Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Methyl 2-Methyl-3-Furoate

    • Product Name Methyl 2-Methyl-3-Furoate
    • Alias methyl_2_methyl_3_furoate
    • Einecs EINECS 256-467-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    992226

    Chemical Name Methyl 2-methyl-3-furoate
    Molecular Formula C7H8O3
    Molecular Weight 140.14 g/mol
    Cas Number 16783-05-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 191-193°C
    Density 1.147 g/cm3
    Refractive Index 1.483
    Smiles CC1=COC=C1C(=O)OC
    Solubility Soluble in organic solvents, slightly soluble in water
    Purity Typically ≥98% (variable by supplier)

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

    Packing & Storage
    Packing Amber glass bottle, 100g, with tamper-evident cap and clear labeling: "Methyl 2-Methyl-3-Furoate, CAS No. 28564-83-2, For laboratory use."
    Shipping Methyl 2-Methyl-3-Furoate is typically shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported under ambient conditions, away from heat and direct sunlight. Handle with care, following standard chemical safety protocols. Ensure appropriate labeling and documentation according to local, national, and international shipping regulations for chemicals.
    Storage Methyl 2-Methyl-3-furoate should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and properly labeled. Store separately from incompatible substances such as oxidizing agents. Use appropriate chemical-resistant containers and secondary containment to prevent leaks or spills. Follow standard laboratory chemical storage protocols.
    Application of Methyl 2-Methyl-3-Furoate

    Applications of Methyl 2-Methyl-3-Furoate in Industrial Manufacturing

    Methyl 2-Methyl-3-Furoate is an organic intermediate with high purity, consistency, and traceability, suited for the synthesis of fine chemicals. Our facility ensures controlled quality and supply, supporting primary sectors that demand reliable input for downstream chemical transformations. Below are critical application segments with relevant standards, usage parameters, integration stages, and typical end products.

    1. Pharmaceutical Intermediate for Heterocyclic Drug Synthesis

    This furoic acid methyl ester serves as a central building block in the multi-step synthesis of several pharmaceuticals, especially those requiring a furan moiety in the active compound structure. Leading API manufacturers utilize it in the early stages of synthetic schemes where controlled reactivity and minimal batch-to-batch variation are required for regulatory filings and scaling to cGMP production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP Guidelines
    • US Pharmacopeia (USP) Chapter <797>
    • EDQM CEP Process Traceability Requirements

    Typical usage ratio

    • Ranges from 0.5% to 2.5% of total synthesis substrate mass, adjusted based on target API yield and furan incorporation efficiency, usually determined during scale-up validation batches.

    Downstream process integration

    • Introduced during Stage-1 intermediate synthesis using controlled addition protocols in batch reactors, typically under nitrogen at mild temperatures. Process controls monitor concentration to prevent side-product formation impacting API downstream purity.

    Final product types

    • Furan-containing antibiotic APIs
    • Antifungal drug intermediates
    • Anti-inflammatory heterocyclic compounds
    • Small molecule clinical development candidates

    2. Fine Fragrance and Flavors Intermediates

    Long-established in aroma chemical manufacturing, this compound acts as a precursor for synthesized musk, balsamic, and caramelic notes. Flavors and fragrance formulators use it as a key matrix reactant for constructing stable, food-grade aroma binders. Production requires adherence to food safety and purity certification to meet international F&F supply chain requirements.

    Industry compliance standards

    • IFRA Global Standards for Fragrance Ingredient Safety
    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • US FDA 21 CFR 172.515 for Flavor Additives
    • ISO 9235 (Natural Aromatic Substances) for labeling control

    Typical usage ratio

    • Used at 0.02% to 0.35% of batch mass for fine fragrance bases; up to 0.1% in flavor formulations, adjusted according to target aroma intensity, product stability, and regional regulatory restrictions.

    Downstream process integration

    • Standard addition to esterification or etherification vessel under acid catalysis, often in the synthesis of specialty aroma intermediates. Inline sampling for GC analysis tracks conversion and ensures minimal off-note generations.

