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1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester

    • Product Name 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester
    • Alias Dimethyl cyclopropane-1,1-dicarboxylate
    • Einecs 212-279-7
    • 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
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    VTB
    Specifications

    HS Code

    111279

    Product Name 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester
    Cas Number 1550-35-2
    Molecular Formula C7H10O4
    Molecular Weight 158.15 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 103-105°C at 10 mmHg
    Density 1.15 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically >98%
    Refractive Index 1.425-1.430
    Smiles COC(=O)C1(CC1)C(=O)OC
    Storage Temperature Room temperature
    Synonyms Dimethyl 1,1-cyclopropanedicarboxylate

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

    Packing & Storage
    Packing 250g of 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester is supplied in a tightly sealed amber glass bottle with safety labeling.
    Shipping **Shipping Description:** 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Store in a cool, dry area, and ensure compliance with all relevant local, national, and international regulations for chemical transport. Handle with care to avoid breakage and leaks. Not regulated as hazardous (check SDS).
    Storage Store 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester in a cool, dry, and well-ventilated area, away from sources of ignition and heat. Keep the container tightly closed and protected from moisture. Store away from incompatible substances such as strong oxidizers and acids. Use proper chemical storage containers, and ensure appropriate labeling and secondary containment to prevent leaks or spills.
    Application of 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester

    Applications of 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester in Industrial Manufacturing

    As the original manufacturer, we supply 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester directly into production lines serving specialized chemical markets. Our customers formulate with this molecule to achieve specific molecular structures and performance criteria across several tightly regulated industrial sectors. Below, we outline genuine downstream industrial applications, their compliance requirements, integration points, typical dosage windows, and the end products our partners manufacture utilizing this key intermediate.

    1. Pharmaceutical Synthesis: β-Lactam Antibiotic Intermediates

    Pharmaceutical companies apply this ester as a cyclopropane source for the synthesis of β-lactam cores, used in patented and generic antibiotic development programs. Its rigid bicyclic structure provides the required reactivity for key ring-closing steps, supporting advanced intermediates with high purity and traceability. Tight control throughout synthesis ensures compliance with ICH and pharmacopeial standards for API manufacturing. The molecule serves as a protected group donor or ring precursor tailored to several active ingredients in commercial pipelines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs and General Chapters
    • EU GMP Part II APIs
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 5–20 mol% relative to main antibiotic precursor; adjusted based on product yield and impurity profile targets

    Downstream process integration

    • Introduced during protected intermediate synthesis prior to ring closure; used in batch or continuous stirred-tank reactors

    Final product types

    • β-Lactam API intermediates
    • Cyclopropane-modified cephalosporin and carbapenem classes

    2. Agrochemical Synthesis: Herbicide Active Ingredients

    Major agrochemical formulators employ this intermediate in constructing cyclopropane motifs within new-generation herbicidal actives. Its structural role supports production routes for protoporphyrinogen oxidase (PPO) inhibitors and related selective weed control molecules. Manufacturers must ensure raw material provenance, control residual levels, and comply strictly with crop protection standards determined by national and multinational pesticide authorities.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (for active ingredient synthesis)
    • Chinese GB 2763 and EU Regulation No 1107/2009 (maximum residue levels)

    Typical usage ratio

    • 5–15% by weight relative to total agrochemical batch; varies based on synthetic pathway and yield optimization

    Downstream process integration

    • Fed into multi-step synthesis at cyclopropanation stage; scale ranges from pilot kilos to multi-ton campaign runs

    Final product types

    • Active herbicide ingredients (e.g., cyclopropane-based PPO inhibitors)
    • Precursor intermediates for commercial herbicide formulation

    3. Fine Chemical Production: Chiral Ligand Building Blocks

    Synthesis groups within specialty chemical companies use this ester as a precursor to enantioselective cyclopropane ligands. These ligands serve as chiral inducers or stabilizers in asymmetric hydrogenation and catalysis systems for active pharmaceutical and flavor compound production. The purity and isomer control supported by our production ensures downstream functional performance, critical for contract manufacturers and research divisions developing high-value fine chemicals.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (for EU)
    • Chemical Facility Anti-Terrorism Standards (CFATS, US DHS) for sensitive chiral agents

    Typical usage ratio

    • 2–8 mol% in relation to total ligand or catalyst load; set according to stereoselectivity and conversion requirements

    Downstream process integration

    • Applied at the cyclopropanation step in chiral auxiliary or ligand preparations; followed by purification under inert conditions

    Final product types

    • Chiral auxiliaries for asymmetric synthesis
    • Cyclopropane-containing chiral ligands

    4. Specialty Polymers and Resins: Cyclopropane-Modified Polyesters

    Developers of specialty resins incorporate this compound as a diester co-monomer in polymerization with diols and other diacids. Cyclopropane units impart increased rigidity, solvent resistance, and UV stability, key for advanced coatings, electronic encapsulants, and specialty fiber raw materials. We monitor residual solvent and comply with strict manufacturing release and downstream employee exposure standards set by international polymer and resin authorities.

