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2,4,4-Trimethyl-2-Pentene

    • Product Name 2,4,4-Trimethyl-2-Pentene
    • Alias Isooctene
    • Einecs 209-753-1
    • 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
    VTB
    Specifications

    HS Code

    769464

    Cas Number 107-40-4
    Molecular Formula C8H16
    Molecular Weight 112.21 g/mol
    Iupac Name 2,4,4-Trimethylpent-2-ene
    Boiling Point 102-103 °C
    Melting Point -135 °C
    Density 0.724 g/mL at 25 °C
    Appearance Colorless liquid
    Refractive Index 1.406 at 20 °C
    Flash Point -2 °C (closed cup)
    Solubility In Water Insoluble
    Odor Hydrocarbon-like

    As an accredited 2,4,4-Trimethyl-2-Pentene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle securely sealed, labeled with “2,4,4-Trimethyl-2-Pentene,” hazard warnings, and handling instructions.
    Shipping **Shipping Description for 2,4,4-Trimethyl-2-Pentene:** This chemical should be shipped in tightly sealed containers, away from heat, sparks, and open flames, as it is flammable. Ensure proper labeling according to hazardous material regulations. Store upright and avoid contact with strong oxidizers. Appropriate personal protective equipment should be used during handling and transport.
    Storage 2,4,4-Trimethyl-2-pentene should be stored in a cool, dry, well-ventilated area away from incompatible materials such as oxidizers and acids. Keep the container tightly closed when not in use, and store away from direct sunlight and sources of ignition. Use approved, clearly labeled containers designed for flammable liquids, and ensure proper grounding to prevent static discharge.
    Application of 2,4,4-Trimethyl-2-Pentene

    Applications of 2,4,4-Trimethyl-2-Pentene in Industrial Manufacturing

    As a direct manufacturer, we supply 2,4,4-Trimethyl-2-Pentene to leading chemical industries with specialized use cases. Our production experience ensures technical compatibility, steady formulation guidance, and quality traceability across downstream segments. Below we outline the main industrial domains utilizing this molecule, along with relevant compliance, usage ratio recommendations, integration stages, and end product examples.

    1. Synthesis of Lube Oil Additives

    Lubricant manufacturers incorporate 2,4,4-Trimethyl-2-Pentene primarily in the alkylation stage for producing key intermediate chemicals like alkylated phenols and zinc dialkyl dithiophosphates (ZDDP). These derivatives serve as essential antioxidants and anti-wear agents in automotive and industrial lubricants. The compound’s high isomeric purity and reactivity profile allow for consistent additive quality and effective functional group modification during synthesis.

    Industry compliance standards

    • ASTM D4485 (Engine Oil Performance)
    • API SN/CF Lubricant Standards
    • SAE J306 (Gear Lubricant Classifications)
    • ISO 9001:2015 for process control

    Typical usage ratio

    • Typically 10–15% w/w in alkylation feed mixtures for additive synthesis; adjusts to control molecular weight and branching of the final additive.

    Downstream process integration

    • Feeds into alkylation or condensation reactors with phenol or dithiophosphoric acid.
    • Process temperature and catalyst ratios calibrated for target viscosity improvers and wear inhibitors.
    • Raw material qualified by GC purity and isomer content before blending.

    Final product types

    • Motor oil additives
    • Gear oil package components
    • Hydraulic fluid additive concentrates
    • Industrial gear and compressor lubricants

    2. Production of Alkylated Aromatic Hydrocarbons for Detergent Manufacturing

    Detergent alkylbenzene plants employ 2,4,4-Trimethyl-2-Pentene as an alkylating agent for producing branched-chain linear alkylbenzene (LAB) intermediates. These intermediates exhibit better cold flow and soil release characteristics in finished cleaning products. Our material enables controlled chain branching during Friedel–Crafts alkylation, impacting final surfactant solubility and bio-degradability.

    Industry compliance standards

    • REACH 1907/2006 (EU Chemicals Regulation)
    • US EPA TSCA compliance for surfactant ingredients
    • ISO 14001 Environmental Management (waste stream control)
    • EC No 648/2004 (Detergent Regulation)

    Typical usage ratio

    • Varies from 5–25% w/w of total alkyl group source in alkyl benzene synthesis; ratio adjusted according to required side-chain branching and pour point.

    Downstream process integration

    • Introduced during the aromatic alkylation reaction with benzene under Lewis acid catalysis.
    • Purity and isomer distribution monitored by GC–FID to meet surfactant performance criteria.
    • Effluent neutralization and recovery as per effluent permits.

