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2-Ethoxy-3,4-Dihydro-2H-Pyran

    • Product Name 2-Ethoxy-3,4-Dihydro-2H-Pyran
    • Alias 2-Ethoxytetrahydropyran
    • Einecs EINECS 211-248-7
    • 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

    981531

    Iupac Name 2-Ethoxy-3,4-dihydro-2H-pyran
    Molecular Formula C7H12O2
    Molar Mass 128.17 g/mol
    Cas Number 7432-40-2
    Appearance Colorless liquid
    Boiling Point 160-162 °C
    Density 0.973 g/cm³
    Refractive Index 1.437
    Flash Point 51 °C
    Solubility In Water Slightly soluble
    Smiles CCOC1=CCCOC1
    Inchi InChI=1S/C7H12O2/c1-2-8-7-5-3-4-6-9-7/h3-4,7H,2,5-6H2,1H3
    Synonyms 2-Ethoxytetrahydropyran
    Melting Point -51 °C
    Vapor Pressure 2.3 mmHg at 25 °C

    As an accredited 2-Ethoxy-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 100g amber glass bottle with a tightly sealed cap, labeled "2-Ethoxy-3,4-Dihydro-2H-Pyran", includes hazard and handling information.
    Shipping 2-Ethoxy-3,4-Dihydro-2H-Pyran is shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It is transported under ambient conditions unless otherwise specified, with standard labeling for identification and hazard warnings. Shipping complies with local and international regulations for the transport of chemicals. Handle with care to avoid spills.
    Storage 2-Ethoxy-3,4-dihydro-2H-pyran should be stored in a tightly sealed container, under a dry and inert atmosphere such as nitrogen. Keep the container in a cool, well-ventilated area away from sources of ignition, moisture, acids, and strong oxidizers. Avoid direct sunlight and store at temperatures recommended by the manufacturer, typically at room temperature or below.
    Application of 2-Ethoxy-3,4-Dihydro-2H-Pyran

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

    2-Ethoxy-3,4-Dihydro-2H-Pyran serves as a specialty intermediate for various synthesis and protection steps in industrial organic chemistry. As the direct manufacturer, we supply this compound for downstream processes in pharmaceuticals, crop protection, specialty monomers, and fine chemical sectors. Below, we outline several key industrial scenarios and the associated technical integration details.

    1. Pharmaceutical Intermediate in API Synthesis

    This material supports the selective protection of hydroxyl groups during the multi-step synthesis of active pharmaceutical ingredients. Our clients use it to generate protected intermediates which facilitate cleaner reaction sequences, higher yields, and streamlined purification in mid- and late-stage synthesis for oral solid dosage manufacturing. Downstream, it is applied during scalable cGMP processing of antibacterial and antiviral compounds, following validated route-of-synthesis schemes governed by regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <941> Bulk Pharmaceutical Chemicals
    • EU EudraLex Vol 4, Part II GMP
    • FDA 21 CFR Part 211

    Typical usage ratio

    • 0.9–1.3 molar equivalents per target hydroxyl group, based on API synthesis protocols and impurity control requirements.

    Downstream process integration

    • Added during the protection phase after initial substrate activation but prior to condensation or cyclization steps in API route development.

    Final product types

    • Antiviral drug raw materials
    • Cephalosporin antibiotic intermediates
    • Custom pharmaceutical contract synthesis products

    2. Building Block for Specialty Monomers in Polymer Manufacturing

    Manufacturers in the specialty polymer sector incorporate this compound for monomer functionalization, particularly in the modification of polyacrylates and polyurethane prepolymers. It introduces cyclic acetal/protective functionalities that enable precise post-polymerization processing, enhancing material properties such as hydrophilicity and flexibility. Process engineers benefit from its controllable reactivity and compatibility with continuous or batch reactors for scale-up production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • EU REACH Regulation (EC) No 1907/2006
    • ASTM D256 Standard Test Methods for Plastic Materials
    • FDA 21 CFR 177.1680 (where final polymers may contact food)

    Typical usage ratio

    • 2–6 wt% relative to total monomer content, adjusted according to desired copolymer architecture and sequence distribution.