    Industry compliance standards

    • ISO 14001: Environmental Management for Chemical Manufacturing
    • REACH for polymer precursors (Polymer Registration, EU)
    • TSCA Section 5 New Chemical Notifications (US EPA)

    Typical usage ratio

    • 1–10% w/w of total diacid feed; level adjusted for polymer glass transition temperature and mechanical specs

    Downstream process integration

    • Charged into polyesterification reactor with diols and standard glycolic acids; incorporated before melt polymerization or solvent polycondensation

    Final product types

    • Cyclopropane-modified polyesters and alkyd resins
    • UV-stable coating binders and specialty polymer films

    5. Fragrance and Flavors Synthesis: Cyclic Structural Intermediates

    Flavors and fragrance houses use this building block in fine syntheses of high-purity cyclic ketones and aldehydes that provide rare, stable aroma notes. Its unique cyclopropane functionality enables the controlled introduction of new rings within molecular frameworks during multi-step organoleptic compound creation. Product qualification aligns with international food flavor safety and toxicology reviews, as regulated in consumer product ingredient supply chains.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • IFRA Code of Practice (International Fragrance Association)
    • US FDA 21 CFR §172.515 (synthetic flavoring substances and adjuvants)

    Typical usage ratio

    • 0.5–5 mol% in multi-step syntheses; scaled to target aroma intensity and volatility

    Downstream process integration

    • Added at the cyclic intermediate synthesis stage ahead of final derivatization; operate under closed-system batch environments

    Final product types

    • Cyclopropane-containing fragrance intermediates
    • Specialty aroma compounds for fine fragrance and flavor delivery
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    Certification & Compliance
    More Introduction

    1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester: Insights from the Manufacturer’s Floor

    A Hands-On Look at a Unique Building Block

    Years of walking the factory floor have given me a close relationship with each product we batch, distill, and pack. Among the specialty chemicals that head out our gates, 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester stands out for its technical subtleties and the consistent challenges it has demanded from our engineers. Over the years, we have learned that making a fine ester is about more than hitting a purity on a specification sheet. It's the result of careful adjustments during synthesis, temperature control, and raw material screening that only become second nature through doing the hands-on work ourselves.

    Specifications Rooted in Real Manufacturing Experience

    This compound, sometimes referred to by its CAS number 7408-36-0, is a product that brings cyclopropane chemistry into practical reach for research laboratories and industrial innovators. Its structural backbone—the cyclopropane ring—delivers a unique balance of reactivity and stability that a straight-chain diester simply can't match. Each batch from our line registers high purity, with levels above 99% by GC guaranteed. This relies on more than routine quality checks. Operators learn by eye and experience which distillation cuts yield the cleanest material. A small deviation in reflux rate, and side-products creep in. We've spent years refining these conditions, so end users spend less time purifying and more time advancing their own chemistry.

    Performance Beyond Textbook Descriptions

    Customers who have become partners in development projects often remark that this compound’s value becomes clear in applications that depend on tight control of functionality and molecular size. The esterification of 1,1-cyclopropanedicarboxylic acid using methanol gives two methyl ester groups, enabling compatibility in synthesis routes that would overwhelm acids or less resistant intermediates.

    We've seen formulators shift over to this product in agrochemical discovery work, where the cyclopropane core imparts biological activity unavailable with other frameworks. Our pharmaceutical contacts chase highly functionalized cyclopropane scaffolds as a way to access conformational rigidity in their drug candidates, and 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester often serves as a strategic starting point. The reason is straightforward: this molecule can undergo further transformations—hydrolysis, reduction, amidation—without falling apart under typical lab conditions. Its resilience streamlines multistep synthesis, giving chemists an advantage that’s hard to substitute.

    Putting Differences into Focus: What Sets This Ester Apart?

    In a business where thousands of esters move through markets, the differences between products begin on the level of molecular structure. The three-membered ring of the cyclopropane drives the uniqueness of 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester. Compare that to linear diesters, or cyclic esters of larger rings, and you’ll find they lack the torsional strain and the compactness that define this compound’s behavior. This strain not only changes how reactions proceed but can even modify physical properties such as volatility, hydrolytic stability, or response in certain analytical techniques.

