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3,4-Dihydro-2H-Pyran

    • Product Name 3,4-Dihydro-2H-Pyran
    • Alias Dihydropyran
    • Einecs 203-950-6
    • 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

    679106

    Chemical Name 3,4-Dihydro-2H-pyran
    Molecular Formula C5H8O
    Molar Mass 84.12 g/mol
    Cas Number 110-87-2
    Appearance Colorless liquid
    Density 0.925 g/mL at 25°C
    Boiling Point 84-86°C
    Melting Point -88°C
    Refractive Index 1.448 at 20°C
    Flash Point -6°C
    Solubility In Water Slightly soluble
    Odor Ether-like odor

    As an accredited 3,4-Dihydro-2H-Pyran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100 mL amber glass bottle labeled "3,4-Dihydro-2H-Pyran, ≥99%". Features hazard pictograms and tamper-evident seal.
    Shipping 3,4-Dihydro-2H-pyran is typically shipped in tightly sealed containers to prevent leakage and evaporation, as it is volatile and flammable. It should be handled and transported in compliance with relevant regulations (e.g., DOT, IATA, IMDG), using appropriate hazard labels and documentation, and kept away from heat, sparks, and incompatible substances.
    Storage 3,4-Dihydro-2H-pyran should be stored in a cool, dry, and well-ventilated area, away from sources of ignition or heat. Keep the container tightly closed and protect it from moisture. Store separately from acids, oxidizing agents, and strong bases. Use only in a chemical fume hood and avoid prolonged exposure to air, as the compound may form peroxides.
    Application of 3,4-Dihydro-2H-Pyran

    Applications of 3,4-Dihydro-2H-Pyran in Industrial Manufacturing

    3,4-Dihydro-2H-Pyran serves as a valuable building block in multiple chemical manufacturing sectors, supporting efficient protection strategies, intermediate synthesis, and downstream value-adding processes. Our expertise as a direct producer ensures reliable supply and consistent quality aligned to precise industrial standards.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical manufacturers incorporate 3,4-Dihydro-2H-Pyran to protect alcohol functions during multi-stage API synthesis, particularly in the production of nucleoside analogs and macrolide antibiotics. As a temporary protecting agent, this compound ensures sensitive hydroxyl groups remain stable throughout rigorous downstream transformations and deprotections. Our material supports controlled, reproducible yields as demanded by mature GMP-regulated sites worldwide.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (API)
    • European Pharmacopoeia (Ph. Eur.) regulations on residual solvents and starting materials
    • US FDA cGMP 21 CFR Parts 210/211
    • Chinese Pharmacopoeia standards for pharmaceutical excipient quality

    Typical usage ratio

    • 1.05–1.2 molar equivalents per hydroxyl group to be protected, adjusted for substrate reactivity and stepwise synthesis demands

    Downstream process integration

    • Charged during the early-stage protection step in stepwise organometallic synthesis, usually in anhydrous solvents with an acid catalyst before further functional group manipulations and purification

    Final product types

    • Antiviral API intermediates (e.g., protected nucleosides for HIV/HBV drugs)
    • Protected macrolide antibiotic precursors (e.g., erythromycin derivatives)
    • Advanced pharmaceutical intermediate supplies for contract API manufacturing

    2. Agrochemical Intermediate Production

    Agrochemical formulators use 3,4-Dihydro-2H-Pyran in multi-step synthesis routes for crop protection agents, especially for compounds requiring selective functional group protection. Its controlled reactivity enables the preparation of protected alcohol intermediates, which downstream producers later deprotect to yield target pesticides, herbicides, or fungicides with improved handling and conversion efficiency.

