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5-Chloro-2-Methoxybenzaldehyde

    • Product Name 5-Chloro-2-Methoxybenzaldehyde
    • Alias 5-Chloro-o-anisaldehyde
    • Einecs 401-210-7
    • 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

    532445

    Product Name 5-Chloro-2-Methoxybenzaldehyde
    Cas Number 6627-51-4
    Molecular Formula C8H7ClO2
    Molecular Weight 170.6 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 57-61°C
    Boiling Point 282°C
    Density 1.29 g/cm3
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC(C=O)=CC(Cl)=C1
    Inchi InChI=1S/C8H7ClO2/c1-11-8-3-6(5-10)2-7(9)4-8/h2-5H,1H3
    Synonyms 5-Chloro-o-anisaldehyde; 2-Methoxy-5-chlorobenzaldehyde

    As an accredited 5-Chloro-2-Methoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g amber glass bottle features a secure screw cap and white label reading "5-Chloro-2-Methoxybenzaldehyde, CAS 13432-28-7, 25g."
    Shipping 5-Chloro-2-Methoxybenzaldehyde is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be protected from moisture, heat, and direct sunlight during transit. The packaging is clearly labeled with hazard information. Only authorized personnel should handle the shipment, and all relevant paperwork, including safety data sheets, accompanies the product.
    Storage **5-Chloro-2-Methoxybenzaldehyde** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid moisture. Clearly label the container and follow all relevant safety and regulatory guidelines for chemical storage.
    Application of 5-Chloro-2-Methoxybenzaldehyde

    Applications of 5-Chloro-2-Methoxybenzaldehyde in Industrial Manufacturing

    5-Chloro-2-Methoxybenzaldehyde serves as a valuable intermediate in specialized organic synthesis, especially within the pharmaceutical, fragrance, agricultural chemical, and dye sectors. Our manufacturing expertise supports clients in integrating this compound into their advanced formulations under strictly controlled processing conditions. Below, we outline several precisely validated downstream scenarios, detailing industry norms, formulation strategies, integration steps, and real-world end product applications.

    1. Pharmaceutical Intermediate for Second-Generation Antihypertensive APIs

    Within pharmaceutical synthesis, 5-Chloro-2-Methoxybenzaldehyde is used as a key building block in the synthesis of certain antihypertensive agents, particularly imidazoline-based compounds. Its role in key condensation and subsequent heterocyclic ring closure steps ensures stringent purity requirements and traceability across all stages, addressing strict regulatory controls from raw material selection to the finished API. Pharmaceutical manufacturers rely on documented impurity profiles and consistent reactivity during multi-step active compound synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) substance monographs
    • United States Pharmacopeia (USP) General Chapter <941> for organic impurities
    • China GMP 2010/2020 for production process control

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents relative to core heterocyclic intermediates, adjusted based on target yield and purity demands in each batch.

    Downstream process integration

    • Introduced during the early condensation stage of API synthesis, allowing further transformations such as cyclization or reductive amination. Specific conditions (e.g., acid/base, solvent choice) vary by manufacturer’s process optimization.

    Final product types

    • Bulk and formulated antihypertensive active pharmaceutical ingredients (APIs), including for combination therapies.
    • Subsequent intermediate compounds with imidazoline, benzimidazole, or related moieties.

    2. Synthesis of Aroma Chemicals for Fine Fragrances

    Producers of high-grade fragrance compositions utilize 5-Chloro-2-Methoxybenzaldehyde as a precursor for aldehydic and floral note enhancers. Its electron-rich aromatic structure serves for selective derivatization, leading to specialty fragrance molecules used in luxury perfumery bases and aroma compounded oils. Batch traceability and reactivity profiling matter for consistent scent profiles across production campaigns.

    Industry compliance standards

    • IFRA standards and QRA (Quantitative Risk Assessment) guidelines for fragrance ingredients
    • REACH (EC No 1907/2006) registration and use conditions
    • ISO 9235:2013 on aroma chemical definitions and purity
    • Cosmetic Ingredient Review (CIR) assessments

    Typical usage ratio

    • Generally between 0.5% and 2% in reaction blends for downstream aldehyde modification, with exact values set by volatility, olfactive intensity, and complete conversion in final step reactions.

    Downstream process integration

    • Added at the condensation or acylation stage to produce substituted benzene derivatives, which are then further processed via reduction or acetalization into stable perfume ingredients. Monitored for residual aldehyde content and trace impurity analysis.

    Final product types

    • Luxury perfume bases and accord concentrates
    • Custom-built aroma molecules for toiletries and high-end skin care
    • Functional fragrance additives for personal care formulations

    3. Plant Growth Regulator and Crop Protection Synthesis

    Manufacturers of advanced agrochemical actives employ 5-Chloro-2-Methoxybenzaldehyde for its selective reactivity during the production of growth regulators and certain fungicide and herbicide intermediates. The aldehyde’s halogen and methoxy substituents improve downstream activity spectrum and target specificity after functional group transformation. Full lifecycle assessment is performed to comply with current agrochemical directives.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticides and technical materials
    • OECD Guidelines for Testing of Chemicals (residue and metabolism)
    • Regulation (EC) No 1107/2009 (Plant Protection Products Regulation)
    • China Ministry of Agriculture GB/T standards for pesticide production

    Typical usage ratio

    • Typically dosed between 1.0% and 3.5% on a molar basis in multi-step syntheses, subject to crop-specific efficacy assays and environmental impact studies.

    Downstream process integration

    • Used as an input in the aromatic condensation or aromatic substitution phase for synthesis of plant growth actives or triazole-based fungicide precursors. Process steps emphasize controlled reaction temperature and pH to maintain product selectivity.

    Final product types

    • Plant growth regulator actives for cereals and vegetables
    • Intermediates for systemic fungicide technical concentrates
    • Herbicide precursor compounds for broadleaf weed management products

    4. Intermediate for Synthesis of Specialty Dyes and Pigments

    Producers of high-performance dyes for plastics, inks, and fiber applications rely on 5-Chloro-2-Methoxybenzaldehyde for generating advanced colorant intermediates. The compound’s functional groups facilitate focused transformations such as diazotization or aldol condensation, supporting the consistent chromophore construction required for color stability and process robustness. Here, quality control emphasizes spectral uniformity and absence of byproducts that affect chromatic intensity.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • ISO 9001:2015 for pigment and dyestuff production quality systems
    • REACH compliance (ANNEX XVII, restriction on substances)
    • EN 71-3 for colorant safety in toys and consumer goods

    Typical usage ratio

    • Commonly incorporated in the range of 0.7 to 1.5 equivalents relative to aromatics undergoing coupling reactions, with ratios tailored for target shade strength and pigment load.

    Downstream process integration

    • Utilized in the primary coupling or condensation step during the synthesis of azo or anthraquinone dye intermediates; subsequent sulfonation or metallation steps create application-ready pigment dispersions.

    Final product types

    • Dyes for polymer and fiber coloration
    • High-energy pigment preparations for plastic color masterbatches
    • Solvent-based and aqueous inks for printing sectors
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