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Diethyl Ethyl(Isoamyl)Malonate

    • Product Name Diethyl Ethyl(Isoamyl)Malonate
    • Alias DEEM
    • Einecs 215-014-2
    • 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

    846066

    Cas Number 87199-14-0
    Molecular Formula C14H26O4
    Molecular Weight 258.35
    Appearance Colorless to pale yellow liquid
    Boiling Point 139-141°C at 15 mmHg
    Density 0.965 g/cm3 at 25°C
    Refractive Index 1.425 - 1.428
    Flash Point 113°C
    Purity Typically >98%
    Solubility Insoluble in water, soluble in organic solvents

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

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of Diethyl Ethyl(Isoamyl)Malonate, tightly sealed, with hazard labeling and product identification.
    Shipping Diethyl Ethyl(Isoamyl)Malonate should be shipped in tightly sealed containers, protected from light and moisture. It must be transported in accordance with local and international regulations for organic chemicals, preferably via ground courier. Proper labeling, including hazard identification, is essential. Keep away from sources of ignition and incompatible substances during shipping.
    Storage **Diethyl Ethyl(Isoamyl)Malonate** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, ignition sources, and direct sunlight. Keep it separate from incompatible materials such as strong oxidizing agents and acids. Store at room temperature and ensure containers are clearly labeled. Handle with gloves and use appropriate personal protective equipment.
    Application of Diethyl Ethyl(Isoamyl)Malonate

    Applications of Diethyl Ethyl(Isoamyl)Malonate in Industrial Manufacturing

    As a manufacturer specializing in high-purity Diethyl Ethyl(Isoamyl)Malonate, we supply this specialty intermediate to several advanced chemical sectors. Our product integrates into high-value downstream processes where its molecular specificity and reaction profile are essential for stringent quality and regulatory demands. Below, we outline the main industrial application scenarios based on verifiable end-use practices.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers select this malonate ester for key building-block reactions in the synthesis of barbiturates and anticonvulsants, as well as select cardiovascular agents. Its tailored structure supports malonic ester synthesis pathways that comply with strict regulatory documentation on traceability and impurity control. The raw material enters at the condensation or alkylation stage, allowing for precision in molecular design and minimization of byproduct formation in GMP environments. Manufacturers perform repeated fractionation and purification directly after the initial reaction step to meet pharmacopeia-grade purity, responding to batch records and validated process controls. The resulting APIs undergo full traceability chain linking back to the origin of the malonate intermediate in regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP, EP, or JP pharmacopeias for relevant APIs
    • FDA 21 CFR Part 211 (Good Manufacturing Practice for Finished Pharmaceuticals)
    • EU EudraLex Volume 4

    Typical usage ratio

    • 5.5 – 11% of total batch mass for malonate condensation stage, depending on specific API target and desired molar excess to ensure completion of dialkylation

    Downstream process integration

    • Utilized as a primary nucleophile or alkyl acceptor in the first or second step of multi-stage condensation or alkylation process chemistry, often followed by hydrolysis and decarboxylation

    Final product types

    • Barbiturate-class sedatives
    • Anticonvulsant active ingredients
    • Intermediate ketones for cardiovascular drugs
    • Pharmaceutical research reference standards

    2. Agrochemical Active Compound Synthesis

    Agrochemical producers introduce Diethyl Ethyl(Isoamyl)Malonate as a core dialkylation intermediate for constructing specific pyrimidine or pyrazole ring structures essential to certain herbicides and fungicides. This intermediate allows for controlled introduction of branched alkyl chains, which tunes the biodegradability and soil mobility of active compounds. To support global registration, producers must document impurity profiles and residual solvent levels back to the original malonate input, requiring precise analytical and process controls directly aligned with downstream technical dossier requirements. The compound enters early in the synthetic sequence, typically during C-alkylation reactions, where its steric properties enable downstream selectivity in cyclization steps.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH registration for chemical intermediates
    • ISO 9001:2015 for process documentation quality
    • Relevant national pesticide registration guidelines (EPA FIFRA in USA, EU Regulation No 1107/2009 in Europe)

