliance checks. No shortcut or workaround substitutes for full traceability; it’s a price our quality auditors insist on for every batch.

    Working with partners who export to the EU, India, and the United States, it became clear early that regulatory harmonization requires a careful paper trail. Any request for additional data — REACH reviews, impurity profiles, or stability data summaries — gets answered directly from our own records. This has prevented more than one customs or dockside holdup on time-sensitive deliveries.

    Customer Solutions: Technical Support and Continuous Improvement

    Open communication with buyers drives ongoing upgrades at each step. One medicinal chemistry group requested narrower impurity specs to match their high-throughput screening needs. In response, our engineers revamped column operation, tuning reflux ratios and plate heights to push out even lower side-product profiles. Joint troubleshooting cut changeover time by over 30%. A polymer segment asked for a drum option with UV-blocking liners for warehouse storage, since they noticed color pickup during prolonged sunlight exposure. We tracked batch appearance in our own storage yard and piloted a packaging upgrade within weeks.

    For most customers, safety data and consistent supply matter as much as price. A few years back, fierce storms stopped one of our external raw suppliers. Fast response meant shifting precursors to our alternate in-house synthesis, and shipments continued without a single interruption. Filling in on plant overtime, our crew delivered without cutting corners. Those are the moments that earn long-term trust in the supply chain, and we don't take them lightly.

    Supporting Innovation in Synthesis

    Emerging breakthroughs in selective catalysis and molecule construction constantly change the demands on specialty esters. Recent work with university partners used Methyl 3,3-dimethylpent-4-enoate toward developing new analogues for crop protection. Hands-on technical exchanges revealed opportunities for scale-dehydration steps, shortening total process time by over a shift per batch. Chemical process engineers now fine-tune crystallization and isolation to cut waste loads below national thresholds, driven by real on-site measurements rather than brochure claims.

    One area where the ester excels: it acts as a versatile intermediate for further elaboration by lithiation or transition-metal catalyzed bonding. Colleagues running Suzuki couplings report that the electronic and steric combination of the ester group supports high selectivity, with less catalyst decomposition and fewer carryover impurities in the isolated product. Feedback from these customers supports ongoing investment in batch analytics and automated sampling systems.

    Continuous Feedback Loop: How the Product Evolves

    Feedback does not stop at technical forms or phone calls. Each technical visit, on-site audit, or review triggers a root-cause analysis from our side. For one customer, low-temperature storage during winter led to higher viscosity, creating headaches for their dosing pumps. After reviewing their plant setup, production shifted to temperature-stable secondary containment drums, reducing their downtime.

    Production operators stay involved in process improvement. Several line engineers proposed transitioning heat exchangers from copper to stainless steel after tracing minor product color issues back to trace metal catalyzed degradation. While initial trials cost more, in-field color and purity data convinced management to roll out the fix site-wide. Data-backed changes have shrugged off the need for vendor guesswork.

    Market and Industry Impact

    Large-scale custom and contract manufacturers bring different priorities to project launches. The flexibility of methyl 3,3-dimethylpent-4-enoate as a workhorse intermediate cuts across sectors, from pharmaceutical pilot plants to specialty materials R&D. Our sales and technical teams see ongoing switches from legacy processes toward those that build on this ester’s branching and allylic reactivity. That move reflects both a push for more finely-tuned intermediates and a shift away from one-size-fits-all chemistry.

    One example: a polymer customer exploring telechelic materials found that the structural rigidity imparted by the 3,3-dimethyl setup gave better property control in subsequent polymerizations, compared to results from linear esters. Researchers in the pharmaceutical sector routinely report improved yields in multi-step target synthesis, thanks in part to the unique migratory aptitude and steric arrangement that this molecule brings.

    Process Safety and Experience-Driven Protocols

    Experienced technicians bring an instinct for risk reduction. Each run-through reinforces how details matter: pump speeds, charge rates, real-time pressure monitoring. Methyl 3,3-dimethylpent-4-enoate responds well to standard procedures but rewards vigilance — a moment’s lapse can shift a clean reaction into a mess of side products.

    On the floor, training focuses on three things: personal protection, closed transfer, and active venting control. Every person with a hand on the batch understands the potential for static buildup around volatile organics. Our team’s discipline, shaped by years in hazardous chemistry, maintains a spotless record across multiple audits. Most of the process controls have also found their way into standard operating procedures for other high-value intermediates, showing that good habits cross over product lines.

    Final Thoughts from the Plant

    Watching a well-made batch of methyl 3,3-dimethylpent-4-enoate move from reactor to drum gives a sense of shared accomplishment. Behind each lot stands not just equipment or automation, but the judgment of operators, engineers, and chemists who know what’s at stake if a shipment falls short. We see high standards paired with restless energy to drive each improvement, both for our own processes and those of our partners.

    This ester’s combination of structural features, well-characterized reactivity, and stable handling have earned it a growing place across a diverse set of industries. As new applications emerge and synthetic routes evolve, the core commitment remains: rigor in production, honesty in technical support, and genuine collaboration with every customer or research partner. Each barrel shipped represents not just a product, but a reputation, built batch by batch and story by story across the plant.