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Ε-Caprolactone

    • Product Name Ε-Caprolactone
    • Alias ε-CL
    • Einecs 201-500-4
    • 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
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    Specifications

    HS Code

    418953

    Chemicalname ε-Caprolactone
    Casnumber 502-44-3
    Molecularformula C6H10O2
    Molarmass 114.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 237 °C
    Meltingpoint -1 °C
    Density 1.07 g/cm3
    Refractiveindex 1.449
    Solubilityinwater Slightly soluble
    Flashpoint 113 °C

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

    Packing & Storage
    Packing The packaging for ε-Caprolactone (1 kg) is a sealed amber glass bottle with hazard labels, chemical identification, and handling instructions.
    Shipping Ε-Caprolactone should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be transported according to local, national, and international regulations for chemicals. Store at a cool, dry location. Ensure proper labeling and documentation. Avoid contact with incompatible substances and handle with appropriate personal protective equipment.
    Storage Ε-Caprolactone should be stored in a cool, dry, and well-ventilated area, away from heat sources, open flames, and direct sunlight. Keep the container tightly closed and avoid moisture exposure. Store away from incompatible materials such as strong acids and bases. Use appropriate chemical-resistant containers, and ensure proper labeling. Follow local regulations and safety guidelines for chemical storage.
    Application of Ε-Caprolactone

    Applications of Ε-Caprolactone in Industrial Manufacturing

    As a direct manufacturer, we provide Ε-Caprolactone to major sectors that require high-purity monomers for polymer synthesis, elastomer production, specialty coatings, and advanced adhesives. Our material supports precise processing environments and integrates into established regulatory frameworks for quality and safety.

    1. Polycaprolactone Polyol Manufacturing for PU Elastomers

    Leading producers in the polyurethane elastomer sector use Ε-Caprolactone as a key monomer to synthesize polycaprolactone (PCL) polyols, which imparts improved hydrolysis resistance, enhanced flexibility in low-temperature environments, and extended service life in final PU elastomer applications. The chemical enters synthesis during ring-opening polymerization processes, carefully monitored for molecular weight and functional group control. Downstream, these tailored polyols react with diisocyanates in controlled formulations for footwear soles, cables, industrial rollers, and seal components.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 compliance for raw material control
    • ISO 9001:2015-certified quality management throughout manufacturing
    • RoHS Directive 2011/65/EU for restricted substances in electronics components
    • Automotive OEM specifications for elastomeric parts (e.g., Volkswagen TL 52424, GM GMW16311)

    Typical usage ratio

    • 60–100% E-Caprolactone based on target polyol molecular weight and application durability
    • Ratio adjusted for hardness and elongation specifications of end product

    Downstream process integration

    • Ring-opening polymerization with glycol initiators under controlled temperature and vacuum
    • Incorporated into PU prepolymer manufacturing post-synthesis
    • Dispensed to elastomer reaction injection molding or casting lines

    Final product types

    • High-performance footwear sole compounds
    • Oil-resistant cable insulation jackets
    • High-tensile drive belts and roller coatings
    • Precision automotive suspension bushings

    2. Biodegradable Surgical Suture and Implant Materials

    Medical device manufacturers leverage Ε-Caprolactone as a principal constituent in synthesizing medical-grade polycaprolactone polymers used for producing absorbable sutures, tissue scaffolds, and controlled-release drug delivery matrices. Stringent process validation ensures monomer purity and consistent polymer molecular weight to meet medical regulatory demands. In implementation, downstream compounding and extrusion convert the polymer to fibers or molded components for sterile surgical use.

    Industry compliance standards

    • ISO 13485:2016 for medical device manufacturing
    • USP Class VI biological reactivity testing
    • ISO 10993 biological evaluation of medical devices
    • FDA CFR 21 Part 820 for medical device quality systems

    Typical usage ratio

    • 90–100% E-Caprolactone for base polymerization, with minor ratios of lactide, glycolide, or copolymerizing monomers depending on degradation rate and mechanical profile

    Downstream process integration

    • Polymerization reactor for controlled ring-opening in sterile-grade environment
    • Granulation, melt-spinning, and fiber drawing operations for medical fibers
    • Injection molding or solvent casting for implantable shapes

    Final product types

    • Absorbable monofilament and braided surgical sutures
    • Drug-eluting implantable scaffolds
    • Biodegradable staples and anchoring devices
    • Tissue engineering films and porous matrices

    3. Specialty Coatings and Surface Protection Systems

    Coating manufacturers use Ε-Caprolactone to modify polyester polyols for two-component and UV-curable coating systems, improving abrasion resistance, low VOC emissions, and coatings flexibility for floors, automotive parts, and electronic housings. The raw material enables customization of molecular structure for specific film properties and chemical resistance profiles based on downstream application requirements. Carefully tuned ratios and reaction conditions control crosslink density and polishing performance.

