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2-Adamantanone

    • Product Name 2-Adamantanone
    • Einecs 204-838-5
    • 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

    243599

    Iupac Name Adamantan-2-one
    Molecular Formula C10H14O
    Molar Mass 150.22 g/mol
    Cas Number 700-58-3
    Appearance White crystalline solid
    Melting Point 174-178 °C
    Boiling Point 251-254 °C
    Density 1.11 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.548
    Smiles O=C1C2CC3CC1CC(C2)C3
    Pubchem Cid 13484

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

    Packing & Storage
    Packing 250 g of 2-Adamantanone is supplied in a sealed amber glass bottle with a white screw cap and detailed hazard labeling.
    Shipping 2-Adamantanone is shipped in tightly sealed containers under ambient conditions. It should be protected from moisture, heat, and direct sunlight. The packaging complies with relevant regulations for chemical transport. Handling instructions and safety data sheets are provided, ensuring safe and secure delivery to laboratories or industrial destinations.
    Storage 2-Adamantanone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container protected from direct sunlight and moisture. Proper labeling and secondary containment are recommended to prevent spills or accidental exposure. Always follow standard safety protocols for handling organic compounds.
    Application of 2-Adamantanone

    Applications of 2-Adamantanone in Industrial Manufacturing

    As a direct manufacturer of high-purity 2-Adamantanone, we supply this specialty ketone to industrial partners with established downstream demand across advanced organic synthesis, pharmaceutical intermediates, and specialty polymer additives. Select end-use sectors rely on its unique cage structure for reactivity and molecular modification, supporting innovation in material performance, drug discovery, and precision electronic chemicals. Below, we detail authentic industrial scenarios with operational details for effective integration.

    1. Pharmaceutical Intermediate Synthesis: Antiviral API Production

    Pharmaceutical developers utilize 2-Adamantanone for structural transformation and construction of macrocyclic frameworks in antiviral active pharmaceutical ingredients, including amantadine derivatives. Its rigid adamantane structure enables precise functional group insertion for target molecular moieties. R&D and commercial scale production employ this raw material at designated synthesis stages, controlled by pharmacopoeial and regulatory quality requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF Monographs for relevant API
    • European Pharmacopeia (Ph. Eur.) standards
    • China Pharmacopoeia (ChP) API requirements

    Typical usage ratio

    • 0.8%–2.5% molar ratio relative to primary reactant, adjusted based on desired conversion and yield control during cyclization

    Downstream process integration

    • Introduced during the intermediate formation stage; undergoes condensation or reductive amination; requires careful process validation to meet GMP traceability and impurity limits

    Final product types

    • Amantadine hydrochloride API
    • Rimantadine hydrochloride API
    • Related cyclic antiviral intermediates

    2. Advanced Material Synthesis: High-Performance Polymer Additives

    Materials manufacturers incorporate 2-Adamantanone as a comonomer or cage-based modifier in specialty polyimides, polycarbonates, and photoresist resins, often in semiconductor and display film substrates. Its rigid cage structure enhances thermal stability, dimensional control, and dielectric strength in engineering plastics and electronic chemicals.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • RoHS Directive (EU Restriction of Hazardous Substances)
    • IEC 61249-2-21 for halogen-free laminates
    • JEDEC JESD22-B102 for polymer electrical testing

    Typical usage ratio

    • 0.2%–1.5% by weight in polymer resin feed, modified based on end-use dielectric or thermal requirements

    Downstream process integration

    • Added during monomer melt blending or solution copolymerization; requires temperature and residence time control to prevent premature degradation

    Final product types

    • Polyimide films for microelectronic applications
    • Photoresist base resins for lithographic processes
    • High glass transition temperature polycarbonate compounds

    3. Synthetic Organic Chemistry: Grignard and Reductive Amination Reactions

    Contract research organizations and scale-up laboratories employ 2-Adamantanone as a carbonyl source in Grignard additions and for ketone-to-amine conversions in the development of nitrogen-containing proprietary molecules and ligands. Its steric profile and stability benefit controlled selective transformations in complex molecular frameworks, supporting lead candidate optimization.

    Industry compliance standards

    • ISO 17025 Laboratory Quality Standard
    • REACH (EC) No 1907/2006 substance registration compliance
    • Internal SOPs validated for hazard and waste management control
    • CAS analytical purity verification

    Typical usage ratio

    • 1.0–3.0 equivalents in reagent addition, refined according to substrate reactivity and scale (<1 kg to multi-kg pilot batches)

    Downstream process integration

    • Charged after reaction initialization with live monitoring of ketone conversion rate and byproduct suppression; recovered or hydrolyzed for final work-up

    Final product types

    • Cationic ligands
    • Functionalized adamantyl amines for pharmaceutical R&D
    • Custom advanced intermediates for specialty chemicals

    4. Fragrance and Flavors: High-Boiling Musk Ketone Analogue

    Select aroma chemical producers use 2-Adamantanone as a specialty ingredient in molecularly engineered, high-boiling musky odorant compounds, particularly where low volatility and thermal persistence are required for premium fragrance bases or technical perfumery. Production adheres to flavor and fragrance industry purity protocols and IFRA safety regulations.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • ISO 9235 for natural and synthetic odorants
    • FEMA GRAS certification (for flavors, where applicable)
    • Cosmetic Ingredient Review (CIR) safety substantiation

    Typical usage ratio

    • 0.05%–0.3% by weight in fragrance compound, optimized for musk note balance and regulatory threshold compliance

    Downstream process integration

    • Blended post-synthesis into base oil matrix; monitored for residual solvent limits and controlled storage to maintain molecular integrity during compounding

    Final product types

    • Technical musk fragrance bases
    • Long-lasting perfume compositions
    • Specialty aroma ingredients for industrial scent applications

    5. Electronic Chemicals: Advanced Photoresist Formulation

    IC fabrication and advanced display manufacturers implement 2-Adamantanone derivatives as building blocks for negative-tone photoresist resins. Its cage structure imparts UV and thermal resistance, necessary for reliable pattern transfer and defect suppression in sub-micron photolithographic processes, while meeting strict regulatory controls on trace metal and organic impurities.

    Industry compliance standards

    • IATF 16949 for automotive electronics supply chains
    • SEMI C62-0817 purity standards for photoresist materials
    • SEMATECH industry guidelines for critical chemical impurities
    • UL 94 flammability standard (where applicable in resin use)

    Typical usage ratio

    • 0.1%–1.2% by weight in resist formulation, tailored to integrate with photoinitiator system, resin architecture, and target lithographic resolution

    Downstream process integration

    • Incorporated during oligomer synthesis, with downstream purification and QC for metal content (<10 ppb) and byproduct minimization; stability testing under UV exposure

    Final product types

    • Negative-tone photoresist solutions for IC fabrication
    • UV-cured display patterning resins
    • High-precision mask aligner chemicals
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