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Diethyl Isopropylidenemalonate

    • Product Name Diethyl Isopropylidenemalonate
    • Alias diethyl 2-propylidenepropanedioate
    • Einecs 209-803-7
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    144586

    Product Name Diethyl Isopropylidenemalonate
    Cas Number 604-53-5
    Molecular Formula C10H16O4
    Molecular Weight 200.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 120-122°C at 10 mmHg
    Density 1.071 g/cm3 at 25°C
    Refractive Index 1.43-1.435 at 20°C
    Solubility Insoluble in water, soluble in organic solvents
    Flash Point 117°C (closed cup)
    Purity Typically ≥98%
    Melting Point -41°C
    Smiles CCOC(=O)C(C(C)=C)C(=O)OCC

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

    Packing & Storage
    Packing 250g of Diethyl Isopropylidenemalonate is supplied in a tightly sealed amber glass bottle, labeled with safety and handling information.
    Shipping **Shipping Description:** Diethyl Isopropylidenemalonate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be handled as a chemical reagent, with appropriate labeling and documentation. Transport in accordance with local, national, and international regulations for chemicals, ensuring spill prevention and keeping away from incompatible substances and ignition sources.
    Storage Store diethyl isopropylidenemalonate in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Protect from moisture and ignition sources. Ensure proper labeling and restrict access to trained personnel. Use appropriate containment to prevent leaks or spills and comply with local chemical storage regulations.
    Application of Diethyl Isopropylidenemalonate

    Applications of Diethyl Isopropylidenemalonate in Industrial Manufacturing

    As a direct manufacturer with established technical expertise, we enable the integration of Diethyl Isopropylidenemalonate across multiple specialized chemical sectors. Each downstream market leverages its distinct reactivity and selectivity in advanced syntheses, with uniquely engineered processes that demand tight control over formulation, compliance, and performance parameters. Below, we detail specific end-use scenarios substantiated by real-world industry adoption, describing application context, process entry points, and precise formulation standards.

    1. Agrochemical Active Ingredient Synthesis

    Diethyl Isopropylidenemalonate functions as a key building block in the multi-step synthesis of select herbicide and pesticide active compounds, where reliable carbon–carbon bond formation is crucial. Formulators adjust dosage based on targeted crop pest spectrum and subsequent synthetic modifications, with stringent oversight to meet regulatory limits on residual intermediates. This raw material enters at the condensation or cyclization phase and influences the downstream purity of the active molecule prior to final formulation and microencapsulation.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006
    • EPA 40 CFR Part 180 (US pesticide residues)
    • ISO 9001:2015 Quality Management Systems for synthesis traceability

    Typical usage ratio

    • 3–8% w/w in primary active synthesis, adjusted based on targeted active yield and batch size

    Downstream process integration

    • Introduced at the core condensation and acylation step during the active ingredient matrix assembly
    • Subsequently removed or modified via hydrolysis or transesterification

    Final product types

    • Pre-emergent herbicide technical concentrates
    • Insecticide intermediates for methylcarbamate derivatives
    • Fungicide precursor APIs

    2. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical fine chemical manufacturers employ Diethyl Isopropylidenemalonate as a critical intermediate in the synthesis of complex heterocyclic active pharmaceutical ingredients (APIs), notably in the production of certain barbiturate and anticonvulsant scaffolds. With GMP-compliant traceability, the compound enters during the nucleophilic addition or cyclization stage, affecting the purity profile and impurity matrix of the downstream molecule. Its use must conform to stringent pharmacopoeial and validation requirements, and API facilities optimize dosage according to reactivity and downstream throughput.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF Monograph Specifications
    • European Pharmacopoeia standards
    • FDA 21 CFR Part 211 (US cGMP regulations for pharmaceuticals)

    Typical usage ratio

    • 2–6 mol% relative to primary amine reactant, depending on specific API route and scale

    Downstream process integration

    • Added at the enolate alkylation or condensation ring closure stage in multi-step API synthesis
    • Blended in reaction vessel under controlled temperature and solvent system for impurity control

    Final product types

    • Barbituric acid derivatives (e.g., anticonvulsants)
    • Pyrazolone and pyrimidine API intermediates
    • Analgesic and anti-inflammatory pharmaceutical substances

    3. Specialty Polymer Monomer Precursor

    Chemical process plants utilize Diethyl Isopropylidenemalonate as a reactive monomer precursor for synthesizing advanced specialty polymers, including ionic conductive copolymers and high-performance polyesters with tailored glass transition or mechanical properties. The material is dosed according to specific polymer design parameters, and chain propagation is closely monitored to ensure compliance with end-use safety and technical product certifications required in electronics or medical device sectors. Plant operators introduce the compound during bulk or batch polymerization, ensuring consistent feed ratios for desired polymer attributes.