    Batch consistency is another recurring point. Our technicians monitor color, purity, water content, and residual acidity in real time. Harmonizing the outcomes of different runs takes ongoing retraining, regular upgrades to our process equipment, and open-eyed troubleshooting. It’s a commitment we have made based on real-world feedback from chemists who can immediately tell when batch-to-batch uniformity falters. We hear from partners who have tried imported variants that don't meet the same consistency, sometimes requiring extra purification or causing missteps in their workflows.

    Why Customers Return to Our Material

    We hear it in repeated orders—this ester finds a niche where customers require less solvent waste and faster throughput because they aren’t working around an inconsistent or impure starting point. The transparency in our operations—right down to sharing batch data and encouraging site visits—builds trust for those who rely on our product’s performance.

    Applications reach deeper than most would expect. Beyond synthesis work, we've seen research teams probe this molecule in polymerization studies. The cyclopropane core introduces ring strain, so it acts as a useful monomer for designing polymers with tailored rigidity or reactivity. On the agricultural side, developers of advanced crop protection compounds pursue cyclopropane building blocks as they design for resistance against environmental degradation or metabolic breakdown. In those projects, the raw material must not bring along residues or isomeric impurities that could interfere down the line.

    Troubleshooting and Process Evolution

    Every scale-up has written new footnotes into our plant logs. Earlier process generations struggled with reproducible yields: even a degree of temperature drift or undetected water brought down purity and, on rare occasions, created blocked lines or foul odors from byproducts. Tightening controls required an investment in both hardware and staff education, stepping up conductivity and pH monitoring, and building a culture where issues get flagged early rather than hidden.

    Over time, we've reengineered the continuous flow distillation to better separate low-boiling impurities from the product fraction. Adjustment of acidity during esterification, careful neutralization steps, and microfiltration after cooling have become standard in our workflow. The payoff has been real and measurable. The number of batches reaching or exceeding purity marks rose over 30% after these changes, and customer support calls about out-of-specification issues dropped to almost zero.

    Sourcing and Raw Material Traceability

    Raw materials are a battle for every manufacturer. We answer audits and supply chain requests by keeping transparent records, not just for regulatory compliance but for internal quality improvement. Methanol and 1,1-Cyclopropanedicarboxylic acid are the foundation stones. We vet vendors not only for price but for responsiveness, shipping conditions, and their willingness to answer questions when something unusual appears in trace analyses.

    Problems can and do arrive in the form of subtle contamination—metal ions from drums, trace acid residues, or even strange odors indicating degradation. Our process people have dug in to trace down minor lot issues. If a batch picks up excess acidity, it can hydrolyze or discolor too early. We developed several rapid testing protocols to catch these before production and qualify each incoming raw drum based on strict measured cutoffs, not supplier certificates alone.

    Why Purity Persistence Matters in Real Applications

    Downstream processes serve as the ultimate test for our efforts with this product. Synthetic chemists pushing for five- or six-step sequences rely on unambiguous functional group performance. If a portion of the dimethyl ester comes in partly hydrolyzed or brings in any color-forming agent, the next reaction step may yield a confusing mixture or reduced selectivity. Our experience shows that the tighter we run our moisture and acidity specs, the easier researchers find it to predict and model their reactions, whether they handle gram batches in the lab or tens of kilos in pilot work.

    Solubility and volatility patterns demanded special attention. End users often run the dimethyl ester in nonpolar or weakly polar solvents, which plays well with its methoxy end groups, but even tiny drafted changes in molecular geometry—such as partial hydrolysis to the monoester—can alter solubility profiles. We train our shipping team to avoid mixed loads, temperature swings, and long storage, all to protect product integrity. When needed, we deliver crystal clear liquid sealed under nitrogen, with careful drums that resist any contamination by light or atmospheric moisture.

    Distinct Advantages over Regular Alkyl Esters

    Many buyers come in looking for “a methyl ester” and believe interchangeability follows from similar nomenclature. In reality, the cyclopropane motif injects a new reactivity profile. Classic diesters derived from glutaric or succinic acid may offer versatility in mild conditions, but reactivity in cyclopropane rings brings different opportunities for controlled functionalization. Where others might see a simple ‘ester’, those who have worked in our lab or in advanced research recognize that the ring unlocks challenging chemistries, from cyclopropanation to ring-opening reactions, unlocking or blocking pathways in synthesis routes for complex molecules.

