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1-Methyl-1-Cyclopentene

    • Product Name 1-Methyl-1-Cyclopentene
    • Alias 1-methylcyclopentene
    • Einecs 211-251-6
    • 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

    841415

    IUPAC_Name 1-Methyl-1-cyclopentene
    Molecular_Formula C6H10
    Molecular_Weight 82.15 g/mol
    CAS_Number 693-89-0
    Appearance Colorless liquid
    Boiling_Point 92-94 °C
    Density 0.773 g/cm³
    Melting_Point -120 °C
    Refractive_Index 1.423
    Flash_Point −12 °C (closed cup)
    Solubility_in_Water Insoluble
    PubChem_CID 11766

    As an accredited 1-Methyl-1-Cyclopentene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tightly sealed, holding 100 mL of 1-Methyl-1-Cyclopentene; labeled with hazard warnings and chemical details.
    Shipping 1-Methyl-1-Cyclopentene should be shipped in tightly sealed containers, kept away from heat, sparks, or open flames. It must be stored and transported in a cool, well-ventilated area, and handled according to all local, national, and international regulations for flammable liquids. Use appropriate hazardous material labeling and documentation.
    Storage 1-Methyl-1-cyclopentene should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and strong oxidizers. Keep container tightly closed and properly labeled. Store in a flammable liquid storage cabinet and protect from direct sunlight. Use only with proper grounding and bonding. Follow all relevant chemical safety and fire regulations for flammable liquids.
    Application of 1-Methyl-1-Cyclopentene

    Applications of 1-Methyl-1-Cyclopentene in Industrial Manufacturing

    As the direct manufacturer, we supply 1-Methyl-1-Cyclopentene to downstream partners operating in several specialized chemical industries. Below we detail application scenarios, regulatory frameworks, formulation guidance, process integration, and representative end products for key industrial sectors employing this material.

    1. Fine Chemical Synthesis for Pharmaceutical Intermediates

    Pharmaceutical manufacturers utilize 1-Methyl-1-Cyclopentene as a building block in the synthesis of complex intermediates for drug development. Its five-carbon ring structure with a methyl substituent provides unique reactivity in alkylation and cyclization stages, supporting synthetic routes for advanced intermediates in anti-inflammatory and antiviral drugs. Chemists adjust reagent ratios based on reaction yields in pilot and production scale, with strict traceability and batch documentation. The raw material enters multi-step synthesis at designated functionalization phases and is monitored under controlled reaction environments to meet strict impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, relevant to intermediates)
    • European Pharmacopoeia guidelines for residual solvents and purity
    • FDA DMF (Drug Master File) requirements for key intermediates

    Typical usage ratio

    • 5–15 mol% per target compound, depending on route complexity; scale-up validated via process R&D
    • Adjustment based on stoichiometric needs and impurity control

    Downstream process integration

    • Added at the ring functionalization stage in batch or semi-continuous reactors
    • Used with transition metal catalysts for selective hydrogenation or isomerization steps
    • Subject to in-process QC sampling for purity, residual solvents, and reaction kinetics

    Final product types

    • Bulk active pharmaceutical ingredients (API) intermediates
    • Specialty pharmaceutical fine chemicals
    • Precursors for anti-inflammatory pharmaceutical compounds
    • Building blocks for antiviral small-molecule drugs

    2. Agrochemical Synthesis as Precursors for Crop Protection Agents

    Manufacturers of agrochemicals adopt 1-Methyl-1-Cyclopentene as an intermediate in the synthesis of advanced herbicide, fungicide, and insecticide actives. The compound’s structure supports targeted alkylation and ring-opening reactions essential for the creation of active moieties in selective crop protection agents. Formulators optimize ratios to maintain process selectivity while minimizing by-product formation, with close adherence to national and EU-specific chemical production regulations. The material typically enters agrochemical synthesis at initial carbon framework construction stages with documentation for batch-to-batch reproducibility.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical registration in the EU
    • FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act, USA)
    • ISO 9001:2015 for quality management in agrochemical manufacturing
    • Globally Harmonized System (GHS) for hazard communication