    Industry compliance standards

    • UL 94 Flame Retardancy (for electronic polymer use)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 13485:2016 (Medical device polymers)
    • ISO 9001:2015 (Production traceability for specialty chemicals)

    Typical usage ratio

    • 2–12 mol% of total monomer mass, with adjustment for polymer chain length and end-use performance targets

    Downstream process integration

    • Direct feed into polymerization reactor as co-monomer or chain modifier
    • Precipitation or solvent removal downstream to isolate high-molecular-weight product

    Final product types

    • Ionic conductive copolymers for electrolytic membranes
    • Engineered polyesters for medical device housings
    • Functionalized films for electronics encapsulation

    4. Organic Pigment and Dye Synthesis

    In high-performance pigment plants, Diethyl Isopropylidenemalonate participates as a precursor in the controlled synthesis of azo and quinophthalone pigments, delivering specific chromophore frameworks demanded by the plastics, inks, and coatings markets. Operators regulate input quantities to fine-tune hue and lightfastness, with all formulation steps adhering to food contact and environmental safety regulations as applicable. Integration generally occurs at the diazotization and coupling stage, and color formulators leverage its selectivity for achieving batch-to-batch color consistency.

    Industry compliance standards

    • EN 71-3 (Toys Safety – Migration of certain elements, colorant use in toys)
    • US FDA 21 CFR Section 178.3297 (Colorants for polymers and food contact materials)
    • OEKO-TEX Standard 100 (Textile chemical safety)
    • ISO 1248 (Pigment Testing for Coloring Strength and Lightfastness)

    Typical usage ratio

    • 1–5% w/w in coupling phase, depending on colorant strength and desired pigment load

    Downstream process integration

    • Added to the coupling reaction vessel post-diazotization, under strict pH and temperature control
    • Crystallization and filtration downstream for pigment isolation

    Final product types

    • High-performance yellow and orange pigments for plastics
    • Azo dyes for industrial inks
    • Specialty colorants for coatings and printing applications

    5. Fine Chemical Intermediate for Flavors & Fragrances

    Leading aroma chemistry manufacturers incorporate Diethyl Isopropylidenemalonate during the key fragrance precursor synthesis stages, especially for musky and floral macrocyclic ester assemblies. All raw material entries must meet IFRA and food-grade additive guidelines, and blending rates are determined by reactivity, odorant concentration targets, and residual solvent removal specifications. Typically, the compound is introduced during esterification or cyclization with strict analytical profile monitoring to verify olfactory performance and regulatory conformity.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association Guidelines)
    • EU Regulation No 1334/2008 (Flavourings and certain food ingredients)
    • US FDA 21 CFR 172.515 (Flavoring agents and related substances)
    • ISO 22000:2018 (Food Safety Management Systems)

    Typical usage ratio

    • 1.5–4% of total reaction mass, controlled to align with final aroma concentration and regulatory residue limits

    Downstream process integration

    • Charged to the main esterification or ring-closing reaction for macrocyclic fragrance intermediates
    • Followed by distillation for purity and odor threshold optimization

    Final product types

    • Macrocyclic ester-based musky fragrances
    • Floral aroma building blocks for perfumery
    • Fine flavoring agents for food and beverage industries
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    Certification & Compliance
    More Introduction

    Diethyl Isopropylidenemalonate: Advanced Solutions from a Manufacturer’s Experience

    A Closer Look at Our Core Product

    Every day in the plant, we deal with a spectrum of chemicals that serve as essential ingredients in the world’s vital industries. Diethyl Isopropylidenemalonate, with the model label sometimes indexed as “DIPM99”, stands out as one of those rare intermediates that brings precision and reliability to a process, not just for its high purity but for the consistency we’ve been able to achieve through years of careful control and incremental improvements. Our batches, targeting a purity above 99%, reflect raw material optimization and a synthesis route crafted around actual feedback from teams working on complex syntheses, not just theoretical yields from academic literature.

    How We See Diethyl Isopropylidenemalonate at Work

    On the production floor, folks handling Diethyl Isopropylidenemalonate rarely talk about it as an abstract “building block.” To those who mix, react, and refine it, DIPM means a cleaner reaction stage, an easier downstream separation, and less troubleshooting in process development. It is known amongst our team as a reliable agent in synthesizing pharmaceuticals, agrochemicals, advanced dyes, and some high-performance pigments. Chemists value its ability to undergo condensation and alkylation without leaving side product headaches that cause yield loss or unexpected byproducts. Process engineers appreciate its liquid stability—at controlled ranges—packed in high-grade tins that cut contamination or evaporation worries to a minimum.

