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5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile

    • Product Name 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile
    • Alias MF3Y
    • Einecs 674-708-5
    • 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

    477097

    Chemical Name 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile
    Cas Number 120624-45-7
    Molecular Formula C8H5F3NO
    Molecular Weight 189.13
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and DMF
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled “5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile, 25 g,” hazard and safety symbols displayed.
    Shipping Shipping of **5-Methyl-2-(Trifluoromethyl)furo-3-ylacetonitrile** requires secure, airtight containers to prevent moisture or air exposure. Proper hazardous material labeling must be used in compliance with local regulations. Transport should be via certified carriers for chemicals, with documentation detailing its chemical nature and emergency procedures. Store and ship at ambient temperature unless otherwise specified.
    Storage Store **5-Methyl-2-(trifluoromethyl)furo-3-ylacetonitrile** in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator). Avoid contact with oxidizing agents, acids, and bases. Clearly label the container and handle under an inert atmosphere if sensitive to air or moisture.
    Application of 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile

    Applications of 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile in Industrial Manufacturing

    As a specialized manufacturer, we supply 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile to a range of advanced sectors that demand high-purity intermediates with reliable traceability. Below, we detail critical downstream applications, with a focus on compliance, dosage control, processing, and the nature of terminal products.

    1. Pharmaceutical Intermediate for Antiviral API Synthesis

    This molecule serves as a selective intermediate in the synthesis pathway for trifluoromethylated heterocyclic APIs, especially in the production of nucleoside analog antiviral agents. Use in GMP-compliant facilities ensures high purity for further reaction, particularly in step-growth reactions involving selective alkylation or condensation. Precise stoichiometric addition at the intermediate stage supports tight batch quality monitoring, which is essential for regulatory dossier submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia Ph.Eur. General Texts 5.12
    • ISO 9001:2015 for Quality Management in API Production

    Typical usage ratio

    • 0.8–1.2 equivalents, adjusted based on substrate reactivity and targeted yield in specific coupling reactions.

    Downstream process integration

    • Added during the early-to-mid synthetic stage in multi-step API manufacturing; reacts under anhydrous conditions in polar aprotic solvents with metal catalysis.

    Final product types

    • Purified nucleoside-type antiviral drug substances
    • Registered pharmaceutical active intermediates

    2. Agrochemical Intermediate for Herbicide Synthesis

    In crop protection chemistry, this raw material acts as a core scaffold for synthesizing fluorinated furan-based herbicides. Downstream formulators incorporate the compound at defined steps to enable selective weed-control efficacy. Manufacturers must control carryover of the nitrile impurity profile, document traceability, and follow explicit process control as required for regulated agrochemical submission batches.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for Technical Material
    • REACH Registration (EC 1907/2006, relevant annexes for plant protection intermediates)
    • ISO 9001:2015 (Certified Raw Material Sourcing)

    Typical usage ratio

    • 10–15% w/w as a reactive intermediate, typically stoichiometric with co-reactants during heterocyclic condensation for herbicide backbone assembly.

    Downstream process integration

    • Introduced during the condensation or cyclization phase preceding active ingredient formation; monitored via HPLC to control conversion rates.

    Final product types

    • Precursor compounds for selective broadleaf herbicide products
    • Technical-grade active ingredients for agrochemical registrants

    3. Fine Chemical Intermediate for Fluorinated Dye Synthesis

    The nitrile structure enables further chemical modification in dye manufacturing for electronics-grade marking and specialty pigments. Exact metering is essential to achieve target chromophore properties, and the feedstock must meet stringent analytical criteria to avoid process interruptions at scale. Downstream, the furan-based segment imparts distinct absorption and improved photostability for pigments used in high-durability labeling.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for Chemical Manufacturing)
    • RoHS Directive (2011/65/EU) on restricted substances in dyes for electronic marking
    • QC protocols per ASTM D1200 (Viscosity Measurement in Dye Solutions)

    Typical usage ratio

    • 2–5% mol/mol relative to primary aromatic feedstocks in dye coupling; adjusted for chromophore extension and color match requirements.

