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HS Code |
814915 |
| Chemical Name | Methyl 1-Cyclopentene-1-Carboxylate |
| Molecular Formula | C7H10O2 |
| Molecular Weight | 126.16 g/mol |
| Cas Number | 20833-12-3 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 163-165°C |
| Density | 1.03 g/cm³ |
| Refractive Index | 1.464-1.466 |
| Melting Point | -33°C |
| Flash Point | 53°C |
| Solubility In Water | Insoluble |
| Smiles | CC(=O)C1=CCCC1 |
| Pubchem Cid | 14011735 |
As an accredited Methyl 1-Cyclopentene-1-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of Methyl 1-Cyclopentene-1-Carboxylate, tightly sealed with a screw cap, labeled with safety information. |
| Shipping | Methyl 1-Cyclopentene-1-Carboxylate is typically shipped in tightly sealed containers under cool, dry conditions. Packaging must prevent leaks or exposure to moisture. For safety, comply with regulations for transporting flammable liquids, including clear labeling and appropriate documentation. Avoid shipping with incompatible substances such as strong oxidizers to prevent hazardous reactions. |
| Storage | **Methyl 1-cyclopentene-1-carboxylate** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Avoid exposure to heat, oxidizing agents, and moisture. Use appropriate chemical-resistant shelving, and label containers clearly. Employ proper secondary containment to prevent spills and environmental contamination. Store in accordance with local chemical regulations. |
Applications of Methyl 1-Cyclopentene-1-Carboxylate in Industrial ManufacturingMethyl 1-Cyclopentene-1-Carboxylate finds precise and specialized use in several chemical manufacturing sectors, serving as a key intermediate in demanding downstream syntheses. We directly supply this raw material to industrial partners engaged in pharmaceutical, agrochemical, polymer, and fine chemical production. Each application segment below details its distinct regulatory, formulation, and processing profile, enabling technical decision-makers to evaluate suitability and necessary control points for integration. 1. Pharmaceutical Intermediate for Cardiovascular SynthesisThis specialty ester is widely utilized as a building block in the multi-step synthesis of cardiovascular active pharmaceutical ingredients (APIs), including certain calcium channel blockers and antiarrhythmic agents. Process chemists employ its highly reactive cyclopentene core to introduce bespoke functional groups during early-stage molecule construction. Rigorous control over process contamination and trace impurity content is maintained throughout handling and transformation, supporting high-purity requirements of the API route. Industry compliance standards
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2. Precursor in Insecticide and Fungicide Active SynthesisMajor agrochemical companies leverage Methyl 1-Cyclopentene-1-Carboxylate as a core intermediate in the synthesis of cyclopentene-derived pesticide actives. Its structural motif introduces chemical stability and activity to final active molecules, particularly in proprietary fungicide and insecticide families. Formulators carefully optimize its concentration to manage both reactivity and process yield. All facilities observe strict standards regarding process effluent and downstream product residual analysis. Industry compliance standards
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3. Functional Monomer for Specialty Polymer SynthesisPolymer producers incorporate this chemical as a comonomer in the synthesis of specialty polyesters and polyamides, introducing unique flexibility and chemical resistance into advanced resin matrices. During copolymerization, its reactive double bond and carboxylate moiety facilitate grafting and crosslinking, produced via controlled process variables. Final polymer grades are then processed into engineering plastics or coatings with tailored end-use requirements. Industry compliance standards
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4. Building Block for Fragrance and Fine Chemical SynthesisFine chemical and fragrance formulators employ this cyclopentene-based ester as a synthetic intermediate to build complex musk and macrocyclic odors. Its cyclic backbone and ester functionality allow selective derivatization, yielding fragrance intermediates with enhanced persistence and stability for both perfumery and flavor applications. Customers value batch consistency and low odorous byproduct profiles, maintained by stringent in-process controls and analytical verification. Industry compliance standards
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As a chemical manufacturer, every batch of Methyl 1-Cyclopentene-1-Carboxylate reflects a blend of careful control, repeatable process, and problem-solving driven by real-world lab and plant experience. This compound, known in labs for its clean ring structure and reactive ester group, shows up on our lines as a clear liquid with a distinct aroma. The CAS number gives it a place in chemical registries, but in actual production and downstream work, it’s the molecular behavior that matters. Over the last years of producing and refining this material, our crews have addressed challenges—both expected and surprising—that have shaped how we talk about quality, purity, and application.
Methyl 1-Cyclopentene-1-Carboxylate runs with a chemical formula of C7H10O2. We consistently target a purity of ≥99 percent GC, since subpar lots introduce headaches for synthesis teams downstream. Density, boiling range, and refractive index form the pillars for acceptance and use. Each run stays dry and free from trace acids, since even a slight contamination leads to off-notes in the final product. Managing moisture content means active intervention at the filtration and packaging step. Our process teams track these details with routine check-ins and run QC on every batch before it leaves the drum. The physical traits matter beyond numbers on a spec sheet—solvent residue, trace impurities, and color can make or break a project, especially in pharmaceutical and flavor development.
