Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Methyl-3-Furoic Acid

    • Product Name 2-Methyl-3-Furoic Acid
    • Alias 2-Methyl-3-Carboxyfuran
    • Einecs 242-646-8
    • 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

    815539

    Chemical Name 2-Methyl-3-Furoic Acid
    Cas Number 874-57-9
    Molecular Formula C6H6O3
    Molecular Weight 126.11 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 57-61 °C
    Boiling Point 255 °C (estimated)
    Density 1.28 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles CC1=COC=C1C(=O)O
    Synonyms 2-Methylfuran-3-carboxylic acid
    Flash Point 131.9 °C (estimated)
    Pka 3.5 (approximate for carboxylic acid group)
    Storage Conditions Store at room temperature, tightly sealed

    As an accredited 2-Methyl-3-Furoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Methyl-3-Furoic Acid, tightly sealed, with hazard labels and product information.
    Shipping 2-Methyl-3-Furoic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be stored and transported in a cool, dry place, away from incompatible substances. Ensure compliance with local chemical handling regulations, including proper labeling and documentation for safe transit. Handle with appropriate personal protective equipment.
    Storage 2-Methyl-3-furoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Ensure proper labeling and avoid sources of ignition. Store at room temperature and handle using appropriate personal protective equipment (PPE) to prevent skin and eye contact.
    Application of 2-Methyl-3-Furoic Acid

    Applications of 2-Methyl-3-Furoic Acid in Industrial Manufacturing

    As a dedicated manufacturer of 2-Methyl-3-Furoic Acid, we support a focused range of downstream industries. This fine chemical serves as a building block for chemical synthesis, flavor production, active pharmaceutical ingredients, and polymer modification. Below we present its industrial applications with detailed reference to processing standards, actual formulation ratios, and end-use products.

    1. Pharmaceutical Intermediate Synthesis

    2-Methyl-3-Furoic Acid acts as a key intermediate in the synthesis of specific APIs, especially heterocyclic drugs. Medicinal chemistry utilizes it during multi-step reactions, including amide coupling or esterification when constructing bioactive molecules like antidiabetic agents and CNS-active compounds. Production batches follow validated documentation and traceable sourcing throughout each synthesis stage.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) – reference for precursor substances
    • European Pharmacopoeia (Ph. Eur.) – precursors for API synthesis
    • FDA 21 CFR Part 211 – Finished Pharmaceuticals standards (applicable to raw material traceability)

    Typical usage ratio

    • 0.1–0.4 molar equivalents relative to main scaffold (adjusted based on yield optimization and byproduct control)

    Downstream process integration

    • Incorporation during intermediate condensation or amidation steps
    • Integration with automated reactor charging systems
    • Pre-dissolved or as solid charge, depending on downstream solubility constraints
    • Analytical QC for residual acid and impurity profiling post-reaction

    Final product types

    • Antidiabetic small molecule intermediates
    • CNS-active pharmaceutical raw materials
    • Research grade peptide intermediates
    • Clinical trial drug precursors

    2. Flavor and Fragrance Ingredient Manufacturing

    This compound supplies a furan-based aromatic note, functioning as a precursor for synthetic flavorants and fragrance aldehydes. Producers use controlled chemical transformation (often via decarboxylation or reduction) in the formulation of food-safe or perfumery ingredients. Strict documentation and trace-level impurity limits are necessary in final batches.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association, Generally Recognized as Safe)
    • European Union Regulation (EC) No 1334/2008 on flavorings
    • JECFA specification for food additives
    • ISO 9235:2013 (Aromatic natural raw materials and derived chemical substances)

    Typical usage ratio

    • 0.05–0.2% w/w in reaction charge, depending on targeted flavor/aroma intensity and subsequent downstream dilution

    Downstream process integration

    • Charge at the precursor synthesis stage via batch or continuous feed
    • Reduction or decarboxylation under controlled temperature (stationary or flow reactor)
    • Final QC for odor threshold and purity assessment, GC-MS based
    • Safe handling and trace documentation per flavor house protocol

    Final product types

    • Furan-based flavoring ingredients for bakery or beverage use
    • Top-note perfume aldehydes
    • Artificial fruit aroma chemicals
    • Compounded flavor bases for confectionery