    Typical usage ratio

    • 2 – 6% mass percent in target formulation lines, with adjustments based on target ring system and desired substitution pattern in the final active

    Downstream process integration

    • Reacted as a malonate nucleophile in an early-stage C–C bond forming reaction before cyclization and oxidative steps leading to heterocyclic scaffolds

    Final product types

    • Pre-emergent herbicide actives (e.g., with branched alkyl substituents)
    • Fungicidal intermediates for seed dressing formulations
    • Fine chemical intermediates for crop protection R&D
    • Technical-grade pesticide precursors

    3. Flavors and Fragrance Ester Synthesis

    Producers of fine fragrances and specialty flavors utilize this malonate variant in the preparation of complex esters and lactones, where controlled transesterification produces flavoring agents with specific volatility and sensory notes. The raw material supports flavor houses in achieving precise aroma profiles with strict compliance to global flavoring additive frameworks. It enters downstream synthesis during selective esterification or lactonization reactions, where minor byproducts must be stringently controlled to meet IFRA and FEMA standards. The final esters are purified via fractional distillation and undergo comprehensive organoleptic evaluation prior to R&D or commercial blending.

    Industry compliance standards

    • FEMA GRAS (Generally Recognized As Safe) for flavoring substances
    • IFRA (International Fragrance Association) Standards
    • EU Regulation No 1334/2008 on flavorings and certain food ingredients
    • ISO 22000:2018 Food Safety Management

    Typical usage ratio

    • 0.2 – 3% of total reaction mass for esterification or lactone synthesis, with dosage refined based on volatility and target odor threshold in the final concentrate

    Downstream process integration

    • Integrated as an acyl component during selective esterification reactions with alcohols, followed by vacuum distillation and GC analysis

    Final product types

    • Specialty fruit aroma esters (e.g., pear, banana, apple notes)
    • Lactone intermediates for creamy and coconut flavor compositions
    • High-purity base notes in fine fragrance formulations
    • Food-grade flavoring substances for beverage and confection applications

    4. Polymer Modifier and Specialty Plasticizer Production

    Manufacturers specializing in specialty plastics and polymeric coatings employ Diethyl Ethyl(Isoamyl)Malonate as a monomeric building block or external plasticizer, particularly for systems requiring a balance of flexibility and UV resistance. When used as a molecular modifier, it provides well-defined side chains that influence Tg and migration properties in PVC copolymers and acrylate-based resins. Regulatory requirements for migration and extractables control the product’s entry point and quality monitoring throughout compounding and extrusion. Downstream processors introduce the material in controlled hot-melt blending or solution copolymerization stages, ensuring in-process testing aligns with regulatory migration and residual organics limits.

    Industry compliance standards

    • EU Regulation No 10/2011 on plastic materials and articles intended to come into contact with food
    • FDA 21 CFR 177.2600 (Rubber articles for repeated use)
    • ISO 9001:2015 for production traceability
    • REACH Annex XVII (Restricted Substances List)

    Typical usage ratio

    • 1 – 8% by weight of total polymer formulation, varied based on flexibility target, UV resistance requirement, and migration specification for end-use

    Downstream process integration

    • Added during the compounding stage prior to melt mixing, or fed as a reactive diluent during acrylate polymer precursor synthesis

    Final product types

    • Flexible PVC compounds for wire and cable jackets
    • Specialty acrylate-polymers used in UV-curable coatings
    • Plasticized sheets for food contact or medical packaging
    • Custom polymer blends for technical films and foils
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    Certification & Compliance
    More Introduction

    Introducing Diethyl Ethyl(Isoamyl)Malonate

    Understanding Our Diethyl Ethyl(Isoamyl)Malonate

    Inside our plant, Diethyl Ethyl(Isoamyl)Malonate does not stay long on the shelves; chemists and formulating teams rely on this highly specialized dialkyl malonate for its distinctive structure and versatility. The product carries the mark of hands-on quality control that sets our batches apart from the broad, more generic listings on the market. Every drum delivers the exact profile chemists seek out, so customers know what they are working with and can plan projects with real-world predictability.

