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2-Propylfuran

    • Product Name 2-Propylfuran
    • Alias 2-Propylfuran
    • Einecs 207-518-6
    • 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

    339744

    Chemicalname 2-Propylfuran
    Casnumber 42043-39-4
    Molecularformula C7H10O
    Molecularweight 110.16
    Appearance Colorless to pale yellow liquid
    Boilingpoint 131-134°C
    Density 0.892 g/cm3 at 25°C
    Refractiveindex 1.461-1.465
    Flashpoint 19°C (closed cup)
    Solubilityinwater Insoluble
    Smiles CCCC1=COC=C1
    Pubchemcid 62290

    As an accredited 2-Propylfuran 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 mL of 2-Propylfuran, securely sealed with a screw cap and labeled with safety information.
    Shipping 2-Propylfuran should be shipped in tightly sealed containers, protected from light and incompatible materials. Transport under cool, dry conditions using appropriate packaging compliant with local and international regulations. It is classified as a flammable liquid and may require labeling and documentation as hazardous material during shipping. Handle with care to prevent leaks or spills.
    Storage 2-Propylfuran should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use proper chemical storage containers, and label them clearly. Store at ambient temperature, following local regulations for flammable liquids. Ensure proper grounding and bonding for bulk storage.
    Application of 2-Propylfuran

    Applications of 2-Propylfuran in Industrial Manufacturing

    2-Propylfuran, as a manufacturer-supplied heterocyclic compound, enables value creation in several specialty industrial sectors. This section details precise downstream use cases, compliance needs, dosage rationales, processing entry points, and definitive end-product classes based on confirmed applications.

    1. Fine Fragrance and Flavor Additive Formulations

    Perfumers and flavor houses incorporate 2-Propylfuran for green, nutty, and roasted flavor notes in select gourmet flavorings and fine fragrance accords. After sensory QC, the compound enters proprietary blends, supporting nuanced aroma in food and luxury fragrance products. Flavorists adjust dosing based on product category (food or fragrance) and targeted region, considering both safety and organoleptic requirements.

    Industry compliance standards

    • FCC (Food Chemicals Codex) monograph standards for flavor ingredients
    • IFRA (International Fragrance Association) guidelines for safe use in fragrance compounds
    • Regulation (EC) No 1334/2008 on flavorings and certain food ingredients
    • FDA 21 CFR Part 172.515—Synthetic flavoring substances and adjuvants (GRAS listing)

    Typical usage ratio

    • Flavor additive: 0.1–10 ppm, adjusted for food matrix and application (beverages, confectionery, bakery)
    • Fragrance compounding: 0.05–2% of fragrance oil formulation, dependent on end-use (fine fragrance, personal care, air care)

    Downstream process integration

    • Directly blended post-filtration into flavor bases or fragrance oil bases
    • Batch mixing under nitrogen atmosphere to preserve volatility and aroma profile
    • QC via HS-GC-MS (headspace gas chromatography-mass spectrometry) for trace analysis
    • Sealed in inert-packaging lines to prevent cross-contamination before dispatch

    Final product types

    • Premium flavor blends for gourmet food service
    • Niche fragrances for eau de parfum and luxury scented products
    • Flavored beverage concentrates and ready-to-drink mixes
    • Bakery and confectionery flavor enhancers

    2. Pharmaceutical Intermediate Synthesis

    Chemical synthesis routes for certain heterocyclic APIs utilize 2-Propylfuran as a functionalized building block. Process chemists select it for its reactivity in cross-coupling or cyclization reactions for antifungal, antineoplastic, or CNS agent precursors. Purity and reactivity assessment follow GMP protocols, controlling for trace metal and residual solvent compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) as an intermediate substance
    • European Pharmacopoeia 10.0 guidelines for synthesis constituents
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) registration for precursor use

    Typical usage ratio

    • 1.0–15.0 mol% relative to limiting reagent per API pilot route, as determined by yield/impurity endpoint in scale-up
    • Adjusted during process optimization to minimize by-products and maximize conversion rate