    Typical usage ratio

    • 8–20 wt% as part of intermediate synthesis; precise charge determined by downstream molecule requirements
    • Ratio optimized in pilot reactions based on target agrochemical efficiency and regulatory impurity thresholds

    Downstream process integration

    • Incorporated during the ring-construction stage in multi-step agrochemical synthesis
    • Processed in closed reactors with thermal controls to ensure conversion rates and minimize emissions
    • Purge and yield data captured for regulatory and process audit trails

    Final product types

    • Precursor intermediates for selective herbicides
    • Building blocks for systemic fungicides
    • Active ingredients for targeted insecticides
    • Crop protection molecules with cyclopentyl functionality

    3. Specialty Polymer and Resin Modifiers

    In advanced material production, formulators use 1-Methyl-1-Cyclopentene to create specialty monomers and as a reactive diluent in polymer synthesis. The compound introduces cyclopentyl moieties into polymer chains, modifying glass transition temperature, impact properties, and UV stability for high-performance engineering plastics and coatings. Ratios are established through lab formulations and validated in full-scale polymerization reactors. Producers conform to global materials safety and environmentally relevant standards applicable to end-use segments such as automotive or electronics.

    Industry compliance standards

    • ISO 14001 for Environmental Management Systems
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • UL 94 for flammability in plastics (for downstream use)
    • REACH SVHC screening if used in consumer-contact applications

    Typical usage ratio

    • 2–12 phr (parts per hundred resin) as monomer or comonomer modifier
    • Tailored based on target polymer properties and mechanical testing results

    Downstream process integration

    • Introduced during co-polymerization, often via bulk or solution polymerization processes
    • Monitored by in-line FT-IR or chromatography for conversion rate
    • Finished resin compounded with performance additives at extrusion or mixing step

    Final product types

    • High-impact engineering plastics for automotive housings
    • Modified epoxy and polyurethane resins for electronic encapsulation
    • UV-resistant exterior industrial coatings
    • Specialty thermoset composites and adhesives

    4. Fragrance and Flavor Intermediate Synthesis

    Producers in the aroma chemicals sector incorporate 1-Methyl-1-Cyclopentene into the synthesis of key fragrance and flavor intermediates. Its base structure supports preparation of cyclopentyl-based ketones and aldehydes, valued in fine perfumery and beverage applications. Quality and trace level control adhere to regional food safety and IFRA guidelines, and usage ratios are balanced by target yield and olfactory strength requirements. The raw material enters multi-step organic synthesis as an alkylated substrate typically following distillation and purification to ensure low impurity burden for downstream conversion.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • US FDA 21 CFR 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption, where applicable)
    • ISO 9001:2015 for quality systems in aroma chemical synthesis
    • EU Food Flavouring Regulation (EC) No 1334/2008

    Typical usage ratio

    • 3–10 wt% per batch, titrated according to fragrance/odorant crystallization curves and flavor formulation labs
    • Adjustment based on downstream perfumery and food additive strength targets

    Downstream process integration

    • Charged in the early-stage, cyclization or alkylation steps of aroma intermediate syntheses
    • Crude product refined via vacuum distillation and analysis for sensory purity
    • Quality assurance via GC-MS for impurity profiling and batch record‐keeping

    Final product types

    • Fragrance ketones for fine fragrance blends
    • Flavor cyclopentyl aldehydes used in beverage concentrates
    • Modifying agents in synthetic musk ingredients
    • Cyclopentyl-based aroma boosters for consumer products

    5. Fuel Additive Intermediate for High-Performance Fuels

    Manufacturers of high-octane fuel additives incorporate 1-Methyl-1-Cyclopentene as a core hydrocarbon building block in octane-boosting agent synthesis. Its molecular backbone enables formation of alkylated cyclopentanes, which display favorable detonation characteristics under engine-operating conditions. Technologists set formulation ratios based on empirical fuel testing and regional additive limits. Refineries and additive blenders must comply with both international and country-specific standards for automotive and aviation fuel use. The compound is integrated during preparative alkylation or ring-hydrogenation reactions prior to downstream blending.

