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2,3-Epoxy-1-Propanal

    • Product Name 2,3-Epoxy-1-Propanal
    • Alias Glycidol
    • Einecs 219-378-4
    • 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
    VTB
    Specifications

    HS Code

    686628

    Chemical Name 2,3-Epoxy-1-Propanal
    Cas Number 6054-89-1
    Molecular Formula C3H4O2
    Molar Mass 72.06 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.144 g/cm3
    Boiling Point 52-53 °C at 20 mmHg
    Melting Point -54 °C
    Flash Point 40 °C (closed cup)
    Refractive Index 1.418 at 20 °C
    Solubility In Water Miscible

    As an accredited 2,3-Epoxy-1-Propanal factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a secure screw cap, labeled “2,3-Epoxy-1-Propanal,” includes hazard symbols and safety information.
    Shipping 2,3-Epoxy-1-Propanal should be shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. It must be labeled as a hazardous chemical, protected from heat, light, and moisture, and transported according to local, national, and international regulations for hazardous substances. Use appropriate protective packaging to prevent leaks or spills.
    Storage 2,3-Epoxy-1-Propanal should be stored in a cool, dry, well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong acids, bases, and oxidizing agents. Store in a tightly sealed, appropriately labeled container, preferably under inert gas to prevent moisture uptake and polymerization. Follow all relevant safety regulations and use secondary containment where necessary to prevent spills or leaks.
    Application of 2,3-Epoxy-1-Propanal

    Applications of 2,3-Epoxy-1-Propanal in Industrial Manufacturing

    2,3-Epoxy-1-Propanal serves as a specialized reactive intermediate across several industrial value chains. We supply this raw material to established downstream producers who require its unique aldehyde-epoxide functionality for controlled synthesis, polymer modification, and fine chemical transformation. Below, we detail precisely how industry customers integrate our material into their finished product lines under real-world conditions.

    1. Pharmaceutical Intermediate Synthesis

    Producers of pharmaceutical actives and intermediates rely on 2,3-Epoxy-1-Propanal as an electrophilic building block during multi-step synthesis, particularly for constructing chiral or functionally dense molecules. The compound frequently features as a precursor during the alkylation or ring-opening stage, providing a scaffold for further molecular elaboration. Formulators adjust addition ratios based on substrate reactivity, product purity requirements, and scale-up considerations.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210 and 211)
    • ICH Q7 Guidelines for Active Pharmaceutical Ingredients
    • Relevant USP, Ph. Eur., or JP monographs (for intermediate purity/control only)
    • Drug Master File (DMF) reference protocols where required

    Typical usage ratio

    • Typically 0.2–2 molar equivalents per target molecule, adjusted according to reaction scale and purification efficiency. Lower ratios are used in high-yield cascade reactions; higher equivalents accommodate substrate excess to drive conversion.

    Downstream process integration

    • Raw material charging occurs during stage-specific nucleophilic addition or oxirane ring opening, usually under anhydrous conditions. Reaction is controlled with stoichiometric dosing via calibrated pumps or microreactor input; post-reaction, solution is neutralized and intermediates isolated by in-line chromatography.

    Final product types

    • Chiral amino alcohols
    • Antiviral or antifungal agent precursors
    • Key intermediates for semi-synthetic antibiotics
    • Custom fine chemical building blocks for contract research programs

    2. Waterborne Epoxy Resin Modifier

    Formulators in the coatings and adhesives sector use 2,3-Epoxy-1-Propanal as a chain extender and reactive modifier within waterborne epoxy resin systems. Its bifunctional epoxide and aldehyde groups allow precise tailoring of crosslink density and film properties, especially in low-VOC formulations or specialty applications where fine-tuned hardness and flexibility are required. Production plants monitor input levels and reaction timing based on resin solid content and end-user technical specifications.

    Industry compliance standards

    • REACH (EC No. 1907/2006) substance registration
    • ISO 9001:2015 certified QMS for resin and coatings manufacture
    • GB 18582-2020 (China mandatory standards for coatings, indoor)
    • ASTM D3960 (VOC Content of Paints and Coatings)

    Typical usage ratio

    • Incorporated at 0.5–3% by weight of total resin solids; level increases with desired crosslinking strength or for targeted adhesion improvement. Formulators may adjust down to 0.2% for applications requiring reduced yellowing or higher flexibility.

    Downstream process integration

    • Added post-emulsification, immediately prior to resin crosslinking stage via inline dosing, typically under high-shear agitation. Reacts with polyamine hardeners; chain extension is monitored via viscosity control and spectroscopic endpoint analysis.