    Final product types

    • Perfumery aldehyde blends
    • Creamy and caramelic food flavors
    • Natural-identical flavor additives
    • Personal care fragrance bases

    3. Agrochemical Synthesis (Furan-Derived Herbicide & Fungicide Intermediates)

    Producers of advanced agrochemicals frequently apply this methyl furoate for constructing selective furan-containing herbicide and fungicide molecules. The compound’s reactivity profile supports functional group transformations needed for synthesizing active agents suited to regulated crop protection markets. Its traceable origin ensures reliable documentation for global product registrations.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Residues: 501–505)
    • US EPA 40 CFR Part 158 (Registration of Pesticide Products)
    • FAO/WHO Codex Alimentarius (Maximum Residue Limits)
    • ISO 17025-compliant QC for analytical testing

    Typical usage ratio

    • Between 1.2% and 3.7% of total reactant mass depending on the molecular structure of the target furan-substituted pesticidal agent and specific transformation route—optimized during process R&D with field trial feedback.

    Downstream process integration

    • Added at Stage-2 condensation or cyclization, typically after initial precursor preparation. Inclusion timing ensures selectivity for furan ring formation and downstream purification.

    Final product types

    • Furan-derived pre-emergence herbicides
    • Systemic triazole fungicides with furan sidechains
    • Seed treatment actives incorporating furan esters
    • Post-harvest crop protection agents

    4. Polyester and Polyamide Monomer Synthesis for High-Performance Polymers

    Leading polymer manufacturers transform this furoate into diacid or diamine monomers through catalytic hydrogenation and oxidation routes to produce bio-based polyesters and specialty polyamides. The compound’s well-defined structure supports integration in co-monomer feedstock for engineering plastics, contributing to enhanced thermal and barrier properties in final polymer goods.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for Raw Material Control
    • EU Regulation No 10/2011 (Food Contact Materials: Plastics)
    • REACH Annex XVII (Restriction of Chemicals in Polymers)
    • ASTM D6866 (Bio-based Content Certification)

    Typical usage ratio

    • Utilized from 3.5% to 11% of total monomer mix by weight, composition varying based on desired copolymer characteristics, such as melting point and hydrophobicity. QC feedback from pilot extrusion guides adjustment during product development.

    Downstream process integration

    • Feeding directly into ester interchange or polycondensation reactors, following monomer pre-purification. Monomer blending strictly monitored for moisture and impurity levels before continuous polymerization.

    Final product types

    • High-barrier bio-based PET packaging films
    • Specialty automotive polyamides
    • Biosourced engineering plastics
    • Food-contact multilayer containers

    5. Advanced Solvent Precursor in Electronics Manufacturing Chemicals

    Electronics and functional material companies use this compound as a precursor for synthesizing polar aprotic solvents and functionalized furan additives, which enable efficient metal-cleaning and thin film deposition steps. The molecule’s controlled reactivity makes it compatible with ultra-trace impurity specifications widely enforced in high-value electronics supply chains.

    Industry compliance standards

    • SEMI C1-101 (Chemical Quality for Semiconductor Device Manufacturing)
    • IEC 62474 (Material Declaration for Electrical/Electronic Products)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances)
    • JIS K 0102 (General Rules for Chemical Testing)

    Typical usage ratio

    • Formulated at 0.9–2.1% of synthesis mixture as a precursor for generating functionalized solvents; ratio tailored according to solvent polarity targets and endpoint process yield.

    Downstream process integration

    • Introduced at high-purity synthesis or distillation step, under anhydrous conditions, enabling the stepwise build-up of targeted solvent structures while maintaining compliance with trace metal and ionic impurity thresholds.

    Final product types

    • Specialized electronic-grade cleaning solvents
    • Photoresist developer additives
    • Planarization slurry vehicles
    • Dielectric thin film deposition aids
    Free Quote

    Competitive Methyl 2-Methyl-3-Furoate 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 sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    Introducing Methyl 2-Methyl-3-Furoate: Chemistry That Drives Creative Synthesis

    An Authentic Manufacturer’s Perspective

    Methyl 2-Methyl-3-Furoate comes off our lines with quality that reflects decades of practical chemical manufacturing. Many research labs and industrial plants rely on a steady, defined supply. Over the years at our facility, we have refined the way we produce this compound, chipping away at inefficiencies and finding the right balance between consistency and adaptability.