    Industry compliance standards

    • ASTM D4814 for motor gasoline
    • EN 228:2012 for unleaded petrol requirements (Europe)
    • US EPA Fuel Additive Certification Protocol
    • ISO/TS 16949 relevant to automotive sector chemical quality

    Typical usage ratio

    • 1–5 vol% in alkylation, optimized for desired octane increase and anti-knock properties
    • Ratio adjusted with pilot blends and knock engine tests

    Downstream process integration

    • Added at the precursor alkylation or hydrogenation unit
    • Octane value monitored using CFR engines before downstream blending
    • Final additive prepared for bulk transport under hazardous goods protocols

    Final product types

    • High-octane blending agents for gasoline
    • Anti-knock fuel additives
    • Performance aviation fuel components
    • Octane enhancer packages for motorsport
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    Certification & Compliance
    More Introduction

    1-Methyl-1-Cyclopentene: Our Experience as a Chemical Manufacturer

    Over the years, we’ve worked with hundreds of different hydrocarbons, each offering its own advantages and quirks in the plant. 1-Methyl-1-Cyclopentene holds a special place in our catalog, not only because of its unique molecular structure but also because of the consistent results it delivers in downstream reactions. We manufacture this compound with a focus on purity and reliability, supporting a range of industries from pharma to advanced materials. Our team’s experience with process chemistry and hands-on synthesis gives us a practical perspective on how real-world production impacts quality, safety, and efficiency.

    Model and Specifications: Meeting Real Production Needs

    Looking at 1-Methyl-1-Cyclopentene compared to a broader group of cycloalkenes, it stands out through its methyl substitution on the ring. In our facilities, the compound is synthesized under well-controlled temperature and pressure conditions, which keeps isomerization in check. We pay close attention to the purification steps—distillation and inert gas blanketing—to ensure a high-purity product. Most users request material with GC purity above 99%, and our batches regularly meet or exceed this mark. In-house analytical work uses both GC and NMR for verification since minor impurities can affect performance in fine chemical applications.

    The chemical formula, C6H10, and its structure—a five-membered cyclopentene ring with a methyl group at the top—aren’t just academic. Differences in methyl group position have real consequences during synthesis and downstream use. Technicians in our lab handle 1-Methyl-1-Cyclopentene in standard metal drums or HDPE containers. Storage advice comes from years of seeing small leaks evolve into larger problems. Sealed, dry conditions away from direct sunlight prevent peroxide formation and minimize the risk of polymerization. Our logistics team coordinates quick shipment schedules because delays can impact sensitive downstream timelines, especially when the compound feeds directly into pharmaceutical intermediates or agricultural chemical syntheses.

    Why Choose 1-Methyl-1-Cyclopentene?

    In practice, the decision to use 1-Methyl-1-Cyclopentene usually arises at the project stage, where synthetic chemists or process engineers weigh its benefits against similar cycloalkenes like standard cyclopentene or 1,2-dimethyl-1-cyclopentene. The single methyl group at the ring’s first position influences both physical and chemical properties. Volatility, boiling point, and reactivity profiles differ from the straight cyclopentene, leading to fewer byproducts in certain Diels-Alder or catalytic alkylation reactions. We’ve seen more consistent yields and easier purification for adduct formation, which can be a constant pain point with some of the isomeric options.

    By talking directly with customers, not just distributors, we gain feedback from the actual bench work—how the compound performs inside reactors, how aggressive cleanup steps must be, and whether handling precautions align with real-world worker experience. One R&D chemist at a major pharma plant once told us that switching to our 1-Methyl-1-Cyclopentene reduced time lost to column purification. Less time on purification translates directly to more productive hours and fewer headaches on regulatory compliance. Safety managers find the material easier to store due to its lower vapor pressure, compared to lighter unsaturated hydrocarbons, which helps cut fugitive emissions and maintain cleaner atmosphere in the work area.

    Production Challenges We’ve Overcome

    Consistency doesn't happen by chance, especially when dealing with unsaturated hydrocarbons. Our years of producing 1-Methyl-1-Cyclopentene taught us lessons on both the chemistry and the logistics of large-scale synthesis. Polymerization risk always lurks with cycloalkenes, so we run tight controls on stabilizer content. Even minor contaminants can cause off-spec batches. We learned to invest in top-end instrumentation—analyzers and moisture meters—for process streams, not just finished product. This level of attention prevents chain-termination reactions and reduces waste, something any operator watching the bottom line will understand.

