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HS Code |
909921 |
| Cas Number | 20847-99-0 |
| Molecular Formula | C16H32O |
| Molecular Weight | 240.42 g/mol |
| Iupac Name | 1,2-epoxyhexadecane |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 330-332 °C |
| Density | 0.842 g/mL at 25 °C |
| Flash Point | 165 °C |
| Solubility In Water | Insoluble |
| Refractive Index | 1.440-1.444 at 20 °C |
As an accredited 1,2-Epoxyhexadecane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 1,2-Epoxyhexadecane, tightly sealed, with hazard labels and product identification details. |
| Shipping | 1,2-Epoxyhexadecane should be shipped in tightly sealed containers, protected from light, heat, and incompatible substances. It must be labeled according to relevant safety regulations, transported in accordance with hazardous material guidelines, and kept upright to prevent leaks. Ensure all handling personnel are equipped with appropriate protective equipment. |
| Storage | 1,2-Epoxyhexadecane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong acids, bases, and oxidizers. Protect from direct sunlight and moisture. Use secondary containment if necessary, and ensure proper labeling. Store at room temperature and follow all relevant safety regulations. |
Applications of 1,2-Epoxyhexadecane in Industrial ManufacturingAs a specialized manufacturer of 1,2-epoxyhexadecane, we support diverse industrial clients in downstream production. Below we detail specific, substantiated applications in key industries, with direct insights into compliance, typical formulation ratios, process points, and final product outputs. 1. Alkyl Glycidyl Ether Modifier for Epoxy Resin SystemsProducers of advanced thermoset polymer systems employ this material as a reactive diluent and flexibilizer for epoxy resins. It enhances mechanical flexibility, reduces viscosity, and adjusts curing characteristics of both bisphenol-A and bisphenol-F-based matrices. It serves critical roles in coatings, electronic encapsulants, and high-performance adhesives where controlled elongation and resistance to fracture are required. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Surfactant Intermediate for Industrial Emulsifier SynthesisOleochemical manufacturers use this chemical as a lipophilic building block for synthesizing non-ionic surfactants. Its long-chain structure enables tailored hydrophobe-lipophile balance required for food-grade, textile, and agrochemical emulsifier development. The material undergoes further functionalization including ethoxylation or sulfonation during surfactant formulation. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Synthesis Intermediate for Specialty Lubricant Base OilsIn the lubricant and metalworking industry, formulators use this material as a precursor to ether-based synthetic oils and additives with tailored viscosity and oxidation stability. Its molecular structure enables downstream hydrogenation or controlled ring-opening, resulting in polyalkylene glycol ethers or novel ester lubricants. These base stocks improve high-temperature lubricity and deposit control in demanding systems. Industry compliance standards
Typical usage ratio
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4. Organic Synthesis Intermediate for Fragrance and Cosmetic EsterificationFragrance and cosmetic ingredient manufacturers utilize this raw material as a foundation for producing long-chain esters, used as fragrance carriers, skin-conditioning agents, and fixatives. Its epoxide ring undergoes selective opening under mild acid catalysis, generating alcohol or acid precursors for further derivatization. The specific use depends on the required olfactory profile, emollience, and stability within personal care formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Reactive Intermediate for Polyurethane Foam AdditivesIn flexible and semi-rigid polyurethane foam production, this chemical serves as a specialty chain extender and modifier. It alters cell morphology, compressive strength, and flexibility of foam matrices produced for automotive, insulation, and acoustic applications. Reacts with isocyanates to produce polyether polyols with unique performance benefits in tailored end-use foam systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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For over two decades, we have been devoted to the practical synthesis and industrial manufacturing of specialized long-chain epoxides. Among our flagship products stands 1,2-epoxyhexadecane, also referred to by its CAS number 2435-35-4. This C16 epoxide has made real-world impacts across chemical synthesis, surfactant, and material modification applications. From the earliest pilot batches to modern, full-scale reactor runs, every lot tells a story that combines daily discipline, an appreciation for purity, and a drive for consistent quality.
We produce 1,2-epoxyhexadecane with a focus on reliability and straightforward sourcing. Anyone involved in fine chemical manufacturing, polymer modification, or pharmaceutical intermediate synthesis will appreciate the value of this particular epoxide. Its appeal grows with each processing line we supply, as plant engineers and chemists rely on repeatable product performance.
Our process engineers understand that the smallest impurities can disrupt high-volume production. We ensure a minimum purity of 98% through distillation and proprietary purification steps. Consistency in appearance and viscosity matters, especially for customers formulating high-performance surfactants or specialty lubricants. 1,2-Epoxyhexadecane presents as a colorless to light yellow liquid, free from sediment, and our standard analysis confirms a GC area percent with traceable documentation for every supply batch.