    3. Agrochemical Active Ingredient Synthesis

    Chemical manufacturers use 2-Methyl-3-Furoic Acid as a coupling partner for the synthesis of heterocyclic agrochemicals, including herbicide and insecticide precursors. The compound is fed into catalytic or acylation stages, generating active scaffolds with target binding properties. Material controls, storage, and handling are operated under established agrochemical quality systems.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for active ingredient development
    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC No 1907/2006) for chemical substances
    • ISO 9001:2015 (Quality management for agrochemical production)

    Typical usage ratio

    • 1.2–1.5 equivalents relative to coupling partner, controlled to avoid unreacted acid in downstream formulations

    Downstream process integration

    • Direct addition during cyclization or amidation with nitrogen or sulfur heterocycles
    • Inline solid or solution addition during continuous process operations
    • Analytical verification with HPLC detection of byproducts
    • Formulation into technical-grade or formulated products after synthesis

    Final product types

    • Herbicidal active ingredient intermediates
    • Precursor molecules for synthetic pyrethroids
    • Custom crop protection chemical building blocks
    • R&D reference standards for agrochemical discovery

    4. Polymer and Resin Modification Additive

    2-Methyl-3-Furoic Acid finds usage in advanced polymer chemistry, where technicians introduce it to impart rigidity, UV resistance, or unique solubility profiles to specialty resins. This material enters pre-polymer mix tanks or post-polymerization blends, with careful monitoring for residual monomer and end-group analysis. Regulatory oversight addresses both worker safety and material tracking throughout composite production.

    Industry compliance standards

    • ISO 9001:2015 (Quality control in polymer processing)
    • ASTM D883: Standard Terminology Relating to Plastics
    • EU REACH compliance for industrial monomeric additives
    • OSHA 29 CFR 1910 (Chemical Hazard Communication)

    Typical usage ratio

    • 0.3–1.5% by weight in total batch, adjustable based on required physical property enhancement and compatibility

    Downstream process integration

    • Addition prior to or during polycondensation for thermosets
    • Dispersion in pre-polymer blend followed by extrusion or casting
    • Residual acid content and molecular weight monitored as critical quality attributes
    • Post-modification with other crosslinkers as per final specification

    Final product types

    • UV-stabilized thermosetting resins
    • Specialty films with moisture barrier properties
    • Polymer coatings for electronics
    • Advanced composites for automotive or aerospace use

    5. Fine Chemical Custom Synthesis

    Fine chemical companies frequently specify this acid for the preparation of custom heterocycles and bi-functional synthons used in advanced organic syntheses. Contract and catalog manufacturers require assured purity and batch-to-batch consistency when employing this material in complex, multi-step synthesis routes. Stringent procedural documentation and analytical control systems ensure specification alignment throughout the production lifecycle.

    Industry compliance standards

    • ISO 9001:2015 (Quality management in fine chemical synthesis)
    • RoHS Directive 2011/65/EU (For chemicals destined for electronics)
    • GMP for chemical intermediates when supplied upstream to regulated industries
    • FDA 21 CFR Part 210/211 (For raw material handling in pharma-oriented projects)

    Typical usage ratio

    • 0.15–0.6 equivalents, tailored to the stoichiometry of individual client synthesis schemes

    Downstream process integration

    • Integrated via batch or microfluidic synthesis lines
    • Charged in precursor formation steps, often via protected carboxylic acid variants
    • QC checks: melting point, GC/HPLC purity, and residual solvent profile for every lot
    • Full traceability and COA support for contract synthesis projects

    Final product types

    • Catalog fine chemicals for research
    • Custom heterocycle compounds for pharma, material science, and electronics
    • Substituted furan derivatives
    • Advanced organic intermediates for pilot-scale synthesis
    Free Quote

    Competitive 2-Methyl-3-Furoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Methyl-3-Furoic Acid: A Closer Look at Its Value in Chemical Manufacturing

    From Workshop to Industry: The Journey of 2-Methyl-3-Furoic Acid

    Working directly at the core of chemical production, every product carries a story—not just in structure, but also in how we manage synthesis, quality, and real-world use. 2-Methyl-3-Furoic Acid stands out not just for what it is, but for what it does and the reliability it delivers to demanding applications. This compound, recognized by its CAS number 1003-92-5, is more than a raw material; its stability and performance support advanced work in pharmaceuticals, flavors, and specialty materials.

