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Ethyl 10-Undecenoate

    • Product Name Ethyl 10-Undecenoate
    • Alias Ethyl undecylenate
    • Einecs 203-329-8
    • 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

    514182

    Cas Number 692-86-4
    Molecular Formula C13H24O2
    Molecular Weight 212.33 g/mol
    Iupac Name Ethyl undec-10-enoate
    Appearance Colorless to pale yellow liquid
    Boiling Point 262 °C
    Density 0.872 g/mL at 25 °C
    Refractive Index 1.432 - 1.436 at 20 °C
    Flash Point 117 °C
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Odor Characteristic, fatty

    As an accredited Ethyl 10-Undecenoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl 10-Undecenoate is supplied in a 100 mL amber glass bottle with a secure screw cap, labeled for laboratory use.
    Shipping Ethyl 10-Undecenoate is shipped in tightly sealed containers, protected from light, heat, and moisture to prevent decomposition. Transport complies with local and international regulations for chemical safety. The chemical should be labeled with appropriate hazard information and handled by trained personnel, ensuring secure packaging to avoid leaks or spills during transit.
    Storage Ethyl 10-Undecenoate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep the storage area free of ignition sources and avoid moisture exposure. Properly label the container and follow all safety protocols to prevent spills and accidental exposure.
    Application of Ethyl 10-Undecenoate

    Applications of Ethyl 10-Undecenoate in Industrial Manufacturing

    Ethyl 10-Undecenoate serves as a specialized chemical intermediate in various industrial sectors. Its unique chemical structure, reactivity profile, and compatibility with established processes have driven its adoption in selected high-value manufacturing pipelines. As a direct producer, we support stringent downstream compliance, offer technical guidance on ratios, and maintain strict lot traceability for all application segments described below.

    1. Synthesis of Polyamide and Polyester Precursors

    Ethyl 10-Undecenoate is widely used in the chemical synthesis of monomers that form specialty polyamides and polyesters. The double bond at omega position allows facile functionalization in the initial oligomerization, while the ester moiety supports transesterification reactions required in high-performance bulk polymers. Producers incorporate the material in controlled feed processes to regulate molecular weight and branching, required for demanding fiber and engineering plastic specifications. Downstream formulators benefit from precise integration at the prepolymer stage, benefiting finished optical and mechanical properties.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for polymer intermediates)
    • EU REACH Regulation (EC) No 1907/2006 - Registration and evaluation of chemical substances
    • EN ISO 16103 (Plastics – Monomers for polymer production – Determination of impurities and purity)
    • China GB/T 21866-2008 (Technical requirements for synthetic monomers)

    Typical usage ratio

    • 5%–25% by weight of total monomer input, adjustable by desired monomer chain length and functionalization; increased ratios used for higher aliphatic content polyamides.

    Downstream process integration

    • Fed to polymerization reactors after pre-drying and in-situ purification; participates in condensation or radical addition reactions; downstream fractionation used to control residual monomer content.

    Final product types

    • High-length polyamide fibers for automotive textiles
    • Aliphatic polyester resins for coatings and packaging
    • High-clarity casting polyamides for electronics and optics
    • Copolymer resins for technical films and sheets

    2. Synthesis of Antimicrobial Agents for Personal Care

    Ethyl 10-Undecenoate acts as a key starting ester for producing undecylenic acid derivatives with established antimicrobial activity. The ester serves in transesterification routes to create undecylenate salts and custom derivatives. Downstream, these are crucial in ingredient compositions where regulatory limits target heavy metals, residual reactants, and endocrine disruptors. The product is used under monitored GMP conditions with routine stability and purity checks pre-blending.

    Industry compliance standards

    • EU Cosmetic Regulation (EC) No 1223/2009
    • US FDA 21 CFR 172.860 (Fatty acids; permitted use in personal care actives)
    • ISO 22716:2007 (Cosmetic GMP)
    • Health Canada Cosmetic Ingredient Hotlist

    Typical usage ratio

    • 2%–8% active equivalent in pre-final formulation, typically saponified or salted in-situ. Ratio varies with class of finished personal care product and local regulatory residue limits.

    Downstream process integration

    • Fed to saponification or salt-forming vessels; distilled intermediates are isolated and further purified before personal care formulation blending; full tracking of side products via batch release.