    We keep our process anchored on meticulous handling of each esterification and ester variant. Decades ago, we discovered that even subtle changes in raw material purity or process temperature lead to unwanted byproducts and yield loss. Our reactors run with a tight temperature window while monitoring acidity and distillation purity throughout the day. This keeps our Diethyl Ethyl(Isoamyl)Malonate free from the kind of minor contaminants that hinder reactivity or skew downstream analytical results.

    Precise Model and Specifications From Actual Operations

    Chemistry rewards rigor. We manufacture Diethyl Ethyl(Isoamyl)Malonate to strict internal specifications reflecting real production experience, not only catalog entries. We consistently achieve a purity above 99.2% by GC, rarely letting it fall below this mark. Moisture sits low, under 0.05%. Color remains nearly water-white, thanks to in-process filtration and careful exclusion of oxidizing agents. By keeping density, boiling range, and acidity within narrow ranges (measured per batch, not assumed), we ensure each container matches our internal reference materials. This attention to detail spares laboratories and plants from the kind of troubleshooting that often slows product launches or disrupts scale-up.

    No batch leaves the door without both in-process and final analytical profiles. We run full GC scans to check for both common and unexpected side esters. By comparing every lot to reference standards, we verify the ethyl and isoamyl substitution is precisely placed, so structure-driven properties – such as solubility, volatility for distillation, and reactivity in alkylation or condensation reactions – stay as predictable as your process demands.

    Observed Usage Across Industries

    Over the years, we have observed Diethyl Ethyl(Isoamyl)Malonate earning its spot in several applications where structure makes the difference. For synthetic chemists, the mixed ester groups open up options in malonic ester syntheses that neither simple diethyl nor dibutyl malonate provide. Reactions proceed at temperatures and times well-suited to multi-step procedures, saving time in routes where selectivity matters. We regularly ship to pharmaceutical synthesis teams who value the differential ester groups for use in active pharmaceutical ingredient intermediates where selective alkylation reduces protecting group strategies downstream.

    Perfume and fine aroma makers use our compound for accord construction and as a building block in essential oil derivatives where controlled hydrolysis and re-esterification yield specific olfactory notes. Because we control the profile tightly, batch-to-batch aroma shifts are nearly eliminated, letting perfumers scale ideas from lab to production without setbacks. Agrochemical developers have come back with feedback about the compound’s ease of transformation into target molecules with higher overall yield, particularly when reacting under basic or transition-metal catalyzed conditions.

    Our records trace other uses as well, including specialty polymer modification and surface chemistry innovations. Certain research groups have highlighted the importance of this malonate’s low residual acidity and uniform ester profile in fine-tuning monomer blends, something less pure versions struggle to deliver.

    What Distinguishes Diethyl Ethyl(Isoamyl)Malonate From Other Malonates

    Manufacturing Diethyl Ethyl(Isoamyl)Malonate has taught us to appreciate its subtle, practical differences. While diethyl and dibutyl malonate both appear regularly in catalogs and have their place in fields like varnish additives and general ester synthesis, neither matches the mixed-ester system’s balance of reactivity and selectivity. The presence of both ethyl and isoamyl groups creates a malonate slower to hydrolyze than diethyl but easier to manipulate than pure isoamyl esters, which show higher viscosity and make solvent handling less predictable.

    Researchers using simple diesters often report side reactions or lower selectivity when targeting mono- or di-alkylated derivatives. In our experience, the mixed-ester design of Diethyl Ethyl(Isoamyl)Malonate cuts down on both, lowering unwanted byproduct levels during controlled alkylations. This benefits both pharmaceuticals and advanced materials research, where regulatory and cost constraints prohibit inefficient reaction conditions.

