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3-(4-Methoxyphenyl)Propionitrile

    • Product Name 3-(4-Methoxyphenyl)Propionitrile
    • Alias 4-Methoxybenzeneacetonitrile
    • Einecs 249-015-6
    • 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

    509187

    Chemical Name 3-(4-Methoxyphenyl)propionitrile
    Molecular Formula C10H11NO
    Molecular Weight 161.20 g/mol
    Cas Number 3710-43-8
    Appearance White to off-white solid
    Boiling Point 306-308°C
    Melting Point 52-55°C
    Density 1.09 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC=C(C=C1)CCC#N
    Inchi InChI=1S/C10H11NO/c1-12-10-5-3-9(4-6-10)7-2-8-11/h3-6H,2,7H2,1H3
    Pubchem Cid 16744

    As an accredited 3-(4-Methoxyphenyl)Propionitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, with tamper-evident cap; white label displays product name, CAS number, hazard pictograms, supplier, and handling instructions.
    Shipping **Shipping Description:** 3-(4-Methoxyphenyl)propionitrile is shipped in tightly sealed containers, protected from moisture and light. Packages are clearly labeled, complying with chemical transport regulations. It is shipped as a non-hazardous material under standard chemical shipping guidelines, ensuring safe, prompt delivery at ambient temperature with supporting safety data and documentation included.
    Storage Store 3-(4-Methoxyphenyl)propionitrile in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and properly labeled. Protect from moisture and incompatible substances such as strong oxidizers and acids. Use appropriate chemical-resistant containers. Follow all standard laboratory safety protocols for handling and storage.
    Application of 3-(4-Methoxyphenyl)Propionitrile

    Applications of 3-(4-Methoxyphenyl)Propionitrile in Industrial Manufacturing

    As a primary producer of 3-(4-Methoxyphenyl)Propionitrile, we supply this chemical intermediate to diverse industrial sectors. Our raw material supports synthesis routes in pharmaceutical, agrochemical, and performance material manufacturing, playing a critical role in finished product quality and regulatory compliance. With direct integration experience and process optimization, we guide downstream partners for controlled and reproducible end-use.

    1. Pharmaceutical Intermediate for Antidepressant Synthesis

    Many pharmaceutical companies use 3-(4-Methoxyphenyl)Propionitrile as a synthetic intermediate in the manufacture of active pharmaceutical ingredients (APIs) for antidepressant compounds, particularly for drugs containing phenylpropylamine structures. Typical synthesis routes require the nitrile group for subsequent amine or acid transformations under GMP-controlled conditions. Reaction monitoring and impurity control are critical for regulatory and market acceptance.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) guidelines for APIs
    • US FDA drug master file (DMF) standards
    • ICH Q3A/B impurity profile limits

    Typical usage ratio

    • Used at 0.8 – 1.3 molar equivalents per 1 mol API backbone unit, fine-tuned according to reaction stoichiometry and impurity specs

    Downstream process integration

    • Enters after initial condensation but before reduction or hydrolysis
    • Typically handled in closed reactor systems with in-process analytical controls
    • Isolated crude is then purified by distillation or crystallization

    Final product types

    • Antidepressant API bulk material (e.g., Duloxetine, Fluoxetine intermediates)
    • Pharmaceutical fine chemicals for contract manufacturing

    2. Agrochemical Intermediate for Selective Herbicide Production

    Major crop-protection manufacturers utilize this compound to construct heterocyclic ring systems in selective herbicide molecules. The aromatic structure and nitrile functionality serve as coupling points for further alkylation and cyclization steps in the synthesis of pre- and post-emergent herbicides. Purity and concentration are tightly monitored to prevent downstream catalyst poisoning or off-spec residues in the end product.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • REACH (EC 1907/2006) registration for chemical safety
    • ISO 9001:2015 for quality management in agrochemical supply
    • OECD guidelines for testing of chemicals

    Typical usage ratio

    • Applied at 0.7 – 1.1 molar equivalents per target active, based on crop selectivity and downstream conversion yield

    Downstream process integration

    • Added during the main heterocycle formation stage, prior to final oxidation or esterification
    • Blended in solvent matrices (e.g., acetonitrile, DMF) for batch or semi-continuous conversion
    • Multistep syntheses require in-process HPLC monitoring

    Final product types

    • Selective herbicide active ingredients
    • Technical grade pesticide formulations
    • Pre-emergent and post-emergent crop protection agents

    3. Fragrance Intermediate in Aroma Chemical Synthesis

    Fragrance manufacturers process 3-(4-Methoxyphenyl)Propionitrile during specialty aroma chemical synthesis, especially for musk and balsamic note derivatives. Its controlled reactivity allows transformation via hydrogenation or hydrolysis into aldehyde, alcohol, or acid functionalities, which then serve as core building blocks for perfume ingredients. High purity minimizes unwanted odor notes and off-flavors in final blends.