The boiling point hovers around 365°C, providing valuable range for downstream reactions that demand thermal resilience. With a molecular weight fixed at 254.44 g/mol, it integrates predictably into chain extension, etherification, and ring-opening protocols. Each delivery meets ROHS, REACH, and key export requirements, removing uncertainties for clients navigating global compliance frameworks.
The faint odor of epoxide comes from the ring but rarely persists through standard air extraction in the plant. Drums and intermediate bulk containers remain sealed to maintain integrity. From loading the reactor with raw hexadecanol to handling sensitive raw material batches, we document every parameter, recording temperature, pressure, and pH to support full traceability—a necessity for chemical producers serving audited sectors.
1,2-Epoxyhexadecane often becomes the go-to choice for chemists targeting long-chain modifications in polymer systems. Its extended hydrocarbon tail opens doors for manufacturing nonionic surfactants where mild foaming and strong emulsification are key, especially in personal care and specialty detergent applications. Beyond surfactants, the molecule finds frequent use in producing cationic intermediates and as a chain-extending reactant in block copolymer synthesis.
Our customers in the plastics sector appreciate its performance for hydrophobizing additives in molding resins, as the epoxide facilitates efficient coupling reactions and durable bonding. The length of the carbon chain, compared to shorter-chain analogs, gives end plastics stronger water resistance, lower surface energy, and better durability across repeated cleaning cycles. These properties help formulators address the rigorous demands of modern agriculture films, food packaging, and wire insulation.
Lubricant blenders choose our product for tailored oils and greases, aiming to boost stability without sacrificing flow properties. In practical blending sessions, the difference between a C12 epoxide and our C16 compound becomes clear: 1,2-epoxyhexadecane supports the formulation’s thickness and temperature tolerance without introducing volatility or breakdown over months of heavy mechanical use. The product’s relatively low volatility and excellent light and chemical stability make it a staple in industrial lubricant formulations seeking longer service life.
We hear regularly from R&D centers experimenting with ring-opening reactions to produce surfactants for textiles and leather finishing. These teams note that 1,2-epoxyhexadecane contributes unmatched smoothness and softening to finished fibers—benefits that can’t be replicated with shorter-chain or aromatic epoxides. The alkyl tail length becomes essential here, imparting hydrophobicity and mild hand feel without the tack or residue observed in alternative approaches.
Plenty of options exist for epoxides. Shorter-chain compounds such as 1,2-epoxyoctane or 1,2-epoxydodecane offer utility but behave differently in large-scale synthesis. Operators working with volatile, low-boiling epoxides struggle with containment and odor control, while those using aromatic-based varieties trade off processability for reactivity. The difference comes down to chain length, oxidation stability, and compatibility with downstream chemistries.
A sixteen-carbon backbone delivers more than just increased hydrophobicity. Its molecular weight translates to lower volatility, giving better yield retention in heated reactors and extended shelf life in warehouse inventories. That’s a metric we track through real storage tests: after 12 months, samples remain clear, with no detectable by-products or crystallization at typical warehouse conditions. Short-chain epoxides often degrade or discolor long before that time frame expires.
Formulation chemists aiming for nonionic surfactants value high chain uniformity to avoid fouling reactor walls or creating off-odors in finished products. Our production line adopts continuous distillation, separating 1,2-epoxyhexadecane from any shorter-chain by-products or isomeric traces. This precision in cut point means every kilogram reacts predictably, and no customer wastes time filtering or cleaning scale from their reactors. Lower-grade imports from other markets often fail on this front, introducing warranty and process upsets that become clear only after drums are opened.
Another frequent comparison focuses on the epoxide ring itself. The 1,2-epoxy structure resists nucleophilic and acid-catalyzed cleavage far better than many aromatic or unsaturated alternatives. In practice, this stability proves crucial in production lines facing variable pH, catalyst shots, or fast heat-up ramps. The reliability of our material means fewer batch failures, less reworking, and tighter consistency for every run.
Crafting 1,2-epoxyhexadecane at industrial scale demands more than textbook chemistry. Each run begins with the procurement of high-purity hexadecanol or brominated intermediates, both of which require tight control to minimize side-reactions in the epoxidation stage. Our team watches for traces of halide, peroxide, or unsaturation that could trigger coloring or instability during storage. Over the years, we improved batch flow by switching to continuous feed reactors, removing hot spots, and automating stage cooling—a response to customer feedback seeking more consistent color and lower peroxide content in the final product.
Handling epoxides imposes unique challenges. The material must be shielded from prolonged UV light and strong acids, yet this isn’t a laboratory exercise. On the shop floor, technicians inspect drums for any color shifts, test random samples for viscosity, and run fresh FTIR scans, even for repeat orders. By keeping a hand on every lot from synthesis to shipment, we prevent surprises from interfering with customer schedules.
