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Trans-2,3-Epoxybutane

    • Product Name Trans-2,3-Epoxybutane
    • Alias trans-2,3-Butylene oxide
    • Einecs 205-523-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    419266

    Cas Number 15149-10-7
    Iupac Name trans-2,3-Epoxybutane
    Molecular Formula C4H8O
    Molar Mass 72.11 g/mol
    Appearance Colorless liquid
    Boiling Point 63-65°C
    Density 0.831 g/cm3
    Refractive Index 1.399
    Flash Point -10°C
    Smiles C/C1OC1/C
    Pubchem Cid 13586
    Solubility In Water Slightly soluble
    Canonical Inchi InChI=1S/C4H8O/c1-3-4(2)5-3/h3-4H,1-2H3/t3-,4+
    Melting Point -102°C

    As an accredited Trans-2,3-Epoxybutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Trans-2,3-Epoxybutane, 500 mL: Supplied in an amber glass bottle with a tight-sealing cap, featuring a hazard-labeled chemical-resistant label.
    Shipping Trans-2,3-Epoxybutane is shipped as a flammable liquid under well-ventilated conditions, in tightly sealed, suitable chemical containers, and in accordance with relevant hazardous material transport regulations. Proper labeling, documentation, and packaging are required. It should be kept away from heat sources, sparks, and incompatible substances during transit.
    Storage Trans-2,3-Epoxybutane should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong acids, bases, or oxidizing agents. Protect from moisture and ignition sources. Proper labeling and secondary containment are recommended. Only trained personnel should handle and store this volatile, flammable chemical.
    Application of Trans-2,3-Epoxybutane

    Applications of Trans-2,3-Epoxybutane in Industrial Manufacturing

    We supply high-purity trans-2,3-epoxybutane for established industrial sectors where its reactive epoxide group delivers value in precision synthesis, specialty polymerization, and advanced intermediate manufacturing. The following sections outline typical downstream applications in leading manufacturing segments, including regulatory requirements, process integration, specific compositional ratios, and common end product categories from real industry practice.

    1. Pharmaceutical Intermediate Synthesis

    Trans-2,3-epoxybutane serves as a targeted building block for synthesis of specific chiral pharmaceutical intermediates, where its oxirane ring facilitates regioselective ring-opening reactions for beta-amino alcohol or beta-hydroxy derivative formation. Process chemists in APIs and fine chemical segments use this epoxide for the introduction of functional groups at the controlled stereochemistry required by regulatory filings, as well as in the preparation of optically active intermediates for cardiovascular and antiviral compounds.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) purity requirements
    • USP <823> for radiopharmaceuticals, applicable if used in labeled drug synthesis
    • REACH registration for supply in the European Union

    Typical usage ratio

    • Used at 0.02–0.10 molar equivalents relative to amine or alcohol nucleophile
    • Adjusted based on stoichiometry and required reaction yield for batch or continuous processes

    Downstream process integration

    • Charged during nucleophilic addition stage of multi-step API synthesis
    • Dosed in jacketed glass-lined reactors with control of reaction temperature and pressure
    • Followed by controlled workup and product extraction for further purification

    Final product types

    • Chiral beta-amino alcohols for antiretroviral drug synthesis
    • Intermediates for cardiovascular drug synthesis
    • Precursors to specialty pharmaceutical active substances
    • Custom-designed fine chemical intermediates for CRO and CDMO clients

    2. Epoxy Resin Modifier for Advanced Composites

    Chemical manufacturers use trans-2,3-epoxybutane as a chain extender or reactivity modifier within advanced epoxy systems intended for aerospace-grade composites, electrical laminates, and specialty coatings. Its shorter alkyl backbone imparts improved toughness, flexibility, and controlled cross-link density in the resulting thermosets, while reaction kinetics can be tuned by varying process conditions and resin formulations to meet end-user technical requirements.

    Industry compliance standards

    • EN 60243-1 for electrical insulating materials (Europe)
    • ASTM D1651 and D1763 for epoxy resin modification
    • RoHS Directive (EU) for finished electronic and aerospace components
    • UL 94 flammability requirements for plastics

    Typical usage ratio

    • 1–6 weight % relative to total epoxy blend
    • Adjusted for resin/filler ratios and targeted glass transition temperature (Tg)
    • Lower ratios used in high-modulus, high-temperature applications

    Downstream process integration

    • Introduced during initial mixing of base epoxy resin and reactive diluent phase
    • Incorporated prior to cure catalyst addition to control network structure
    • Direct addition via metering pumps in continuous resin production lines

    Final product types

    • Aerospace composite parts (structural panels, interior components)
    • Electrical circuit board laminates
    • Flowable floor coatings
    • Specialty adhesives requiring enhanced impact resistance

    3. Fine Flavor and Fragrance Intermediates

    In the specialty fragrance and aroma industry, trans-2,3-epoxybutane is valued as a precursor for assembling complex oxygenated molecules used in unique flavor creation. Manufacturers exploit its electrophilic center to build lactone, ester, or hydroxy structure scaffolds essential for fresh, fruity, or green notes, while consistent product identity facilitates reproducibility and quality for global food and fragrance brands.