    Industry compliance standards

    • IFRA Code of Practice and Guidelines
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9001:2015 for quality assurance in flavor and fragrance chemicals
    • RIFM standards for raw material safety

    Typical usage ratio

    • Generally 1.0 equivalent per main musk derivative structure, adjusted based on the conversion efficiency for each aroma target

    Downstream process integration

    • Fed into hydrogenation or acidic hydrolysis unit operations
    • Subject to staged distillation for purity adjustment
    • Intermediates are subsequently esterified or combined with alcohols or acids

    Final product types

    • Musk and balsamic fragrance ingredients
    • Cosmetic fragrance bases
    • Luxury perfume compound concentrates

    4. Building Block for Liquid Crystal Monomer Synthesis

    Advanced materials manufacturers apply this intermediate to produce custom monomers for high-performance liquid crystalline polymers (LCPs) used in electronics and display technologies. The aromatic and para-methoxy substituents aid in controlling mesogenic alignment and optical clarity. Consistent nitrile content and trace impurity levels are vital for maintaining dielectric properties and panel reliability.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for specialty material production
    • JIS standards for liquid crystal compounds (e.g., JIS C6263)
    • RoHS (2011/65/EU) and REACH restrictions on hazardous substances
    • IEC 61249 for materials in printed circuit assemblies

    Typical usage ratio

    • Dosage control at 0.9 – 1.05 equivalents per monomer repeat unit, with process analytical confirmation by NMR and GC-MS

    Downstream process integration

    • Polymer backbone assembly via aromatic coupling and subsequent functionalization steps
    • Incorporated in batch reactor or continuous flow systems for precise alignment
    • Post-polymerization purification to reduce residual organic impurities

    Final product types

    • Liquid crystal display (LCD) panel monomers
    • LCP resins for electronics
    • Smartphone and flat-panel display films

    5. Intermediate for Specialty Coatings Precursors

    Manufacturers of advanced surface coatings employ this compound as a key intermediate in producing film-forming resins with targeted optical and weathering characteristics. Its molecular structure allows precise integration into aliphatic or aromatic systems, supporting gloss and durability for industrial and automotive coatings. Low color index and impurity grade are necessary for clear and high-performance applications.

    Industry compliance standards

    • ASTM D16 Standard Terminology for Paint, Related Coatings and Materials
    • EU Regulation (EC) No 1907/2006 (REACH) for chemical classification
    • ISO 12944 for protective paint systems
    • VOC content limitations per EPA Title 40 CFR Part 59

    Typical usage ratio

    • Utilized at 1.0 – 1.2 mol per resin backbone unit, depending on targeted molecular weight and film properties

    Downstream process integration

    • Polymerized within prepolymer synthesis reactions
    • Subsequent crosslinking and curing stages integrate functionalized fragments
    • Quality controlled by IR spectroscopy and chromatographic analysis

    Final product types

    • Weather-resistant automotive clearcoats
    • Protective industrial coating resins
    • High-gloss architectural paints

    6. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Colorant producers use 3-(4-Methoxyphenyl)Propionitrile as a precursor for synthesizing specialty dyes and pigments, including azo, anthraquinone, and phthalonitrile derivatives. The methoxy substitution facilitates electronic tuning and colorfastness. Accurate dosing and impurity removal are essential for brightness, shade stability, and lightfastness in finished pigment dispersions for textiles and plastics.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes
    • EN 71-3 (Safety of Toys – migration of certain elements) for pigments
    • CFR Title 21 for food-contact compliant colorants
    • REACH SVHC (Substance of Very High Concern) regulations

    Typical usage ratio

    • Active at 0.8 – 1.2 mol per pigment or dye core, variation based on targeted hue and conversion efficiency

    Downstream process integration

    • Fed during diazotization, coupling, or cyclization stages in dye synthesis
    • Isolated pigment intermediates undergo purification via filtration or solvent extraction
    • Final dispersions are milled and standardized for application

    Final product types

    • Textile fiber dyes
    • High-performance organic pigments
    • Thermoplastic color masterbatches
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