    Industry compliance standards

    • FAO/WHO Technical Specifications for pesticide intermediates
    • REACH (EC 1907/2006) chemical safety requirements
    • ISO 9001:2015 certified quality management in agrochemical synthesis
    • Chinese National Standards (GB) for active ingredient precursors

    Typical usage ratio

    • Approximately 1:1 mole ratio versus alcohol to be protected; adjusted up to 1.3 equivalent for complete conversion in challenging matrices

    Downstream process integration

    • Used in a dedicated protection step within the intermediate plant; product then isolated and transferred for follow-up transformations such as halogenation, amidation, or ring closure before final deprotection

    Final product types

    • Pesticide active intermediates (e.g., protected hydroxyphenols, phenoxyacetic acid derivatives)
    • Pre-formulated herbicide intermediates
    • Seed treatment and crop coating additive components

    3. Fine Chemical Synthesis for Flavors and Fragrances

    The fine chemical sector employs 3,4-Dihydro-2H-Pyran for the targeted protection of alcohols in the stepwise assembly of synthetic aroma compounds and fragrance precursors. The controlled, selective reactivity safeguards oxidation-sensitive moieties, facilitating downstream aldehyde or acid formation without undesired side reactions. This protection is subsequently removed under mild acidic conditions to afford high-purity, low-residue formulations meeting global flavor additive standards.

    Industry compliance standards

    • IFRA (International Fragrance Association) guidelines
    • FDA 21 CFR 172.515 (Flavoring Substances and Adjuvants)
    • EU Regulation (EC) No 1334/2008 (Food Flavorings)
    • FEMA GRAS (Generally Recognized as Safe) evaluations

    Typical usage ratio

    • 0.95–1.15 equivalents per target alcohol functional group; optimized based on substrate and batch scale to limit residuals in finished aroma materials

    Downstream process integration

    • Introduced during the early formation of protected synthetic intermediates; protection removed via aqueous acidolysis before purification and compounding into final fragrances or flavors

    Final product types

    • Cyclohexanone-based fragrance ingredients
    • Naturally-inspired aroma intermediates (e.g., protected citronellol derivatives)
    • Complex flavoring agents for beverage and confectionery bases

    4. Custom Monomer & Polymer Synthesis

    Producers of specialty polymers and resins leverage 3,4-Dihydro-2H-Pyran to control reactive alcohol functionalities during the pre-polymerization stages of acrylate, vinyl, and oxirane-based materials. Protective group chemistry ensures precise control over polymer architecture and molecular weight distribution, enabling the design of advanced coatings, adhesives, and functional polymers with tailored application properties.

    Industry compliance standards

    • ISO 14001 (Environmental management for chemical manufacturers)
    • EU REACH for monomer registration and safety
    • ASTM D256 (Polymer impact resistance standards)
    • Japan Chemical Substances Control Law (CSCL) notification

    Typical usage ratio

    • 0.8–1.2 equivalents depending on the reactivity of the alcohol and subsequent polymerization sequence; fine-tuned to modulate reactivity during multi-monomer pre-assembly

    Downstream process integration

    • Protection step occurs prior to bulk polymerization; after polymer chain assembly, deprotection yields functional hydroxyl groups for subsequent cross-linking, curing, or end-group modifications

    Final product types

    • Functional resin intermediates with terminal hydroxy groups
    • Specialty adhesives for automotive and electronics applications
    • Custom acrylate and vinyl polymer materials for industrial coatings

    5. Laboratory and Pilot-Scale Synthesis Support

    Process development laboratories and custom synthesis units in the pharmaceutical, fine chemical, and material science fields routinely apply 3,4-Dihydro-2H-Pyran for the temporary masking of alcohol groups in multi-step synthetic campaigns. Its use supports rapid route scouting, impurity profile studies, and intermediate isolation—crucial for scaling new chemical entities and accessing specialized intermediates efficiently for further scale-up.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for non-clinical safety assessment
    • ISO/IEC 17025 (Laboratory competence accreditation)
    • Internal corporate HSE guidelines for handling protective agents
    • OECD Chemicals Test Guidelines for pilot synthesis

    Typical usage ratio

    • Ranges from 1.0 to 2.0 equivalents per hydroxyl function depending on experiment scale, desired conversion, and methodology under investigation

    Downstream process integration

    • Protection introduced at molecule design or early route exploration; subsequent process development cycles optimize removal and evaluate byproduct profiles prior to kilogram-scale validation