    Final product types

    • Household laundry detergent surfactants
    • Industrial cleaning agents
    • Dishwashing liquid raw materials
    • Cement and concrete admixtures (as plasticizer intermediates)

    3. Precursor for Antioxidant Production in Polymer Manufacturing

    Polymers such as polyolefins require robust thermal and oxidative stabilization. 2,4,4-Trimethyl-2-Pentene serves as a building block for manufacturing bisphenolic antioxidants like 2,4,4-trimethylpentyl phenol. These antioxidants are crucial in extending polymer life, reducing processing discoloration, and supporting non-migratory stabilization in automotive and packaging plastics. Our supply meets batch-to-batch traceability and controlled hydrocarbon profile essential for polymer grade raw materials.

    Industry compliance standards

    • FDA 21 CFR 177.1520 (Polyolefins for food contact)
    • EU Regulation 10/2011 (Plastics Food Contact Materials)
    • ISO 9001/14001 in polymer compounding
    • GB 9685-2016 (China Food Contact Additives)

    Typical usage ratio

    • Usually 8–20% w/w in alkylphenol reaction mixture; adjusted depending on polymer processing temperature and required antioxidant loading.

    Downstream process integration

    • Integrates during synthesis of alkylphenols via acid-catalyzed alkylation steps.
    • Antioxidant intermediates are further processed and blended into masterbatch or resin melt blending lines.
    • Full traceability ensured from raw material tank to final additive packaging.

    Final product types

    • Polypropylene and polyethylene stabilizers
    • ABS resin antioxidants
    • Automotive plastic masterbatches
    • BOPP film packaging materials

    4. Intermediate for Agrochemical Synthesis

    Agrochemical formulators use our product as an intermediate for targeted synthesis of organic compounds exhibiting selective herbicidal and pesticidal activity. The trimethylpentene structure undergoes specific functionalization, creating chemical motifs integral for modulating soil degradation rates and leaf cuticle penetration in crop protection formulations. Stringent control over impurity profiles ensures agriculture sector compatibility and downstream regulatory filings.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius pesticide specification
    • ISO 17025 in agricultural chemical testing
    • EPA FIFRA (US Federal Insecticide, Fungicide, and Rodenticide Act)
    • OECD GLP for field and residue trials

    Typical usage ratio

    • 5–18% w/w in alkylation or cycloaddition reactions; tuned according to active ingredient chain length and functional group introduction requirements.

    Downstream process integration

    • Raw material loaded into synthesis reactors for alkylation, oxidation, or cyclization with aromatic or heterocyclic cores.
    • Post-reaction fractions separated before formulation and co-formulant blending.
    • Residual QC performed for unknowns and non-target isomers.

    Final product types

    • Grass pre-emergent herbicide active ingredients
    • Selective insecticide intermediates
    • Paddy field herbicidal agents
    • Vegetable crop protection blends
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    Certification & Compliance
    More Introduction

    Introducing 2,4,4-Trimethyl-2-Pentene: A Closer Look at a Core Intermediate

    What 2,4,4-Trimethyl-2-Pentene Brings to the Table

    In the chemical industry, practical experience often reveals the real value of each compound. With decades spent sourcing, synthesizing, and supplying key intermediates, our experience with 2,4,4-Trimethyl-2-Pentene shows how much impact a single molecule can have on diverse production lines. We produce 2,4,4-Trimethyl-2-Pentene to a purity of at least 98%, typically exceeding that target by a comfortable margin. Years spent refining the distillation process have paid off in terms of both reliability and quality, supporting customers who work in plant-scale production just as well as those still running pilot batches.

    The molecular formula C8H16 points to its clear structure—a branched olefin that stands apart from standard alkenes in the same carbon range. Its low reactivity toward many acid-catalyzed reactions, yet moderate readiness for alkylation, makes it a versatile choice for chemists who need very specific selectivity. We see most activity with customers in the synthesis of specialty chemicals, oil additives, and pharmaceutical intermediates.

    With a boiling range typically just above 110°C, this compound has proven much less volatile than lighter alkenes like isobutene or propene. Labs appreciate the combination of manageable vapor pressure with solid liquid-phase stability. The compound remains a colorless liquid over a wide temperature range, which makes it much easier to handle without complex cooling or containment. Such handling advantages make a difference when customers rely on large-volume drum supplies, railcar deliveries, or even specialty tote packaging.

    Why Pentenes Matter: Real-World Performance from the Factory Floor

    Manufacturing chemists see a steady demand for 2,4,4-Trimethyl-2-Pentene for a few practical reasons. Many routes to high-value target molecules begin with a consistent double-bond configuration or a precisely branched carbon skeleton; this compound checks both boxes. Our process starts with thorough selection of precursor streams so customers can trust the composition from lot to lot. Trace impurities—especially other C8 isomers, low-boiling C7 hydrocarbons, and trace organosulfur—get pushed well below 0.5% total, as confirmed by continuous GC monitoring. That degree of purity means far fewer downstream surprises, whether someone is working with aluminum alkyls or enolate intermediates.

