|
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 | 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. |
Applications of Methyl 3,3-Dimethylpent-4-enoate in Industrial ManufacturingMethyl 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 SynthesisOur 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
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical API SynthesisThis 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
Typical usage ratio
Downstream process integration
Final product types
3. Fragrance and Aroma Molecule ProductionPerfume 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
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer SynthesisPolymer 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
Typical usage ratio
Downstream process integration
Final product types
5. Advanced Materials Science Research and DevelopmentR&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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Methyl 3,3-Dimethylpent-4-Enoate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.