    Industry compliance standards

    • VOC content in compliance with EU Directive 2004/42/EC
    • ISO 16000 series for indoor air quality and emission limits
    • EN 71-3 (Toy Safety) for coatings in children’s products
    • ISO 12944 for corrosion protection coatings

    Typical usage ratio

    • 10–60% E-Caprolactone-derived polyol content depending on system flexibility and crosslink density required for performance specification

    Downstream process integration

    • Introduced during polyester polyol synthesis prior to resin blending phase
    • Blended with curing agents (isocyanates or acrylic photoinitiators) to achieve target application viscosity and film characteristics
    • Applied through spray, roll, or dip coating systems onto various substrates

    Final product types

    • High-wear industrial floor coatings
    • Automotive plastic and metal component coatings
    • Consumer electronics housings finishes
    • UV-cured wood and furniture topcoats

    4. Hot Melt and Structural Adhesive Formulation

    Producers of industrial adhesives rely on Ε-Caprolactone to synthesize thermoplastic polyurethane (TPU) and polycaprolactone-based hot melt adhesives designed for flexible assembly, packaging, footwear, and automotive applications. The monomer enables controlled polymer chain length and melting point targeting. Robust process control during polymerization and compounding ensures predictable tack, adhesion, and performance tailored to automated dosing and high-throughput assembly lines.

    Industry compliance standards

    • ISO 9001:2015 quality systems in adhesive raw material manufacturing
    • FDA 21 CFR 175.105 for adhesives in indirect food contact
    • ASTM D1002 for lap shear strength in metal-to-metal bonding
    • GB/T 2793-1995 for Chinese industrial adhesive performance

    Typical usage ratio

    • 30–75% E-Caprolactone-derived segments, variable based on viscosity, open time, and cohesive strength required in downstream operations

    Downstream process integration

    • Reacted with polyisocyanates in melt or solution phase to form elastomeric blocks
    • Compounded with tackifiers, plasticizers, and stabilizers for thermoplastic adhesive pellets or films
    • Supplied as granules or films for hot melt or pressure-sensitive application equipment

    Final product types

    • Bookbinding and packaging adhesives
    • Footwear assembly bonding systems
    • Automotive trim and interior mounting adhesives
    • Industrial lamination adhesives for textiles and films

    5. Biodegradable Packaging Films and Agricultural Mulch Materials

    Packaging and agricultural film manufacturers integrate Ε-Caprolactone into copolymer blends to achieve controlled biodegradation, flexibility, and clarity in final films. Processing in dedicated reactors allows for precise adjustment of degradation profiles, mechanical strength, and optical properties to meet specific end-user needs while passing compostability certifications. Downstream operations include compounding, extrusion, and blowing or casting film, followed by slitting and print coating.

    Industry compliance standards

    • EN 13432:2000 certification for industrial compostability of packaging
    • ASTM D6400 for biodegradable plastics
    • FDA 21 CFR 177.1520 for polymer items in food contact
    • ISO 17088 for compostable plastics product labeling

    Typical usage ratio

    • 15–45% in PCL/PLA or PCL/PBAT blends, adjusted according to transparent or opaque film requirements and targeted degradation time

    Downstream process integration

    • Blending in twin-screw extruders during masterbatch preparation
    • Blown film extrusion or cast film production lines
    • Conversion into sheets or rolls for agricultural or packaging films

    Final product types

    • Biodegradable shopping and produce bags
    • Compostable agricultural mulch films
    • Food packaging wraps with certified compostability
    • Disposable single-use packaging liners
    Free Quote

    Competitive Ε-Caprolactone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Εpsilon-Caprolactone: Practical Insights from the Manufacturer’s Floor

    Bringing ε-Caprolactone to the Industry Table

    From small batch synthesis to large scale reactors, few monomers deliver the versatility of ε-caprolactone. We know this material up close, from the loading of cyclohexanone in the reactor to the point when the pure, colorless liquid emerges, practically ready for caprolactone-based polyester synthesis or custom bio-based polymer projects. Our facilities in this line carry decades of expertise in the ring-opening polymerization route, where just the right catalyst—usually a stannous octoate or an organic acid—turns ε-caprolactone into the backbone for many advanced materials.