    From a logistical and supply-chain perspective, the more common diesters can be sourced through commodity channels. Diethyl Ethyl(Isoamyl)Malonate, on the other hand, rarely surfaces with consistent quality or clear provenance unless it comes from an experienced manufacturer. Chemists cannot risk a solvent batch or reaction sequence falling apart over inconsistent minor components. That is why we commit to keeping full batch histories, long-term raw material partnerships, and reliable custom packaging for temperature-sensitive deliveries.

    The Importance of Structure and Handling in Manufacturing

    We have learned that the structure of the product dictates the complexity of the manufacturing process. Diethyl Ethyl(Isoamyl)Malonate requires balancing multiple feedstocks, matching catalyst efficiency, and countering the higher boiling range that mixed-ester intermediates display. If water content creeps up, minor hydrolysis begins to degrade yield and structure, so routines like vacuum-drying, nitrogen purging, and closed-loop transfers have become ingrained in our plant’s standard operating procedures.

    A key lesson: clean equipment and phase separation techniques must be monitored batch by batch. We maintain regular acid-wash schedules because even trace acid or base left from previous runs can catalyze side reactions. Each week, our operators log checks on valve integrity and storage tank linings because residue from previous campaigns gradually shifts color and purity, a problem many commodity producers overlook.

    We built our product quality assumptions from practical trials, not just chemical theory. Early on, trial customers told us about unexplained reactivity losses when using equal purity malonates from varied sources. By making regular shipments to high-purity requirements, we spotted the culprits: minor isoamyl isomers and higher alcohols, which disrupt planned synthetic steps. Our continuous reviews and process upgrades – including cold-chain logistics and QA sample archiving – arose from these real-world trials.

    Supply Consistency: A Manufacturer’s Perspective

    Over time, we have recognized that consistent supply affects more than simple delivery windows. Downstream users base entire projects on forecasted availability, sometimes planning months of work on promised arrival times. A missed shipment means not just lost material, but wasted labor, capital, and customer trust. Many distributors list products without direct access to actual stock or batch control, so the end-user faces uncertainty as deadlines approach.

    Running our own production line gives us practical control. Every year, we examine raw material contracts well ahead of time, verifying that our ethanol, isoamyl alcohol, and malonic acid partners are ready to meet projected needs. QA teams push through periodic stress tests, examining everything from drum seal durability in transit to how container airspace affects moisture pick-up on long ocean shipments.

    As the actual manufacturer, we learn the true pace of scale-up and the all-too-common bottlenecks at solvent recovery, catalyst reuse, and energy balancing. No warehouse paperwork can replace the sight of reactor jackets steaming just outside the QA lab. There is no shortcut to trusting what goes into or comes out of every drum. Our product arrives, always with batch numbers and detailed COAs, so project managers and sourcing agents can trace every liter to its origins—no grey area, no compounded risk.

    Quality, Safety, and Environmental Responsibility

    No chemical plant survives long without a sharp focus on safety and environment. In the past, industry sometimes accepted off-spec barrels ending up in less regulated markets or improperly disposed waste. Those days are behind us. Regulatory attention, paired with our own active audits, drives daily improvements. Our solvent recovery systems minimize volatile emissions and cut down significantly on disposal-related costs. In emergency drills, simulated releases give us critical training to contain or neutralize spills before material escapes the site.

    All effluent from our malonate unit routes through multi-stage biological treatment before leaving the facility. Regular reviews identify areas for process water reuse, keeping freshwater input stable while supporting expanding production. Last year, operator ideas led to the addition of a chilled flow header, letting us condense and reclaim more product from the reactor vent streams, supporting not only regulations but also profitability.