    Downstream process integration

    • Charged to glass-lined reactor as a reagent in stepwise organic synthesis
    • Utilized in Grignard or palladium-catalyzed functionalizations with continuous monitoring of exothermicity
    • Conteolled via in-process HPLC or LC-MS for intermediate verification
    • Synthesis residues managed under validated waste handling SOPs

    Final product types

    • API intermediates for oncology and antifungal pharmaceuticals
    • CNS-active small-molecule precursors
    • Key intermediates for furan-based finished APIs
    • Advanced fine chemical blocks for specialty contract development manufacturing

    3. Agrochemical Synthesis for Crop Protection Agents

    Agrochemical manufacturers select 2-Propylfuran as a precursor for the synthesis of certain furan-based herbicide and insecticide actives. Its reactivity enables specific functional group modifications required for crop protection molecules. Blending and dosing depend on the downstream synthetic target and reaction sequence within the technical-grade active manufacturing process.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • U.S. EPA 40 CFR Part 174—Pesticide Registration and Data Requirements
    • OECD Test Guidelines for Chemical Safety of Agrochemicals
    • China GB/T 1606-2001 for testing of pesticide raw materials

    Typical usage ratio

    • 1.5–12 mol% based on target technical active concentration and reaction conversion rate
    • Adjusted according to synthetic step yield, downstream workup loss, and batch scale

    Downstream process integration

    • Added in controlled-release or one-pot synthesis steps for target pesticide actives
    • Monitored for formation of desired substitution patterns in proprietary process schemes
    • Followed by in-process GC-FID (flame ionization detection) for purity assessment post-reaction
    • Technical-grade output undergoes crystallization and solvent removal before formulation

    Final product types

    • Technical herbicide active ingredients for field crop applications
    • Insecticidal actives for seed treatment and foliar spray products
    • Furan-based growth regulators for specialty crop protection uses
    • Blended agrochemical technical concentrates for downstream formulation

    4. Polymer Modifier in High-Performance Resin Systems

    Material scientists and formulation chemists utilize 2-Propylfuran as a reactive modifier or co-monomer in the manufacturing of specialized furanic resins and thermoset polymers. The compound supports network flexibility and crosslinking in composite laminates or adhesives. Dosing is set based on desired mechanical strength and thermal stability for aerospace, automotive, or industrial composite end-uses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for manufacturing and compounding processes
    • RoHS (Restriction of Hazardous Substances) for electronics and automotive compounds
    • ASTM D638 for tensile properties of plastics
    • EU Regulation No 1907/2006 (REACH) substance registration—polymer intermediates

    Typical usage ratio

    • 2–10 wt% of polymer precursors or resin blend, according to specification sheet targets
    • Dose adjusted depending on glass transition temperature and flexibility requirements

    Downstream process integration

    • Incorporated during polymerization or resin prep by direct mixing prior to curing stage
    • QC checks for degree of cure and crosslink density after mold release
    • Analyzed for molecular weight distribution by GPC (gel permeation chromatography)
    • Finished composite material subject to ASTM or ISO mechanical/thermal testing

    Final product types

    • Furan-modified thermoset resins for aerospace and automotive structural parts
    • Specialty adhesives with defined flexibility profile
    • High-temperature gaskets and industrial sealing compounds
    • Composite prepregs for technical laminates

    5. Fuel Additive and Alternative Fuel R&D

    Developers in biofuel and advanced fuel sectors research and deploy 2-Propylfuran as a high-octane blending agent or as a model compound in combustion studies for next-generation renewable fuels. Integrators select dosage based on required volatility, compatibility with base fuels, and combustion profile testing. QC applies advanced analytical protocols to verify mixture uniformity and emissions factors.

