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Cyclododecanone

    • Product Name Cyclododecanone
    • Alias Cyclododecan-1-one
    • Einecs 208-871-4
    • 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

    117908

    Cas Number 828-53-1
    Molecular Formula C12H22O
    Molar Mass 182.30 g/mol
    Appearance White crystalline solid
    Melting Point 61-63 °C
    Boiling Point 273-274 °C
    Density 0.962 g/cm3
    Solubility In Water Insoluble
    Flash Point 122 °C
    Refractive Index 1.481 (at 20 °C)
    Iupac Name Cyclododecanone
    Pubchem Cid 13635

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

    Packing & Storage
    Packing Cyclododecanone is packaged in a 100-gram amber glass bottle with a secure screw cap, labeled with hazard and identification details.
    Shipping Cyclododecanone should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. The chemical must be handled as a flammable solid and transported according to local, national, and international regulations for hazardous materials. Ensure compatibility with the packaging, and include appropriate labeling and documentation for safe and compliant shipping.
    Storage Cyclododecanone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed when not in use. Protect from direct sunlight and moisture. Use appropriate chemical storage containers and ensure proper labeling to avoid confusion. Handle using appropriate personal protective equipment to prevent spills or contamination.
    Application of Cyclododecanone

    Applications of Cyclododecanone in Industrial Manufacturing

    Cyclododecanone serves as a foundational ketone intermediate produced and supplied for specialized synthesis routes in multiple chemical sectors. Its consistent quality and established supply base enable demand from clients in industrial-scale polymer, fragrance, lubricant, and pharmaceutical ingredient production. The following sections outline major real-world downstream applications, industrial requirements, and outcome categories.

    1. Nylon 12 Monomer Production

    Downstream nylon manufacturers convert cyclododecanone by oxidative processes to synthesize laurolactam, the critical monomer for Nylon 12. This pathway demands precise oxidation control and impurity management to ensure polymer-grade output suited for high-performance engineering plastics. Quality of received raw material directly impacts subsequent ring-expansion and polymerization stages. Clients require lot-to-lot consistency and comprehensive contaminant screening.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 Annex VII/VIII regarding monomer purity
    • RoHS (EU Directive 2011/65/EU) for electronics-grade end-uses
    • Accredited Analytical Control – GC, NMR for trace impurities

    Typical usage ratio

    • 100 wt% as starting material for ring-expansion or oxidation to laurolactam
    • Overall molar conversion rate: 1:1 basis relative to monomer output
    • Batch adjustment made according to target polymer molecular weight
    • Yield considerations tied to oxygen feed, catalyst loading, and feedstock analytical purity

    Downstream process integration

    • Charged directly into oxidation reactors as primary feedstock
    • Intermediate purification after oxidation to minimize cyclododecenone and over-oxidation byproducts
    • Crude laurolactam isolation follows cyclododecanone consumption
    • Integration with continuous or batch caprolactam and polyamide production lines

    Final product types

    • Nylon 12 polymer chips for extrusion and molding
    • High-barrier packaging films
    • Automotive fuel line and tubing
    • Flexible electronic insulation coatings

    2. Fragrance Macrocyclic Musk Synthesis

    Leading aroma chemical producers utilize cyclododecanone as a key precursor for cyclododecanol, cyclododecanolides, and other macrocyclic musks via reduction and lactonization steps. This application requires low-odor profile, minimized trace metals, and stringent fractionation. End-users formulate the derived musks as signature notes in luxury perfumes and high-volume detergents.

    Industry compliance standards

    • IFRA Code of Practice for fragrance ingredients
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9235:2013 on aromatic raw materials
    • Purity criteria per customer-specific GC-MS archive

    Typical usage ratio

    • 95-100 wt% depending on catalytic hydrogenation or Baeyer–Villiger oxidation route
    • Stoichiometry adjusted for conversion to cyclododecanol, then lactone
    • Reaction scale varies from kilo-lab to several tons per batch, with customized blend ratios for downstream perfume formulation
    • Trace additive use (acid/base catalyst) per process

    Downstream process integration

    • Introduced at crude reduction or oxidative lactonization reactor in fragrance ingredient synthesis
    • Purified by fractional distillation to achieve odor standards
    • Blending with carrier solvents for shipment to blending sites
    • Maintained under inert conditions to prevent flavor contamination

    Final product types

    • Macrocyclic musk perfume bases
    • Luxury fine fragrances
    • Functional musks for household care detergents
    • Personal care product scents

    3. Specialty Lubricant Additive Intermediate

    Manufacturers in synthetic lubricant sectors leverage the ketone for conversion to high-molecular-weight alcohols and esters, crucial for high-performance lubricants in demanding applications. Purity and water content directly influence the efficiency of catalyst-driven reduction and subsequent esterification steps. Final lubricant properties depend on controlled structure of derived molecules from the initial cyclododecanone batch.

    Industry compliance standards

    • SAE J300 viscosity classification
    • OECD Test Guidelines for chemical safety
    • ASTM D4444 specification for base oil materials
    • Quality certificates per EN ISO 21469 for lubricant ingredients

    Typical usage ratio

    • 85-98 wt% converted to alcohol or ester intermediate
    • Byproduct yield managed below 2-5%
    • Dilution adjusted for batch reactor loading and molecular weight target
    • Blending ratios recalculated for each formulation to meet viscosity profiles

    Downstream process integration

    • Feeds catalyst-driven reduction reactors
    • Subsequent reaction with specific acids for ester lubricant base stock
    • Incorporated into semi-synthetic or synthetic blend production lines
    • Filtered and QC-tested prior to downstream additive incorporation

    Final product types

    • High-performance ester lubricants
    • Compressor and vacuum pump fluids
    • Industrial gearbox lubricants
    • Automotive transmission fluids

    4. Pharmaceutical Intermediate in Antifungal Synthesis

    API manufacturers integrate cyclododecanone as a structural block in the multi-step manufacture of patented antifungal compounds, especially azole derivatives. The requirements for this segment include pharmaceutical-grade purity, low residual solvent, and compliance with international pharmacopoeial limits. Downstream synthesis relies on robust, reproducible conversion rates and complete in-process traceability from ketone to final API intermediate.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monographs (as referenced by finished API dossier)
    • EMA Guideline on Residual Solvents in APIs (ICH Q3C)
    • ISO 14644-1 cleanroom certification for integration points

    Typical usage ratio

    • 90-99 wt% as dedicated intermediate for specified step
    • Reaction ratios calculated for stepwise yield optimization
    • Batch scale from pilot quantities (10-100 kg) to full commercial production (tons/month)
    • Adjustments made per synthetic route, with validated analytical controls

    Downstream process integration

    • Introduced into target heterocyclization reaction as substrate
    • Subjected to purification via recrystallization/column chromatography as per GMP
    • Process analytical technology (PAT) used for in-line monitoring
    • Isolated intermediate forwarded to API finishing stage

    Final product types

    • Pharmaceutical-grade azole intermediates
    • Active pharmaceutical ingredients for topical antifungals
    • Systemic antifungal formulations
    • Research compounds for pre-clinical development
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