    Final product types

    • Medicated anti-fungal creams
    • Dandruff treatment shampoos
    • Active deodorant bases
    • Antimicrobial wipes

    3. Lubricant Base Stock Modifier for High-Temperature Applications

    Lubricant manufacturers select Ethyl 10-Undecenoate as a modifier for synthetic ester base oils, especially where high temperature and oxidative resistance is mandatory. Its chain structure and terminal unsaturation enable co-polyol reaction and formation of stable, low-volatility lubricants. The integration optimize viscosity index, reduce volatility loss, and assure compatibility with specialty additive packages in synthetic engine and compressor lubricant applications.

    Industry compliance standards

    • DIN 51517 (Lubricants for industrial gear units)
    • ASTM D445 (Kinematic viscosity methods for oils)
    • ISO 21469:2006 (Hygiene requirements for the formulation of lubricants)
    • SAE J300 (Engine oil classification by viscosity grade)

    Typical usage ratio

    • 3%–15% by volume in base oil blend; dose level varies with desired pour point, stability, and exposure temperature profile.

    Downstream process integration

    • Integrated in the esterification and polyol blending stage; real-time viscosity and volatility monitoring during batch blending; post-formulation vacuum stripping for purity assurance.

    Final product types

    • High-temp compressor oil formulations
    • Automotive synthetic engine oils
    • Industrial gear lubricants
    • Specialty chain oils for food machinery (NSF H1 base)

    4. Perfume Intermediate for Specialty Fragrances

    Leading fragrance compounders employ Ethyl 10-Undecenoate as a key intermediate in the synthesis of macrocyclic musks and select lactones. Its molecular geometry provides a functional foundation for ring-closing metathesis, conjugation, and subsequent derivatization. The downstream pathway maximizes olfactory specificity while meeting strict residual solvent and purity constraints in luxury and fine fragrance formulations.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • IFRA/IOFI Labelling Manual for flavor and fragrance substances
    • ISO 9235:2013 (Aromatic raw materials)
    • EU Regulation (EC) No 1223/2009 (for finished fragrances in personal care)

    Typical usage ratio

    • 2%–10% of reactant molality at macrocycle synthesis stage. Differentiation depends on musk intensity thresholds and target final aroma profile.

    Downstream process integration

    • Reacted in metathesis or esterification reactors under inert atmosphere; multi-stage distillation and crystallization for isolating pure intermediate; technical support on odor quality release testing.

    Final product types

    • Luxury perfume concentrate bases
    • Fine fragrance compounds for branded products
    • Personal care musk and lactone notes
    • Encapsulated aromatic ingredients for detergents

    5. Surface Modifier in Silicone Release Coatings

    Within the pressure-sensitive release liner segment, formulators use Ethyl 10-Undecenoate as a sacrificial hydrophobe and chain transfer agent to tailor migration and surface properties of silicone polymers. Incorporated at the crosslinking stage, it fine-tunes migration rates, partially blocks silicone transfer, and delivers stable, low-energy surfaces for technical label and film applications that demand high-fidelity release without adhesive bleed.

    Industry compliance standards

    • FDA 21 CFR 175.320 (Resinous and polymeric coatings for food contact surfaces)
    • EN 12316-1 (Adhesives – Test methods for release liner performance)
    • TAPPI T541 (Release liner base paper properties)
    • ISO 14001:2015 (Environmental management for coating production)

    Typical usage ratio

    • 1%–4% by total silicone solids; precise adjustment according to balance of release strength and cross-link density.

    Downstream process integration

    • Pre-blended with silicone precursor prior to crosslinker addition; cured thermally on in-line roll coaters; post-cure QC includes migration and release value testing by peel methods.

    Final product types

    • Pressure-sensitive adhesive (PSA) release liners
    • Graphic lamination backing films
    • Medical wound dressing release papers
    • Protective masking films for industrial use
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    Certification & Compliance
    More Introduction

    Ethyl 10-Undecenoate: A Versatile Building Block Straight from Our Reactors

    A decade back, hardly anyone in our lab talked in detail about ethyl 10-undecenoate. Most folks stuck with established fatty acid esters, not quite seeing the need for an unsaturated chain as esoteric as C11 with a terminal double bond. In the years since, everything’s changed. I have seen R&D teams, from large flavor houses to tiny labs, demand the sort of precision and purity that only a focused manufacturer can maintain. Through those years, we built our production flow around the practical, day-to-day needs of formulators and synthetic chemists.

    What Sets Ethyl 10-Undecenoate Apart?

