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2-(3-Benzoylphenyl)Propionitrile

    • Product Name 2-(3-Benzoylphenyl)Propionitrile
    • Alias CN-09547
    • Einecs 260-119-7
    • 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
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    Specifications

    HS Code

    661526

    Product Name 2-(3-Benzoylphenyl)Propionitrile
    Cas Number 60170-46-9
    Molecular Formula C16H13NO
    Molecular Weight 235.28 g/mol
    Appearance White to off-white solid
    Melting Point 98-102 °C
    Solubility Soluble in common organic solvents (e.g. DMSO, methanol)
    Purity Typically ≥98%
    Iupac Name 2-[3-(benzoyl)phenyl]propanenitrile
    Smiles CC(C#N)C1=CC=CC(=C1)C(=O)C2=CC=CC=C2
    Storage Conditions Store at room temperature, protected from light and moisture

    As an accredited 2-(3-Benzoylphenyl)Propionitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with screw cap, labeled with "2-(3-Benzoylphenyl)propionitrile," chemical formula, and hazard symbols.
    Shipping 2-(3-Benzoylphenyl)propionitrile is shipped in tightly sealed, chemically-resistant containers, protected from light and moisture. Packaging ensures minimal exposure to air, and all relevant hazard and handling labels are included. Transportation complies with local and international regulations regarding hazardous chemicals, ensuring safe and secure delivery to the customer’s designated location.
    Storage Store 2-(3-Benzoylphenyl)propionitrile in a tightly sealed container at room temperature, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and moisture. Keep away from incompatible materials such as strong oxidizing agents. Ensure proper labeling, and follow standard laboratory safety protocols. Use personal protective equipment when handling and avoid generating dust or vapors.
    Application of 2-(3-Benzoylphenyl)Propionitrile

    Applications of 2-(3-Benzoylphenyl)Propionitrile in Industrial Manufacturing

    2-(3-Benzoylphenyl)Propionitrile is a specialty intermediate favored by key manufacturing sectors for its performance as a core building block in high-value synthetic routes. As a direct manufacturer, we supply this compound to downstream industries relying on advanced chemical transformations for pharmaceuticals, agrochemicals, and specialty chemical production. We ensure regulatory alignment, high consistency in composition, and precise support for each identified end-use application.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis

    This compound plays a critical role as an intermediate during the multi-step synthesis of specific NSAIDs, especially for APIs requiring a benzoylphenylpropionitrile core. Downstream pharmaceutical plants integrate this intermediate after initial aromatic nitrile formation, introducing the benzoyl moiety to provide structural backbone for active compounds. Stringent regulatory inspection governs its specification, purity levels, and traceability at every transfer stage up to the final API production. Its consistent quality supports final purification, crystallization, and formulation of finished drug products.

    Industry compliance standards

    • United States Pharmacopeia (USP) Reference Standards
    • European Pharmacopoeia (Ph. Eur.) Section 2.2.46
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Ranges from 0.15 mol to 1.1 mol per 1 mol target API, adjusted based on process yield and batch size
    • Excess reagent not recommended due to post-reaction purification constraints

    Downstream process integration

    • Introduced after initial aromatic ring nitrile construction stage
    • In-line with acylation or coupling steps forming the final NSAID structure
    • Subjected to HPLC analysis for residual impurities before downstream reactions
    • Purified through solvent extraction prior to formulation

    Final product types

    • Non-steroidal anti-inflammatory drug tablets
    • Injectable NSAID formulations
    • Active pharmaceutical ingredient bulk powder
    • Topical anti-inflammatory pharmaceutical creams

    2. Agrochemical Synthesis: Precursor for Selective Herbicide Compounds

    Agrochemical manufacturers employ this nitrile intermediate in the synthetic pathway for certain benzoylphenylpropionic acid-based herbicides. The compound is introduced in early-stage syntheses leading to ring-substituted active herbicidal ingredients. Its use requires precise stoichiometric control to reduce side-products and optimize downstream chlorination or amidation reactions. Regulatory authorities enforce detailed traceability and purity limits due to the stringent requirements for safe use in crop protection agents.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Production
    • REACH Annex II for registration, evaluation, authorization

    Typical usage ratio

    • 0.9–1.25 mole per mole of target herbicidal active ingredient
    • Ratio varies according to targeted substitution pattern and catalyst system

    Downstream process integration

    • Mixed with other aromatic intermediates in controlled batch reactors
    • Chlorination or oxidation performed directly following nitrile addition
    • Monitored through GC and MS methods for side-product minimization
    • Herbicide actives isolated post-crystallization and dried under vacuum

    Final product types

    • Granulated selective herbicides for cereal crops
    • Emulsifiable concentrate herbicide formulations
    • Water-dispersible powder herbicide packs
    • Technical-grade agrochemical actives for export formulation

    3. Specialty Chemicals for UV-Absorber and Photoinitiator Manufacturing

    Chemical producers utilize the phenylpropionitrile skeleton during synthesis of UV-absorbing additives and photoinitiators. The compound introduces aromatic rigidity and electron-withdrawing features necessary for high-performance UV stabilizers, which require tightly controlled impurity profiles. Integration occurs in the intermediate condensation or alkylation phases, with tailored adjustment based on target optical absorbance properties. Continuous QC ensures the absence of volatile contaminants that could affect performance in polymer matrices.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical quality
    • RoHS Directive 2011/65/EU for substance restrictions
    • ASTM D5201 for UV absorber chemical testing
    • EN 71-3 safety of toys where UV stabilizers are included

    Typical usage ratio

    • 0.1–0.25 mol per mol of final stabilizer system, adjustable for target absorption range 270–360 nm
    • Lower dosages used for high-purity or thin film polymer requirements

    Downstream process integration

    • Enter alkylation or condensation stages to build UV-absorbing chromophores
    • Inline solvent extractions remove color bodies
    • UV-VIS spectrophotometry tracks product performance
    • Pelletization or microencapsulation follows final blending

    Final product types

    • UV absorber blended masterbatches for plastics extrusion
    • Photoinitiator powders for ink and coating industries
    • Clear polymer films with integrated UV stabilization
    • Automotive and architectural coating additives

    4. Fine Chemical Intermediate in Liquid Crystal Material Synthesis

    This compound functions as a specialized intermediate in the synthesis of liquid crystalline molecules needed for advanced display materials. Downstream processing facilities introduce the compound during the esterification or aryl coupling reactions that impart anisotropic optical properties to final liquid crystal monomers. Quality must support narrow batch-to-batch consistency, with stringent evaluation for low ionic and particulate contaminants. Compliance with electronics sector purity demands is required to support manufacturing of high-resolution display modules.

    Industry compliance standards

    • JEDEC JESD96 for purity specifications in electronic chemicals
    • IEC 61249-2-21 for material content in electronics
    • ISO 14001:2015 for environmental management systems
    • RoHS Directive for hazardous substance limits in electronic devices

    Typical usage ratio

    • 0.05–0.12 mole per mole of target liquid crystal monomer compound
    • Precise measurement due to high-purity and high-cost end products

    Downstream process integration

    • Entered during multi-step coupling or esterification with halogenated aromatics
    • Material filtered to sub-micron levels before process entry
    • Thin-film purity checks through HPLC and NMR spectroscopy
    • Inline control prevents cross-contamination and supports device reliability

    Final product types

    • Twisted nematic liquid crystal materials for TFT display production
    • Liquid crystal alignment layers in LCD module assembly
    • Advanced phase retarders and compensators for optical devices
    • Organic compounds for OLED and next-gen display technologies
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