    Downstream process integration

    • Dosed during the arylation or substitution stage, typically under controlled temperature and inert atmosphere to preserve product purity.

    Final product types

    • UV-resistant inkjet colorants for electronics
    • High-performance furan-derived pigment concentrates

    4. Specialty Polymer Modifier for Fluoropolymer Blends

    This specialty intermediate finds application in the modification of advanced fluoropolymer composites, particularly for wire and cable coatings demanding non-flammable, chemically-resistant finishes. The cyano and trifluoromethyl groups enable strong compatibility and covalent bonding in radical polymerization systems. Process teams monitor integration for optimum chain transfer and dispersion with tight batch-scale controls, especially in systems aiming to meet international fire resistance criteria.

    Industry compliance standards

    • UL 94 Flammability Test for Plastic Materials
    • IEC 60811 for Cable Insulation & Sheath Material Testing
    • ISO 9001:2015 for Polymer Compound Quality

    Typical usage ratio

    • 0.5–2 phr (parts per hundred resin), with ratio based on polymer resin grade and flame-retardancy targets.

    Downstream process integration

    • Employed during melt-blending or solution polymerization before extrusion; monitored by FTIR for molecular incorporation.

    Final product types

    • Insulation materials for automotive and industrial wiring harnesses
    • Chemically resistant jacketing for control cables

    5. Intermediate for Crop Growth Regulator Synthesis

    Formulators utilize this furan-based nitrile as a building block for the development of new-generation crop growth regulators that require tight control of trifluoromethyl substitution. It provides essential reactivity for subsequent functional group conversion, offering precision in the tailoring of plant growth modulation effects. Downstream manufacturers deploy strict, audited synthesis routes to ensure compliance with agricultural chemical registration frameworks and residue standards.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals – Crop Regulator Assessment
    • FAO Specifications for Plant Growth Regulators
    • ISO 17025 for Analytical Testing Laboratories

    Typical usage ratio

    • 8–12% of active reaction mass, with adjustments based on desired regulator structural outcome and agronomic bioactivity requirements.

    Downstream process integration

    • Input during the key condensation stage, often under inert atmosphere; product confirmation by NMR before formulation release.

    Final product types

    • Active crop growth regulating agents
    • Custom plant metabolic pathway modifiers for field use
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    Certification & Compliance
    More Introduction

    Introducing 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile: A Chemist's View from the Factory Floor

    Meet a Compound That Moves Projects Forward

    Here in the synthesis hall, hands are stained with the work it takes to build molecules like 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile. We know its full name trips up chemists fresh to fluorinated furan chemistry, but for those of us behind the reactors, this compound represents the result of countless hours optimizing yields, cleaning glass, and coaxing stubborn intermediates to react. As a manufacturer, each batch reflects attention to detail, well-tracked process control, and learning from what other acetonitrile derivatives failed to deliver.

    What Surfaces in Production

    Daily, we weigh, stir, and analyze, watching for pure white or pale crystals with an unmistakable sharp scent. The acetonitrile group at the tail binds tightly, and that trifluoromethyl cluster—once a headache for isolation—grants both chemical stability and a unique profile for further synthesis. Unlike the mass-produced building blocks that crowd the catalogs, this compound springs from a tricky balance of reaction conditions. Getting the furan to survive, letting the methyl group land on just the right carbon, and securing the trifluoromethyl motif means tuning processes at every step. Even tiny shifts in temperature or solvent choice show up in the final yield. That’s the difference between running a plant and ordering a bottle off a website.

    Learning from Each Run: Why Purity Matters

    Years in chemical manufacturing blunt any tolerance for unpredictable impurities. Each time we tighten control over reactant additions or slow down a crystallization, the next HPLC trace returns fewer shoulders, sharper peaks. For 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile, complex byproducts can complicate downstream derivatization. Clean material makes life easier later — whether customers plan to transform it into agrochemical candidates or slip it into a medicinal lead series. As scale increases, consistency matters more than throughput. Colleagues running smaller labs sometimes wrestle with inconsistent outcomes when sourcing this molecule from resellers who lack direct control over inputs. Direct manufacturing fixes these gaps through process discipline and knowing exactly what landed in the reactor.