Over time, customers have asked for lower peroxide residue and tighter specifications in color and clarity. These requests led us to invest in extra purification columns and stricter analytical monitoring at each batch release. Our quality team backs every drum and IBC with a transparent stack of COAs, internal test reports, and—upon request—archived retention samples. For clients keeping their lines compliant with ISO, FDA, or other product standards, such documentation reduces audit risks.
Our in-house analytical lab supports this commitment. Routine GC-MS and FTIR checks flag impurities as low as 50 ppm, not because regulators demand it, but because real-world blending and downstream processing demands it. This isn’t just about regulatory compliance—it’s about delivering a material that meets the real expectations and deadlines of chemical operators and formulators counting on every lot to perform the same way as the last.
Customers switching from alternate suppliers or substituting other long-chain epoxides often report time-consuming revalidation cycles and yield losses. By offering production consistency and lot traceability, we help smooth this transition. Technical support matters as much as the chemical itself. When a formulator’s blend separates after storage or when copolymerization fails due to trace saturated byproducts, our technical engineers respond with root-cause insight and workable process tweaks—sometimes as simple as a slightly longer pre-mix stage at a specific temperature, sometimes as detailed as adjusting the order of raw material addition.
Real-world manufacturing never stays static. Scale-ups expose hidden variables in reactivity, impurity carryover, or storage handling. Our experience points to the need for ongoing dialogue between supplier and user. Providing reference batches and facilitating comparison tests on-site have proven more valuable than reams of generic data sheets. For example: one food packaging client struggled with haze in their films when substituting from a generic C16 epoxide. Side-by-side testing with retained samples revealed subtle differences in side-chain branching. Our higher-cutpoint refinement eliminated the haze, kept melt-flow intact, and met their migration requirements—without changing their production method or requiring new approvals.
Efforts to reduce downtime and improve yield depend just as much on order reliability and supply chain transparency as they do on underlying chemistry. Colleagues in procurement repeatedly tell us how difficult it has become to source consistent, high-purity specialty intermediates when shipping lines or customs clearance introduce delays. We have responded by keeping safety stock, increasing batch frequency, and integrating digital ordering systems with key clients to provide delivery and stock updates in real time. Production schedules can adjust, but not when a missing drum halts a multi-million-dollar line for a week.
Chemical manufacturers must anticipate not just present usage but how future regulations and sustainability demands shape the specialty epoxide landscape. 1,2-Epoxyhexadecane contains no halogens, heavy metals, or persistent organic pollutants, simplifying both handling and disposal. Our teams maintain up-to-date REACH registrations and ensure every outgoing batch includes a complete regulatory profile.
Customers with environmental targets seek assurance about lifecycle impacts. Long-chain epoxides typically show better biodegradability than aromatic or halogenated analogs. Their residues break down more predictably under controlled waste treatment, reducing longer-term liability for formulators. We continue to support client efforts to certify finished goods under emerging eco-labels and voluntary assessment schemes.
Worker safety stands at the foundation of every successful plant operation. Our SDS documentation and training extend beyond paper requirements to include on-site visits and refresher courses by technicians who have mixed, pumped, and handled these chemicals themselves. This approach eliminates surprises on the factory floor and helps production managers keep their safety records incident-free.
Our R&D group remains committed to pushing the limits of what C16 epoxides can do. Innovations in catalyst technology and green chemistry hold the promise of even purer, more environmentally friendly pathways. We invest in closed-loop systems that cut solvent use, recycle unreacted starting materials, and minimize waste—practical steps that keep our competitive edge sharp while aligning with industry goals for cleaner, safer chemical production.
More customers are evaluating the benefits of long-chain 1,2-epoxides in new applications: medical coatings that require skin-friendly profiles, electronics encapsulation materials that resist humidity, and plant-based lubricants for greener mechanical operations. These requests push us to fine-tune each parameter—chain linearity, trace peroxide level, residual water content—because formulation errors on the micro-scale translate into big dollars when lines run 24/7.
Every advancement, from automation in distillation columns to the adoption of real-time in-line monitoring tools, arises from our day-to-day experience. Supporting clients through technical trials, responding to the inevitable hiccups of scale-up, and guaranteeing the same predictable material in every shipment remains at the core of our philosophy.
Serving as both a producer and long-standing partner, we believe that quality, transparency, and technical partnership remain more valuable than marketing promises. The story of 1,2-epoxyhexadecane—whether in surfactants, polymers, or lubricants—is written not by brochures but by steady improvements in purification, process control, and hands-on support to the chemical industry. The path forward will demand even tighter collaboration and more robust supply chain responses. As chemical markets evolve, the combination of technical know-how, experience-driven insights, and dedication to every lot shipped will continue to drive us—and our customers—toward greater efficiency, safety, and innovation.