    Our focus stays on the details that matter. The molecular structure — 10-undecenoic acid, esterified with ethanol — means it carries an 11-carbon chain and a double bond on the terminal carbon. The typical shipment leaves our loading dock at a purity consistently above 98%, based on GC analysis. This subtle arrangement — an ester head and a reactive terminal — makes the material stand out for both flexibility and reliability. We control each stage from raw acid through final drums, ensuring specs hit the mark batch after batch.

    Direct contact with this compound tells a story different from the generic C11 esters available on secondary markets. Many companies grab large-volume undecanoic acid esters in commodity grades, but our team tweaks each parameter — from catalyst system to fractional distillation temps — to preserve the unsaturation. This is never just a commodity molecule. Chemists looking for a customized starting point for polyamide or fragrance synthesis count on that double bond being exactly where it should be, and that our product won’t introduce contamination or byproducts.

    Decisions in Production: Purity, Stability, and Consistency

    Every batch faces hurdles in two directions: chemical stability under shipping conditions, and the maintenance of appropriate isomer ratios. It’s easy to over-purify or under-distill this ester; we see the difference immediately when side chain isomers creep in. Using calibrated packed columns and refined vacuum protocols, our operators catch instability before it passes QC. After a decade of scaling up, we learned that cutting corners here—on energy, time, or people—always introduces margin calls in downstream applications.

    Direct sunlight, improper drum liners, and even ambient warehouse heat can start polymerizing some unsaturated esters. We keep real-world storage conditions in mind. By fine-tuning antioxidant treatment and selecting HDPE-lined drums, we cut the risk of in-drum gelling or off-odors. This level of detail rarely shows up on spec sheets, but it decides whether a customer’s project succeeds or fails.

    Uses in Synthesis: More Than Just a Flavor Precursor

    Formulators reach for ethyl 10-undecenoate in more areas than you’d expect. Its most recognized role lands in the flavor and fragrance sector, where its structure lets R&D teams design musk intermediates and macrocyclic ketone scents. The terminal double bond enables ring-closing metathesis, allowing for the creation of high-value ingredients used in high-end perfumes.

    Beyond scent creation, polymer chemists often call on this ester for specialty nylon or polyamide resins. Here, the double bond is essential. Unlike saturated esters, this product’s unsaturation supports functionalization through epoxidation, hydrosilylation, or Diels-Alder reactions. In my own experience, the yield and consistency of downstream resins shift dramatically with small impurities. Only the cleanest batches, prepared by continuous-flow esterification rather than batch processes, achieve reliable molecular weights in polymer runs.

    Another camp comes from the agrochemical intermediates and specialty lubricant fields. Ethyl 10-undecenoate, with a manageable boiling point and decent thermal stability, gives synthesis teams a cleaner route to long-chain, functionalized molecules—much harder with shorter or saturated esters. Our clients often mention success in developing anti-fungal agents and high-performance base oils, singling out our material’s low color index and absence of residual acid.

    Differentiation: Why Not Just 'Any' Undecenoate?

    Working on the ground floor, we come across plenty of ethyl esters of undecenoic acid that don’t fit demanding jobs. Many traders and resellers repackage mixed-feed oils with varying levels of unsaturation or hidden residual moisture. Most users don’t see issues until their reactions foul or their products fall out of spec. This gets tricky, especially in fragrance and pharma work, where trace impurities matter.

    The way we run our reactors minimizes re-esterification byproducts. Throughout the year, we tweak feedstock ratios by season—early summer fatty acids differ in iodine value from winter fractions, so we monitor every incoming truckload for exact match. On a bad day, if we get off by a few percentage points, our stabilization tanks catch it. A third-party trader rarely even asks about iodine value or double bond placement.

    Most of our competition weighs purity from an analytical, not functional, standpoint. The difference only surfaces in end use. I’ve spoken directly to customers running high-throughput parallel synthesis, who notice subtle shifts in boiling points or reactivity based on where the double bond lands. With mass-market undecenoates, that control slips. We keep documentation open and QC transparent, so the trail back to every reactor charge is unbroken.

    Real World Application Stories: Learning from the Lab Floor

    Focusing on practical impact has pulled our chemists closer to project partners. A polymer scientist from southern Europe called me, worried about sticking during their monomer synthesis runs. After comparing gas chromatograms, we traced issues back to slight excess in residual water content that went unnoticed in a sub-supplier’s product. Switching to material kept under inert nitrogen from our own drums cut out the polymerization problems.

