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Cyclopentanecarbonitrile

    • Product Name Cyclopentanecarbonitrile
    • Alias Cyclopentanenitrile
    • Einecs 207-963-6
    • 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

    584708

    Cas Number 5449-60-7
    Molecular Formula C6H9N
    Molar Mass 95.15 g/mol
    Appearance Colorless to pale yellow liquid
    Density 0.945 g/mL at 25°C
    Boiling Point 192-194°C
    Melting Point -19°C
    Refractive Index 1.4570 (20°C)
    Flash Point 82°C (closed cup)
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Synonyms Cyclopentyl cyanide
    Smiles C1CCC(C1)C#N

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

    Packing & Storage
    Packing Cyclopentanecarbonitrile is supplied in a 100g amber glass bottle with a secure screw cap and hazard labeling for laboratory use.
    Shipping Cyclopentanecarbonitrile should be shipped in tightly sealed containers, protected from heat and moisture. It must comply with all local, national, and international regulations for transporting hazardous chemicals. Proper labeling and documentation are essential, and the substance should be handled by trained personnel using appropriate safety measures to prevent leaks or exposure during transit.
    Storage **Cyclopentanecarbonitrile** should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizing agents. Keep away from direct sunlight. Use appropriate chemical-resistant containers and ensure proper labeling. Follow all relevant regulations and safety guidelines for storage to prevent leaks or accidental exposure.
    Application of Cyclopentanecarbonitrile

    Applications of Cyclopentanecarbonitrile in Industrial Manufacturing

    Cyclopentanecarbonitrile is an advanced nitrile compound produced in our ISO-certified facility and utilized as a crucial intermediate in several high-value industrial manufacturing sectors. Its unique alicyclic structure and chemical reactivity deliver performance advantages in specific synthesis routes, leading to more efficient production and consistent product quality. The following application scenarios reflect its established use in key downstream industries, with process, compliance, ratio, and final product details based on actual customer integration.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Cardiovascular Agents

    Major pharmaceutical manufacturers employ cyclopentanecarbonitrile as a key intermediate during the multi-step synthesis of targeted cardiovascular APIs, especially where selective nitrile functionality is required for subsequent heterocycle formation. It undergoes controlled reactions such as catalytic hydrogenation or amide conversion steps, forming core scaffolds found in authorized antihypertensive and antiarrhythmic drug molecules. QC integration requires batch traceability and strict impurity control to meet the high purity demands of regulated drug substance manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current US and EU Pharmacopoeia Monographs (USP, EP)
    • FDA cGMP 21 CFR Part 210 & 211
    • EDQM TSE (transmissible spongiform encephalopathies) and EMA Substances of Human Origin regulations

    Typical usage ratio

    • Stoichiometric or slight excess relative to corresponding precursor (usually 1.0–1.2 molar equivalents), adjusted according to downstream target yield and reaction kinetics

    Downstream process integration

    • Added at the intermediate coupling, cyclization, or amide-hydrolysis reaction stage within the controlled synthesis route, frequently under nitrogen with catalytic agents or in polar aprotic solvents

    Final product types

    • Regulated cardiovascular APIs, such as antiarrhythmic drugs and antihypertensive pharmaceuticals
    • Finished pharmaceutical tablets and injectable formulations

    2. Crop Protection Arylpyrazole Synthesis

    Leading agrochemical companies incorporate cyclopentanecarbonitrile during the targeted synthesis of complex arylpyrazole structures used as the active substances in next-generation insecticides and miticides. It serves as a critical nitrile-functional building block for cyclization, enabling high-purity pyrazole core assembly with consistent transformation yields. Process control is vital at the condensation and cyclization stages to minimize by-product formation and secure regulatory acceptance in key agricultural markets.

    Industry compliance standards

    • FAO Specification for Agrochemicals
    • ISO 9001:2015 and ISO 14001:2015 Quality/Environment Management
    • National regulatory approval (EPA, EU REACH, China Pesticide Registration Regulation GB 20815-2021)
    • Global Harmonized System (GHS) for classification, labeling, and safety

    Typical usage ratio

    • 0.8–1.3 mol per equivalent of downstream arylhydrazine or diketone intermediate, adjusted for process scale and desired crop protection active content

    Downstream process integration

    • Introduced during the condensation step with arylhydrazine, followed by cyclization and functional group modification in batch or semi-continuous agrochemical synthesis lines

    Final product types

    • Technical-grade insecticide and miticide active ingredient concentrates
    • Formulated crop protection products (e.g., wettable powders, EC, SC formulations)
    • Pre-mixed granules for field application

    3. Aroma Chemicals and Fragrance Synthesis

    Specialty chemical companies utilize cyclopentanecarbonitrile as a precursor in the synthesis of select macrocyclic musks and related fragrance intermediates. Its cyclopentyl core and nitrile group enable it to participate in controlled catalytic hydrogenation, oximation, and ring-functionalization reactions, leading to high-purity macrocycle fragrance molecules used in perfumery and fine fragrance markets. Material traceability, odor purity analysis, and compliance with international IFRA standards must be met to secure downstream approval for consumer scent products.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals
    • ISO 9001 Certified Quality Systems
    • EU Cosmetic Regulation (EC) No. 1223/2009

    Typical usage ratio

    • Typically 0.5–1.5 molar equivalents in relation to ring-closure or chain extension partners, fine-tuned for yield, odor threshold, and TPC (total purity control)

    Downstream process integration

    • Added during skeleton-building or terminating steps in macrocyclic musk synthesis, followed by purification and multi-stage distillation or crystallization

    Final product types

    • Macrocyclic musk intermediates for perfumery bases
    • Blended fragrance oils for fine fragrances and personal care

    4. Specialty Polymer Modifier Synthesis

    High-performance polymer producers employ cyclopentanecarbonitrile in the synthesis of tailored specialty monomers for niche engineering plastics and copolymers. Its nitrile moiety facilitates polymer backbone functionalization by copolymerization or post-polymer modification, imparting specific rigidity, solvent resistance, or thermal properties. Compliance requires full batch documentation for downstream ROHS and REACH assessments before integration into consumer product plastics.

    Industry compliance standards

    • EU REACH and SVHC (Substance of Very High Concern) compliance
    • RoHS Directive (2011/65/EU) for environmental safety in plastics
    • ISO 9001/14001 Quality and Environmental Management Systems
    • UL 94 Flammability Safety for final polymer products

    Typical usage ratio

    • Generally 0.2–0.5 molar equivalents as comonomer relative to main monomer feed in copolymerization, adjusted for desired polymer attribute intensity; higher ratios for masterbatch or reactive blend applications

    Downstream process integration

    • Introduced at first or second monomer feed stage in batch and continuous polymerization reactors, or added during reactive blending of high-performance resins

    Final product types

    • Modified engineering plastics with enhanced resistance or functionalized surfaces
    • Thermoplastic copolymer pellets and masterbatches for automotive, electronics, or specialty textile markets
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