    To get here, we listen closely to the kinds of requirements organic chemists and fragrance engineers talk about. The material flows clear and colorless, usually presenting a faint fruity scent. We see the bulk of interest coming from people synthesizing fine chemicals, working in agrochemical intermediates, or chasing next-generation flavors and fragrances.

    Our Production Model and What Sets It Apart

    We’ve always believed you get quality through stability at every step, not by leaning on buzzwords or vague assurances. Every batch starts with furfural derivatives that pass a strict entry checkpoint. Our technicians keep an eye on moisture and impurity levels throughout, since even a slight deviation can throw off reaction routes. Methyl 2-Methyl-3-Furoate demands a carefully tuned esterification, then a purification set-up that doesn’t cut corners. Extensive sample-taking keeps the process honest. The resulting liquid measures above 98.5% by purity, with water content usually well below 0.2%, and GC trace analysis down to the last tenth of a percent for any side aromatics. Those margins come from actually running the line, not just writing it into paper specs.

    In the day-to-day of the plant, we notice customers don’t just want a certificate—they want confidence that each drum or bottle inside their facility will match the last one. This means investing as much in repeat verification and hands-on material handling as in analytical instrumentation. It’s easy to overlook, but anyone in scale chemistry knows repeatability often matters as much as the published grade or purity.

    How Chemists Use This Molecule

    The real story behind Methyl 2-Methyl-3-Furoate lives in bench-top discovery as well as pilot-plant scale-up. Chemists in flavor and fragrance labs use it to bring out subtle undertones—an extra note in a fruit blend or a background character in a green-apple or berry profile. We’ve had clients experimenting with it in new perfume launches, often seeking out a more authentic, less synthetic furan ring flavor. The methyl substitution tweaking the backbone of the molecule creates a lighter, more vibrant profile than standard methyl furoates.

    Agrochemical developers come back to Methyl 2-Methyl-3-Furoate when they look for intermediates that can undergo further functionalization. Its reactivity around the furan ring makes for versatile possibilities—opening the door to oxime, amide, and other derivative syntheses. During custom synthesis consultations, we’ve discussed with clients how this exact setup can reduce step count in their process. Sometimes that means a shorter path to a key pesticide intermediate or a specialty fine chemical.

    Technical Characteristics: Real-World Details

    Chemistry runs on trust and reproducibility. The furoate’s molecular structure—C6H6O3—makes it more than a recipe component. It shapes boiling and melting point data that actually hold up under day-to-day batch conditions. The boiling point sits comfortably around 200–205°C, and the flash point runs safely for flavor/fragrance blending environments, provided standard precautions stay in place. Specific gravity readings remain tight around 1.17 at 25°C. This makes volumetric formulation more manageable compared with some of the less stable, heavier esters.

    Our QA team puts each lot through GC-MS and IR to confirm identity, while Karl Fischer analysis keeps water at bay. Over the years, we’ve found customers work best with lighter moisture loads, since the furoate can hydrolyze easily if improperly stored or handled. Tanks and drums inside our warehouse stay purged with dry nitrogen after every batch, no exceptions.

    Some new clients ask how our Methyl 2-Methyl-3-Furoate stands up over months of storage. In our direct tests, samples held in sealed, light-blocked containers at 20°C stay well within spec even after a year. This is a big reason why R&D labs that don’t burn through stock monthly keep coming back—they know what they start with will be what hits the flask months later.

    Comparing with Other Furoate Compounds

    The furoate family covers a big range. Many buyers and process chemists wonder how Methyl 2-Methyl-3-Furoate fits in with methyl furoate, ethyl 2-methyl-3-furoate, and related molecules. The methyl group at the 2-position in our product shifts its solvent compatibility and alters its volatility. Unlike plain methyl furoate, which tends toward a simpler fruity note and a bit more volatility, 2-methyl substitution adds stability to the molecular backbone. This nuance lets blend specialists create longer-lasting fragrance notes.

    The main difference you’ll sense isn’t just academic—it’s practical. In trial runs with flavorists, Methyl 2-Methyl-3-Furoate resisted rapid oxidation and didn’t generate off-aromas under regular storage. Compared with ethyl furoate cousins, you get a different volatility curve and tighter control on ester hydrolysis over time.