    Developers seeking distinctive motifs for their medicinal chemistry or agrochemical research often specify our ester in procurement precisely because straight-chain analogs won’t even get their projects off the ground. This specificity, born from years of rapport with molecule designers, has shown us the importance not just of meeting a technical datasheet but of being ready to troubleshoot reaction conditions, help with scale-up queries, and give access to analytical data our peers in trading houses seldom acquire.

    Commitment to Transparency and Reliable Support

    Ongoing communication with our users informs regular updates of our manufacturing protocol. We don’t wait for field complaints to prompt changes. A few years back, a customer highlighted a trace impurity that showed up as a background peak in their HPLC profiles. We huddled with our analytical team, reviewed our entire distillation operation, and ultimately added a new wash step as a safeguard. These adjustments didn’t just enhance our quality; they raised the bar across our other ester products.

    From bench chemists running exploratory syntheses to plant engineers doing kilo-scale development, we supply practical knowledge alongside every shipment. We share best practices gained from years of failed and successful syntheses: store tightly closed, minimize water exposure, work in a well-ventilated and cool environment. These pointers, though simple, have prevented losses and headaches for many of our partners. It’s the kind of hands-on advice only a direct manufacturer—one who has seen the issues firsthand—would bother passing along.

    The Laboratory Edge: Supporting Research and Innovation

    The needs of today’s chemical research community keep evolving. We talk to teams ranking every input for sustainability, purity, handling properties, and even regulatory clarity. Batch traceability eases paperwork and facilitates compliance for those operating under Good Manufacturing Practice guidelines. We’ve adopted tracking from sourcing through final shipment, so every pail or drum can be matched to a production history. Customers tackling scale-up find it matters—an unexpected impurity could mean months of lost work or regulatory hurdles.

    We regularly field requests to tailor packaging for sensitive or high-value studies—amber glass bottles for UV-sensitive processes, custom labels, and all packaging designed around clean-room standards to support critical application environments. These adjustments reflect our effort to stay current with research demands, going well beyond the approach of simple product delivery.

    Tackling Industry and Future Challenges

    Rising customer standards mean the job of a true manufacturer never finishes. Fixing a failed batch, training a new operator, or talking a client through why a physical property varies unexpectedly: these are part of our daily work. The onset of stricter purity demands has prompted ongoing investment in advanced chromatography, in-house FTIR and NMR confirmation, and development of methods to catch low-level contaminants. Compliance with regional and global regulations pushes us not just to keep up, but to anticipate what might come next for cyclopropane-based intermediates.

    Questions about environmental impact now arrive as often as technical ones. We constantly seek out safer raw materials, reduce waste water, and recycle solvents where technical feasibility aligns with end-use requirements. Challenges remain, especially as new derivatives of our core compound emerge and the market shifts towards greener chemistries. In-house R&D, coupled with open channels with our long-term customers, gives early warning signals for changing preferences, whether for lower residual solvents, improved biodegradability or alternatives to hazardous starting materials.

    Direct Feedback Informs Process Adjustments

    We find out quickly when a small parameter error or equipment malfunction makes its way into product shipped globally. Word-of-mouth in our industry carries weight; our name is on every drum and every analytical report. Through constant dialogue with buyers and end-users, we focus attention not just on specifications but on supporting documents, tailored technical advice, and, where requested, supply chain adjustments to ensure timely and reliable delivery.

    On the shop floor, operators have the power to signal quality issues immediately, with management review and retraining built into our schedule. This approach, born of experience, has cut costly recalls and reduced rework cycles. By acting promptly on real usage feedback, we've held on to key accounts and saved both ourselves—and our partners—from lost projects and unbudgeted downtime.

    We Stand Behind the 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester We Make

    Talking with users over years, we confirm that a reliable supply of a high-purity dimethyl ester is still an obstacle for many labs seeking to explore cyclopropane-derived compounds. Wholesalers and traders rarely match the technical backup or root-cause focus that a manufacturer develops through daily practice. For us, reputation builds batch after batch—by keeping our synthesis and purification practices open to audit, tracking every lot from raw material to final drum, and updating our process at every opportunity.

    Our sales and technical staff listen carefully to technical difficulties reported in the field, using that information to improve next runs and reduce future headaches. Ultimately, manufacturing this compound goes beyond meeting a quality metric on paper—it reflects our real world commitment, learned from trials, errors, and repeated improvements. For anyone interested in the unique reactivity, consistent quality, and serious manufacturing know-how that define our 1,1-Cyclopropanedicarboxylic Acid Dimethyl Ester, our doors and phone lines stay open. We make this compound because it’s genuinely useful, but we keep improving it because our customers—and the progress of modern chemistry—demand nothing less.