    Not every feedstock delivers the clean polymerization profile of ε-caprolactone. Compared to traditional lactones, this one stands out for its high purity and low color index, achieved through vacuum distillation and well-controlled crystal purification. Spec-grade ε-caprolactone always presents itself as a clear, nearly water-white liquid at room temperature, with negligible residual acid content and minimal moisture. We hold moisture under 0.05% by constant in-line monitoring, because even small traces can throw off molecular weight distribution in polymerization runs.

    Our 4-liter and 200-liter units process this monomer to exceed standard ASTM-D2566 purity tests, meeting or surpassing 99.5% assay where the residuals—cyclohexanone, caproic acid, caprolactam—are kept at sub-100ppm by our purification steps. Many customers arrive with the same question: how does caprolactone behave in synthesis compared to more common lactones, such as δ-valerolactone or even glycolide? We have spent years compiling practical comparisons under real process conditions.

    From Synthesis to Performance: Why ε-Caprolactone Delivers More Than Just Polymer

    Our own teams use ε-caprolactone mainly in ring-opening polymerizations through tin-based or enzymatic catalysis. In these reactions, caprolactone opens up its ring to form polycaprolactone with predictable molecular weights and low polydispersity indices, making it an ideal building block for medical device resins, biodegradable films, and specialty adhesives. Unlike some structurally related lactones, ε-caprolactone structures afford slower hydrolysis in vivo, which appeals to biomedical applications needing a balance between strength and controlled degradation.

    Having guided hundreds of synthesis campaigns, we see a clear distinction: ε-caprolactone based polymers exhibit a lower melting point, around 60°C, than PLA sourced from lactide or glycolide, and this directly influences processability. The native flexibility of ε-caprolactone-derived polymers means easier melt-processing and fewer surprises on extrusion lines, especially when blending with natural polymers or soft touch plastics. Our technical staff diagnose challenges with molecular weight control, rheology, and end-group functionality every day, which often traces back to source monomer quality. We run caprolactone through Karl Fischer titration, GC-MS, and NMR to guard against rogue impurities that tend to catalyze undesirable side-reactions.

    Competitors in the market sometimes focus solely on lactide or glycolide, but our hands-on work demonstrates why ε-caprolactone is the workhorse for elastic, durable polyesters. Its reactivity under mild conditions—polymerization at 120-180°C—means lower technical barriers and often, less costly plant retrofitting. Even our most experienced operators notice fewer fouling events and cleaner reactor outputs thanks to caprolactone’s consistent boiling point and purity. This reliability translates to fewer shutdowns and tight lot-to-lot variance—critical for high-value applications like surgical sutures and medical-grade foams.

    Real-World Usage: In the Trenches of Research, Medicine, and Industry

    Every inquiry about ε-caprolactone seems to arrive with a different end-use in mind. Biodegradable packaging, industrial adhesives, resorbable medical implants, and even functional coatings all draw on its physical and chemical flexibility. Our R&D partners often request custom bulk quantities with specific residual monomer targets, which we deliver using customized distillation steps and nitrogen-blanketed drums to prevent oxidation. Through repeated collaboration with research clients, we’ve supported polymer chemists chasing narrow molecular weight distributions, or those who need to functionalize end-groups for click chemistry reactions—a capability strongly enabled by the low reactivity toward non-specific side-products.

    It’s common knowledge in our labs that ε-caprolactone outperforms in blending with lactides, glycolides, and even polyester-based polyols. Our proprietary purification allows for high-clarity copolymers that sit at the core of controlled drug release matrices, or as soft segments in polyurethane design, where traditional caprolactam or butyrolactone fall short due to either a too-high melting point or less predictable degradation.