    Material traceability extends to MSDS and label updates, which reflect latest toxicology and regulatory data. Our staff attends not just industry training but also specialty symposia to follow new research on malonate safety, decomposition routes, and potential environmental impacts. This culture means fewer surprises downstream, whether a customer needs support for a regulatory audit or runs into unexpected questions from their own health and safety teams.

    Facing Market Pressures and Innovation

    Markets do not stand still. Our malonate’s value depends on our ability to anticipate, not just react to, user needs. Sometimes, demand fluctuates based on pharmaceutical approvals in large markets, or swings with changes in agricultural chemical registrations. We buffer swings with finished inventory and raw material hedging, so our supply stays robust across economic cycles.

    Continuous improvement is not just a slogan in the chemical industry. Each year, our technical team meets with academic and industrial partners exploring new, more sustainable routes. In recent collaborations, we have trialed alternative esterification catalysts and bio-based feedstocks. These projects are weighed not just by laboratory merit, but by how robustly they handle scale, raw material price swings, and regional logistics. Our plant upgrades result directly from lessons learned—not just from our own trials, but from sharing knowledge with customers who push their syntheses further.

    We do not see chemical manufacturing as static. Fine-tuning process controls, adopting greener solvents, and running pilot-scale demonstrations all support a product that evolves along with the needs of specialized users. Rather than compete strictly on price, we align with project managers, procurement teams, and technical departments to develop solutions that work beyond the laboratory—real synthesis, at commercial scale.

    Supporting Customers Beyond the Shipment

    Our role does not end once the drums are loaded. Many customer calls come during pilot-scale manufacturing trial runs, or in troubleshooting meetings when something unexpected stalls a project. If a purification unexpectedly yields off-color oil, our technical team can reference both the batch run data and the previous production trends to determine if a subtle shift in process variables needs to be addressed. With real-world product histories logged on site, we are able to confirm lot trends over time, supporting research teams and process scale-up managers by sharing data in real time.

    Technical support includes helping customers optimize their own handling and storage. We have collaborated on changing packaging, recommending inert headspace precautions for sensitive applications, or advising on shelf-life adjustments needed when storage conditions fall outside normal laboratory practice. Larger-scale customers have implemented our suggestions for on-site filtration and drum-heating setups that lower wintertime viscosity for uninterrupted dosing. We back up every technical question with internally validated data, because nobody benefits from unreliable information.

    Customers sometimes approach us to develop tailored grades of Diethyl Ethyl(Isoamyl)Malonate, aligning analytical profiles to match proprietary reactions or end products. Our plant’s flexibility allows us to tweak reaction time, distillation approach, or filter sequence according to mutually agreed trial parameters. These projects underline the importance of working directly with a manufacturer over indirect channels, which rarely offer the same depth of technical alignment.

    Looking Forward: Meeting Future Needs

    In our experience, innovation in chemical feedstocks often arises from sustained dialogue with users committed to stretching what a material can do, not just how cheaply it can be supplied. As markets move toward greener solutions, our R&D initiatives focus on lowering the carbon footprint of malonate production and optimizing water and energy use. We engage closely with universities and research consortia to benchmark new catalyst systems, alternative raw materials, and advanced purification technologies.

    Large-scale change always brings challenges—balancing process economics with sustainability, or weighing labor and automation for complex tasks. Since our plant runs these processes daily, we test proposed changes not only in bitesize lab settings but in the more realistic world of around-the-clock production. Drawing on years of experience—dealing with seasonal raw material variability, contract logistics, and stricter global compliance—we aim to introduce evolutionary advances rather than risky, unproven shortcuts.

    As new projects emerge in specialty pharma, agricultural sciences, and fine fragrance chemistry, we expect Diethyl Ethyl(Isoamyl)Malonate’s importance to deepen. Our commitment remains to manufacture with pride, attention, and openness—ensuring the material not only supports today’s complex syntheses, but sets a standard for future innovation in ester chemistry.