    Industry compliance standards

    • ASTM D4806 for denatured fuel ethanol blending
    • EU Directive 2009/30/EC relating to the quality of petrol and diesel fuels
    • EPA Tier 3 fuel regulations for oxygenate blending agents
    • ISO 17025 for accredited fuel analysis laboratories

    Typical usage ratio

    • 0.5–5 vol% in fuel test blends for engine and emissions trials, as specified by lab protocol
    • Mid-range adjusted for pilot studies to evaluate performance under varied load conditions

    Downstream process integration

    • Blended into gasoline or alternative base stocks in fuel pilot plants
    • Employed in engine testbench environments under controlled conditions
    • Component concentration verified via GC-MS to ensure batch-to-batch repeatability
    • Emissions measured according to regulatory engine cycles post-combustion

    Final product types

    • Octane-boosted petrol blends for research use
    • Developmental biofuel formulations
    • Reference blends for engine emission benchmarking
    • Patentable alternative fuel compositions
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    Certification & Compliance
    More Introduction

    2-Propylfuran: A Practical Perspective from the Manufacturing Floor

    Introducing Our 2-Propylfuran

    In our plant, we’ve worked with a wide variety of furan derivatives, and 2-Propylfuran stands out as one of the more distinctive offerings in our lineup. This compound carries the CAS number 42046-98-6. Chemically, it takes the structural formula of C7H10O, and on a basic level, it's a five-membered furan ring with a three-carbon propyl side chain at the second position. We typically produce it in clear, colorless liquid form, usually with a purity above 98%, which supports consistent performance applications. There’s nothing particularly magical about its appearance—what really matters goes deeper than that.

    As a chemical manufacturer, real difference appears in what you handle, not just the specifications on a PDF. 2-Propylfuran brings a nuanced odor reminiscent of nutty or bready notes—subtle, sure, but noticeable to anyone who has spent hours around the distillation columns. Its boiling point sits around 137°C, which is higher than unsubstituted furan. This change matters during both handling and storage on-site, as its volatility is more manageable, making it less prone to aggressive evaporation compared with other low-boiling furans.

    How 2-Propylfuran Is Produced On-Site

    We handle production in a closely controlled environment. Manufacturing typically starts from furfural or another suitable furan ring precursor. Side-chain alkylation introduces the propyl group selectively. Our team relies on optimized catalysts and temperature management to favor high yields, minimizing by-products you’d rather not deal with. Any impurities that might arise can throw off downstream processes; careful purification avoids these headaches. Every batch undergoes rigorous GC analysis before it ever makes its way off-site.

    We’ve refined our technique over the years to achieve reproducibility, which our long-term clients notice. That’s the result of continuous batch monitoring, equipment upgrades, and technician know-how, far more than any line on a technical sheet can capture.

    Why 2-Propylfuran Gets Attention in Research and Industry

    What gets the R&D teams talking is the molecule’s versatility. We’ve shipped 2-Propylfuran to flavor and fragrance labs, polymer developers, and agrochemical researchers. While not all uses are equally publicized, one of the best-recognized applications sits in its function as a high-impact flavor and fragrance compound. Experienced perfumers sometimes refer to it as a building block for nut, coffee, or baked profiles, adding complexity where other molecules fall flat.

    On the industrial chemistry side, this furan derivative finds use as an intermediate, helping to introduce oxygen-rich rings into more complex molecules. Its higher boiling point compared to other furans allows for distillation integration in multi-step syntheses, providing tighter control over separation and yield. The propyl group’s size and non-polarity shift reactivity and partition coefficients, bringing options that methyl- or ethylfuran cannot. These small structural differences create significant changes in performance when integrated into more advanced targets, especially those targeting hydrophobic environments or long-term stability.

    Comparison to Other Furan Derivatives

    Being on the manufacturing side, we end up evaluating and producing several furans in parallel: furan itself, 2-methylfuran, tetrahydrofuran, and others. Once you step into the plant, practical differences quickly overshadow mere technicalities. Furan and its lower alkyl derivatives, like 2-methylfuran, boil much lower and bring more volatility hazards. In practice, furan can be tougher to keep contained at room temperature, and gives off a greater vapor load, which means more demands on our ventilation and safety systems. 2-Propylfuran, with its intermediate boiling point, allows for safer open-handling operations under our regular controls.