    What Sets Our Material Apart

    Over the years, plenty of hands have shaped the process behind our DIPM. Our technical group continually adapts to the reality that every step, from esterification to distillation, leaves an imprint on the end product. Higher-purity DIPM runs cleaner in catalyst-driven reactions. Customers chasing multi-step targets see less waste and fewer hiccups when the input meets exacting parameters—low water content, minimized residual alcohols, repeatable acidity. Through this lens, our Diethyl Isopropylidenemalonate is less about a CAS number and more about a guarantee of consistency for demanding chemistry routes.

    From a manufacturer’s eye, the competition leaves room for improvement. Generic DIPM on the open market often comes out at purity claims above 95% but carries trace solvents, higher acidity, and color variability from batch to batch. That bit of extra care in our process—tighter column control, focused drying, rigorous sampling—delivers a product that works more predictably. Pharmaceutical clients cite fewer crystalline impurities in isolation stages. Agrochemical partners often send word that they see a drop in reprocessing or rejected material when using our stock compared to larger, less detail-oriented factories.

    Listening to Users and Adapting Process

    What separates a manufacturer from a repackager becomes clear when users push for process data, traceability, and repeat supply. Over years of feedback loops, we adapted our drying protocols and exhaustive GC evaluation to catch variations even a seasoned chemist might miss by sight or scent. Every change we make, no matter how small, starts with a practical concern voiced by a user: “My final product color is yellowing in storage,” or “Yield drops when I switch batches.”

    One fidelity check we swear by includes random sampling, checked not just for purity but for batch-to-batch consistency in refractive index and UV-Vis transparency. That approach cuts down blind spots—you catch a material that looks fine on paper but deviates in less-obvious parameters. The end user might notice these changes in their own yields or impurity profiles, but from our bench, such shifts come under the microscope long before they can throw off a downstream reaction.

    Filling a Gap Where Precision Matters

    Our Diethyl Isopropylidenemalonate works in organics synthesis where the margin for error shrinks, especially in pharmaceutical and specialty chemical platforms. Typical processes using it target carbon-carbon bond formation through Knoevenagel condensations and Michael-type additions—both of which expose weaknesses in inconsistent feedstock. Our manufacturing teams review these application specifics, tracking how purification strategies at our end trickle down to cleaner product at the customer’s plant.

    It’s clear to us after decades in the field: the little improvements—the extra drying cycle, the thorough removal of trace acids, the vigilance about atmospheric exposure—accumulate into measurable differences on your analytical sheets and, more importantly, your final product’s reliability in the market.

    How Our Standards Arise from Experience, Not Romantic Claims

    The drive to improve comes from a blend of failed batches, unexpected shutdowns, and customer calls that set you back on your heels. We have weathered them all. One round of crystals clogging a filter press can set a plant back a day, so our team will shift a process variable, document the change, and stay up late testing runoff from each stage before releasing even a kilogram for sale. Over time, these experiences bake traceability and transparency into our workflow.

    Another real-world lesson: packaging and transport leave as much mark on product quality as the initial chemical reactions. Improper sealing or a few hours in uncontrolled conditions can knock a pristine batch down a few notches. We switched to more robust steel drums with inert gas blanketing, ensuring our DIPM arrives within the same tight specs we send it. Every so often, we get a call about subtle streaks or color shifts; our traceability system lets us pinpoint the exact day, operator, shift, and even the specific distillation run behind that drum.

    Where Diethyl Isopropylidenemalonate Succeeds—and Where It Doesn’t Fit

    No chemical does it all. DIPM excels where those precise C–C couplings and malonic ester derivatives are required—active pharmaceutical ingredients, fine chemical building blocks, and designer pigments. In broader commodity reactions where cost trumps purity or when users look for less sensitive esters, alternatives often fulfill the role at a lower price or with less evolving hazard management.

    In our experience, DIPM finds few true substitutes for specialty malonate chemistry calling for high selectivity and clarity. Other dicarbonyl intermediates step in for general alkylations but bring with them greater likelihood of byproduct scaffolds, more difficult purification, or incompatibility with certain downstream groups. Our material remains the choice in custom molecule development pipelines built for reliability, speed, and final trace specs—whereas cheaper materials often wind up in lower tiers of dye, pigment, or broad commodity synthesis.

    Feedback, Not Guesswork: How We Use the Market’s Voice

    End-use companies—from pharmaceutical R&D pilot plants to small-batch pigment houses—helped us tune our DIPM. Through repeated supply cycles, we notice patterns: users blending DIPM for stepwise reactions call back with their analytical data, noting clean conversion rates and drop-off of unknown peaks in their NMR spectra. On the other end, some customers challenge our team when inconsistencies show up, expecting answers that go deeper than surface-level fixes.

    We draw on those experiences—a product’s real journey outside our doors, used by hands that demand results, not just specification sheets. Open technical partnerships with clients push us to keep analytical instruments calibrated, HPLC traces archived, and every process tweak recorded in run logs available upon request. That culture, driven by external pressure and internal accountability, sets the stage for the next-generation grades we bring to market.