    Not all applications tolerate residual acid or unreacted monomer, so our process innovations—like in-situ vacuum stripping and platinum-cured polishing—directly respond to demands from GMP-grade resin markets. As a manufacturer, we work hand-in-hand with our customers’ chemists, designing caprolactone streams with micro-filtration protocols and rigorous tank sampling schedules. Each production log pairs batch identity with impurity profiles by GC, a practice that ensures traceability throughout downstream processing.

    Unpacking the Differences: Beyond the CAS Numbers

    Polymer labs often ask: why select ε-caprolactone over δ-valerolactone or γ-butyrolactone? From our vantage, the structural difference may appear slight, but the process implications are large. Polycaprolactone offers not only higher hydrophobicity but also forms more flexible chains, which is crucial for elastomers and shape-memory thermoplastics. Unlike δ-valerolactone-derived polymers—whose mechanical properties quickly degrade in moist environments—ε-caprolactone-based materials hold up under prolonged mechanical cycling and resist hydrolytic scission much longer.

    From an operator’s perspective, ε-caprolactone also brings less volatility and a narrower boiling range under industrial reactor pressures, simplifying distillation and condensation control. In direct comparison, γ-butyrolactone tends to slip into side-reactions, forming cyclic oligomers or inciting unwanted crosslinks. Here, we give our process engineers a simpler path to scale-up, fewer offcuts in downstream conversion steps, and more freedom in molecular design. This sort of consistency matters for regulatory audits, custom order fulfillment, and real-world user safety.

    Functionalization is another key difference. ε-caprolactone copolymers enter into chain-extension or end-capping with less effort, responding well to controlled nucleophilic additions or grafting with PEG, for example. Our in-house research staff validate reactive blending protocols for medical-grade applications, submitting every batch to both chemical and biomechanical stress testing. The result: polymers with uniform degradation rates, targeted molecular weights, and a proven safety track record.

    Specification Details as Lived in Production

    We stand behind our technical specs not as a formality, but as a lived necessity. Over the years, the ε-caprolactone tanks in our plants have changed—automated level sensors, broader data logging, tighter environmental control—but the core specification profile remains unchanged. Purity levels, water content, color, and residuals undergo real-time checks at both synthesis and storage stages. We experiment with novel catalysts all the time, but the best results still arise when all trace acids and peroxides are minimized, because even a 0.1% bump in water can throw off entire polymer runs with gel formation or runaway exotherms.

    Polymer viscosity is at the mercy of our monomer’s consistency. A casual approach on storage or shifting for shipping containers can degrade final performance, so we fill and seal all drums inerted with dry nitrogen or argon. We have built a steady workflow for sampling—using closed systems, certified glassware, and low-temperature extraction—so batch data remains trustworthy from reactor start to last drop used in the customer’s tank. Our teams log and trend all critical parameters, and offer full batch data transparency for audit or troubleshooting.

    Across the range, we offer ε-caprolactone in multiple bulk and pre-packed sizes, with specialized packaging for sensitive end-uses such as medical, food-adjacent packaging, or pilot line scale-up. Our long-term partners value that we maintain segregated lines for pharma and industrial material, protecting against cross-contamination. Every product leaving the site comes with full COA, with GC-mapped impurity curves and rapid spectral reference for incoming quality checks.

    Delivering Practical Value for Advanced Application

    There’s a growing demand for biodegradable polymers, and ε-caprolactone is right at the center of this shift. Our on-site application lab routinely supports start-ups and major firms designing polycaprolactone-based packaging films, joint coatings, or 3D-printed scaffolds. For engineers working on solvent welding or reactive blending, the low glass transition temperature (around -60°C) translates to resilience in chilly storage and flexibility at typical handling temperatures. Our formulation scientists perform aging studies—dry/ambient, wet cycles, UV exposure—to publish realistic service expectation data for you.

    In the adhesives sector, ε-caprolactone is prized for its balance of melt strength and easy incorporation into hot melt and reactive adhesive systems. Unlike many commodity monomers, it tolerates the inclusion of toughening agents, tackifiers, and even reclaimed polyols without catastrophic loss of performance. Our staff troubleshoot blending, polyester resin formation, and even compounding for UV-cured acrylics by adjusting molecular fragment ratios at the monomer feed stage, with attention to storage stability and downstream process timing.