    Working directly with flavor companies, I have witnessed how the consistency of the C11 backbone affects musk performance. Small impurities, undetectable by the naked eye, degrade the subtlety of end fragrances. Over time, formulators request tighter specs for color and peroxide values — something we have adapted to by refining our column setups and monitoring batch logs. This feedback cycle rolls directly into production tweaks.

    Once, an innovative team sought to use ethyl 10-undecenoate for controlled-release agrochemical capsules. The success of their design depended on the slow, predictable reactivity of the terminal double bond. Our production experience told us that thermal history in storage plays a crucial part; together, we adapted our shipping and local warehousing profile, tracking each container and switching from metal to food-safe PE liners to eliminate rogue polymerization.

    Common Questions and Industry Challenges

    People often ask whether slight differences in specification matter for practical applications. In our experience, trace metals, isomer ratios, and leftover acidity change the path of a reaction. Several years back, I remember a batch that passed standard chromatography but still fouled a client’s hydrogenation catalyst. Root cause analysis zeroed in on trace iron from legacy transfer lines that we now replace annually.

    One recurring challenge remains: shipping and storing unsaturated esters without darkening or thickening. Continuous attention to oxygen exposure, temperature swings during transit, and drum hygiene pays dividends. We’ve recently begun using oxygen-absorbing sachets for longer export shipments and track storage conditions with digital data loggers. Feedback from loyal customers tells us that these steps keep our product stable and workable across a broader geographic range.

    Environmental Responsibility from Ground Up

    From year one, our team put environmental health at the front of production decisions. By investing in ethanol recovery and catalyst recycling units, we’ve cut down process waste that traditionally built up in the sector. Supporting responsible sourcing, we work closely with our partner refineries to purchase fatty acids from plantations certified against illegal clearing — not just for marketing, but because batch records show better consistency with traceable feedstocks.

    We know large end-users raise concerns about lifecycle and biodegradability. Pure ethyl 10-undecenoate, derived from plant-based undecylenic acid, fits into most renewable chemistry goals. The terminal double bond allows downstream products to be more easily broken down via oxidative processes. Sharing LCAs with clients provides transparency: sustainable sourcing reduces not only carbon footprint but also minimizes conflict over raw material security.

    From the Manufacturing Floor: Difficulties Faced and Lessons Learned

    A day’s work in producing functional esters isn’t simple. Scaling up from pilot runs to commercial loads revealed dozens of process shortcuts that looked fine at flask scale, but produced yield slippage and color instability as the tonnage ramped. Our lineup of column stills, backed by digital process control and regular recalibration, became critical for repeatability. Direct feedback from packing room staff — spotting yellowing before drums get sealed — matters more than printouts.

    It’s common for customers to request tighter impurity profiles as application needs shift. Our work with R&D clients, who sometimes prototype with 100 gram lots before moving up to hundreds of kilograms, has taught us to leave flexibility in planning. We maintain small-batch glass reactors for quick runs, and keep analytical staff cross-trained for fast turnarounds. This way, new process tweaks or spec changes don’t throw off schedules for committed deliveries.

    Regulatory Trends and Customer Expectations

    We follow emerging rules on raw material stewardship and process disclosure, not just to stay compliant but to build lasting trust. Our documentation includes certificate-of-analysis with each load, plus optional certificates for kosher, halal, or RSPO compliance on request. These aren’t legal requirements, but today’s brands want full visibility from molecule to shelf.

    Since the global supply chain turbulence of recent years, customers increasingly ask about stock buffers and backup routes for key inputs. In response, we have diversified our fatty acid sourcing by region and built long-term volume agreements with plant oil partners. By maintaining direct tolling relationships, we set aside enough raw stock, avoiding the shortfall risks that come from outsourced arrangements.

    Continuous Evolution in Manufacturing and Customer Relationships

    No matter the changes in scientific trends or market conditions, strong customer partnerships guide process evolution. Through regular production reviews and open report sharing, both sides catch inefficiencies early. My technical team runs periodic ‘open batch’ days for major buyers, letting customers examine process controls on-site and walk through analytical findings the way our staff does. These sessions drive deeper collaboration and faster troubleshooting.

    Our experience tells us that each new technical challenge — from green chemistry benchmarks to new performance specs — brings opportunities for better chemistry and stronger partnerships. In this way, the work behind every kilogram of ethyl 10-undecenoate extends far beyond generic chemical supply. On the manufacturing floor, these lessons grow from the hands-on trials and errors of the team, dedicated to building reliability one batch at a time.