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1-Phenyl-2-Hexanone

    • Product Name 1-Phenyl-2-Hexanone
    • Einecs 213-915-7
    • 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

    392946

    Name 1-Phenyl-2-Hexanone
    Cas Number 943-80-6
    Molecular Formula C12H16O
    Molar Mass 176.26 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 265-267 °C
    Melting Point N/A
    Density 0.982 g/cm³
    Refractive Index n20/D 1.515
    Flash Point 111 °C
    Smiles CCCC(C=O)Cc1ccccc1
    Synonyms α-Hexanoylbenzene; 2-Hexoanone, 1-phenyl-
    Solubility In Water Insoluble
    Pubchem Cid 110565
    Un Number N/A

    As an accredited 1-Phenyl-2-Hexanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Phenyl-2-Hexanone, 100g: Supplied in a sealed amber glass bottle with tamper-evident cap and hazard labels for safe storage.
    Shipping 1-Phenyl-2-Hexanone is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical, so transportation complies with relevant regulations (e.g., DOT, IATA). Packages are clearly labeled and handled by trained personnel to prevent leaks, spills, or exposure during transit. Safety data sheets are included.
    Storage Store 1-Phenyl-2-hexanone in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Use appropriate safety measures, including labeling and secondary containment, to prevent spills and exposure. Ensure storage complies with local chemical safety regulations.
    Application of 1-Phenyl-2-Hexanone

    Applications of 1-Phenyl-2-Hexanone in Industrial Manufacturing

    As a chemical raw material manufacturer, we specialize in supplying 1-Phenyl-2-Hexanone for downstream industries demanding high purity and performance in synthesis, particularly where aromatic ketones serve as critical intermediates. On this page, we present the key application sectors where this material is truly deployed, highlighting the compliance standards, application ratios, integration points in customer processes, and typical finished products.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical synthesis processes integrate 1-Phenyl-2-Hexanone as a core building block for specialty APIs, especially those requiring aryl ketone motifs within non-chiral or racemic frameworks. Customers in the small molecule sector apply it for constructing advanced intermediates preceding heterocycle formation or further functional group transformations. The choice of this compound depends on its reactivity within specific Grignard, acylation, or reductive amination protocols, where reliability of supply and trace impurities profoundly impact downstream yields and regulatory audits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP–NF Monograph Reference for Starting Materials
    • EU GMP Part II for Bulk Pharmaceutical Chemicals
    • 21 CFR Part 210/211 (FDA-US) site validation

    Typical usage ratio

    • Typically 1–8 mol% relative to final API mass, adjusted according to step conversion efficiency and isolated intermediate yield.

    Downstream process integration

    • Charged to the initial reactor during carbonyl coupling, or introduced during the condensation stage as the limiting reagent, followed by subsequent purification via distillation or chromatography at the customer’s facility.

    Final product types

    • Aromatic ketone-core APIs (e.g. intermediate for nonsteroidal anti-inflammatory drugs or antimicrobial agents)
    • Pharmaceutical intermediates requiring aryl substitutions for synthetic elaboration

    2. Fragrance Ingredient Manufacturing

    Fragrance producers incorporate this aromatic ketone in the formulation of perfume bases and specialty odorants, exploiting both its own mild floral character and its function as a precursor to musks and other luxury fragrance molecules. The raw material enters the batch at the blending or synthesis stage, where its compatibility with aldehydes and alcohols is critical for achieving the target sensory profile in fine fragrances, air care, and personal care products. Customers regularly require compliance with IFRA and traceability for each lot due to strict end-market requirements.

    Industry compliance standards

    • IFRA Amended Standards (latest applicable amendments)
    • ISO 9235: Aromatic Raw Materials for Fragrance
    • EU Cosmetics Regulation (EC) No. 1223/2009
    • REACH Registration (EC 1907/2006) for traceability

    Typical usage ratio

    • Generally 0.5–3 wt% of total fragrance oil concentrate, modulated based on finished scent intensity and regulatory limits per end application.

    Downstream process integration

    • Added during batch blending, custom synthesis of musk intermediates, or directly as a fixative or modifier, followed by vacuum distillation or solvent removal.

    Final product types

    • Fine fragrance oils for perfumery
    • Air freshener essential blends
    • Personal care and cosmetic perfuming compositions

    3. Agrochemical Synthesis Intermediate

    Agrochemical manufacturers utilize 1-Phenyl-2-Hexanone in the development of certain herbicide and pesticide precursors, particularly those featuring aryl-alkyl-ketone substructures that provide distinctive activity and stability. It is applied in the early stages of multi-step organic synthesis, influencing both yield and selectivity of the agrochemical active ingredient. Precise documentation supports registration dossiers submitted to crop protection authorities, and the integration of this raw material is subject to rigid QC at every critical synthetic step.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Chemical Control Legislation: EPA PRIA (US) and Regulation (EC) No 1107/2009 (EU)
    • ISO 9001:2015 for production traceability
    • REACH Pre-registration and ongoing SIEF obligations

    Typical usage ratio

    • Standard range 2–12 wt% of the total reaction mass in intermediate synthesis, modulated by targeted batch scale and specific conversion route.

    Downstream process integration

    • Charged during coupling or alkylation steps, followed by sequential purification, assay confirmation, and incorporation into subsequent formulation stages at the agrochemical plant.

    Final product types

    • Precursor intermediates for selective herbicides
    • Key building blocks for insecticide actives

    4. Fine Chemical Synthesis (Specialty Resins & Polymers)

    Chemical processors employing 1-Phenyl-2-Hexanone in specialty resin systems leverage its structure as a functional monomer or modifier, particularly within advanced coatings and binder applications. Its controlled addition strengthens polymer chain propagation and contributes to the steric/toughness profile of the finished resin. Only manufacturers of certain performance resins and adhesives deploy this ketone at scale, and all shipments receive full COA and batch traceability to satisfy end-use quality audits and technical requirements for downstream formula approval.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems for production facilities
    • RoHS Directive 2011/65/EU for finished goods entering electronics or toys
    • GB/T 19001 (China) or ISO 9001:2015 (International) for QC
    • VOC content reporting per regional industrial regulations

    Typical usage ratio

    • Added at 0.8–5 wt% of total polymer batch, tuned according to viscosity, reactivity, and target resin characteristics.

    Downstream process integration

    • Incorporated during resin pre-polymerization or chain modification steps, followed by curing or polymer work-up according to customer formula type (solvent-based, waterborne, or hot melt).

    Final product types

    • High-performance industrial resins for coatings and adhesives
    • Specialty polymers for advanced material applications
    Free Quote

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