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Isomannide

    • Product Name Isomannide
    • Alias 1,4:3,6-dianhydro-D-mannitol
    • Einecs 204-821-7
    • 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

    237935

    Cas Number 24155-42-8
    Molecular Formula C6H10O4
    Molar Mass 146.14 g/mol
    Appearance White crystalline solid
    Melting Point 64-66°C
    Solubility In Water Soluble
    Boiling Point Decomposes before boiling
    Density 1.54 g/cm³
    Synonyms 1,4:3,6-Dianhydro-D-mannitol
    Structure Bicyclic diol (isomer of isosorbide)
    Chemical Family Sugar alcohol, dianhydrohexitol
    Odor Odorless

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

    Packing & Storage
    Packing A white, sealed HDPE bottle labeled "Isomannide, 100g", with hazard pictograms, lot number, and safety instructions printed on the label.
    Shipping Isomannide should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically transported as a stable, non-hazardous solid at ambient temperature. Ensure the package is clearly labeled, handled with appropriate personal protective equipment, and complies with regional and international shipping regulations for chemicals.
    Storage Isomannide should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed when not in use to prevent moisture absorption and contamination. Store at room temperature and avoid excessive heat. Ensure proper labeling and compliance with local regulations for chemical storage.
    Application of Isomannide

    Applications of Isomannide in Industrial Manufacturing

    Isomannide, a bicyclic diol derived from renewable carbohydrate sources, delivers essential structural and functional benefits in multiple high-value industrial formulations. As the original manufacturer, we support global downstream partners in strict compliance with quality systems and exacting processing requirements. Below, we detail primary commercial application scenarios, specific compliance frameworks, precision formulation practices, and process integration considerations for successful downstream production.

    1. Biodegradable Polyesters for Packaging Materials

    Producers of next-generation biodegradable packaging incorporate isomannide as a key diol component in aliphatic polyester synthesis, using it to introduce rigidity, tune crystallinity, and enhance hydrolysis profiles. The material consistently enables transparent films and thermoformable substrates with targeted compostability characteristics. Formulators adjust isomannide input to balance performance and regulatory requirements across rigid trays and flexible wraps.

    Industry compliance standards

    • EU Regulation (EC) No 1935/2004 on materials and articles intended for food contact
    • FDA 21 CFR 177.1630 for polyesters intended for packaging
    • EN 13432:2000 for requirements of packaging recoverable through composting and biodegradation
    • ISO 17088:2021 for specifications of compostable plastics

    Typical usage ratio

    • 10–30 mol% in the diol component of the polyester synthesis; ratio adjusted based on mechanical and degradability targets

    Downstream process integration

    • Directly fed into melt polycondensation reactors during polyester backbone formation
    • Incorporated alongside aliphatic diacids and comonomers before film extrusion or sheet molding

    Final product types

    • Compostable food trays and clamshells
    • Biodegradable shopping bags and produce films
    • Flexible wrapping films for dry goods
    • Disposable cutlery and straws

    2. Polycarbonate-Based Engineering Plastics

    Manufacturers of high-transparency, BPA-free polycarbonate resins use isomannide for its distinctive rigid backbone, which increases glass transition temperature and yields polymers with improved dimensional stability. Its stereochemical configuration supports the addition of renewable content within engineering polymers for applications such as medical devices and optical discs, where clarity and durability are critical.

    Industry compliance standards

    • ISO 10993 biocompatibility (medical applications)
    • USP Class VI for plastics used in biological and medical devices
    • REACH Regulation (EC) No 1907/2006 for substances in articles
    • UL 94 flammability standards for plastics

    Typical usage ratio

    • 15–40 mol% of total diol content in melt polycondensation, depending on desired optical clarity and heat performance

    Downstream process integration

    • Incorporated during phosgene-free polycarbonate transesterification reactions
    • Used as a co-monomer with diphenyl carbonate and other diols prior to extrusion or injection molding

    Final product types

    • Optical storage media (CDs, DVDs, Blu-ray discs)
    • Laboratory and surgical instrument handles
    • Transparent machine safety shields
    • Medical tubing and device housings

    3. Eco-Friendly Plasticizers for PVC Compounds

    Plasticizer formulators in the wire & cable and coated fabric sectors select isomannide-based esters as effective non-phthalate alternatives to conventional plasticizers, prioritizing low migration and reduced volatility. These bio-based plasticizers increase permanent flexibility while ensuring long-term performance in demanding interior and exterior applications, and are compatible with both general-purpose and specialty PVC formulations.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 Annex XVII—restriction on phthalates
    • RoHS Directive 2011/65/EU on hazardous substances
    • EN 50363-3 for insulating and sheathing materials of electrical cables
    • IEC 60811 for physical testing of insulating and sheathing compounds

