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Isopropylmalonic Acid

    • Product Name Isopropylmalonic Acid
    • Alias Methylsuccinic acid
    • Einecs 212-142-0
    • 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

    491230

    Chemical Name Isopropylmalonic Acid
    Cas Number 498-20-2
    Molecular Formula C6H10O4
    Molecular Weight 146.14 g/mol
    Appearance White crystalline powder
    Melting Point 128-131°C
    Solubility In Water Soluble
    Boiling Point Decomposes before boiling
    Density 1.25 g/cm3 (approximate)
    Pubchem Cid 77597
    Iupac Name 2-isopropylpropanedioic acid
    Smiles CC(C)C(C(=O)O)C(=O)O
    Inchi InChI=1S/C6H10O4/c1-3(2)4(5(7)8)6(9)10/h3-4H,1-2H3,(H,7,8)(H,9,10)
    Synonyms 2-Isopropylmalonic acid

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

    Packing & Storage
    Packing Isopropylmalonic Acid is supplied in a sealed, amber glass bottle containing 25 grams, labeled with hazard information and chemical details.
    Shipping Isopropylmalonic Acid should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport in accordance with local, national, and international regulations for chemicals. Use appropriate cushioning and labeling, ensuring the package is secure to prevent leaks or contamination during transit. Store at room temperature, away from direct sunlight.
    Storage Isopropylmalonic acid should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances. Keep the container tightly closed and protected from moisture. Store at room temperature, avoiding excessive heat and direct sunlight. Ensure proper labeling and keep away from strong oxidizers and bases. Use appropriate safety measures to prevent inhalation, ingestion, or contact with skin and eyes.
    Application of Isopropylmalonic Acid

    Applications of Isopropylmalonic Acid in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply isopropylmalonic acid specifically designed for industrial sectors that demand strict quality control, precise formulation, and regulatory compliance. The following application scenarios demonstrate the material's documented roles in advanced synthesis and specialty molecule production, each supported by real industry requirements and standards.

    1. Pharmaceutical Intermediate Synthesis

    Isopropylmalonic acid serves as a critical C3-building block for the synthesis of various active pharmaceutical ingredients (APIs), particularly in the creation of specialized beta-amino acids and substituted succinic acid derivatives. Manufacturers employ its unique branched structure to achieve selectivity in stepwise alkylation, condensation, and decarboxylation processes necessary for chiral center development in small-molecule drug intermediates. Its controlled reactivity supports both batch and continuous API manufacturing lines, where scale, reproducibility, and purity are paramount.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) for intermediates reference specifications
    • EU GMP Part II for APIs and intermediates
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (if imported to EU)

    Typical usage ratio

    • Generally 0.6–1.2 molar equivalents per API target structure, adjusted according to stoichiometry of the condensation or alkylation steps. Excess addition is minimized to reduce purification challenges.

    Downstream process integration

    • Raw acid introduced post-preactivation or as its sodium salt variant in multi-step organic synthesis routes, typically during nucleophilic substitution and carbon–carbon bond construction steps preceding intermediate crystallization and purification.

    Final product types

    • Intermediates for beta-blockers
    • Pyrrolidine-based drugs
    • Substituted succinic acid pharmaceuticals
    • Custom chiral molecules for medicinal chemistry programs

    2. Agrochemical Precursor Manufacturing

    Agrochemical producers apply isopropylmalonic acid as a specialized alkylating agent in the synthesis of advanced herbicide and insecticide intermediates. Its well-defined molecular structure enables regioselective modifications within the target molecule backbone, contributing to improved field performance and metabolic stability in crop protection agents. Downstream operators depend on this compound when manufacturing scalable, high-purity intermediates that meet regulatory review for large-scale agricultural use.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • REACH compliance for agrochemicals
    • GLP (Good Laboratory Practice) for test and pilot production

    Typical usage ratio

    • Employed at 0.9–1.3 equivalents relative to parent aryl or alkyl halide substrates, with adjustments made for conversion efficiency in target molecule synthesis as evaluated during process validation.

    Downstream process integration

    • Added directly after formation of core pesticide skeleton during the key alkylation, cyclization, or side-chain modification stages of synthetic agrochemical production, particularly before separation and formulation into technical-grade intermediates.

