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Methyl 2-Nonynoate

    • Product Name Methyl 2-Nonynoate
    • Alias Methyl non-2-ynoate
    • Einecs 246-815-3
    • 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

    929116

    Cas Number 111-80-8
    Molecular Formula C10H16O2
    Molecular Weight 168.23 g/mol
    Iupac Name Methyl non-2-ynoate
    Appearance Colorless to pale yellow liquid
    Boiling Point 222-224 °C
    Density 0.917 g/mL at 25 °C
    Refractive Index 1.431
    Flash Point 94 °C
    Solubility In Water Insoluble
    Smiles CCCCCC#CC(=O)OC
    Melting Point -51 °C

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of Methyl 2-Nonynoate, sealed with screw cap, labeled with hazard warnings and product details.
    Shipping Methyl 2-Nonynoate is typically shipped in sealed, chemical-resistant containers to prevent leaks and exposure. It should be transported according to applicable hazardous material regulations, kept cool, dry, and away from sources of ignition. Proper labeling and safety data sheets (SDS) must accompany the shipment for safe handling and compliance.
    Storage Methyl 2-Nonynoate should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from light. Recommended storage is in a chemical safety cabinet, preferably flammable-proof, at temperatures below 30°C. Proper labeling and secondary containment are advised to prevent accidental release or exposure.
    Application of Methyl 2-Nonynoate

    Applications of Methyl 2-Nonynoate in Industrial Manufacturing

    Methyl 2-Nonynoate is an alkyne-containing ester applied in select sectors of the chemical industry. As an original manufacturer, we focus on its integration in downstream synthesis, flavor ingredient preparation, agricultural chemical production, and advanced organic intermediates. Each application involves industry-specific regulatory considerations, prescribed usage proportions, and defined processing windows to support high-value end products.

    1. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers employ Methyl 2-Nonynoate as an alkyne-functional building block for drugs containing propargyl or nonynyl motifs. The controlled reactivity of its terminal alkyne enables selective cross-coupling in heterocycle formation and expanded ring synthesis, supporting the production of antitumor and antiviral compound intermediates. Formulators use this ester in custom reaction sequences, balancing purity, lot-to-lot consistency, and trace metal content to meet pharmaceutical synthesis requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs for related intermediates
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals (for facilities incorporating intermediates)
    • USP General Notices and Requirements (trace impurity limits)

    Typical usage ratio

    • 5–12 mol% relative to total reactants in alkyne cross-coupling reactions, depending on target intermediate structure and catalyst selection
    • Adjusted according to scale, reaction kinetics, and downstream purification requirements

    Downstream process integration

    • Introduced during the advanced synthetic step after initial backbone construction
    • Acts as a coupling partner in Sonogashira or Glaser–Hay reactions
    • Requires anhydrous environment with nitrogen blanket to avoid side reactions
    • Route to further conversion or deprotection without intermediate isolation in flow or batch reactors

    Final product types

    • Propargyl-containing pharmaceutical intermediates
    • Azido-alkyne functionalized APIs (in final step or as precursor)
    • Nonynoic acid derivatives for medicinal chemistry programs
    • Branched polyketide scaffolds

    2. Flavor and Fragrance Ingredient Synthesis

    Within the flavors and fragrance industry, formulators use Methyl 2-Nonynoate for the preparation of alkyne-based aroma compounds and advanced esters. Its unique odor profile contributes fresh, fruity, and green notes in complex blends. Synthesizers react this ester to broaden fragrance raw material palettes and as a key intermediate for creating specialty scents. Product batches require verification of residual solvents and allergen status to comply with global fragrance regulations.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Regulation (EC) 1223/2009 on Cosmetic Products
    • US Food and Drug Administration 21 CFR 172.515 (Flavoring Agents and Related Substances)
    • REACH (EC) No 1907/2006—Substance Registration for Use in Consumer Products

    Typical usage ratio

    • 0.05–0.5% in fragrance concentrate
    • As low as 0.01% in finished consumer products depending on final evaluation and IFRA limits per specific perfume base

    Downstream process integration

    • Injected at the esterification stage for aroma chemical manufacture
    • Purified by fractional distillation to remove impurities affecting flavor profile
    • Subjected to GC/MS quality control for odor purity
    • Integrated as a modifier or top note agent in compound blending

    Final product types

    • Fragrance bases for fine perfumes and cosmetics
    • Flavored beverage syrups (non-direct ingestion)
    • Industrial air fresheners and odor control agents
    • Floral perfume oil compounds

    3. Crop Protection Active Ingredient Synthesis

    Producers of agrochemical actives utilize Methyl 2-Nonynoate as a precursor in the construction of plant growth regulators and insect pheromone mimics. The terminal alkyne functional group enables specific reaction pathways for synthesizing long-chain analogues used in integrated pest management. Careful formulation is necessary to align with regulatory residue limits and toxicological assessment when manufacturing substances intended for crop application.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • US EPA 40 CFR Part 180—Tolerances and Exemptions for Pesticide Chemical Residues in Food
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • OECD Test Guidelines for Chemical Safety

    Typical usage ratio

    • 0.5–3.0% w/w relative to total batch in active ingredient synthesis route
    • Batch size and final substance design determine exact input

    Downstream process integration

    • Added following initial chain elongation of fatty acid derivatives
    • Modified through selective hydrogenation or halogenation, depending on biological mode of action required
    • QC by HPLC for process contaminants and yield verification
    • Conversion to salt form if required for formulation stability

    Final product types

    • Synthetic pheromone mimics for pest monitoring traps
    • Modified fatty acid-based plant growth regulators
    • Active ingredient precursors for selective herbicide formulations
    • Minor component in complex insect attractant blends

    4. Fine Chemical and Polymer Intermediate Production

    In fine chemical manufacture, Methyl 2-Nonynoate serves as a versatile intermediate for specialty condensation reactions, including the preparation of conjugated polymers and functionalized surfactant products. Chemical engineers value its alkyne moiety for designing monomers with precise backbone rigidity. Processing requires controlled temperature profiles and solvent selection to avoid unwanted polymerization. Batch records document feed ratios for consistent downstream properties.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems (for chemical production)
    • EN 71-3:2019 (Migration of certain elements in finished polymer goods)
    • REACH Annex XVII restrictions (when used in manufacturing consumer-accessible polymers)
    • Custom MSDS, hazard classification per GHS/CLP

    Typical usage ratio

    • 0.2–2.0 eq relative to secondary monomer for condensation polymer synthesis
    • Exact ratio determined by target molecular weight, end group functionalization, and process optimization data

    Downstream process integration

    • Charged at the pre-polymerization or grafting stage in solvent or bulk systems
    • Subjected to temperature ramping with metal-based catalysts for chain propagation
    • Followed by purification steps such as precipitation or solvent stripping
    • Integrated into QC release workflow for viscosity, color, and terminal group analysis

    Final product types

    • Functional block copolymers for adhesives and sealants
    • Alkyne-terminated surfactants and specialty detergents
    • Molecular probes for analytical chemistry kits
    • Advanced materials for electronics encapsulation
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