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HS Code |
709709 |
| ChemicalName | 2,3-Dimethyl-1-butene |
| MolecularFormula | C6H12 |
| MolecularWeight | 84.16 g/mol |
| CASNumber | 563-78-0 |
| Appearance | Colorless liquid |
| Density | 0.693 g/mL at 25°C |
| BoilingPoint | 64-66°C |
| MeltingPoint | -119°C |
| RefractiveIndex | 1.394 at 20°C |
| FlashPoint | -23°C |
| SolubilityInWater | Insoluble |
As an accredited 2,3-Dimethyl-1-Butene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,3-Dimethyl-1-Butene is packaged in a 500 mL amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2,3-Dimethyl-1-butene should be shipped in tightly sealed, chemical-resistant containers under cool, well-ventilated conditions. It is flammable and volatile, requiring classification as a hazardous material. During transport, it must comply with relevant regulations (such as DOT or ADR), avoiding sources of ignition and incompatible substances to ensure safety. |
| Storage | 2,3-Dimethyl-1-butene should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, or direct sunlight. Store in tightly closed, properly labeled containers made of compatible materials. Keep away from oxidizing agents, acids, and halogens. Ensure proper grounding and bonding during transfer. Use within a chemical fume hood if opened frequently to limit vapor exposure. |
Applications of 2,3-Dimethyl-1-Butene in Industrial Manufacturing2,3-Dimethyl-1-butene is a specialized alkene intermediate that plays a critical role in select chemical manufacturing sectors. As the direct producer, we supply this material to downstream partners who require consistent batch quality for precise applications in fine chemicals, performance materials, and specialty synthesis. The following sections outline established industrial scenarios where 2,3-dimethyl-1-butene is crucial, with application details relevant to process engineers and QC professionals in each field. 1. Synthesis of High-Performance Lubricant AdditivesDownstream formulators rely on 2,3-dimethyl-1-butene as an advanced alkylating agent in the manufacture of polyalphaolefin (PAO) oils and specialty lubricant additives. Its unique branching profile delivers improved viscosity indices and enhances low-temperature fluidity compared to linear olefin precursors. Our raw material integrates at the oligomerization or alkylation phase, where strict molecular weight control and consistent purity underpin additive performance in demanding mechanical environments. Industry compliance standards
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2. Pharmaceutical Alkylation Intermediate ProductionCROs and pharmaceutical manufacturers select 2,3-dimethyl-1-butene for its controlled reactivity in targeted alkylation reactions, especially in the synthesis of complex intermediates for high-value APIs. Its defined double bond position and steric hindrance support regioselective transformations, helping end users minimize by-products in multistep syntheses while satisfying strict impurity profiles mandated by regulatory bodies. Industry compliance standards
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3. Manufacture of Specialty Polymer ModifiersProducers of impact modifiers and specialty copolymers incorporate 2,3-dimethyl-1-butene to impart high flexibility, improved low-temperature elastomeric properties, and tailored molecular branching in polymer blends. Its reactive alkene functionality supports copolymerization with vinyl monomers in continuous or batch reactors, enabling precise control over branching and end-group incorporation at scale. Industry compliance standards
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4. Advanced Organic Synthesis in Agrochemical ProductionAgrochemical producers use 2,3-dimethyl-1-butene in the synthesis of highly branched intermediates for selective herbicides and growth regulators. Its stable structure lends effective alkylating properties for the attachment of side chains that modulate biological activity. Our manufacturing process guarantees minimal side-products, which supports robust downstream quality control especially where residue limits are tightly controlled. Industry compliance standards
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5. Fine Flavors and Fragrance Intermediate ProductionManufacturers in the aroma chemical sector utilize 2,3-dimethyl-1-butene for synthesizing alkylated aroma intermediates with distinctive scent notes, thanks to its highly branched structure. This material supports downstream Friedel-Crafts alkylation and hydroformylation processes, producing odorant molecules required in specialty fragrance compositions and high-impact flavor bases under compliant, food-approved reaction parameters. Industry compliance standards
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As a team that has spent decades fine-tuning production lines and batch consistency, we know the difference hands-on experience makes with every kilo that leaves our reactors. 2,3-Dimethyl-1-butene stands out in our portfolio for both its purity profile and the controlled conditions under which we manufacture it. This alpha-olefin, with the molecular formula C6H12, is built around a distinct structure: a butene backbone substituted with two methyl groups at the 2 and 3 carbon positions.