    Why Purity and Consistency Actually Matter

    Inside a laboratory, and more so in scaled manufacturing, unpredictable feeds spell trouble. Even the slightest water content change, a few ppm higher on the acid number, or a lone impurity peaking in GC can set back an entire project. Whether making an active pharmaceutical ingredient or a delicate pigment, batches are only as good as their least controlled variable.

    By working out the kinks at our production location—controlling for moisture intrusion, regular calibration cycles, and taking quick action on any odd analytical results—we minimize those surprises for users. For us, the cost of extra attention is much lower than the cost and reputation loss from returning material or pausing a customer’s project.

    Pharmaceutical intermediates call for the tightest trace levels, so we often run DIPM through more than one stage of distillation, drying, and filtration, removing even trace residual ethanol or acidic signals. We chose protocols based not on abstract compliance but based on actual cases where deviation meant real-world loss for a user. Those experiences shape production for each new lot—an evolutionary process, not a static recipe.

    Comparing DIPM to Related Malonates and Alternatives

    Our technical teams often receive comparison requests: “Why choose Diethyl Isopropylidenemalonate over diethyl malonate, dimethyl malonate, or other derivatives?” The answer boils down not just to chemical structure but to how each profile reacts in practical use. DIPM stands out for its isopropylidene substitution, which steers reactivity, providing more selectivity in key condensation processes and often a more defined product in specialized synthesis work.

    Standard diethyl malonate, a workhorse for basic malonate chemistry, suffices in broad applications but misses the remarkable selectivity DIPM brings to table. Analytical chemists recognize DIPM’s unique reactivity in forming highly substituted intermediates with minimized byproducts. That property makes the difference in research-scale optimization and scale-up where even trace side products can complicate regulatory filings or process validation.

    We never recommend DIPM for processes requiring high volatility or rapid, broad ester response—its more stable profile proves a strength in targeted yield, but not in rapid, brute-force alkylations where cost and speed matter above everything else. Our DIPM models run with high isomeric control and minimal solvent residue, thanks in part to our closed-system purification protocols and rapid, sample-backed verification at every step. That extra care means the compound can perform in stereoselective syntheses, advanced dye linkages, and select pharmaceutical builds where other malonates fall short.

    Listening, Adapting, and The Path Forward

    Real manufacturing rewards patience, feedback, and a healthy respect for how small adjustments in process echo downstream. With every client report, every delay traced to a lot issue, and each improvement delivered, we get one lesson closer to a process that won’t leave users guessing. Our DIPM sets its standard as part of that cycle—a result of open ears, tested traceability, and willingness to invest in the steps other plants might skip to hit the lowest price.

    In practice, our approach to Diethyl Isopropylidenemalonate does not rely on chasing buzzwords. We seek to protect every batch against batch-to-batch swings through real hands-on vigilance: temperature and pressure logs at every key step, transparency about every run deviation, and direct lines with users able to point out improvements we can act on. From our team’s point of view, that’s worth a lot more than just another compliance certificate or a generic statement about product “quality.”

    Supporting the People Who Rely on Advanced Materials

    Our journey with DIPM taught us that real reliability is nothing you can fake with paperwork or empty marketing. Every lot packed, every feedback call taken, every surprise analyzed in the lab opens the door for a sturdier chain between plant and customer. We’ve learned the value of vigilance, the importance of saying “not good enough” and pushing for one more rinse or one tighter distillation fraction. Users pick up on this difference—sometimes with relief, sometimes with their own questions—but always knowing their process will start on firmer ground.

    DIPM, in our hands, amounts to more than a chemical—it represents a commitment between the work done in our process bays and the projects you’ll run in yours. No matter how specialized or broad the application, our model arises from decades of hard-earned trial, customer feedback, and the never-ending pursuit of more predictable performance. That builds trust, saves money in the long run, and earns us a place not just as another supplier but as a known, proven origin for a critical building block in complex chemistry.

    Building for Tomorrow, One Lot at a Time

    Diethyl Isopropylidenemalonate will continue evolving in the years to come. With each generation, we update methods, re-check analytical standards, and work hand-in-hand with users facing new challenges and higher bars for reliability. As a manufacturer connected directly to the realities of chemical synthesis, our success relies on both relentless standardization and an openness to adapt. The DIPM we offer today stands as a product of this ongoing dialogue—a material shaped not in isolation but in cooperation with those who turn its potential into finished goods.

    For us, that is the true measure of value: not how much we push out the door, but how sure we all are—manufacturer and customer together—that every batch supports another successful outcome, another complete process, another trusted result. Diethyl Isopropylidenemalonate earns its place not from price lists or standard features, but from years of purpose-driven manufacturing, user-driven adaptation, and a shared goal to take on more challenges, one reaction at a time.