Some manufacturers push throughput at the expense of lot-to-lot consistency, but solvent traces and variable refractive indices show up fast during downstream coupling reactions. When customers run hydrogenation or condensation, the clean removal of our methyl ester group ensures smooth conversion. We run retention samples and crash tests with key reagents to judge stability and performance, not just by the numbers in a document but by the compound's actual behavior in benches and reactors.
Each drum or flask of Methyl 1-Cyclopentene-1-Carboxylate brings performance to organic chemistry rooms—whether that's at kilo lab scale or full-blown continuous process. For research chemists, esterification of the cyclopentene ring structure creates a proven building block for synthesizing advanced molecules. Medicinal teams use it as a key intermediate, channeling the ring’s reactivity to form complex active pharmaceutical ingredients. Agrochemical projects lean on it to step toward crop-protection scaffolds. The cyclopentene backbone keeps backbone rigidity, offering both conformational stability and a pathway to functionalized compounds. Fragrance houses use it to introduce a saturated note and as a stepping stone toward bicyclic and tricyclic motifs.
Having spent years working the process lines and collaborating with customers at scale, some patterns stand out. Customers use Methyl 1-Cyclopentene-1-Carboxylate in Grignard reactions, Heck coupling, and palladium-catalyzed functionalizations, ringing out both the ester and the double bond. It’s not just a matter of shipping a canister and closing the book. Upstream choices and small differences in raw material quality feed into the yield and selectivity of downstream chemistry. Feedback from researchers and process directors reinforces the value of consistent, low-residual-byproduct material in scaling up, reducing side reactions, and achieving high-value transformations.
Plenty of cyclopentene derivatives cross our desks, ranging from simple cyclopentenes to more involved diesters and substituted carboxylates. Yet, the methyl ester brings a unique profile that changes both its reactivity and its handling. Cyclopentene alone, lacking the ester, shows higher volatility, more flammability, and lower solubility in polar schemes. Substituting the methyl ester raises the boiling point, bringing greater control in batch or flow reactors.
Compare this to ethyl, tert-butyl, or benzyl cyclopentene carboxylates—methyl sits right in the Goldilocks zone. Smaller than ethyl or bulkier substituents, the methyl group yields a steeper loss on ignition and a brisker hydrolysis rate when teams run the next step in aqueous or basic conditions. Tert-butyl esters, for example, offer more bulk but demand harsher deprotection. For teams working in harsh or catalytic settings, the methyl ester often outperforms alternatives, either by speed of cleavage or by minimizing unwanted tarring.
Many times, chemists face decisions about ester choice based on downstream hydrolysis ease, solubility, or reactivity. Methyl 1-Cyclopentene-1-Carboxylate threads the needle between easy hydrolysis and manageable volatility. Labs working on acridines, spiro-compounds, or bicyclic structures use it because methyl esters resist hydrolysis long enough for multistep coupling—unlike more labile esters—while remaining cleanly convertible under mild base or acid.
The chemistry isn’t the whole story. Bringing Methyl 1-Cyclopentene-1-Carboxylate from bench to drum needs vigilance in every part of the process. Every time we switch from a pilot run to production, the risk of byproduct formation jumps. Even small temperature drifts along the cyclization or esterification route leave signatures in the impurity profile. As a result, we track GC-MS, NMR, and Karl Fischer water checks—not just at the endpoint, but during key inflection points mid-process.
On the plant floor, a large part of our work involves securing raw material supply and preventing cross-contamination. During times of supply-chain disruption or rising solvent costs, some producers cut corners to boost yields or manage costs. The resulting off-quality material comes out in yield losses and waste downstream for customers. Our own protocols mean running double checks during dissolving, washing, and fractionation. For new applications, both scale-up teams and long-standing customers want to see full breakdowns of impurity profiles, not just summary specs, so our teams maintain data archives and batch-tracking that cover every production run.
Over the years, we’ve faced our share of bottlenecks and technical setbacks. Early on, thermal degradation during esterification posed a consistent problem, with traces of acidic by-product causing significant yield loss for users focused on medicinal synthesis. The fix involved a simple—but overlooked—step of tighter temperature control and adding specific scavengers. Later, rising energy costs forced us to rethink solvent recycling protocols. Recovering solvents with minimal cross-contamination and tracking spent acid reduced both cost and environmental impact.
Shipping conditions for this compound can impact stability. Extended storage above room temperature may lead to gradual decomposition, but rigorous containment and handling minimize product breakdown. Moisture pickup during transit led to a switch from standard closures to more robust, tamper-evident seals—lessening batch returns and reducing customer complaints about water content. Routine feedback pushes us to make practical improvements, not simply rely on supplier guarantees.
The last two decades have brought changes in how teams approach molecule construction, both in industry and academic settings. Green chemistry calls for tighter atom economy, safer handling, and lower emissions. Methyl 1-Cyclopentene-1-Carboxylate, with its ring and ester, fills a unique role by allowing semi-stable intermediate isolation while keeping options open for rapid downstream transformation. Its moderate boiling point and manageable vapor pressure allow scale-up teams to work safely, even in facilities lacking high-vacuum infrastructure.