We give special attention to controlling isomeric purity. The positional isomer, 2,3-dimethyl-2-butene, slips through in typical synthetic routes due to similar boiling points and close reactivity. Our process engineers adapted separation steps that minimize this risk, making our stream high in target content and low in unwanted by-products. Most intermediates are checked inline, rather than only in final product testing, because a weak spot at any stage quickly ripples through downstream performance.
Experience teaches that partners want transparency, not just a certificate of analysis. We regularly open our process logs, discussing chromatograms, GC trace data, and purity readings—especially when a feedstock batch requires adjustment or new analytical methods come online. Our standard specification keeps isomeric purity above 97%, with contaminants—like traces of C5 or C7 hydrocarbons, or over-hydrogenated fractions—well below 1%. Whether the shipment is a few hundred grams for R&D or several metric tons, we inspect all tanks for reactivity, and pre-load all vessels under inert gas to avoid peroxide formation.
Our 2,3-dimethyl-1-butene comes as a clear, colorless liquid. Boiling point falls within the 63–64°C range, which aligns with published literature. Densities hover between 0.69 and 0.71 g/cm³ (20°C). Chemists in our own application development team rely on this consistency for internal projects, from synthesis of fragrance intermediates to custom polymerization cycles in our pilot labs.
Demand for 2,3-dimethyl-1-butene often comes from specialty synthesis. Our experience touches several market areas:
We keep up with how clients adapt our material for pilot work—turnaround time matters, and so does having the same source for each batch to ensure reproducibility. Field feedback shapes our own QC protocol updates. Our analytical chemists regularly tune retention times and MS fragmentation patterns, spotting batch-specific nuances we document and share when requested.
It’s easy to confuse 2,3-dimethyl-1-butene with other C6 olefins at a glance, especially for teams not immersed in day-to-day chemical handling. Structural cousins like 2,3-dimethyl-2-butene or 2-methyl-2-butene look similar on paper but behave differently in lab and plant settings. Isomeric placement changes how the molecule undergoes addition, oxidation, or polymerization steps.
For example, 2,3-dimethyl-2-butene—sometimes called tetramethylethylene—is symmetrical and less reactive at the central double bond, often favoring highly substituted carbocation formation. Our product, with the double bond at the terminal carbon, shows greater reactivity towards electrophilic additions and oligomerizations. Synthesis requiring high selectivity usually chooses the terminal isomer for cleaner conversion rates, with fewer regioisomeric by-products.
2-methyl-2-butene, another structural variant, bears only one methyl branch at the 2-position, limiting steric hindrance and altering addition site preferences. Chemists worried about branching-induced selectivity shifts tend to lay side-by-side comparison runs, and our batches have served as standards in such trials. We work with customers to match their specification sheets, often sending both isomers for side-by-side benchwork.
A major lesson from scaling up production comes from watching how small process deviations undermine batch reproducibility. Over the years, moving from glassware to pilot reactors to full plant operation, we saw how feed purity and temperature control spill into the finished product specs. Consistently low moisture content, iron-free process piping, and periodic catalyst replacement all help tighten batch-to-batch consistency. Control loops on our distillation columns track column head temperature with real-time feedback to avoid tailing or smearing from co-boiling isomers or over-hydrogenated fractions.
Some clients use our material in multi-step syntheses, where any impurity amplifies downstream, bloating cost or time for reprocessing. For their sake and ours, we maintain transparency: field engineers often phone us from site, reviewing visible impurities or minor color tinge. In those cases, we review reactor cleaning logs and investigate any deviations in raw material batches. The difference between a good and an average batch often boils down to those phone calls and the cooperation between technical teams.
Stability of 2,3-dimethyl-1-butene is a concern for any bulk user. Olefins have a reputation for forming peroxides if exposed to oxygen, especially after months in storage. To prevent off-spec degradation, our logistics team blankets all drums and tankers with nitrogen, loading them under slight positive pressure. Tanks vent through catch filters, and we recommend storage in a cool, shaded area away from ignition sources.
Old product—left unused for over a year—should be checked with peroxide test strips. Small amounts of peroxide can wreak havoc in polymerization runs or catalytic reactions, and we share our best practices for on-site screening. Occasional clients request material packaged under argon, or glass ampoules for milligram-scale analytical work. We accommodate these needs, leveraging our on-site analytical lab to check for traces of oxygenated by-products.