    Industry compliance standards

    • IFRA Code of Practice for safety and allergen labeling
    • Food Chemicals Codex (FCC) for applicable flavor intermediates
    • EU Regulation (EC) No 1334/2008 on flavorings
    • ISO 9235 for natural and synthetic aromatic raw materials

    Typical usage ratio

    • 0.015–0.080 molar equivalents relative to aldehyde or alcohol reactants
    • Ratio set according to desired yield, target sensory profile, and side-product minimization

    Downstream process integration

    • Fed during epoxide ring-opening with Grignard, alcohol, or acid species
    • Used in batch or semi-continuous coupling processes
    • Workup includes distillation and chromatography to isolate pure organoleptics

    Final product types

    • Green-note aroma intermediates
    • Fresh/fruity flavor ingredients for beverages, confectionery, and bakery
    • Lactone precursors for luxury perfumery
    • Functionalized fragrance bases for detergent and air care markets

    4. Agrochemical Synthesis Building Block

    Active agrochemical manufacturers rely on trans-2,3-epoxybutane as a compact epoxide input in the synthesis of heterocyclic intermediates for some herbicides and growth regulators. Technical teams use its reactivity to construct complex carbon frameworks by ring-opening with nucleophilic species, supporting the tailored synthesis of selective actives for commercial crop protection products.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for agricultural pesticides
    • ISO 9001 quality management system (for technical-grade synthesis plants)
    • REACH (EC 1907/2006) registration where placed on the EU market
    • National pesticide act compliances (e.g., US FIFRA GMP for inputs used in USA)

    Typical usage ratio

    • 0.025–0.12 molar ratio vs. target nucleophile, as per synthetic step
    • Adjusted by desired throughput, product batch size, and downstream dilution strategy

    Downstream process integration

    • Dosed in closed-system reactors during construction of heterocyclic structures
    • Charged directly after pre-mix or catalyst introduction, temperature controlled
    • Streamlined for automated, multipurpose synthesis lines

    Final product types

    • Herbicide intermediates for broadleaf control products
    • Selective plant growth regulator building blocks
    • Specialty safener intermediates for crop tolerance formulations
    • Fine chemical inputs for biorational pesticide actives
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    Certification & Compliance
    More Introduction

    Trans-2,3-Epoxybutane: A Manufacturer’s Perspective on Its Value and Application

    As a chemical manufacturer with decades invested in producing specialty epoxide intermediates, we’ve watched product requirements shift with each new wave in downstream industries. Trans-2,3-Epoxybutane stands out in that evolution. Known to many as 2,3-epoxy-2-butene, its formula C4H6O sets it apart from other small epoxides like ethylene oxide or propylene oxide. The experience behind its production, much like the compound itself, reveals subtle challenges and significant advantages that only consistent, hands-on work can bring to light.

    Characteristics and Production Realities

    Trans-2,3-Epoxybutane can’t be mistaken for a bulk commodity. Its rings are tight, with a specific trans configuration giving it unique reactivity and selectivity. We regularly achieve liquid product of high clarity, with a purity exceeding 99%. Our controlled processes keep moisture below 0.1%. This strict specification comes from lessons learned: even trace water content triggers ring opening, compromising both yield and the user’s process reliability. Small changes during synthesis—like catalyst selection or temperature profile—alter isomer ratios. Therefore, we’ve stuck with a proprietary multi-step epoxidation approach built for consistency at scale.

    Our operation never cuts corners on packing either. Trans-2,3-Epoxybutane reacts with acids, water, and some common polymers. Epoxy-specific drums, lined to prevent contamination, keep product stable for transport and longer storage. Shipment often goes straight to project sites or custom formulators, bypassing extensive warehousing, more due to customer demand than any intrinsic instability of the material.

    What Makes This Epoxide Different?

    We’ve synthesized and, more importantly, worked through production bottlenecks for the major epoxies and oxiranes. Ethylene oxide carries hazardous vapor pressure, often demanding elaborate containment. Propylene oxide dominates in polyurethane and glycols, but misses key selectivity for chiral or fine synthesis tasks. Cis-2,3-Epoxybutane offers different spatial orientation, leading to alternate reactivity, but in practice, trans-2,3 is favored for certain syntheses, especially where the geometry impacts downstream catalysis or pharmaceutical building block integrity.

    Veteran users ask about the racemic mixture, but our batches maintain trans-selectivity above 99% because downstream complexity climbs fast with isomeric contamination. In pilot projects for agrochemical derivatives, one group using commodity-grade mixes hit yield and separation losses that didn’t show up once they shifted to our trans-pure supply.