    Final product types

    • Herbicidal acid intermediates
    • Precursor molecules for pyrethroid insecticides
    • Building blocks for aromatic fungicides
    • Seed treatment chemical intermediates

    3. Specialty Polymer Monomer Production

    Advanced materials manufacturers utilize isopropylmalonic acid in the creation of bespoke monomers for high-performance polymer systems. Its unique dicarboxylic acid functionality, coupled with isopropyl branching, allows introduction of targeted amorphous or crystalline domains in specialty copolymers. This is particularly relevant in the electronics, membrane, and engineering plastic segments, where molecular design directly influences dielectric, mechanical, or permeability properties.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restricted substances in electrical and electronic equipment
    • ISO 9001:2015 Quality Management System for polymer production
    • UL 94 Flammability testing (for final plastics)
    • REACH/TSCA inventory listing (for monomers and finished polymers)

    Typical usage ratio

    • Between 1–10 wt% as a comonomer, or up to 30 mol% in specialty copolymer formulations, with proportions fine-tuned according to required flexibility, glass transition temperature, or polarity in the final polymer matrix.

    Downstream process integration

    • Incorporation of acid in melt or solution polycondensation stages, typically reacted with diols, diamines, or epoxides, followed by extrusion or solvent-casting to generate the copolymer base resin.

    Final product types

    • High-temperature engineering plastic films
    • Membrane separation media for gas or liquid filtration
    • Dielectric layers in microelectronic devices
    • Specialty coatings with tailored surface energy

    4. Organic Synthesis Reagent Supply for Fine Chemicals

    Producers of fine specialty chemicals leverage isopropylmalonic acid as a precise C3 extender in iterative organic synthesis, enabling targeted functional group transformations for custom molecule discovery, flavors, fragrances, or advanced laboratory reagents. Its defined structure and reactivity profile benefit research pilot batches and industrial campaigns aiming for process efficiency and product purity across custom synthesis projects and catalog material production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • IUPAC analytical reference documentation
    • REACH/TSCA registration for exported materials
    • ISO/IEC 17025:2017 for designated contract analytical labs

    Typical usage ratio

    • Ranges from 0.8–1.0 equivalents relative to nucleophilic or electrophilic reaction partners, adjusted to optimize reaction conversion or selectivity in stepwise organic transformations.

    Downstream process integration

    • Charged to the reactor during chain elongation, substitution, or esterification steps, either in solution phase (laboratory synthesis) or continuous flow reactors for industrial-scale fine chemical output, with subsequent purification via chromatography or crystallization.

    Final product types

    • Chiral alpha-alkylated diacids
    • Custom ketones for fragrance compounds
    • Laboratory standard reagents
    • Novel fine chemicals for R&D, catalog or pilot-scale applications
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    Certification & Compliance
    More Introduction

    Introducing Isopropylmalonic Acid: Practical Applications and Manufacturing Insights

    Our Perspective as Chemical Producers

    Daily, our team faces a new set of expectations from research laboratories, industrial partners, and fine chemical users searching for building blocks that drive modern synthesis. Working at the manufacturing stage, we witness first-hand how choices upstream affect every step of process and product quality. Isopropylmalonic acid continues to prove its versatility, thanks to a stable structure and a carboxyl functional group arrangement that provides value during complex organic transformations. Unlike more basic dicarboxylic acids, this compound brings a unique branching that translates into subtle but significant differences in reactivity and downstream compatibility.

    Product Characteristics From Years at the Plant

    Isopropylmalonic acid, with a molecular formula of C6H10O4, appears as an off-white crystalline powder. Produced in our controlled reaction vessels, purity often exceeds 98%, which we confirm by high-performance liquid chromatography and nuclear magnetic resonance. Chemists appreciate this material because isopropyl substituents add steric bulk, steering reactions and helping maintain selectivity during alkylation, acylation, and cyclization. Through multiple cycles of crystallization and controlled drying, we keep water content and related impurities low enough for sensitive research settings.

    From a manufacturing point of view, isopropylmalonic acid represents more than a synthetic intermediate. Our operators encounter varying physical characteristics, such as clumping and dusting, which we address through optimized particle sizing and precise drying protocols. Each production batch receives rigorous filtration and packaging steps, protecting it from moisture ingress that would otherwise induce hydrolysis. Stability studies show excellent shelf-life under ambient conditions, especially with our specialized anti-caking techniques.

