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2-Chloroadamantane

    • Product Name 2-Chloroadamantane
    • Alias 2-Chlortricyclo[3.3.1.1^3,7^]decane
    • Einecs 247-392-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    427608

    Cas Number 768-90-1
    Molecular Formula C10H15Cl
    Molecular Weight 170.68 g/mol
    Appearance White to off-white crystalline solid
    Melting Point 156-159 °C
    Boiling Point 274 °C (estimated)
    Density 1.09 g/cm³
    Solubility In Water Insoluble
    Flash Point 134 °C
    Refractive Index 1.547 (at 20 °C)
    Synonyms 1-Adamantyl chloride, Adamantane, 2-chloro-
    Pubchem Cid 13857

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

    Packing & Storage
    Packing 2-Chloroadamantane, 25g, supplied in a tightly sealed amber glass bottle with hazard labeling and tamper-evident cap, for laboratory use.
    Shipping 2-Chloroadamantane is shipped in tightly sealed containers, protected from moisture and light. It should be transported in compliance with local regulations for hazardous chemicals, with appropriate labeling. Store at room temperature, away from incompatible substances. Ensure proper documentation, and handle with gloves and protective eyewear to prevent exposure during shipping and handling.
    Storage 2-Chloroadamantane should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, well-ventilated area, separate from incompatible materials such as strong oxidizers. Proper labeling and secure storage are essential to prevent accidental exposure. Personal protective equipment should be used when handling to minimize risk.
    Application of 2-Chloroadamantane

    Applications of 2-Chloroadamantane in Industrial Manufacturing

    2-Chloroadamantane serves as a critical intermediate in advanced synthesis for several specialized sectors. Our manufacturing operations supply this material directly for use in technically demanding downstream applications requiring consistent purity and compliance with global standards. Below we detail its utility across distinct industrial fields, specifying standards, dosing, production steps, and resulting products in each application domain.

    1. Pharmaceutical Synthesis: Antiviral and Antiparkinsonian Drug Intermediates

    Pharmaceutical manufacturers use 2-Chloroadamantane as a key halogenated precursor in the synthesis of adamantane-derived actives, including antiviral compounds and antiparkinsonian APIs. Production environments demand precise handling to ensure regulatory conformity throughout the value chain, especially when scaling up halogenation chemistry for registered pharmaceutical substances. The material integrates into N-alkylation or subsequent substitution stages, serving as a building block for commercial molecules such as amantadine analogues or rimantadine derivatives. End products include finished APIs after further transformation and purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Volume 4
    • 21 CFR Part 211 (US cGMP for Finished Pharmaceuticals)
    • USP, EP, and JP monographs where applicable for related substances

    Typical usage ratio

    • 0.95–1.15 molar equivalents as process intermediate, adjusted on target substitution yield and impurity profile requirements

    Downstream process integration

    • Introduced after initial adamantane halogenation for amine or ether formation via nucleophilic substitution, followed by API isolation and characterization

    Final product types

    • Active pharmaceutical ingredients for antivirals
    • Parkinson’s disease treatments
    • Bulk intermediates for registered drug master files (DMF/CEP systems)

    2. Advanced Organic Synthesis: Specialty Chemical Building Block

    The chemical industry employs 2-Chloroadamantane in the construction of rigid, sterically demanding frameworks for high-performance molecules. R&D and commercial plants select this compound for specific haloadamantane scaffolds where enhanced thermal stability or hydrophobicity is required, such as in the synthesis of novel ligands, organic catalysts, or dendrimer cores. Integration occurs at the coupling or substitution stage, commonly under controlled, anhydrous conditions to manage selectivity and limit byproduct formation during multi-step syntheses. Custom molecules built with adamantane cores enable further innovations in multiple specialty chemical sectors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • REACH Regulation (EC) No 1907/2006, compliance for substance registration and traceability in the EU
    • Responsible Care® global chemical industry initiative