    Final product types

    • Research-grade protected intermediates for structure-activity studies
    • Process route candidates for commercial drug or agrochemical synthesis
    • Pilot-plant demonstration batches for downstream engineering studies
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    Certification & Compliance
    More Introduction

    3,4-Dihydro-2H-Pyran: The Unsung Backbone of Many Transformations

    The Product Behind Cleaner Chemistry

    Next time you walk through a pharmacy or use a cleaning product at home, you might not realize how deeply the success of those everyday essentials depends on a small, colorless liquid: 3,4-Dihydro-2H-Pyran, often labeled as DHP in the lab. We make this compound in our own facilities, day in and day out, following a process honed by decades of chemical manufacturing experience. The structure might look simple to the untrained eye—a six-membered ring with an oxygen atom that gives it a certain reactive spark. Yet DHP rarely emerges in the discussion outside synthetic chemists’ circles, even though it plays an essential role in shaping the way chemists protect and uncover new possibilities in organic molecules.

    Uniquely Positioned in Modern Synthesis

    DHP’s value has always been about its balance of reactivity and selectivity. In our plants, purity runs high and water traces are low—because for DHP, cutting corners translates into problematic side reactions. Many laboratories count on us to deliver material that won’t compromise yields or introduce unnecessary impurities. This level of reliability translates directly to the benchtop, where researchers need a reagent that consistently forms acetal or ketal protecting groups with alcohols, giving them the freedom to carry out tougher jobs downstream.

    Some protecting reagents work fast but leave behind stubborn by-products. Others demand harsh conditions, risking the integrity of sensitive molecules. DHP falls in a special category: it can be coaxed to form a tetrahydropyranyl (THP) ether with mild acid catalysis, typically at room temperature, and it reverses easily with acid and a little water. There’s minimal fuss, low color formation, and, most importantly, it hardly stirs up any side products that would muddy the next step. The neat circle of reversible reactivity is a testament to smart design—not a random fluke. Our process trims the peroxide and aldehyde content to trace levels, so you don’t have to wrestle with contaminants downstream.

    Far Beyond Lab Curiosity: Industrial Impact

    In large-scale manufacturing, small differences in reagent quality can snowball into inconsistent batches or, worse, entire shipments rejected by quality control. For DHP, issues like excess acidity, oxidative by-products, or even minor color traces all matter, and production teams have learned to respect these limits. Our reactors run under strict atmosphere control, and we use distillation techniques that squeeze out unwanted volatility. The result—steady, predictable results from kilogram batches to metric tons, always supported by certificates of analysis pulled from real batch data, not assumptions.

    Pharmaceutical chemistry is probably the area with the highest standards, often because a single impurity can block a regulatory filing. DHP repeatedly comes up as the protecting agent of choice, not because it is flashy, but because it adds a layer of confidence. It helps keep critical building blocks shielded, right up until the final stages of drug assembly, then slips away quietly during the unmasking stage—a process we have supported for clinical and process chemists both at small and large scales.

    Quality Beyond the Drum

    Practical issues sometimes slip through the cracks in pure research articles, but chemists in the production environment don’t forget them. Moisture absorption, peroxide formation during storage, and incompatibility with certain materials are all problems seen with poorly handled or low-grade DHP. We keep water content to a minimum (Karl Fischer analysis below 0.05%), and every drum is filled under nitrogen. Containers are tested for leachable interaction with DHP. Since even a few parts per million of water can slow down acetal formation or hydrolyze the product prematurely, these practices are necessary, not just luxury.

    Quality assurance teams know that color can be a quick warning sign of deeper trouble—usually degradation—and we monitor both initial and aged appearance. A transparent liquid might seem trivial, but minor yellowing could mean the beginning of a contamination chain that will echo down the process. Because DHP is volatile and a moderate peroxide former, we include stability data with each batch so users can plan storage rotation instead of just hoping their stock survives. Every reprocessed kilogram and every discarded drum due to low-grade source material represents cost, delay, and frustration—troubles we have learned to avoid through consistency and attention to the small details.