    Understanding 2-Methyl-3-Furoic Acid

    At a glance, 2-Methyl-3-Furoic Acid offers a chemical structure derived from the furan ring, substituted with a methyl group at the 2-position and a carboxylic acid at the 3-position. What makes our process unique is the focus on both purity and reproducibility. Over years of manufacturing in controlled facilities, we've seen how even small inconsistencies in starting materials or reaction control can lead to variability—something end-users do not tolerate, especially in pharmaceutical synthesis or when used as an intermediate in crop protection agents.

    Getting the Details Right: Specifications and Purity

    Chemistry rewards precision. Our batches of 2-Methyl-3-Furoic Acid regularly exceed 99% purity after recrystallization and chromatographic refinement, leaving only trace impurities measured in parts per million. Color and odor indicators align tightly with expectations for commodity-grade organic acids: a faint off-white crystal with a subtle earthy furan note.

    Moisture, a common pitfall in carboxylic acids, often leads to instability or unwanted side reactions. Through careful vacuum drying and packaging under inert atmosphere, we’ve managed to keep moisture levels below 0.1%. Cheaper alternatives often cut corners, relying on open air drying or bulk handling, which might introduce hidden variables.

    Consistency—From the Reactor to Delivery

    On the manufacturing floor, we inspect parameters like melting point, color index, and spectral signatures (NMR, GC-MS) for every batch. Having seen both small-batch and continuous-flow production, I know firsthand how scale can throw curveballs: solvent retention, by-product formation, and heat management all change as volumes rise. Sticking to standardized protocols pays dividends for customers who expect their synthetic planning to go off without a hitch.

    Material is packed in high-barrier containers, preventing light and air from affecting the acid’s stability over time. Each drum is batch-tracked and sealed immediately after final QC. The aim is to deliver a product that performs the same way months after it leaves our plant as it does the day we pack it.

    Applications in Fine Chemicals, Pharmaceuticals, and Beyond

    Many buyers are looking for materials that either form a base for advanced molecule building or act as critical intermediates in their own right. 2-Methyl-3-Furoic Acid strikes a useful balance: reactive enough for derivatization, stable enough to handle the rigors of multi-step synthesis. Active pharmaceutical ingredient (API) manufacturers use it to build heterocyclic cores, exploiting its conjugated system to carry specific functional groups to the right place in a molecule.

    Flavor and fragrance chemists appreciate its mild furan note, adding a subtle depth to certain formulations. The agricultural sector sometimes calls on it when designing crop protection agents that need both activity and selective environmental breakdown. Years of moving this acid from one application to another—field trials, regulatory submissions, process optimization—have shown us the importance of adaptability in a raw material.

    Comparing Alternatives: Why Not Just Any Furoic Acid?

    It’s tempting to lump all furoic acids together. In practice, differences in substitution—whether at the 2-, 3-, or 5-position—change polarity, reactivity, and physical handling. For instance, 3-Furoic Acid or 5-Methylfuroic Acid have similar frameworks, but customer feedback and repeated trials have underlined how reaction yields change considerably depending on positional isomer. We’ve seen separation challenges escalate and side-product profiles shift simply by running the same synthesis route with a slightly different furoic acid.

    Experience teaches that method validation (in both small- and large-scale runs) hinges on controlling these differences. Reactivity in esterification, amidation, or coupling steps shows noticeable improvement with our 2-Methyl derivative, compared to other isomers we’ve produced. Beyond chemical behavior, every customer wants fewer surprises in physical form—bulk density, flow properties, rate of dissolution in typical organic solvents—since each property affects downstream automation and formulation.

    Insights From the Manufacturing Process

    Building 2-Methyl-3-Furoic Acid at significant volume doesn’t just mean scaling up glassware reactions. We’ve had to solve challenges ranging from catalytic efficiency to safe solvent recovery. For instance, temperature control remains critical; furan derivatives tend to form impurities through overreaction or degradation if heating profiles go astray. Years of pilot and plant-scale experience pushed us to deploy real-time temperature monitors, and feedback-driven adjustments based on the purity of in-process samples.

    Chromatography and crystallization stages demand patience. Overly rapid cooling can lock in solvates or trap impurities—a headache we often see from less careful producers. Only through methodical adjustment have we refined our protocols to deliver consistent, high-purity product. Batch-to-batch comparison drives every improvement: we keep reference samples and trend analyses on key analytical figures, so if something drifts, we catch it before it leaves the door.