    Another challenge comes from the raw materials and their quality. Sourcing methylated cyclopentenes with the right isomeric ratios means trusting only suppliers with robust analytical backing. Early in the game, using substandard precursors cost us weeks of investigation and off-line capacity. We now run a battery of tests before a drum even gets near a reactor, drawing on close-knit relationships with only vetted partners. It’s easy to see which suppliers genuinely understand our requirements versus those just selling bulk commodity stock. Having a single methyl group in the right location makes all the difference, especially as downstream users push for higher reactivity and lower residuals in finished goods.

    Industrial and Research Applications

    We have seen this compound serve both established and emerging markets. In pharmaceuticals, 1-Methyl-1-Cyclopentene becomes a building block for specialty intermediates, thanks to the ring’s stability and the added methyl group’s influence on reactivity. Process chemists exploit its properties to design more robust synthetic routes, sometimes replacing open-chain alkenes to avoid rearrangement issues.

    On the polymer side, specialty elastomers often call for cycloalkene monomers with precise substitution patterns. A customer working in elastomer research once shared their struggle to achieve certain thermal and mechanical properties in block copolymers. Switching feedstock to our material enabled them to finally dial in the cross-linking density they needed, opening up a new class of performance materials. Small changes in the monomer—such as that single methyl group—have ripple effects on polymer architecture and, ultimately, product performance in end uses like hoses, diaphragms, and vibration-damping components.

    Academic researchers working on fundamental cycloaddition chemistry also appreciate the clean profile provided by a well-made batch. Less background noise in spectroscopic data means faster reaction development and easier publication of reproducible results. By focusing on precise manufacturing and vigilant lot tracking, we support these users going from two-gram reactions up to kilo-scale pilot runs. We keep communication simple and direct so lab managers get consistent outcomes, whether working on bench-scale innovation or planning scale up for industrial trials.

    Understanding the Differences: 1-Methyl-1-Cyclopentene Versus the Alternatives

    It’s easy to assume that all cyclopentenes behave alike, but we see every day the real-world differences methylation brings. This compound brings moderate steric hindrance compared to unsubstituted cyclopentene. That means reaction conditions adjust in subtle but important ways—for example, in electrophilic addition or selectivity during ring-opening reactions. Technicians running hydrogenation or oxidation steps notice fewer side reactions and unwanted polymers, simplifying downstream purification. Our experience tells us that users switching from less substituted rings notice measurable gains in selectivity and process stability.

    Other methylated cyclopentenes add more than one methyl group, changing how the ring behaves in both basic and acidic media. Some isomers show much higher volatility or tendency to form byproducts under strong acid catalysis. Users seeking a clean transformation or predictable ring closure often find 1-Methyl-1-Cyclopentene to be the better balance. We’ve validated this both through feedback from chemical engineers and our own rigorously monitored pilot runs, which track overall material balance and impurity profiles hour by hour. The ease of handling—less sensitivity to air and moisture than some other cycloalkenes—makes it popular in both basic research and demanding industrial setups.

    For those in the agricultural space, the stability of this compound shortens production cycles for agrochemical precursors. The more predictable behavior in alkylation and acylation steps enables higher yields, so formulators spend less time troubleshooting variable conversion rates. That saves both materials and man-hours. Plants using older feedstocks often face fouling or build-up in reactors; switching to a high-purity 1-Methyl-1-Cyclopentene helped customers run longer between shutdowns. Many of these learnings emerged during hands-on trouble-shooting with plant crews, where the difference between theory and day-to-day plant operation becomes clear.

    Safety Considerations in Handling and Use

    With any unsaturated hydrocarbon, safe handling depends not just on the material but also on the systems in place. We insist on detailed hazard communication and have built up a set of practical recommendations after years in the field. Even with its lower vapor pressure, 1-Methyl-1-Cyclopentene requires controlled atmosphere workstations for sampling and transfer. Drips and spills harden over time, making thorough wipe-down and inspection routines key to a well-run operation. Having seen the bottlenecks created by inconsistent housekeeping, our plant managers push for strict following of supervision and checklist protocols.