    Why Not Use Alternatives?

    Some chemists point to other protecting agents like methyl ethers, benzyl groups, or silyl derivatives. Each has its place. DHP’s THP group often wins for its gentle installation and removal: you don’t need large excesses or exotic catalysts, and you can usually recover valuable intermediates without the hard shock of hydrogenolysis, heavy metals, or fluoride salts. The ease of both application and reversal shaves days off method development, a huge asset when time and resources are tight. Plus, the waste streams generated from THP group removal typically pose fewer regulatory headaches than some organotin or chlorinated by-products.

    Another clear edge is tolerance. The THP protection offered by DHP stands up well against many oxidizing and reducing conditions, as well as mild bases. Strong acids or bases can remove the protection, but in our hands and those of our customers, DHP hits the sweet spot between robust protection and easy deprotection. That’s subtraction of complexity, not just swapping one set of issues for another. When you look for alternatives, most either tip the scale toward hard-to-remove or hard-to-install, or they cost significantly more both in purchase price and required purification steps.

    Handling and Safety: Hard Lessons Learned

    Safety is not just a checkbox on a regulatory form in our business. Exposure to DHP’s vapors can cause respiratory irritation, and its flammability means every batch comes out of the reactor into completely sealed, grounded systems. Over the years, we’ve learned the hard way that storing DHP in bulk near direct sunlight or in contact with air accelerates peroxide buildup, raising both handling and storage risks. Standard practice in our facilities now means periodic peroxide checks and pre-treatment with stabilizers, fully documented so customers can track the origin and chain of custody of every shipment.

    Small batch chemists often ask about the “right way” to store and transfer DHP, especially if they only open a container once every few months. Our advice, shaped by years of hands-on experience: transfer in a fume hood with dry, inert gas cover, use amber bottles to cut down on light exposure, and prep for use as soon as practical after opening. We use these same standards in our shipping departments, and it’s made the difference between repeated complaints and steady praise from some of the world’s most critical quality controllers.

    Real-World Uses: Where DHP Shows Its Value

    Synthetic organic chemistry, especially pharmaceutical and fine chemical synthesis, counts on reproducibility above all. Each protecting group must play its role perfectly, and DHP consistently picks up the slack in multi-step routes. In our production logs, protecting both primary and secondary alcohols for extended sequences comes up again and again: peptides, steroids, antibiotics, fragrances—THP ethers pop up in project after project, from blockbusters on the market to molecules still in the development pipeline.

    The correct DHP, at spec and delivered fresh, means those protecting groups work as promised every time. In specialty polymers and advanced materials, DHP comes in for strategic addition and removal of functional handles. Researchers scaling promising bench results to the pilot plant have relayed many stories of so-called “identical” DHP from outside sources causing color changes, reduced yields, or extended purification times. Through it all, our product line has provided the baseline that R&D, process, and production chemists expect—not just acceptable, but reliable enough to take through FDA audits and international plant inspections.

    Differences That Matter: DHP Versus the Crowd

    The market offers an increasing range of products under the general umbrella of protecting group chemistry. DHP’s competitors include tetrahydrofuran, 1,3-dioxolane, and even isopropylidene acetal reagents. What usually separates DHP, and our particular batches, is the combination of moderate activation energy, compatibility with numerous functional groups, and ease of downstream removal. Many alternatives either need stronger acid or base, or produce more persistent impurities that complicate workups. For customers synthesizing sensitive or highly functionalized intermediates, every side product matters—our refinements and real-world batch experience translate directly into cleaner results.

    Other sources often cut corners on drying or try to market solvent-grade DHP as reagent quality. We stick to higher standards: water, aldehyde, and peroxide control, proof-of-origin, and traceability built into every batch record. Every outgoing drum is tied to in-process QA, and our team reviews every result before sign-off. This attention to production integrity is what separates factory producers from simple repackagers or traders. In our experience, the best way to guarantee reliable chemistry downstream is to start with material whose history and technical profile match the original order, every time.