    One of the other ways 2-Propylfuran stands apart involves its sensory impact. The other low-molecular furans tend toward pungent ether or solvent-like odors. 2-Propylfuran, by contrast, lends itself well to food-adjacent applications, opening up markets and experimentation outside of pure industrial chemistry. Customers working in flavor technology consistently request this molecule when they want more subtlety, warmth, or complexity. If we switch over to the technical side, 2-Propylfuran’s molecular structure makes it less reactive in many harsh reaction conditions. Where rapid ring cleavage or oxidation threatens yield, the propyl side chain adds a degree of stability, stretching the range of possible downstream modifications.

    Challenges in Production and Handling

    No new batch of 2-Propylfuran ships without its hurdles. We still see supply chain uncertainties creeping in, especially for certain upstream base chemicals. Markets may fluctuate, and regulatory scrutiny can shift with little notice, especially given food and fragrance end-uses. Getting to high purity helps, but the additional cost must always be balanced against changing customer requirements. We’ve had to build greater flexibility into our warehousing and logistics, which in practice means stockpiling base chemicals and maintaining delivery commitments even during tight periods.

    From a daily operations standpoint, 2-Propylfuran behaves nicely if standard solvent containment procedures are in place. It doesn’t demand the sub-zero storage or inert gas blankets of some more unstable furan derivatives. Our staff uses standard polypropylene drums or glass bottles for short-term storage, and stainless holding tanks as needed. Safety systems clock spills or fugitive emissions before they matter. Toxicity remains low at industrial exposure levels, though inhalation over extended shifts is still avoided in our plant, with appropriate respirators in secondary containment areas and regular air monitoring as standard policy.

    Real-World Usage: Industry Experience

    Years of experience tell us not all 2-Propylfuran ends up in the same final applications. The range of usage evolves as new research surfaces and formulations change. In food chemistry, the compound serves as one of several “impact aroma” molecules that can transform chocolate, nut, or baked product profiles. Most customers in this market look for natural-identical flavor profiles, and we have adapted both the origin and purity pathways accordingly. Our food-graders want non-GMO feedstocks whenever possible, and we’ve pivoted raw material sourcing to accommodate that trend.

    Outside flavor houses, certain polymer researchers keep coming back for our highest-purity batches. 2-Propylfuran acts as an intermediate for more specific ring-substituted macromolecules, especially when building oxygenated frameworks that resist UV or thermal breakdown. In these cases, any minor by-product can change the downstream polymer’s color or mechanical attributes. That’s why we’ve doubled down on in-line purification equipment and trace-level product analytics, building on feedback from technical meetings with our polymer customers.

    Another small but growing segment involves pharmaceuticals and fine chemicals. Some research projects incorporate 2-Propylfuran for synthesizing heterocyclic scaffolds or exploring new lead structures. Access to high-purity, well-documented material often acts as the decider, since even minor residual solvents or side products can affect pharmacological screening. We maintain detailed batch history and supply full certificates of analysis, not just for client assurance but for our own internal standards.

    Our Quality Approach: From The Ground Up

    Quality for us never starts or ends at a certificate. Every operator on our team knows where things actually go wrong in the day-to-day—leaks at a pump, minor temperature drift, or a shipment delay can all make the difference between a top-tier product and a rework batch.

    Raw material selection has grown more sophisticated. We screen upstream furan ring providers for both reliability and contaminant background. Trace metals, waters, or halides from previous runs can all contaminate a sensitive batch. We work with suppliers to provide regular test results, while our own incoming QC station performs independent checks. This investment pays off in both yield and reputation. From cracking open the drum to charging the reactor, our production crew pays attention to both automation alarms and sensory clues. Vapor pressure, odor notes, or slight visual changes each tell their own story long before any lab analytics catch up.

    On purification, we take care to avoid “overworking” the product, as excessive heat or distillation cycles tend to degrade both yield and scent profile. Each batch passes through multiple-stage vacuum distillation, and we utilize inert atmospheres during processing to avoid oxidative damage that could impact both fragrance and downstream chemistry. The packed distillation columns remain cleaned and validated to prevent carryover between production runs.

    Final product gets sampled at every critical stage. Along with routine GC/MS and NMR analyses, we employ trained sensory analysts for food and fragrance batches. Their input has guided more gradual process adjustments than any written SOP ever could. Certificates released with our product cover all relevant metrics: purity, isomer content, and trace residues. Clients have told us our documentation helps them cut weeks off their own validation cycles, particularly when dealing with new regulations or internal audits.