Pharmaceutical teams, facing regulatory pressure for better impurity profiles, choose methyl over other esters to streamline purification and cut down on related substances write-ups. Fragrance designers, seeking unique cyclopentyl notes, appreciate the versatility in creating fused ring structures while keeping synthetic sequences efficient. Each time a new process comes over the transom from a partner—acylation, reductive amination, or catalytic rearrangement—we validate with small-scale trials and back-calculate best-fit usage.
Route selection at the manufacturing site drives impurity profile and cost. Some suppliers still use batchwise acid-catalyzed esterification, which brings higher risk of oligomerization and residual acid traces. Instead, our site moved toward continuous flow protocols, which afford tighter control and lower byproduct creation. This swap didn’t happen overnight—it followed months of troubleshooting, equipment re-tooling, and operator training. Each improvement paid off in lower waste streams and better yields not just for us, but for our clients scaling up their downstream syntheses.
Years of supporting scale-ups have shown us that reputation comes from accumulated experience, not advertising. Teams return for more product because they see tangible results—clean reaction profiles, predictable downstream transformations, and reduced post-reaction purification. Small differences in methyl ester quality translate directly into fewer headaches in late-stage synthesis. Process directors, especially in high-throughput environments or regulated sectors, report fewer deviations when ester lots hold tight to proposed specs. Sales wins, in the long run, come when word gets around about solid material—pointing to better purity, minimized waste, and reliable on-time delivery.
Every chemical producer fields questions about environmental impact. For Methyl 1-Cyclopentene-1-Carboxylate, managing emissions, reducing solvent footprints, and closing material balances go beyond regulatory reporting. We regularly review how to trap and reuse organic vapors, cut water consumption, and avoid single-use drums wherever possible. End users facing sustainability targets ask for input, and we respond by providing life cycle data, waste reduction plans, and, when feasible, integrating renewable feedstocks.
All this work aligns with regulatory requirements surrounding waste, emissions, and transportation for organic esters. In some regions, authorities demand rigorous monitoring of volatile organic compound emissions and require tracking of all waste generated from production. Such demands push us to constantly modify protocols and maintain a transparent chain-of-custody, so product users can track sourcing and disposal data throughout their supply chains.
Research teams sometimes face struggle sourcing consistent lots of Methyl 1-Cyclopentene-1-Carboxylate during early discovery. We bridge this gap by providing small trial quantities and scale-up support, running extra analyses to backstop customers breaking new ground. For process chemists, the focus shifts to tonnage, stability, and integration into existing synthetic routes. Our technical staff collaborate closely, suggesting modified packaging, optimal shipping conditions, and storage advice grounded in real experience—right down to container materials and lot tracking.
Feedback rarely comes in tidy forms—issues surface as vague complaints about conversions or color, not bullet-point lists. Sorting through customer off-notes, failed HPLC batches, or acid number spikes often leads to real process improvement that benefits everyone using the material in advanced chemistry. Rarely do two years pass without another tweak to filtration, distillation, or shipment, based on inquiries or customer lab data.
The demand for this ester keeps expanding, especially with more complex and nitrogen-rich molecules entering agrochemical and API pipelines. We anticipate more scrutiny of even trace-level impurities as regulatory guidelines evolve, and continue to refine our purification steps. Balancing new supply chain pressures with time-tested process reliability means staying nimble—adding new drying technologies, refining distillation setups, and regularly retraining plant staff on best practices.
Unexpected changes in energy markets or raw material supply have pushed us to hold greater material in reserve and build buffer production capacity. By collaborating with downstream customers, we ensure stock meets their project timelines without settling for off-spec or rush-produced material. Research groups working on next-generation intermediates increasingly request custom modifications to the methyl ester framework—sometimes requiring co-development of new technology or real-time process troubleshooting.
From a manufacturer’s perspective, the advice for first-time users centers on testing the product in intended synthetic schemes before full commitment. Checking baseline moisture content, running a trial purification, and reviewing the latest batch data helps guarantee a smooth start. For repetitive use, plan out inventory rotations to avoid long-term storage’s slow decomposition risks. Don’t underestimate the impact of small changes in material grade—what seems like a minor difference in residual water or acid content can create outsized headaches in multi-step synthesis or scale-up.
Staying in open communication with your supplier solves problems faster; we frequently troubleshoot together with customers’ technical teams. Honest feedback—whether complaints or success stories—guides improvements that reach all end users. After years of partnership, we find that these conversations lead to concrete action, not just paperwork or compliance efforts.
Every batch echoes back the craft, skill, and accumulated learning of the manufacturing team. Challenges will always come, whether from new regulations, market disruptions, or applications never seen before. Our process relies on seeing the material not just as a chemical, but as a product of human effort, ingenuity, and continual adaptation. Manufacturing Methyl 1-Cyclopentene-1-Carboxylate means more than producing a commodity. It’s a matter of building lasting relationships, supporting scientific progress, and delivering practical value for customers—whether they work at a research bench, on the production line, or at the decision table shaping tomorrow’s molecules.