    Specification Snapshots: What the Right DHP Looks Like

    While ultimately the molecule itself carries the bulk of the value, specifications matter in ways that show up clearly in plant performance and customer feedback. Good reagent-grade DHP should arrive as a clear, colorless to very pale yellow liquid, free from suspended solids, and with a faint, unobtrusive odor. Boiling point hovers around 83–85 °C under atmospheric pressure. Specific gravity and refractive index also serve as routine checkpoints, and we calibrate our equipment to detect drift in either for every production cycle.

    Purity sits above 99%, usually monitored by gas chromatography using calibrated standards. Peroxide readings come in below 0.001%, as peroxide buildup signals either production or storage problems. We test aldehyde content regularly; even traces can influence downstream reactions and color. Customer requests sometimes call for custom batch splits or specialty packaging—small glass bottles for research labs and steel drums for bulk process use—so we maintain flexible production and filling lines that keep pace without losing quality control.

    Future-Proofing DHP: Regulatory and Sustainability Considerations

    Regulatory scrutiny never stops, and we keep ahead by periodic review of emerging environmental regulations, both within our own region and for international destinations. DHP, like most reactive intermediates, runs afoul of strict air quality rules if handled loosely. Our closed handling systems, solvent recovery loops, and container tracking guide each drum from production through delivery, limiting fugitive emissions and minimizing waste. As a chemical manufacturer, we know regulators look for evidence of control, not just promised compliance. Every year brings updated documentation and periodic audits, so our team cycles through process risk reviews and operator training as an everyday discipline.

    Demand for more sustainable batch operations is rising, even for classic reagents like DHP. We’ve trimmed our waste streams, recycled process solvents, and shifted toward greater energy efficiency in distillation and purification lines. Every kilogram saved or recycled means one less kilogram ultimately shipped off for disposal, and our clients—especially those in regulated markets—increasingly ask for audit data and environmental impact statements as part of their supplier reviews. We keep our focus on both short-term performance and long-term site stewardship. Chemists who use our DHP for process development often want to know how it stacks up from a carbon footprint perspective; providing transparent lifecycle snapshots now frames our monthly discussions with clients.

    What We’ve Learned From Years of Manufacturing DHP

    DHP may be a small molecule, but it’s taught us important lessons about batch consistency, quality, and customer needs. We’ve adjusted reactor sizes, improved in-line drying, and scaled analytical checks based on feedback from users in the field. Some early users pushed our technical team for lower residual solvent limits, others demanded documentation on residual metals. We take these requests seriously: the best manufacturing relationships happen when someone on the line knows who’s receiving the next shipment and why small differences matter.

    Clients sometimes ask why our DHP consistently avoids the headaches they’ve had with others—clogged lines, sticky residue, odd color shifts. The answer lies both in production discipline and in a willingness to listen: every reported complaint, whether from a researcher synthesizing micrograms or a production site scaling up to metric tons, feeds into the next batch run. Over time, all these adjustments have made our DHP sharper and more fit for purpose than what’s available from casual repackagers or bulk commodity traders.

    Looking Beyond Specification Sheets

    We don’t consider our job finished just because a batch cleared the final analysis. Supporting DHP means continuing technical assistance—troubleshooting unexpected downstream issues, adjusting pack size, updating safety procedures in response to new regulatory guidance, or providing real-time QA results for urgent shipments. Whether DHP is protecting a precious alcohol in a flagship pharmaceutical or serving as a sturdy tool in the hands of a research chemist, its value hinges on how well it performs day after day, batch after batch.

    In the end, a manufacturer’s perspective adds a layer of respect for the compound itself—not just as another product, but as an enabler of cleaner, safer, and more efficient chemistry. Our DHP holds its ground through process rigor, hard-won experience, and a clear track record of helping chemists do their best work with the least amount of friction. This isn’t just about selling a drum of liquid; it’s about guaranteeing a result, a method, and a promise that every drop carries forward the legacy of serious, responsible manufacturing.