    Typical usage ratio

    • 25–60 phr (parts per hundred resin) blending level in vinyl compound formulations; optimized based on mechanical and migration test results

    Downstream process integration

    • Esterified from isomannide and fed into PVC mixing and plastisol preparation lines
    • Blended with PVC resin and stabilizers, then processed through calendaring or extrusion

    Final product types

    • Flexible electrical cable insulation
    • Synthetic leather upholstery and wall coverings
    • Coated tarpaulins and conveyor belts
    • Protective film for construction materials

    4. Polyurethane Systems for Performance Coatings and Elastomers

    Isomannide is chosen by polyurethane formulators for its rigid diol structure, producing elastomers and coatings with elevated modulus and controlled hydrophilicity. Manufacturers serving the automotive, electronics, and specialty flooring markets utilize it to engineer thermoset and thermoplastic polyurethane systems that meet precise durability and sustainability requirements, especially where hot-cast or waterborne technologies apply.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer manufacturing
    • ISO 12944 for protective coatings
    • RoHS and REACH compliance for E&E coatings
    • DIN EN 15651 for construction sealants

    Typical usage ratio

    • 5–30 mol% of the polyol mixture in prepolymer or one-shot systems; percentage fine-tuned for flexibility and abrasion control

    Downstream process integration

    • Introduced during polyol blend preparation for chain-extension reactions
    • Blended with diisocyanates in prepolymer formation for elastomer casting or coating emulsions

    Final product types

    • High-wear industrial floor coatings
    • Automotive protective topcoats
    • TPU films for textile lamination
    • Technical elastomeric bushings and seals

    5. Performance Polycondensation for Cosmetic and Pharmaceutical Polymers

    Producers of medical-grade and cosmetic excipient polymers select isomannide as an APE-free and phthalate-free monomer to synthesize specialty copolyesters and polycarbonates. The resulting polymers exhibit both biocompatibility and enhanced mechanical properties for use in sustained-release matrices, emulsion stabilizers, and specialty hydrogels in regulated personal care and life science markets.

    Industry compliance standards

    • United States Pharmacopeia (USP) <88> Biological Reactivity
    • European Pharmacopoeia (Ph. Eur.) Validated Excipients Standard
    • FDA CFR Title 21—Part 210, 211 cGMP for pharmaceuticals
    • ISO 22716 Good Manufacturing Practices for cosmetics

    Typical usage ratio

    • 10–25 mol% of diol content in copolyester or polycarbonate excipient synthesis; precise ratio depends on target polymer hydrophilicity and matrix release profile

    Downstream process integration

    • Fed into batch reactor polycondensation or polycarbonate chain extension for polymer excipient production
    • Used prior to granulation, micronization, or emulsion blending steps

    Final product types

    • Sustained-release tablet coatings
    • Ophthalmic hydrogel materials
    • Dermal delivery film-formers
    • Rheology modifiers for topical formulations

    6. Biobased Reactive Diluents for UV-Curable Systems

    For UV-curable coatings, inks, and adhesives, isomannide-derived diacrylates or dimethacrylates are employed as environmentally preferable reactive diluents. These components provide tailored crosslink density and viscosity control, essential for low-odor, low-VOC product lines marketed for flooring, electronics, and packaging. Process engineers value these biobased diluents to meet both technical and sustainability goals imposed by downstream partners and regional regulations.

    Industry compliance standards

    • Directive 2004/42/EC (EU VOC limits in paints and coatings)
    • ISO 11890-2 for determination of low VOC content
    • FDA 21 CFR 175.300 for indirect food contact adhesives
    • GHS classification for labeling and transport

    Typical usage ratio

    • 10–35 wt% in overall formulation, proportion modified according to required cure speed and film hardness

    Downstream process integration

    • Reacted to form acrylate/methacrylate derivatives, then compounded with oligomers and photoinitiators before UV application
    • Blended as reactive thinner for viscosity adjustment in screen, flexo, and digital printing lines

    Final product types

    • UV-cured wood and flexible flooring coatings
    • Overprint varnishes for consumer packaging
    • Digital printing ink vehicles
    • Fast-setting adhesive systems for electronics and displays
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