    Solvent compatibility comes up in nearly every new project, and experience helps here. Our records show that polar protic solvents prompt more rapid side reactions; so, operators working up new process trains usually stick to inert solvents like hexane or heptane during extraction steps. Inerting blanketed bulk tanks with dry nitrogen, then running periodic headspace checks, keeps both product and workers safe. Those who cut corners with lesser stabilizers or ventilation setups often end up with off-spec product or costly downtime due to unplanned maintenance.

    Environmental Responsibility in Manufacturing and Use

    Beyond immediate process concerns, environmental responsibility shapes the way we make and supply this compound. Through closed-loop solvent recovery and recycling, we keep emissions of volatile organics far below reported industry averages. Our team adopted these measures a decade back, after early trials showed significant loss from conventional vented systems. More robust storage vessels and real-time leak monitoring mean our emissions now measure in grams per ton, not kilograms. The effort to minimize flaring of waste streams doesn’t just keep us in regulatory compliance—it pays off in tangible cost savings and reduced energy inputs.

    On the downstream side, customers share our growing interest in cradle-to-gate impacts. With transparent reporting on batch production and raw material sourcing, we support users who need lifecycle analysis for final product reporting. As the shift toward green chemistry gains ground, end-users want assurance not just on product quality but on the environmental profile of upstream processes. Over time, more buyers ask about our energy mix, water footprint, and waste stream handling. It’s part of a broader movement calling for cleaner, more responsible chemical manufacturing, and we’re happy to share details of our journey and ongoing improvements.

    Supporting Innovation Through Technical Collaboration

    One of the most rewarding aspects of providing 1-Methyl-1-Cyclopentene happens away from the reactor—through direct technical discussions and collaborative problem-solving with users. Many customers come to us seeking advice on scaling up new synthesis schemes or troubleshooting unexpected side reactions. Daily interaction between our technical team and on-site plant operators drives continual improvement.

    Process development benefits from this hands-on feedback. For example, we worked with a specialty materials customer struggling with a recurring byproduct in their polymerization process. By tuning stabilizer systems and providing trial volumes with tailored methyl content, we enabled them to keep unwanted oligomers at bay, improving their downstream polymer properties. These success stories stem from honest dialogue and a willingness to adapt our approach. Innovation in chemical manufacturing rarely happens in a vacuum, and many of our best improvements result from working closely with end users, sharing plant data, and tackling obstacles together.

    Our laboratory team supports early development by offering more than just a bottle of product. Researchers running new reaction screens have unique material needs—a specific isomeric composition, a narrow boiling range, or a custom stabilizer blend. Having small teams of process chemists, analytical staff, and logistics coordinators all under one roof allows us to offer these custom solutions in days, not weeks. Rapid response and open lines of communication help projects move through trial runs fast, with fewer delays lost to sourcing, paperwork, or missed delivery windows.

    The Reliable Choice for Forward-Thinking Users

    Across hundreds of projects—ranging from simple intermediates to high-tech polymers—1-Methyl-1-Cyclopentene has earned its place on the production line. Its specific balance of reactivity and stability supports innovation without introducing needless complications. Because we manage every step of the process, from raw material qualification through final shipment, users receive the same consistent quality batch after batch. This makes planning easier for research and production teams alike.

    Over the decades, the collective expertise of our shop-floor operators, process engineers, and technical support staff has built a reputation for dependability. We’ve faced the same headaches our customers do: unplanned downtime, equipment fouling, and unpredictable output. Through continuous improvement and open collaboration, we make sure challenges turn into opportunities for better products and smoother workflow. By focusing on proven strategies—solid analytics, responsive technical support, and strong supply chain management—we keep bringing both innovation and reliability to the market.

    With new regulatory standards and performance targets always on the horizon, industrial customers seek more than just a supplier—they expect true partners who understand not only what 1-Methyl-1-Cyclopentene is, but how it works inside a real plant. Drawing on our front-line perspective as an actual chemical manufacturer, we remain committed to supporting your business and your projects with materials and insights rooted firmly in practical experience.