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4-(2-Methoxyphenyl)Benzaldehyde

    • Product Name 4-(2-Methoxyphenyl)Benzaldehyde
    • Alias 4-(2-Methoxyphenyl)benzaldehyde
    • Einecs 629-662-7
    • 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

    453614

    Product Name 4-(2-Methoxyphenyl)Benzaldehyde
    Cas Number 3218-36-8
    Molecular Formula C14H12O2
    Molecular Weight 212.25
    Appearance White to off-white solid
    Melting Point 85-89°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COc1ccccc1-c2ccc(C=O)cc2
    Inchi InChI=1S/C14H12O2/c1-16-13-6-2-3-10(9-13)12-7-4-11(8-15)5-12/h2-9H,1H3
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 4-(2-Methoxyphenyl)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 4-(2-Methoxyphenyl)benzaldehyde is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Shipping **Shipping Description:** 4-(2-Methoxyphenyl)benzaldehyde is shipped in sealed, chemical-resistant containers, labeled with hazard information according to GHS standards. The package is cushioned to prevent breakage and complies with international shipping regulations for laboratory chemicals. Temperature and handling guidelines are followed to ensure product stability and safety during transit.
    Storage 4-(2-Methoxyphenyl)benzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as oxidizing agents. Store at room temperature or below. Ensure the storage area is free from sources of ignition. Properly label the container, and keep it out of reach of unauthorized personnel.
    Application of 4-(2-Methoxyphenyl)Benzaldehyde

    Applications of 4-(2-Methoxyphenyl)Benzaldehyde in Industrial Manufacturing

    As a dedicated chemical manufacturer, we supply 4-(2-Methoxyphenyl)Benzaldehyde directly to industrial partners for advanced organic synthesis. Below we outline its established applications across specialized manufacturing sectors, covering critical compliance norms, realistic formulation guidance, integration into downstream production lines, and the resulting industrial-grade finished goods.

    1. Synthesis of Specialty Pharmaceutical Intermediates

    This raw material plays a crucial role as a key aromatic aldehyde in multi-step synthesis protocols for a number of specialty pharmaceutical intermediates, especially those used within the development of anti-inflammatory agents and certain neuroactive compounds. Its unique molecular structure supports selective condensation reactions, offering value during late-stage intermediate manufacture under controlled GMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Guide Part II (APIs)
    • US FDA 21 CFR Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Relevant pharmacopeial monographs for intermediates (USP, EP, JP, as applicable)

    Typical usage ratio

    • Dosage typically ranges from 0.12 mol to 0.30 mol per synthesis batch, tailored to pathway molarity and yield targets in downstream active intermediate formations.

    Downstream process integration

    • Incorporated during the key condensation, reductive amination, or cyclization steps in multi-stage bench and pilot scale reactors. Introduced post-activation, prior to catalyst charge, ensuring controlled aldehyde reactivity and downstream yield consistency.

    Final product types

    • Active pharmaceutical ingredient (API) intermediates for further hydrogenation or acylation
    • Fine chemicals for proprietary anti-inflammatory agent synthesis
    • Building blocks for central nervous system drug candidates

    2. Agrochemical Synthesis: Herbicide and Growth Regulator Raw Materials

    Our clients in the agrochemical sector leverage this compound for the elaboration of aromatic building blocks, serving as a controlled aldehyde donor in the production pathway of selective herbicides and advanced plant growth regulators. It supports high-purity conversion yields demanded in bulk agrochemical manufacturing, particularly where phenoxy-benzaldehyde motifs are proven for target activity.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Agrochemicals
    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 concerning the placing on the market of plant protection products
    • China Pesticide Registration Standards (GB 2763, GB 28150)

    Typical usage ratio

    • Utilized at 0.5–2.5% w/w of total reactant load, adjustable depending on the specific herbicidal compound and batch scale. Engineers optimize ratio for cost control and reaction endpoint targeting.

    Downstream process integration

    • Dosed after pre-treatment of base reactants, before condensation or Knoevenagel reaction steps, ensuring clean product isolation and minimized byproduct formation under continuous-flow or batch reactors.

    Final product types

    • Selective phenoxy-based herbicide intermediates
    • Precursor molecules for auxin-type plant growth regulators
    • Base chemicals for formulation of new-generation crop protection agents

    3. Fragrance and Fine Perfume Ingredients Manufacturing

    This aromatic aldehyde is valued by downstream fragrance ingredient formulators, where it acts as a specialty note builder in the synthesis of scent base compounds and unique modifiers. The material’s methoxy-phenyl structure provides required olfactory characteristics and performs reliably in continuous aromatic chemical production lines.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredient Use (current amendments)
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (where applicable for fragrance intermediates)
    • ISO 9001:2015 for Fragrance and Cosmetic Raw Materials

    Typical usage ratio

    • Applied at 0.8–2.0% of total blend in specialty aroma chemicals, with batch yield and olfactory target as control parameters.

    Downstream process integration

    • Introduced directly into fragrance compound reactors post-solvent base charge, prior to esterification or acylation, enabling targeted synthesis of aromatic bases and fixatives in industrial blending systems.

    Final product types

    • Specialty aromatic aldehyde intermediates for fine perfumery
    • Fragrance bases for premium home and personal care products
    • Aroma chemical modifiers for air care formulations

    4. Advanced Liquid Crystal Material Synthesis

    Manufacturers of high-purity liquid crystal materials utilize this compound in the production of specific biphenyl precursors for display and optical applications, where high chemical integrity and stable molecular arrangement are mandatory. The raw material’s distinctive substitution pattern supports precise alignment within the downstream synthesis of display-grade liquid crystals.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for display chemicals
    • ISO 14001:2015 for Environmental Management in Specialty Chemicals
    • UL 746A (Polymeric Materials—Short Term Property Evaluations)
    • Customer-specified purity and trace impurity control standards (often >99.5%)

    Typical usage ratio

    • Typically 0.3–1.2 molar equivalents based on total reactant feed for liquid crystal precursor formation, dependent on the exact molecular design and batch scale.

    Downstream process integration

    • Dosed at the key aromatic coupling or Suzuki-Miyaura cross-coupling step, immediately following substrate dissolution and catalyst/initiation charge, supporting reproducible alignment and mesogen structure formation.

    Final product types

    • Nematic and smectic liquid crystal intermediates for TFT-LCD production
    • Custom biphenyl key precursors for field-driven LC modules
    • Bespoke organic compounds for advanced optoelectronic displays

    5. Dye and Pigment Intermediate Production

    Industrial dye manufacturers rely on this compound as a tailored aldehyde donor within the construction of specialty azo- and anthraquinone-based dye intermediates. Its controlled reactivity allows for clean bond-forming steps, facilitating production of high-stability colorants for demanding technical textiles and ink applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 certification for textile dyes
    • REACH Annex XVII restrictions on aromatic amines in dyes
    • ZDHC MRSL (Manufacturing Restricted Substances List) for textile chemical safety
    • ISO 9001:2015 for dye intermediate manufacturing

    Typical usage ratio

    • Used at 1.5–5% of total dye batch mass; chemists adjust ratio based on shade depth, extinction coefficient requirements, and process scale.

    Downstream process integration

    • Dosed into condensation or coupling reactors immediately before initiation of azo bond formation, maintained under temperature and pH control for optimal chromophore development.

    Final product types

    • High-stability dye intermediates for technical textile coloration
    • Colorant precursors for digital and security ink formulations
    • Complex aromatic pigments for automotive and industrial coatings
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