    Where Trans-2,3-Epoxybutane Gets Used

    Customers drive the merit of our product. Pharmaceutical chemists gravitate to trans-2,3-epoxybutane for building chiral intermediates—particularly when the subsequent ring opening demands controlled regioselectivity. Agrochemical teams point to its behavior in heterocycle synthesis, benefiting from the strained ring while sidestepping the overactivity seen in other short-chain epoxides.

    Specialty polymer makers push us for purity and minimal color, as off-stoichiometry shows immediately in batch variability. With over 15 years supplying trans-2,3-epoxybutane for academic research, we saw early attempts in epoxy resin R&D stall until researchers traded up from lower-grade isomeric blends. In collaboration with advanced materials startups, we’ve observed that the targeted geometries of trans over cis in their requirements have led to cleaner reaction profiles. The epoxide ring preserves reactive handles, reducing byproducts in multi-step syntheses.

    The Day-to-Day of Handling and Consistency

    Producing this compound involves more than just following standard epoxidation practices. During scale-up, ring closure triggers exothermicity that only robust thermal control avoids. We tune addition rates and agitation to keep isomer ratios predictable and batches safe. Solvent traces get removed by careful distillation, taking care that elevated vacuum doesn’t lead to polymerization or unpredictable ring opening. Our operators know from experience: slow steps, regular in-line checks, no hope for shortcuts.

    Customers who use trans-2,3-epoxybutane in fine synthesis processes need to avoid residual metallic or organic catalyst traces. Through years of iterative improvement, we’ve achieved analytical breakdowns showing contaminants below detectable limits after distillation, supporting even the most sensitive pharmaceutical or electronic chemical applications. For packaging lines, we monitor drum liners for reactivity, shifting vendors when even minor incompatibilities appear.

    Real-World Issues and Solutions

    Stability concern comes up in new user onboarding. Trans-2,3-epoxybutane, like many strained cyclic ethers, resists degradation under clean, dry conditions. We run real-time stability tests on retained lots, confirming six-month and twelve-month product integrity at standard storage conditions. The main threat remains unexpected acid ingress or trace water. Field feedback once flagged a supplier warehouse with humidity control lapses; split samples revealed hydrolytic ring opening. Now, logistics teams get tailored guidelines and sealed labeling for every drum.

    Batch-to-batch performance matters most for scale-up partners. Each production cycle draws on tight analytical controls, with GC and NMR tracing both isomer purity and non-volatile residues. Streamlined communication between our lab and end-user technical contacts weeds out issues before product reaches site. Sometimes, an R&D chemist’s new downstream route identifies subtle impurities. We’ll sit down, match spectra, and dial in purification steps—not just for that batch, but as part of an ongoing process evolution.

    Comparisons to Alternative Epoxides

    In terms of reactivity, trans-2,3-epoxybutane threads a line between universal and specialized. Ethylene oxide serves big industries where cost and abundance matter most. Propylene oxide finds utility in flexible foam and glycols. For those targeting cycloaddition or regioselective functionalization, our product wins key points. While glycidol and epichlorohydrin open new possibilities, their handling risks and chlorinated profiles add cost and environmental concern. From our vantage point, trans-2,3-epoxybutane achieves a sweet spot: small enough to ensure fast reaction kinetics, large enough to influence stereochemical outcomes in organic synthesis.

    Customers sometimes request both trans and cis isomers for academic comparison studies. Our experience shows that for processes requiring nucleophilic opening, stereochemistry governs yield and selectivity downstream. The trans isomer, with its predictable geometric constraints, allows tighter process window control. We get calls from researchers after failed attempts to substitute propylene oxide—the lower steric hindrance and lack of defined geometry in those analogs just doesn’t translate to matched selectivity or product purity.

    Building Trust through Traceability and Openness

    Complex chemicals build relationships, not just sales. Over the years, customers in pharmaceuticals, specialty coatings, and agrochemical intermediates trust our traceability, knowing every batch links back to archived analytical runs. When a client switched suppliers to chase price before, their downstream process soon ran into variability and actual cost overruns. We stepped in, shared spectra, production parameters, and batch protocols, helping them regain their footing. That incident reinforced our approach—transparency on process, real chemical knowledge, and no hiding issues if they arise.

    We’ve faced regulatory checks and technical audits, always opening our process logs and analytical records. Continuous learning has driven process improvements, not just for output volumes but also for byproduct minimization, worker safety, and waste handling. A consistent regulatory framework doesn’t just build compliance; it enriches how we understand this chemistry in the real world.