    Final product types

    • Low-VOC architectural coatings
    • Automotive refinishing primers
    • High-performance flooring systems
    • Waterborne adhesive binders

    3. Biocidal Agent Synthesis

    Agrochemical and specialty chemical manufacturers integrate 2,3-Epoxy-1-Propanal as a synthetic route intermediate for producing advanced biocidal agents. Its epoxide group enables nucleophilic functionalization for constructing oxazolidine-based and other heterocyclic actives, providing controlled reactivity under mild process conditions to minimize byproduct formation. Quality assurance teams track source and batch consistency for regulatory review.

    Industry compliance standards

    • EU Biocidal Products Regulation (BPR, Regulation (EU) No 528/2012, Article 95)
    • US EPA FIFRA registration for biocide actives
    • ISO 14001:2015 environmental management for synthesis facilities
    • OECD guidelines for chemical testing and safety

    Typical usage ratio

    • 1.0–1.3 molar equivalents per functional group transformation, occasionally increased in iterative syntheses for efficiency at scale. Final input ratio depends on downstream chain length and product activity profile.

    Downstream process integration

    • Charged in controlled micro-reactor or batch system early in synthetic sequence for ring-closure reactions or aminoalkylation. Post-reaction stages include in-line extraction and distillation to purify the biocidal intermediate before formulation.

    Final product types

    • Oxazolidine-based microbicides
    • Bactericidal concentrates for water treatment
    • Disinfectant precursor blends
    • Industrial fungicide intermediates

    4. Specialty Flavors and Fragrance Ingredients

    Flavor and fragrance houses employ 2,3-Epoxy-1-Propanal as a synthetic aldehyde component for constructing high-impact aroma molecules, particularly where an epoxide ring confers unique olfactory profiles. Its controlled reactivity allows precise introduction of carbonyl moieties under mild, food-grade processing, vital for maintaining batch traceability and complying with international additive guidelines.

    Industry compliance standards

    • FEMA GRAS status (Flavor and Extract Manufacturers Association)
    • 21 CFR Part 172 Subpart F (US FDA) for synthetic flavorings
    • IFRA Standards for fragrance ingredient safety
    • ISO 22000:2018 food safety management during production

    Typical usage ratio

    • 0.01–0.1% w/w in concentrated aroma compounds, with lower limits for food-contact applications and higher ratios for specialty perfume bases. Regulatory and sensory panels oversee each batch-level adjustment.

    Downstream process integration

    • Undergoes aldehyde addition or epoxidation in flavor synthesis reactors at controlled temperature/pressure. Final product is fractionated, tested for odor purity, and blended into proprietary compounds or bases for customer-specific formulations.

    Final product types

    • Synthetic flavoring agents for beverages and confectionery
    • Fragrance intermediates for fine perfumery blends
    • Chemically defined aroma impact compounds
    • Specialty aldehyde notes for cleaning and personal care products
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    Certification & Compliance
    More Introduction

    2,3-Epoxy-1-Propanal: Insights from a Dedicated Manufacturer

    Understanding 2,3-Epoxy-1-Propanal from a Production Perspective

    As manufacturers, we rely on years of hands-on experience to keep 2,3-Epoxy-1-Propanal meeting strict quality standards. This compound, also called glycidyl aldehyde, plays a unique role among fine chemicals thanks to its highly reactive epoxide and aldehyde groups. In this industry, users often compare it against compounds like glycidol or glycidyl ethers, yet not every molecule offers the same range of possibilities that 2,3-Epoxy-1-Propanal brings to a lab bench or production line.

    Typical Model and Physical Specifications

    We focus on purity as the core of our production. Typical batches remain colorless and clear, with a faintly pungent odor. Purity often reaches above 98%, with water content kept below 0.5%. Our finished product generally shows a density near 1.05 g/cm³ at 20°C, with a boiling point roughly around 90–95°C (decomposition). Reactivity remains high, so extra care during storage and handling prevents polymerization or degradation. These are the technical details, but in production, even a small deviation in process control can diminish its value for downstream users.

    Value in Synthesis and Chemistry

    Chemists value 2,3-Epoxy-1-Propanal for its bifunctionality. You won’t find the same combination of an aldehyde and an epoxide in most other intermediates used in organic synthesis. Whether reacting through the aldehyde group or attacking the epoxide, researchers enjoy flexibility for introducing new architectures into target molecules. In practice, those who run pilot-scale reactions often observe that other similar compounds demand harsher conditions to reach the same transformations.

    In the pharmaceutical field, scientists consider it a clever building block for custom active ingredient synthesis. Owing to both reactivity and manageable volatility, early-stage R&D selects this material where selectivity and mild processing are must-haves. Experienced lab managers recognize how quickly impurity profiles can change when improper storage introduces moisture—quality assurance keeps a close eye on stability data batch after batch. That oversight benefits firms moving from preclinical development to more robust scale-up, as a process is only as reliable as its raw materials.