    Model and Real-World Specs

    Each lot features a consistent formula and expected physical properties. The melting point remains reliable batch after batch—this speaks to the day-by-day optimization and hands-on monitoring of the whole process. The molecular weight and fluorine content line up exactly with what chemists need for traceable downstream chemistry. Analytical data supports traceability, but we see value in the practical: Ease in handling, clear solubility, and lack of fine dust come from mechanical improvements as much as catalogue specification lines.

    Why 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile Evolved as a Choice

    Early work in the factory focused on simpler nitriles or furan rings, but research shifts in crop protection and pharma meant customers needed more precise fluorinated building blocks. The trifluoromethyl group wasn’t just a decorative appendage—it changed metabolic stability, bioavailability, and occasionally enabled access to properties traditional methyl or ethyl groups couldn’t replicate. The push toward 2-(trifluoromethyl) motifs intersected with a growing demand for robust, not overly sensitive cores. From a manufacturer’s standpoint, adapting to this required a new production line, extra fume treatment, and getting the core synthesis sequence robust enough for scale-up. The performance differences show up in real-world project success, not just on paper.

    Comparing to Related Products

    Standard 2-methylfuran derivatives once filled much of our product list. They proved easier to build and ship, but lacked the unique combination of hydrophobicity and electron-withdrawing effect delivered by trifluoromethyl. Many analogues with other halogens—chlorine or bromine—show early promise in screens, yet can lead to reactive intermediates that behave unpredictably under further transformation steps. We’ve seen development groups turn to our 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile after repeated headaches with low volatility or instability in their early halogenated furo derivatives.

    In early screening reports, pairs of closely related acetonitriles often produce starkly different results. The trifluoromethyl version tends to demonstrate greater chemical inertness and persists under varied process conditions, where methyl-only versions might fall apart or underperform in subsequent substitutions. That comes straight from in-plant troubleshooting feedback, not just literature notes.

    Applications: Beyond Theory and Into the Lab

    The real power of this molecule comes to light once it leaves our doors. In medicinal chemistry, the furan ring and its attached groups offer a flexible platform for introducing new moieties. The nitrile group sits ready for reduction, cyclization, or functional group interchanges. Researchers looking for ways to tune lipophilicity, electronic properties, or binding affinity find this backbone a reliable stepping stone. The trifluoromethyl motif influences not only reactivity but also the fate of the entire molecule in biological systems. Biologists report differences in metabolic pathways—some furan derivatives degrade too quickly or too slowly, but this structure strikes a workable compromise between reactivity and resistance.

    We also support teams working in material science or agrochemical discovery pipelines. Many high-performing actives begin with subtle, hard-to-build skeletons like this one. The integrated acetonitrile side chain, matched with the electron-rich furan, presents a launching pad for complexity. Choosing this molecule reflects a desire for performance—and a willingness to work with products that come from deliberate, quality-focused manufacturing routes.

    Supporting Process Chemistry with Real-World Data

    Often, literature offers promise but not proof. Scalability in the lab does not always guarantee the same in a plant. We document and share the conditions that led to each batch’s consistency, from solvent system to order of additions. Manufacturing 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile at scale involves learning from past deviations, incorporating lessons from failed runs, and making practical modifications. Advanced analytics pick out micro-contaminants and let us adjust purification protocols before back-end problems surface. Every improvement gets folded into the next campaign, tightening the gap between ideal and actual output.

    Technical support teams at our facility field questions from researchers who have struggled with the product’s competitors. Stories come in about clumping, inconsistent melting, or hard-to-purify side products. Our line operators trace the root issues to upstream controls: poorly tracked raw material quality or lack of control over reaction kinetics. Full transparency between line workers, QC personnel, and researchers closes these gaps. Our process design emphasizes solutions, not workarounds: steady temperatures, rigorously documented filtrations, smart solvent choices, and careful wash protocols.