    In actual use, 2,4,4-Trimethyl-2-Pentene often serves as a feedstock for aldehyde and ketone syntheses, especially those aiming for highly branched products or tert-alkyl moieties. The steric environment around the double bond reduces risks of unwanted polymerization, compared with less hindered alkenes such as 1-octene. This protects process reliability during scale-up and minimizes fouling in fixed-bed or continuous reactors.

    Some customers take advantage of its straightforward hydroformylation to make neopentyl-type aldehydes. Others use it in alkylation steps for building specialty lubricants or anti-knock agents for fuels. One interesting feature shows up in how its structure resists isomerization, giving process chemists more precise control over product selectivity during catalytic hydrogenations.

    The Distinction from Other C8 Alkenes and Branched Olefins

    As a producer, we see a range of C8 alkenes move through the plant alongside 2,4,4-Trimethyl-2-Pentene, but few achieve the same balance of reactivity, safety, and supply stability. 1-Octene and 2-octene, still favored for their linearity, can’t deliver the same degree of branching. 2,4,4-Trimethyl-1-pentene, a close isomer, offers alternative reactivity but typically drifts toward less defined downstream selectivity in many synthesis routes. Isobutene-based coupling products often bring higher volatility or require stabilization additives, while our 2,4,4-Trimethyl-2-Pentene runs clean without performance-robbing inhibitors.

    Some customers new to C8 chemistry ask why not just use cycloalkenes or heavier decenes for the same role. Experience teaches that heavier molecules introduce viscosity and higher boiling points, which complicate both storage and product separation. Cyclohexene derivatives behave quite differently under acid and hydrogenation conditions, sending reactions down less predictable pathways. For fine chemicals, pharmaceuticals, and performance fluids, the trimethyl-branched linear olefin structure of our product stays reliable batch after batch—a fact reinforced by the low scatter in test data.

    How 2,4,4-Trimethyl-2-Pentene Flows into Key Sectors

    One of the main reasons producers keep a close eye on this chemical sits in its role as a bridge to higher-weight molecules. In lubricant additive synthesis, it acts as a starting material for alkyl-substituted phenols and sulfonates, each bringing critical oxidation resistance and detergent performance to engine oils. The double bond, easily alkylated but shielded by tertiary carbon branches, allows process engineers to balance reactivity without giving up process margin.

    We’ve seen major blenders of anti-knock compounds reinforce their formulas with 2,4,4-Trimethyl-2-Pentene derivatives. This move—supported by independently tested octane numbers—links directly to more efficient fuel combustion. Some follow up with oxidation to manufacture functionalized alcohols used in synthetic lubricants capable of outperforming conventional mineral oils at both high and low temperatures.

    In fragrance and flavor chemistry, the molecule stands out for its rigid backbone, which can help preserve volatile notes in target aroma compounds. Selective hydrogenation yields branched saturated hydrocarbons that blend smoothly into odor formulation bases. Its high chemical stability eliminates the risk of premature transformation in stored mixture tanks, letting perfumers and blenders scale batches with high reproducibility.

    Process Scale and Technical Details from the Manufacturer’s Viewpoint

    Scaling 2,4,4-Trimethyl-2-Pentene production to commercial levels means confronting a few persistent engineering realities. The feedstock, sourced from precise C8 fractions, often needs pre-treatment with molecular sieves and double-stage drying. Our process relies on atmospheric-pressure distillation paired with careful temperature profiling at each tray stage, pushing the bulk product close to the azeotrope point but never beyond, ensuring color and clarity without introducing degradation artifacts.

    Instrumental analysis—typically GC-FID and occasionally GC-MS for trace speciation—confirms each drum meets strict purity standards. Moisture detection methods, like coulometric Karl Fischer, track sub-100 ppm water to protect downstream reactions in the hands of fine chemical customers. Beyond purity, density and refractive index tests (as done per ASTM D4052 and D1218) allow regular verification of consistency between batches.

    Packages range from bulk iso-tankers intended for global shipments to reusable steel drums for regular regional customers. All drum linings and valves select for high resistance to alkene corrosion; lessons learned the hard way from early years of using less robust shipping materials. Our team runs a real-time logistics update system, so delivery windows rarely slip—critical for customers running on just-in-time production.