    Supporting Sustainability and Future-Proofing Our Process

    Over the past decade, sustainability has gone from a buzzword to a central feature of customer audits. Our team understands that solvent and base chemical supply chains have real, physical sources; they aren’t infinite taps. We’ve implemented several initiatives to reclaim solvents wherever possible, reduce thermal input during distillation, and minimize emissions. The propyl group in our 2-Propylfuran often originates in plant-derived precursors, and we disclose full traceability for clients who require this information.

    We have integrated our process with in-plant recycling and recovery. As a byproduct of some of our longer furan runs, we can redirect offcuts or side fractions for energy generation within the plant. This cuts down on incineration waste and helps with our scope-one carbon reporting. Safe solvent handling is not just regulatory compliance—it’s direct risk reduction for our people.

    We’ve also engaged in regional partnerships to encourage the use of renewable feedstocks. Several upstream partners now provide verified renewable furans, and we track origins through independent third-party certification. Any client who requests detail on chain of custody can get access to the complete run log for their batch.

    Innovation and Client Collaboration: The Future of 2-Propylfuran Applications

    Product development cycles have become more collaborative over time. Increasingly, R&D teams turn to us as more than just a supplier—they include us in the early stages of project planning. We’re sharing real-time process data, adapting purity and packaging, and even adjusting run times to match experimental windows at the client site.

    Recent projects have included fragrance houses exploring more sustainable “green” notes, polymer scientists developing oxygen-rich fibers, and pharmaceutical teams crafting novel heterocycles. Each of these groups specifies different impurity limits, packaging sizes, or even analytical documentation. Our flexibility comes from both large and small-scale production trains, as well as the dedication of process engineers who understand both traditional chemistry and the new demands. Whenever a client’s trial calls for short-turnaround production, our team pivots from bulk drum runs to small, clean glass containers in less than a shift.

    In food and fragrance applications, regulatory expectations keep rising. We stay proactive, not reactive. Hazard analyses go deeper than the minimum, and international compliance becomes part of routine documentation. For years, we watched as new standards from Europe or North America changed labeling, transport, or specification norms—so our internal protocols now anticipate changes rather than chasing enforcement deadlines.

    Responsive manufacturing, in our view, grows from listening to both facility staff and end-users. Our best suggestions have come from the floor—technicians spotting a new impurity profile or plant engineers proposing heat exchanger upgrades that cut energy waste by double digits. Client visits, whether virtual or in person, always bring fresh insights and motivate another round of process improvement.

    Potential and Limitations: Honest Industry Assessment

    2-Propylfuran does not fit every need. Some applications need even lower volatility, crystalline form, or greater solubility in polar phases—that’s where other molecules, such as tetrahydrofuran or more highly alkylated furans, often take the lead. Our teams know these distinctions because we see the consequences directly: certain resins discolor with the wrong furan, or food applications run into regulatory limits. The propyl variation suits applications where aromatic complexity, mid-range volatility, and oxidative resistance rank as top priorities.

    Pricewise, production of 2-Propylfuran remains more demanding than for simple furan or methylfuran, both due to the more controlled alkylation conditions and more robust purification steps required. Still, for specific high-value applications, the cost justifies itself in performance and safety advantages.

    The Manufacturer’s View: Continuous Learning and Adaptability

    Every new application or client brings us back to basics—keep the raw materials flowing, maintain equipment, listen to both the client and the chemist overseeing the reactor. Over the years, we’ve come to respect the unique character of 2-Propylfuran, not just in its performance but also in how it demands careful, attentive production and handling. The lessons learned in one production cycle inform process improvements in the next.

    For anyone searching for a high-quality supply of 2-Propylfuran, our team stands behind each batch. Experience tells us what distinguishes a reliable supplier: transparency, technical rigor, and a willingness to adapt. The chemistry world evolves quickly, but as long as we keep learning and responding, we’re prepared for tomorrow’s requirements, whether in the lab, the plant, or in the hands of a creative formulator.