    Medical device manufacturers struggling to achieve the right rate of absorption in implantable resins have found that our fine-tuned ε-caprolactone lots permit better control than lactide or glycolide blends, giving them latitude to design devices that degrade predictably or stall breakdown in sensitive tissue environments. We run strict bioburden control, and maintain close chain-of-custody on all consumables, with full trace batch history available to device partners and their auditors. Our manufacturing journey has cemented strong relationships with regulatory and standards boards, giving us foresight on upcoming compliance shifts and safety data trends.

    Looking Ahead: ε-Caprolactone in the New Manufacturing Landscape

    As feedstock costs, environmental oversight, and user expectations rise, we keep refining our operations to guarantee every drum of ε-caprolactone meets stringent controls. Our technical teams develop catalysts that eliminate trace color bodies, and optimize reactor systems to slash both reaction time and energy demand. Closed-loop solvent recovery, heat integration, and smart process control define our latest investments. We spot problems in real time by coupling analytics with operator know-how, and adapt production cycles based on partner feedback.

    We see customers pushing boundaries—blending ε-caprolactone into PHAs for compostable plastics, or tailoring caprolactone chain ends for click chemistry drug delivery systems. Our approach draws from a direct understanding of the complexities: water and acid management, product stability in transit, and the many faces of end-use compatibility. We bring a practical eye to market changes—adjusting drum sizes, filtering specs, or introducing higher purity pharmaceutical lines as research shifts toward more advanced uses and stricter compliance.

    For every kilogram of ε-caprolactone leaving our facilities, we log hundreds of technical details and problem-solving milestones. Over time, the relationships built with polymer scientists, formulation specialists, and production engineers feed into future improvements—real lessons that let us keep this monomer front and center in the evolution of materials science. The most critical factor remains unchanged: working with those who use this monomer in unpredictable, ever-advancing fields, gathering insight from every process hiccup and development breakthrough.

    Addressing Manufacturing Challenges with Real-World Solutions

    Manufacturing advanced monomers like ε-caprolactone at industrial scale never runs on autopilot. Each campaign throws up new hurdles: reactor fouling, peroxide formation, or sudden blips in thermal stability. Our teams have fine-tuned operations—adjusting catalyst loading for clean conversion, modulating pressure profiles to mitigate side reactions, and rolling out redundant inline filtration for ultra-sensitive batches. We learn by doing, keeping error logs and tracking how process tweaks impact downstream polymer behavior.

    Shipping and storage demand just as much attention. We have seen where improper sealing or temperature cycling can spike hydrolysis in only a week. Our solution: every drum gets filled under inert blanket, followed by immediate leak checks and expedited logistics. In the field, customer polymerizations reflecting phase separation or discoloration often trace back to overlooked details in monomer handling. By working directly with users, from R&D to plant managers, we reinforce best handling practices—with quick feedback and emergency support for the rare shipping mishap.

    Regulatory change, particularly regarding medical and food-contact materials, shapes our work every quarter. Our compliance officers navigate the evolving REACH and FDA landscape, investing in early testing and third-party audit readiness. We see the value in proactivity: tight documentation, cross-functional staff training, and inviting partner audits at our sites. Lessons learned in these reviews go into daily production practice, closing knowledge gaps and elevating every future batch.

    End-user chemistry changes often faster than market forecasts predict, so we collaborate with research consortia, major brands, and even university spin-offs to anticipate trends in caprolactone applications. Whether it’s next-gen “smart” packaging or high-performance elastomer design, our plant operators and chemists adapt quickly—rethinking distillation protocol, testing new storage vessels, or batch-segregating for cross-market needs, always with ears open for practical feedback.

    Conclusion

    The everyday job of a chemical manufacturer includes many small details that add up to a superior ε-caprolactone product—details that aren’t visible in standard spec sheets or market brochures. Customers trust us for more than a commodity; they count on insights built over thousands of in-process data points, direct collaboration, and an enduring commitment to quality over expedience. Every sample, drum, or truck-tanker leaves our sites supported not just by documentation, but by the knowledge and troubleshooting skill of teams who work with ε-caprolactone as both science and craft. In this way, we keep the backbone of many advanced polymers reliable, adaptable, and ready for whatever the next customer challenge brings.