We monitor global trends and share insights with downstream users. Production volumes of 2,3-dimethyl-1-butene have edged higher over the last decade, propelled by a push in specialty polymer research and growing interest in structural isomers for green chemistry. Shifts toward sustainable catalysis have prompted inquiries for material with minimized residual metals. As green solutions move from patent literature to production, we supply cleaner, more tightly specified batches for pilot lines and evaluation testing.
Our conversations with research groups indicate new catalytic pathways often demand material with hyper-low sulfur or halide contamination. Rather than treat these requests as special orders, we have phased in new raw material input checks and upgraded our catalyst beds to limit trace element carryover. Years spent fielding unusual requests help us anticipate evolving needs, and our process engineers now proactively build extra cleaning cycles into production runs scheduled for sensitive downstream use.
For those following regulatory updates, our technical office tracks international changes governing process safety and allowable trace impurities. We maintain full documentation for each batch, and our own regulatory team updates local and overseas clients on new labeling or logistics rules that affect safe transport and handling. Having direct access to our process history—rather than relying on an upstream trader—lets us address questions quickly, sharing original raw data when needed for audits or compliance checks.
Direct input from regular users matters as much as published literature. Over the years, researchers in both academia and industry have alerted us to quirks unique to their application space: a fragrance chemist might notice a faint off-note with one supplier’s batch, a polymer chemist logs a change in melt behavior. By working closely with these partners, we fine-tune process controls and investigate reports down to the source tank.
We build long-term relationships by making technical staff available for hands-on troubleshooting. If a batch diverges from historical color or shows trace solvent residue, our QA group reviews incoming logs, double-checks blending records, and proposes joint investigative analysis. Root cause analysis, product replacement, or small-batch resynthesis—these are part of our open-door policy. No batch passes without chromatographic confirmation and routine review, and we encourage clients to trend key specs over the course of consecutive orders.
Having a single-site origin for each lot simplifies troubleshooting. Any minor shift in profile—such as trace hydrocarbon contaminants, or subtle boiling point depression—can be traced to the specific processing sequence. We have watched many examples where imported, third-party sourced material introduces unwanted variability that derails research or production. Our investment in modern analytical hardware reduces this risk and supports quick resolution when issues do crop up.
The wide range of downstream users—from multi-ton plastic producers to boutique fragrance labs—shapes how we operate. We set up small advisory boards made up of trusted application scientists and chemical engineers from client companies, gathering feedback not only about performance in their own systems but the real-world issues they encounter. This two-way feedback loop has changed our material testing routines, led to expanded packaging options, and improved our support programs for training and safety.
Field visits and video troubleshooting help smooth out user-specific problems, such as minimizing transfer line sticking, optimizing storage temperature, or resolving minor foaming during unloading. We document new learnings and recycle them into future production cycles, building institutional knowledge to raise the baseline for all users. This ongoing dialogue, more than any single process tweak, enables a more dependable experience batch after batch.
As the chemical industry pivots toward more sustainable sourcing and manufacturing, we participate by minimizing waste, energy use, and emissions in our own processes. We recover solvents wherever feasible, recycle non-conforming batches through distillation, and are actively developing catalyst regeneration strategies. It’s no longer just about regulatory compliance—it’s cost-effective and better for everyone connected to our supply chain.
We remain attentive to customer requirements as they evolve. If clients express new needs—like reducing residual solvent, or providing more precise batch data for digital traceability—we adapt workflows and invest in instrumentation. Our facility audits and environmental checks are now available for partners to review, matching the rising importance of transparency.
2,3-Dimethyl-1-butene may seem like just another alpha-olefin, but small differences in purity and handling add up quickly in demanding processes. Our experience has shown time and again that attention to detail, clear communication, and honest process assessment do more to ensure reliability than grand promises or flashy marketing. For users who treat each synthesis or production run as a high-stakes investment, the steady hand of a producer who has walked through decades of chemical manufacturing pays real dividends.
We see ourselves not just as a supplier, but as a project partner. Our door stays open for technical conversations, collaborative problem-solving, and practical advice—whether troubleshooting an analytical anomaly, consulting on storage protocol, or sharing long-term usage trends. In a changing landscape where end-users demand more accountability, we welcome the chance to share not just a product, but our accumulated knowledge.