    Process Consistency and Batch Traceability

    Consistency between batches ranks high in fine chemical production. We trace every shipment of raw materials, log process parameters, and reserve retain samples across several years. If an R&D partner contacts us about subtle color variance or slightly different crystallization patterns, we can track the entire lot history. Full transparency and repeatability support reproducible results in pharmaceutical or academic labs. As we constantly fine-tune crystallization speed and solvent recovery, such minor controls accumulate into a record of reliability.

    Breaking Down the Application Landscape

    Users often engage us about the role of isopropylmalonic acid in synthetic routes for pharmaceuticals and agrochemicals. In our own formulation trials, we see the benefits firsthand. The tertiary carbon created by the isopropyl side chain resists overreaction, contributing to high yields when synthesizing substituted malonate derivatives. For example, chemists preparing α-alkylated carboxylic acid intermediates find that isopropylmalonic acid provides a distinct profile versus dimethyl or diethyl malonates, especially when selectivity is crucial. Process development teams confirm lower by-product formation, which helps downstream purification and reduces overall waste.

    Academic partners rely on this compound to explore new methodologies for C–C bond formation, asymmetric catalysis, and chiral auxiliary synthesis. In these fields, our product finds service as a substrate for Knoevenagel condensations and Michael-type reactions. Practitioners highlight how the isopropyl group shapes reaction outcomes, giving cleaner spectra and minimizing the need for labor-intensive column purification. The physical qualities of our batches—dry, controlled particle size—make it easier to weigh and handle in a busy teaching lab or scale-up facility.

    Differences From Common Malonic Acid Derivatives

    Users comparing isopropylmalonic acid to malonic acid or simple dialkyl malonates notice differences even before reactions begin. Malonic acid itself is fully symmetrical and highly water-soluble, leading to easy use in classical decarboxylation reactions but lacking control over product branching. Isopropylmalonic acid features a protective isopropyl side chain at the alpha carbon. This subtle addition shields one proton from abstraction, reducing over-alkylation and limiting side reactions in base-catalyzed processes.

    Among the dialkyl esters, such as diethyl or dimethyl malonate, volatility and odour pose handling challenges on the shop floor. Our isopropylmalonic acid remains solid and stable even on warm days, with a minimal odor profile, which simplifies warehouse and laboratory storage logistics. We have heard from formulation engineers who experience higher yields and more consistent quality in small molecule production when substituting common malonic acid derivatives with our product. Researchers also report that the steric environment creates a more pronounced difference in chiral centers, benefiting asymmetric transformations.

    Solubility and Handling Experience

    Manufacturers always pay attention to solubility profiles since these affect blending, mixing, and eventual conversion yields. Isopropylmalonic acid dissolves moderately well in polar aprotic solvents like dimethylformamide and dimethyl sulfoxide, with limited solubility in water. While we know some applications require adjustments in temperature or pH to reach full dissolution, clear communication and guidance minimize setbacks. Based on decades of feedback, powder sticking and static charge rarely cause problems when handled under normal conditions, though we always recommend sealed containers under dry nitrogen for best practice.

    Health, Environmental, and Stability Considerations

    Safety remains central to any discussion about synthetic chemicals. Our experience at the plant confirms mild irritant properties of isopropylmalonic acid when handled in bulk, but personal protective equipment and extraction booths maintain a safe working environment. Decomposition, if exposed to strong acids or bases for prolonged periods, leads to benign by-products—key when considering environmental fate and worker exposure. We routinely test waste streams and air emissions to ensure they fall well below national standards.

    From a long-term stability perspective, we store sample vials at varied humidity and temperature ranges to verify product robustness. After years of observation, we have not recorded any significant degradation under sealed conditions. Only direct contact with water or highly acidic/alkaline media compromises purity, which we note in technical documentation but rarely see in real-world use.

    Collaboration with Research and Industry

    Every innovation in active pharmaceutical ingredient synthesis or specialty chemical production starts with robust building blocks. Our chemists offer direct access to production data, custom batch sizes, and technical support honed through years of troubleshooting at scale. When a partner attempts a new reaction or needs analytical data for publication, we provide certificate analysis and supporting documents generated from the manufacturing line. Feedback on processability or yield challenges flows back into our pilot plant, guiding future improvements in drying, filtration, or packaging.