    User Experiences and Customer Feedback

    At the end of the day, the feedback from chemists using our acid in demanding synthetic projects gives us the clearest measure of success. Academic researchers need high-purity, structurally unambiguous material for well-controlled experiments. Pharmaceutical groups anticipate rigorous regulatory review of their raw material supply chains—complete transparency on origin, processing, packing, and analytical data matters. Feedback loops have sometimes flagged subtle differences in crystallinity or melting behavior depending on storage or transit timing. Each note from a user, whether glowing or highlighting a snag, goes into our process review system.

    Many repeat customers cite the reliability and traceability of our product—especially important during scale-up phases and tech transfer from lab to plant. Once, a customer flagged a slight shift in IR spectra in samples delivered across different seasons. Digging in, we traced the source to minor changes in solvent moisture content at one stage. Fixing these 'invisible variables' helped restore consistency, and we updated documentation and QA checks across the board.

    Regulatory, Safety, and Environmental Considerations

    From the manufacturing perspective, potential buyers are often surprised by the strict regulatory environment chemicals like 2-Methyl-3-Furoic Acid must navigate. Material traceability, documentation of synthesis steps, impurity profiles, and safe handling procedures aren't just paperwork—they directly affect what applications the product can serve, particularly in pharmaceuticals and food-contact scenarios.

    Hazard identification and material safety data are more than formalities. The furan group lends certain reactivity, requiring containment during production and careful management of vent gases and waste. We have invested in on-site solvent recovery and closed-system filtration to limit emissions and exposure. Waste streams containing by-products or spent solvents are always treated on-site or via accredited partners according to local regulations to avoid environmental release.

    Over the past five years, regulatory audits have steadily increased in number and intensity, pushing us to maintain thorough batch records, real-time process monitoring, and transparent supply chain management. These measures mean more than audit checklists—they build lasting confidence for our customers, who depend on uninterrupted, high-specification supply.

    Market and Supply Challenges

    Securing high-quality raw materials, especially furan base chemicals, requires reliable sourcing; supply chain interruptions have far-reaching consequences. Price spikes for furfural (a key starting material) due to shifts in agricultural output can ripple through every step of the process. We've had years where tight supply has required switching to alternate vendors, sometimes triggering minor process recalibrations to account for slight upstream differences. Long-term supply contracts, built on years of mutual trust with our own partners, stabilize pricing and delivery for customers.

    Global logistics play a role, especially with increased scrutiny on container safety, regulatory declarations, and certification at customs points. Any gap in paperwork or subtle change in product declaration risks delays—or in worst case, the need to re-import material, wasting time and money for everyone. Our longest-standing clients often note that such behind-the-scenes logistics work matters just as much to them as the certified purity of what actually arrives.

    Future Paths for 2-Methyl-3-Furoic Acid Development

    Chemistry evolves as new research sectors arise. As biocatalytic and green synthesis push industry forward, we continually explore milder, less energy-intensive methods for 2-Methyl-3-Furoic Acid production. Traditional oxidation protocols that use heavy metals or high pressure are being replaced by catalyst systems that reduce by-products and lower the ecological footprint. We track advances in electrochemical synthesis and enzymatic routes, keen to adopt those offering both economic and environmental benefits without compromising on purity or performance.

    Our R&D group is testing innovative purification approaches combining membrane technology with established crystallization, aiming to reduce solvent use and improve yield. Advances here could mean faster production, better quality, and a smaller impact on the environment. These technical improvements are not pursued for their own sake, but because real-world customers—whether in pharma, agriscience, or advanced materials—ask for greener, safer, and more sustainable chemicals along with robust documentation.

    Closing Thoughts on Value and Reliability

    2-Methyl-3-Furoic Acid shows every user that attention to detail in manufacturing translates into tangible results in application. Having worked through both smooth and rocky production cycles, guided customers through unexpected challenges, and celebrated breakthroughs, I see this compound as a testament to the power of quality at every link in the supply chain. Every bottle or drum shipped is a reflection of those long lessons. Its enduring reputation in the market is built on dependable process control, practical transparency, and the close collaboration between our teams and end-users.

    Real value shows up in the confidence our partners gain—from the analytical chemist scaling a new synthesis, to the plant engineer relying on timely, specification-matched delivery. In the world of complex chemistry, that kind of reliability stands out. As the chemical landscape shifts, our focus rests on improving how we manufacture, listen, and respond to those who depend on each batch, batch after batch, year after year.