    Differences from Other Epoxy Compounds

    Familiar epoxides such as ethylene oxide or glycidol show significant differences from 2,3-Epoxy-1-Propanal, even though each contains a reactive three-membered ring. In production environments, technicians immediately notice a sharper odor and increased sensitivity to acidic or basic contaminants in glycidyl aldehyde. Using it in polyester or polyether modifications, for example, gives project chemists a direct route for molecular branching and crosslinking that’s tough to replicate with simpler epoxides.

    In direct comparison, the aldehyde group offers advantages in directing reactions toward specific products or in chain extension for specialty resins—a field that sees increasingly strict ingredient requirements. Downstream applications, such as carbohydrate derivatization, or formation of heterocycles, benefit not only from high reactivity but also from the ability to introduce key functional links under mild conditions. These differences have led some polymer chemists to use it in new UV-curable coating systems aimed at minimizing migration or enhancing adhesion. Experience shows the product handles well in pilot reactors designed for minimum exposure to moisture, but shows sensitivity to prolonged storage, which has prompted us to optimize our packaging protocol to maintain integrity throughout distribution.

    Workflow and Quality Control

    Our production team learned over time that tight control over feedstock purity determines final epoxide quality. Impurities such as water, trace metals, or peroxides often catalyze unplanned side reactions that deteriorate both product color and stability. Lab techs run regular spectrometric and chromatographic analyses to confirm batch quality. Deviations get caught early. Close coordination with freight specialists minimizes transit delays that could risk temperature excursions.

    We reinforce strict safety measures. 2,3-Epoxy-1-Propanal can be potent on skin contact or inhalation, and we’ve invested in modernized personal protection infrastructure and ongoing operator training. Our HSE coordinators engage with line workers to share safety learnings from near-misses and regular audits. Manufacturing quality comes from these day-to-day details, not just compliance numbers on a certificate.

    Storage and Stability Concerns

    Anyone handling 2,3-Epoxy-1-Propanal in bulk storage sees how varied storage conditions can cause material to yellow or form byproducts over just a few weeks. We adopted airtight, dark-glass container solutions based on performance in actual field tests, rejecting lower-cost plastics that allowed gradual degradation. Shipments travel with air-tight seals and desiccant packets, helping to keep impurities from entering the supply chain. Temperature-controlled logistics are not an option but a necessity for high-stakes applications—especially in high-purity requirements for advanced manufacturing. Over the years, our technical support teams have guided end users through best-in-class storage routines, saving not only product but reducing costly loss-of-batch issues in busy labs.

    Role in R&D and Commercial Production

    Custom synthesis outfits and R&D laboratories consistently demand materials that perform not only in small bench-top trials but across a growing range of scales. 2,3-Epoxy-1-Propanal has shifted from a niche intermediate in academic research to an essential choice for companies exploring innovative pharmaceutical, agrochemical, or specialty polymer pipelines. The dual function of its core structure—epoxide and aldehyde together—enables project chemists to design reactions with fewer steps and greener solvents. Opportunities to reduce waste or unsafe reaction conditions continue to push the material up the adoption curve in regulated industries.

    In actual manufacturing practice, labs value the ready-handling of the raw material as much as its chemical profile. The product’s volatility enables easy dosing, even in semi-automated continuous processing setups. Unlike some highly viscous intermediates, 2,3-Epoxy-1-Propanal flows and dispenses accurately, reducing the likelihood of dosing errors or equipment blockages. Time saved here means more reliable campaign output for contract manufacturing organizations under tight delivery schedules.

    End Uses: Pharmaceuticals and Specialty Polymers

    Pharma producers see clear benefits for tailoring smaller molecule drugs. The compound’s dual reactivity speeds up the introduction of key functional groups while avoiding extended or harsh processing sequences. Medicinal chemists can take advantage of this flexibility, building new scaffolds or attaching pharmacophores that often require tedious protection and deprotection steps if attempted using traditional alternatives. Feedback from pilot-scale runs often points to increased overall yield and reduced workload for downstream purification units—testament to a reagent that, when produced at high quality, makes a difference on the bottom line.

    In polymer science, research teams value 2,3-Epoxy-1-Propanal during surface functionalization or backbone modification work. Smaller-scale applications in customized coatings, adhesives, and elastomers benefit from precise control over molecular weight and introduction of new branching points. Technicians at our partner firms report a lower threshold for reaction onset compared to simpler epoxides, making formulation work more predictable in high-mix environments.

    Challenges in Process Optimization

    From a production standpoint, fine-tuning reactor conditions over hundreds of batches taught us that glycidyl aldehyde’s balance of reactivity and stability lies in careful management of temperature and pH ranges. Process scaling throws up new issues: milligram-scale success in R&D doesn’t always translate to hundreds of liters. Exothermic surges during addition steps or unexpected polymerization ruined more than one campaign before we established process controls with rapid quenching and in-line monitoring.