    What Sets Our 2,4,4-Trimethyl-2-Pentene Apart

    Maintaining a consistent product calls for more than verifying liters produced and purity checked. Each synthesis batch earns regular review; we work closely with QA teams to monitor color, odor, and trace element readings, and any shift triggers root-cause analysis. Frequent, transparent feedback with end users lets us align practical experience with laboratory data, closing the loop between what works on paper and what delivers in finished goods.

    Some plants in the market lean on external traders for their feedstocks, but vertical integration secures raw material streams for our operation. This not only stabilizes costs and timelines but also builds deep process knowledge, making it easier to respond quickly if impurities, shifting customer specs, or tougher regulatory checks come into play.

    Our safety protocols for handling C8 alkenes have evolved through trial and incremental learning. Experience with spills, planned system shutdowns, and even off-spec incidents has shaped today’s practice. Closed transfer, nitrogen blanketing, active leak detection, and personal protective instruction all limit real-world risks—practices informed as much by years in plant operations as by studying regulatory updates.

    Environmental, Regulatory, and Responsible Production

    As environmental pressure grows on the chemical sector, scrutiny of both process emissions and lifecycle impacts intensifies. We treat every vent stream through catalytic oxidation units, cutting VOC output to the minimum. Wastewater from the purification sequence meets standards before release, and spent carbon beds see responsible disposal through partners equipped for hazardous organic waste.

    Any update to regulations—whether European REACH, American TSCA, or regional standards—pushes the operation to audit SDS files, update shipping paperwork, and make changes to trace systems. We take this as a chance to reinforce training and keep the feedback loop open with both regulators and bulk buyers, ensuring processes meet the spirit as well as the letter of the law.

    Supply chain transparency matters for customers tracing the origin of key intermediates. Our record system ensures tracking from initial batch blending to shipping container, documenting all interventions, testing, and handoffs. Experience shows that end-to-end visibility not only strengthens trust but also helps respond quickly in the event of any quality concern or transport delay.

    Solving Practical Challenges in Application

    A few realities shape the production and end use of 2,4,4-Trimethyl-2-Pentene. Storage stability ranks high on the list, as the branched olefin structure largely resists peroxide formation under standard safe-keeping. Customers looking for longer-term drum or tank storage receive regular advice about optimal headspace, temperature, and light protection, lessons that follow from long-running observations across different climates and facilities.

    In downstream applications, some users initially encounter selectivity issues when running direct alkylations. Sharing best practices, such as careful catalyst choice and temperature ramping, helps customers see improved yields and less unwanted side-product formation. We remain engaged with R&D teams to pass along findings, traceable back to pilot and scaled-up runs at our own site.

    Handling questions on compatibility with process elastomers, lining choice, and safe draining keeps our technical team busy. One example: 2,4,4-Trimethyl-2-Pentene does not attack PTFE or high-performance viton gasket materials, even after months of exposure—a claim proven by repeated soak testing and confirmed with user feedback from both storage and continuous process lines.

    Industry Trends, Research, and Future Directions

    Demand for 2,4,4-Trimethyl-2-Pentene has shifted gradually. New catalyst systems for alkylation and polymerization have made use of its configuration, especially where high branching produces low-pour-point lubricants. The push toward greener syntheses sees new routes emerge using less aggressive Lewis acids and even enzyme-inspired catalysis, broadening downstream options while minimizing environmental burden.

    Academic collaborations in the past decade have shed light on alternative functionalization strategies, such as cross-metathesis and regioselective hydroboration. Information shared between researchers and plants translates into optimized process conditions on the manufacturing side. It is not uncommon to receive updated requests about new purity cutoffs, tailored performance tests, or custom packaging, reflecting the agile and dynamic needs coming from the bench and production floor alike.

    Some industrial chemists are now moving toward more renewable origins for the C8 fraction itself, experimenting with biosynthetic feedstocks or bio-waste streams. The adaptability of the synthetic protocol for 2,4,4-Trimethyl-2-Pentene places it in a favorable spot once those processes scale, ensuring that downstream users seeking “greener” credentials don’t have to compromise on performance or safety.

    Conclusion: Lessons from Real-World Chemical Manufacturing

    Experience with 2,4,4-Trimethyl-2-Pentene goes beyond filling drums and checking off test sheets. Each batch, each customer call, and each regulatory curve alters the way this product fits into the supply chain. Reliable procurement, ongoing technical support, and a commitment to process transparency set the tone. For anyone building complex molecules, pushing performance boundaries in lubricants, or driving selective chemical transformations, this compound proves its worth day in and day out. Our hands-on knowledge comes from decades in plant rooms, shipping yards, and technical back-and-forth with people who depend on every delivery.

    We remain committed to innovation, listening closely to customers’ changing needs, and ensuring that 2,4,4-Trimethyl-2-Pentene continues to deliver above and beyond, from research bench to industrial production line.