    Our experience also reaches into the regulatory spaces. Isopropylmalonic acid’s clear structure and established history contribute to straightforward hazard assessments and documentation for customs and shipping regulations. Unlike less familiar new chemical entities, this product rarely raises questions that would delay delivery to an end user.

    Opportunities for Optimization and Waste Minimization

    Operating as a manufacturer means watching out for both yields and the bottom line. Careful solvent choice, energy use, and waste remediation all factor into the cost and reliability we deliver to partners. Based on in-plant observations, batch crystallization remains the most resource-intensive step, so incremental tuning of solvent use and temperature profiles helps minimize losses. Our latest process improvements rely on in-line monitoring to prevent over-drying, thus cutting energy costs and supporting sustainability benchmarks.

    We treat all process wash streams and spent solvents in-house, recovering and recycling what we can. Residual waste is neutralized before disposal, which reduces environmental loading and aligns with global stewardship principles. Any user concerned about green chemistry or lifecycle impacts can find practical assurance from our integrated approach.

    Real-World Case Studies: Refining Value Beyond the Lab Bench

    Collaborating with a multinational pharmaceutical supplier, we adjusted the particle size distribution of isopropylmalonic acid to match a specific wet-milling process. Our technical liaison exchanged data on dissolution time, and we piloted new drying curves until granule size met their reaction speed requirements. This fine-tuning eliminated the need for their pre-processing, cut cycle time by 12%, and reduced both solvent use and staff hours per batch. Drawing from this type of direct feedback, we have permanently adjusted our production parameters for similar clients operating in high-throughput environments.

    A regional specialty plastics manufacturer came to us after struggling with malonic acid’s reactivity during curing. By trialing isopropylmalonic acid, their R&D team found greater process window flexibility and reduced side products—delivering more reproducible tensile and thermal performance. Through technical exchange, they learned to optimize resin blending by monitoring acid value and using our guidance on mixing conditions, helping scale up new materials for the electronics market.

    Supporting Regulatory, Purity, and Quality Documentation

    As manufacturers, we spend considerable time updating audits, supplier questionnaires, and quality assurance documents to meet customer demands and regulatory compliance. Our analytical capabilities support comprehensive impurity profiles, trace residual solvents, and lot-specific data required by most global regulatory frameworks. Laboratories using our isopropylmalonic acid can draw upon hard copies and digital records going back more than a decade, creating a documented thread from synthesis to end use. This transparency builds confidence and secures relationships with demanding pharmaceutical, cosmetic, and polymer manufacturers.

    Since quality standards evolve, we routinely validate instrumental methods, running cross-checks with both internal and accredited third-party laboratories. Each iteration reveals small improvements, maintaining our reputation for reliability. End users can meet local, national, and international compliance requirements using our document support, including full Material Safety Data Sheets, batch COAs, and origin traceability as requested.

    Thoughts on Market Trends and Future Demand

    Rapid innovation in pharmaceutical chemistry, polymers, and specialty materials keeps demand for isopropylmalonic acid steady. We see a growing focus on selective syntheses that reduce waste and maximize yields—both areas where the isopropyl group brings value. End users increasingly request batch customization, and our plant moves to meet these needs without added downtime. The push for greener chemistry and sustainable processing aligns with our ongoing investments in waste recovery and solvent recycling. Our process flexibility lets us adopt emerging methods, such as continuous-flow synthesis, that could further shrink waste streams and energy use.

    By staying close to both academic and industrial partners, we anticipate changes before they disrupt supply chains. As regulations tighten or research shifts, we keep production methods flexible, scaling from pilot to full capacity as required. Maintaining open lines of communication between lab, line, and logistics keeps us responsive, strengthening the role of isopropylmalonic acid in next-generation material and molecule development.

    Conclusion: Real Impact from the Factory Floor

    Few appreciate the downstream impact of chemical manufacturing decisions as intimately as those who move product from vessel to vessel, pack drums, and answer technical calls at odd hours. Isopropylmalonic acid continues to prove its worth across sectors, from early-stage discovery chemistry to mature industrial processes. Drawing on years of feedback, incremental process improvements, and open communication with users, we keep quality and adaptability at the front of production. Every kilogram reflects not just a molecular formula, but thousands of hours spent tuning purity, minimizing risk, and supporting customer innovation. Our ongoing investment in people, equipment, and technical support ensures future-ready supply for everyone counting on reliability, sustainability, and proven performance in isopropylmalonic acid.