    Incorporating lessons from chemical engineering partners, we invested in automated addition systems and calorimetric sensors that respond to runaway conditions faster than manual checkpoints. This approach decreased rework rates and improved the consistency of our final bulks. We continue adjusting reactor passivation methods, aiming to extend equipment lifespans, reduce downtime, and keep maintenance overheads manageable.

    Customer Collaboration and Technical Support

    No intermediate works in isolation—collaboration with application specialists drives our commitment to ongoing product improvement. Customer pilot teams frequently send inquiries about handling, scale-up, and usage in untested formulations. Rather than offering generic answers, our technical staff maintain open feedback loops, sharing direct support through process guides, troubleshooting advice, and post-delivery QA follow-ups.

    We also receive practical feedback from regular users about bottlenecks in using 2,3-Epoxy-1-Propanal: demands for greater shelf life, easier transfer, and reduced environmental impact often appear near the top of the list. Rather than relying solely on periodic product updates, we integrate this insight into our continuous improvement programs. Live demonstrations, technician-to-technician peer calls, and on-site audits supplement printed documentation. Experience on both sides shows the fastest way to solve issues always comes from open lines of communication between maker and user.

    Solutions to Typical User Challenges

    End users sometimes run into handling issues, such as container gumming, color changes, or non-uniformity in overhead addition. We addressed these by upgrading fill lines and switching to inert gas headspace purging before seal. Early user trials showed that process bottlenecks often developed during transfer, so we worked with equipment suppliers to create custom dispensing attachments compatible with our packaging. This intervention delivered measurable improvements in material throughput and reduced product loss in high-volume applications.

    To combat degradation from minute acid traces, we integrated extra inline drying and purification steps, targeting contaminant levels below detectable limits. We also rolled out advance shipment notifications and expanded our logistics partner network, which has improved on-time delivery during periods of tight supply or holiday slowdowns. Whenever a trending issue surfaces—such as unusual side reactions in polymerization chemistry—the technical team organizes roundtable call-ins with affected customers and provides newly validated protocols, avoiding production delays and costly rework.

    Environmental Responsibility and Safe Disposal

    Responsible handling of 2,3-Epoxy-1-Propanal covers more than just in-process safety. Our environmental commitment calls for regular audits on both in-house and downstream disposal steps. Some clients expressed concerns regarding safe effluent treatment when dealing with trace organics and reactive aldehydes. Our response has included partnering with certified waste handlers and circulating clear guidelines for neutralization using approved aqueous reducing agents, greatly reducing hazardous residue output and improving regulatory compliance rates.

    Our R&D group continues to study process modifications that can limit byproduct generation at source, targeting greener chemistry pathways. As regulations evolve, our teams anticipate stricter limits on emissions and workplace exposures, so production processes adjust to meet and exceed those targets. It’s an industry-wide challenge, but an ongoing one that we address with updated practices and outreach.

    Continuous Improvement and Innovation

    Over time, market requirements for fine chemicals shift. Expectations for traceability, reproducibility, and sustainability become more rigorous. Every improvement in 2,3-Epoxy-1-Propanal manufacturing arises from direct observation—reactor runs, QA outliers, even end user complaints.

    Process innovation can start with small steps: updated instrumentation, or recalibration after surprise measurement drift in a plant batch. Large gains come from major upgrades, whether in digital tracking of production batches or from introducing predictive maintenance routines that flag equipment issues before they affect product. We take pride in applying lessons learned from decades of cumulative production cycles, aiming to serve users looking for greater reliability, consistency, and technical clarity.

    Future Directions: Meeting Changing Industry Needs

    As application landscapes change, experienced buyers and product developers look for sharper specifications, new packaging formats, and ready technical documentation. We regularly consult with downstream partners developing targeted pharmaceuticals, microelectronics materials, or advanced coatings. Their fast-moving projects demand input not just on the product, but on possible process risks, performance trade-offs, and new analytical controls.

    Working directly with these innovators, our process and R&D teams explore formulation trials and design collaborative pilot projects. Regular investments in laboratory tools and skilled personnel keep the pipeline open to new application fields. We keep a close eye on regulatory movement in all major markets, tuning compliance and traceability features to keep customers in good standing during audits.

    Closing Perspective

    Making 2,3-Epoxy-1-Propanal at a high, consistent benchmark isn’t just about formulas and equipment. It grows out of a practice grounded in real-world feedback, technical partnership, and an open-minded attitude to every step—from batch planning through to end use. That perspective underpins every shipment, every technical data sheet, and every support call our team takes. For users looking to advance their own processes, we aim to be more than a supplier: we see ourselves as partners in making each innovative application a practical reality.