    Typical usage ratio

    • 20–85% by molar input relative to final target scaffold, based on synthetic strategy and complexity of downstream transformation

    Downstream process integration

    • Charged as the principal halide intermediate during nucleophilic substitution or palladium-catalyzed cross-coupling, prior to additional functional group installation

    Final product types

    • Dendrimers and advanced polymer initiators
    • Organic synthesis intermediates for R&D portfolios
    • Rigid-core ligands for specialty catalysts

    3. Coating Additives: High-Performance Protectants

    Manufacturers in the coatings sector apply 2-Chloroadamantane as an intermediate precursor in the synthesis of adamantane-functionalized resins and protective agents. The compound enters resin modification or polymerization stages to impart increased hardness, scratch resistance, and chemical inertness in top-tier protective coatings. Such features are crucial for optical materials and aerospace components, where conventional additives fail under harsh physical or chemical exposure. Product quality relies on close control of the adamantane moiety’s stability throughout integration into curing and crosslinking reactions.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management in chemical coatings production)
    • ISO 12944 for protective paint systems in industrial and marine environments
    • RoHS Directive 2011/65/EU for coatings on electronic assemblies

    Typical usage ratio

    • 1–10% by resin weight, tailored to film thickness, mechanical property targets, and crosslinking density

    Downstream process integration

    • Incorporation during prepolymer synthesis or post-polymer modification via nucleophilic substitution, followed by blending and application in solvent- or water-based systems

    Final product types

    • Clear coatings for electronic and optical components
    • Protective layers for military and aerospace applications
    • Scratch-resistant films for display and sensor devices

    4. Fragrance and Flavors: Adamantane-Based Aroma Compounds

    The flavors and fragrances sector utilizes 2-Chloroadamantane in the bespoke synthesis of adamantane-derived aroma ingredients. This material supports the introduction of unique, persistent odor notes in fine fragrance bases and specialty flavorings. Manufacturers introduce it during regioselective substitution reactions to yield finished molecules that meet stringent international sensory and toxicological standards. Its use is tightly regulated, and downstream processing focuses on residue removal and achieving high olfactory purity in the final aroma compound.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • FDA 21 CFR Part 172 (for flavoring substances)
    • EU Regulation (EC) No 1334/2008 on flavorings and food ingredients with flavoring properties

    Typical usage ratio

    • 0.05–0.35% by composition in concentrated aroma intermediates, adjusted for intensity and safety margins as per sensory panel feedback and regulatory limits

    Downstream process integration

    • Charged during selective alkylation or etherification to construct stable, high-impact aroma molecules before downstream distillation and blending

    Final product types

    • Base notes for premium perfumes
    • Flavor modifiers for specialty food products
    • Intermediate building blocks for aroma ingredient production

    5. Polymer and Composite Production: Structural Modifiers

    Producers of specialty polymers and composites incorporate 2-Chloroadamantane to introduce a sterically protected, rigid cage structure that enhances thermal and dimensional stability. The material participates in copolymerization, grafting, or end-group modification steps, conferring improved performance in engineering plastics and high-strength composites for automotive, aerospace, or electronics market segments. Quality assurance focuses on complete reaction incorporation and minimization of residual chlorinated species, especially for electrical applications requiring precise dielectric properties.

    Industry compliance standards

    • UL 94 Vertical Burning Test for flame retardant applications
    • ISO 9001:2015 for polymer manufacture and QC
    • REACH (EC) No 1907/2006 for notification and safe use in industrial polymers

    Typical usage ratio

    • 3–12% by monomer or polymer matrix weight, optimized via mechanical and thermal property tests for each final formulation

    Downstream process integration

    • Added during prepolymer formation or as a post-polymer modification reagent, followed by extrusion or molding processes

    Final product types

    • Engineering plastics for automotive and aerospace
    • Dielectric components for electronics
    • Composite parts for high-performance fabrication
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