    Safety Insights from Years on the Floor

    Trans-2,3-Epoxybutane earns respect from everyone who handles it. The epoxide group means gloves and ventilation, common sense for seasoned chemical operators. In our own facilities, accidents typically tie back to lapses in standard operating procedures, reminding all of us that the little details—drum tightness, sampling valve checks, site walkthroughs—make all the difference. We put equal care into guiding end users: site training, proper labeling, and walking them through safe handling whether for R&D or scaled-up commercial runs.

    Hazard data doesn’t substitute for real-world discipline. Liquid-tight gloves, chemical goggles, and local exhaust—these aren’t suggestions but expectations built through routine and practice. Security seals and tamper detection now form part of each outgoing shipment, based on feedback from transport partners who noticed warehouse pilferage risks with high-value reactives.

    Challenges and Looking Ahead

    Every year, sourcing raw materials for epoxidation grows more competitive, especially as market dynamics shift with energy, feedstocks, and international regulations. We’ve learned not to rely on a single supply chain. Maintaining diverse, qualified partners secures uninterrupted transfers even when geopolitical or natural disruptions arise elsewhere. For sustainability, efforts move beyond compliance to proactive waste reduction and energy recycling on site, lowering emissions while ensuring economic and operational stability.

    Advanced applications keep pushing the boundaries. Recently, we’ve observed increased demand from catalyst manufacturers and specialty pharmaceutical developers. Their questions have become more sophisticated—they request documentation not just on purity but also spectral data, kinetic profiles, and reaction conditions. To keep up, we maintain an R&D team dedicated to both customer support and process development, running test reactions in parallel with clients’ teams to troubleshoot or optimize new routes.

    Lessons from Collaborations and Customization

    Seeing a client’s project evolve from lab notebook sketch to commercial-scale batch offers the kind of satisfaction many outside manufacturing might not appreciate. A recent partnership with a startup chemist brought forward a new nucleophile ring-opening methodology. Their initial results on commercial samples from generalized suppliers showed mixed yields and inconsistent stereochemical outcome. Switching to our tighter-spec, trans-pure batch led to reproducible results, moving the project along to investor-stage pilot. Situations like these remind us how upstream attention to detail pays dividends all down the line.

    Product modification requests also arrive, from dehydration requirements to additional stabilizer inclusion. Each adjustment takes practical experimentation; relying solely on theory often misses the subtle impacts unforeseen during scale-up. We invite partners to witness these changes, auditing process changes and learning alongside our crews. The combined effect builds cross-discipline respect rarely found outside hands-on manufacturing.

    The Importance of Industrial Temperament

    Years of operational work with trans-2,3-epoxybutane have shown that reliability doesn’t come from automated controls alone. Personnel with experience, accountability, and a willingness to share real observations raise a plant’s standards. If a foreman notices a faint color change, or an operator at the distillation skid detects odd vapor behavior, quick action often resolves emerging issues before they move further. These human elements—combined with targeted analytics—create the backbone of true quality assurance.

    Discussions with customers go well beyond product certificates. Questions about reaction temperatures, mixing times, or cleaning protocols receive straightforward answers, born from trial and correction rather than theory alone. Detailed logbooks and photographic evidence support any claims, showing respect for both our process and the chemists downstream who depend on us.

    Continual Improvement and Industry Direction

    Specialty epoxides, including trans-2,3-epoxybutane, get shaped continually by industry direction—toward greener input methods, closed-loop waste controls, and advanced analytics. We now dedicate resources to minimizing energy spent during ring closure and separation steps. Automation in analytics continues to help, but never fully replaces the insight from seasoned hands—especially when unexpected assay results show up. Working closely with regulators and sustainability-motivated partners, we trial lower-carbon epoxidation catalysts and solvent recycling.

    The finest customers keep us honest. They run challenging reactions, document every impurity, and often push for more from each batch. We value this approach, reciprocating with open technical support and willingness to adjust lot specifications as needed. Sometimes, a single lot reveals a new instrumental artifact; instead of evasion, we dig in and figure out both cause and correction, keeping the door open for improvement from both sides.

    Final Thoughts

    Producing trans-2,3-epoxybutane, we see the results show up in improved pharmaceutical intermediates, more reliable specialty polymers, and advanced agricultural chemicals made cleaner and more efficiently. Each drum carries a story—hands-on synthesis, incremental process improvement, and direct collaboration with those who use it every day. Unlike more routine commodities, this product thrives on exacting standards and earned trust. That trust isn’t won through marketing but through daily commitment: handling challenges as they arise, communicating with transparency, and always backing up product claims with facts from the lab and production line.

    In our experience, trans-2,3-epoxybutane will keep finding new uses as fine chemical synthesis grows more precise. As manufacturers, the best contribution we offer is not just consistent, selective product, but ongoing partnership in every aspect of its use—from safe delivery to scale-up troubleshooting and beyond. The work continues, backed by real records and the knowledge built only on production floors, helping customers build, test, and refine the next wave of chemical innovation.