    Downstream process integration

    • Dosed into the monomer blend prior to initiation with radical or ionic catalysts, particularly in staged feed or block copolymer setups.

    Final product types

    • Functional acrylate copolymers used in biomedical coatings
    • Waterborne polyurethane dispersions
    • Custom resins for advanced adhesives

    3. Glycosyl Donor Protecting Agent in Carbohydrate Synthesis

    In carbohydrate synthesis, this compound acts as a protecting agent for glycosyl substrates, preventing unwanted side reactions during elaboration of oligosaccharides and glycoconjugates. It is particularly suitable for use in automated synthesizers and in high-throughput scale-ups, where purity and reaction efficiency are crucial. Downstream, our clients appreciate its compatible cleavage profile, which supports clean deprotection under mild acidic conditions without substrate degradation.

    Industry compliance standards

    • Pharmacopeia of the People’s Republic of China (ChP) for glycoconjugate APIs
    • USP <621> Chromatography for carbohydrate purity
    • ISO 17025 Laboratory Accreditation for analytical verification
    • GMP system audits for oligosaccharide synthesis

    Typical usage ratio

    • 1.0–1.2 equivalents per free hydroxyl, adjusted based on substrate complexity and glycosylation site accessibility.

    Downstream process integration

    • Introduced after core glycosyl moiety preparation, preceding donor/acceptor coupling in stepwise assembly protocols.

    Final product types

    • Therapeutic oligosaccharide APIs
    • Glycoprotein intermediates
    • Specialty carbohydrate reference standards

    4. Synthesis of Crop Protection Ingredient Intermediates

    Agricultural chemistry operations select 2-Ethoxy-3,4-Dihydro-2H-Pyran for the temporary protection of hydroxyl and amine functionalities in the synthesis of herbicide and fungicide active ingredients. Its use allows stepwise assembly and late-stage modification in pesticide technical-grade manufacture. This component supports compliance with ongoing registration requirements and batch reproducibility, key during scale transition from pilot to bulk production in regulated crop input supply chains.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Agricultural Pesticides
    • China Pesticide Registration Requirements (ICAMA)
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17034 Reference Material Producer Accreditation

    Typical usage ratio

    • 2–5 mol% based on the number of reactive functional groups in the pesticide precursor.

    Downstream process integration

    • Introduced after halogenation/aromatic substitution but prior to final deprotection and formulation in technical-grade active centers.

    Final product types

    • Technical-grade herbicide actives
    • Fungicide intermediates for seed treatment APIs
    • Pesticide custom synthesis reference samples

    5. Fine Chemical Synthesis for Fragrance and Flavor Intermediates

    Producers of high-value fragrance and flavor ingredients use this compound in the selective synthesis of cyclic acetals, improving stability and odor profile control. It aids in masking reactive aldehyde or ketone functionalities during multistep fine chemical synthesis, facilitating downstream deprotection and targeted modification. Analytical quality teams appreciate its process compatibility and minimal carryover, supporting finished material conformance with global standards for trace chemical residue.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredients
    • Food Chemicals Codex (FCC) for flavor delivery systems
    • ISO 9001:2015 for fragrance/fine chemical manufacturing
    • EU Regulation 1334/2008 on flavorings and certain food ingredients

    Typical usage ratio

    • 1–4 molar equivalents per aliphatic aldehyde intermediate, with ratios adjusted for scale and odor threshold control.

    Downstream process integration

    • Dosed directly into protection stages prior to condensation or Diels-Alder transformations in fragrance and flavor synthesis workflow.

    Final product types

    • Masked aldehyde aroma complexes
    • Ready-to-use fragrance oil bases
    • Encapsulated food flavor precursors
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