    Process engineers working in intermediates synthesis value the slightly higher boiling point. The furan ring modulates reaction pathways for cycloaddition chemistry or nucleophilic substitution, an advantage when looking for predictable outcomes batch after batch. Many manufacturers overlook these small details, but anyone who’s had to recalibrate for inconsistent volatility or hydrolysis rates knows it eats up time and lowers yield.

    Practical Handling Tips From Our Own Labs

    Our crews handle this liquid throughout daily shifts, so experience brings its own lessons. The compound doesn’t tolerate standing open in humid air; a tight-sealed bottle reduces waste by minimizing hydrolysis, even in a busy bench environment. In medium-scale operations, stainless steel turns out to be the best storage and transfer material. Plastic can pick up lingering odors and is easier to scratch, leading to cross-contamination if you’re managing multiple aroma compounds.

    We rely on slight positive-pressure storage protocols, combined with warehouse monitoring. Every shipment leaves the gate certified, but we also attach a memo with storage advice—not as fine print, but as nuggets drawn from real-life incidents. For example, we saw early failures in aroma retention years ago, traced back to leaky gaskets on storage containers. Swapping out for chemical-resistant rubber solved that long before a technical bulletin could get written.

    Safety Commitment: Lessons From the Floor

    Experience teaches respect for every chemical, and Methyl 2-Methyl-3-Furoate is no exception. Our workforce learned early to use appropriate skin and eye protection, not because the material is aggressive by the book, but to fend off sensitization after repeated splashes and exposure. The compound vapor can give mild irritation with heavy, unventilated use, a lesson reinforced through years of handling drums and blend tanks instead of just reading an MSDS.

    Even experienced handlers get complacent after hundreds of drum transfers. We enforce simple rules: don’t open containers near open flames, ventilate storage, and clear up spills with adsorbent—never dilute with water and wash away, given hydrolysis risk. We take fire drills and chemical handling refreshers seriously, drawing on close calls as concrete reminders instead of general warnings.

    Environmental Considerations: Practiced, Not Just Promised

    Nobody working with furan derivatives can ignore environmental responsibility. Our process lines use closed-loop systems whenever possible, recycling solvents and treating off-gas with catalytic scrubbers. Some years ago, we invested in containment zones to head off run-off, after a single containment breach led to downtime and corrective action. These investments aren’t window dressing—they reduce waste, keep regulatory inspectors satisfied, and prevent headaches for both operations and neighbors.

    Disposal solutions come from partnering with licensed hazardous waste handlers. Early on, we saw how bad disposal practices could shut down a line and hurt reputations. Our staff is trained to distinguish reclaimable waste from discardable residues, ensuring that whatever can be cleaned and reused is, and anything leaving the premises is logged and documented.

    Ongoing Support and Real Communication

    No catalog or glossy brochure reflects what actually works on the production floor or inside the R&D lab. We spend a lot of time on the phone—or replying to customer emails—to help troubleshoot batch inconsistencies, provide retesting data, or just lend a hand with new blend ideas. Our technical staff are also spenders of the product. They design and run application trials, using the same material shipped out to customers.

    Direct dialogue with chemists and flavorists helped us understand where small variances in purity, color, or moisture could tip a blend from “approved” to “rejected.” Based on feedback, our QC system is tuned not for passing formal benchmarks, but for keeping material inside narrower-than-standard windows. If you ever get a drum or a bottle that doesn’t measure up, replacements come out fast, because every lost batch is real cost and real time.

    Why Real-World Perspective Matters

    Chemical manufacturing is not just about filling the pipeline with product. In our experience, it’s about paying close attention at every critical point—handling raw material, listening to user feedback, learning where each compound stands out, and responding fast to problems. Methyl 2-Methyl-3-Furoate captured our attention because it sits at the crossroads of creativity and reliability. Whether your next step is perfume innovation, agricultural chemistry, or specialty synthesis, what you get from us comes with the lessons learned under real plant lights, not just lab fluorescents or marketing spotlights.

    That mindset reflects every shipment, call, or consultation we handle. If you’re working with this molecule, you're tapping into a resource shaped by hands-on chemistry, field troubleshooting, and a shared belief that the story of a chemical—its production, use, and ongoing evolution—is as important as the numbers on a COA. We’re always here to talk shop, dive into application challenges, or try new things together, because the field keeps moving and so do we.