    Safety and Handling: A Manufacturer’s Experience

    From direct experience, anyone who personally weighs and processes kilogram quantities treats this compound with respect. Trifluoromethylated nitriles do not give off any obvious warning except for their spirited aroma. We work in ventilated spaces, run air monitors, and train each new hire with direct, hands-on demonstrations of proper PPE and handling workflows. Over time, these routines translate into a safety record that isn’t just paperwork, but peace of mind for everyone involved.

    Customers who have handled small-scale samples say factory-packed material arrives dry, free-moving, and with no sign of residual moisture that might cause clumping or caking. This means we don’t simply wipe down drums at the end of the day; it takes careful packaging, pre-shipment analysis, and a commitment to shipping only what we’d be confident to use in our own next run.

    What Problems Arise in Scale-Up?

    Any plant manager knows that success at the beaker scale rarely survives first contact with a 500-liter batch. With fluorinated intermediates, the risks only multiply: reaction exotherms, vent scrubber load, peculiar reactivity when impurities creep in. We’ve built our lines to adapt quickly if the reaction misbehaves. We run parallel trials to check new reagent batches before they go into full-scale reactors and log every deviation in detail. Trace metals, minor residual solvents, even batch-to-batch subtlety in fragrance reveals what process textbooks don’t cover.

    Where our synthesis differs from that of traders and small third-party labs lies in repairability: when something goes awry, we don’t blame the last delivery. We troubleshoot in-house, tweak temperatures or reaction orders, and rerun analytics until the final output matches customer specs. Over years, this focus on real-time correction and feedback gives a factory a sort of memory. Each lesson captures a shortcut or warning, saved for the next big run.

    Environmental Responsibility: Our Approach to Byproducts and Waste

    Every kilogram produced produces its own batch of waste. Fluorinated intermediates are notorious for their persistence in the environment, so we respond by tightening plant emissions. Scrubber arrays, liquid effluent recycling, and chemical capture systems all come from listening to environmental chemists’ warnings, not just rulebooks. Careful separation means that the waste stream contains less trace fluorine, less cyano residue, and fewer surprises for the local treatment facilities. This ethos matters more than a badge—it influences process redesign and purchasing choices. We continuously invest in greener solvents, safer alternative reagents, and end-to-end life-cycle tracking.

    Customers increasingly audit upstream handling of sensitive chemicals. Transparency is built on the willingness to discuss both wins and persistent challenges. For 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile, we aim to set a higher standard by being open about both strengths and room for process improvement. Sustainability never finishes—it remains an ongoing challenge, requiring regular investment in R&D, as well as hands-on training for every operator and manager.

    Supporting Your Next Steps: Feedback from the Factory

    Feedback isn’t just something we ask for on a survey. Chemists try new ligations or build new screening libraries using our product, and we hear swiftly if solubility, purity, or stability trip up productivity. Our technical experts live among the reactors and QC equipment. They keep phone lines and inboxes open because they want to know how the molecule performs, not just whether it ships on time. Reports from long-standing pharmaceutical partners help us dial in changes that improve everything from crystal habit to pourability.

    We listen for real outcomes—whether the compound performs under new conditions or fails to deliver the selectivity or reactivity intended. Tight collaboration between production and end-users points out bottlenecks and unexpected reactivity patterns. Whether a formulation gums up at scale or a catalyst test runs surprisingly clean, we value the thousand details that only show up after product leaves our site. This shapes next-generation process improvements and, in turn, helps the broader research community make better progress.

    Between Plant and Research Bench: Building Confidence

    Trust comes from seeing the same performance, day in and day out. Years of continuous improvement, open feedback, and close process management raise this fluorinated furan from a niche catalog curiosity to a preferred tool across a range of industries. The molecule earned its place not just for what’s on paper, but for the silent reliability it brings to hundreds of projects.

    We know the people using this product. Their projects rely on each drum carrying exactly what it says, every shipment arriving in good order, and every run backed with honest data. Building that confidence remains the real work behind every batch of 5-Methyl-2-(Trifluoromethyl)Furo-3-Ylacetonitrile we make. No matter how synthesis trends change, bringing hands-on focus and transparent communication to every lot is what keeps both the factory and the research moving smoothly forward.