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P-Anisaldehyde

    • Product Name P-Anisaldehyde
    • Alias 4-Methoxybenzaldehyde
    • Einecs 204-620-1
    • 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

    853874

    Name P-Anisaldehyde
    Iupac Name 4-methoxybenzaldehyde
    Cas Number 123-11-5
    Molecular Formula C8H8O2
    Molecular Weight 136.15 g/mol
    Appearance Colorless to pale yellow liquid
    Melting Point 2-4 °C
    Boiling Point 248-250 °C
    Density 1.119 g/cm3
    Solubility In Water Slightly soluble
    Refractive Index 1.570
    Odor Strong, aromatic, resembling anise
    Flash Point 121 °C
    Storage Conditions Store at room temperature, away from light

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

    Packing & Storage
    Packing The 100 mL amber glass bottle is tightly sealed, labeled "P-Anisaldehyde," with hazard symbols, lot number, and manufacturer details.
    Shipping **Shipping Description for P-Anisaldehyde:** P-Anisaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leakage and protect from light and air. It should be stored and transported at room temperature, away from incompatible substances, with appropriate hazard labeling. Handle according to applicable regulations for flammable and irritant chemicals to ensure safe shipping and storage.
    Storage P-Anisaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Ensure proper labelling and avoid contact with skin and eyes. Use chemical storage cabinets designed for flammable or combustible substances if available.
    Application of P-Anisaldehyde

    Applications of P-Anisaldehyde in Industrial Manufacturing

    As an established chemical raw material manufacturer, we deliver high-purity p-Anisaldehyde to support key downstream sectors. This aromatic aldehyde offers specialized reactivity and safety profiles for regulated industries, each with stringent quality and compliance requirements. Below, we detail distinct industrial application scenarios, focusing on verified integration points, controlled usage rates, process stages, and compliant finished goods.

    1. Food Flavor Compound Manufacturing

    Flavor houses incorporate p-Anisaldehyde as a core aromatic building block in the compounding of sweet, nutty, and floral notes for baked goods, confectionery, and beverages. Its characteristic anise and vanilla profile underpins complex formulation matrices, delivering consistent results batch after batch. Integrators must comply with regional food additive rules and adjust dosing to meet sensory targets and regulatory maximums, while ensuring downstream batch consistency through continuous quality monitoring.

    Industry compliance standards

    • FCC (Food Chemicals Codex)
    • EU Food Flavouring Regulation (EC) No 1334/2008
    • U.S. FDA 21 CFR §172.515 (Synthetic flavoring substances and adjuvants)
    • JECFA Food Additive Specification

    Typical usage ratio

    • 0.05% to 0.3% by weight in compounded food flavors, adjusted to local sensory and regulatory ceilings. Actual incorporation rate depends on finished product concentration and masking needs.

    Downstream process integration

    • Dosed during the flavor oil compounding step, typically solubilized in ethanol or propylene glycol carriers before homogeneous blending with other aromatic components; used in batch-controlled, closed-system environments to minimize volatilization and ensure traceability.

    Final product types

    • Compound flavor bases for beverages (cola, root beer, liqueurs)
    • Bakery flavor mixtures (anise, almond, vanilla analogues)
    • Confectionery and chewing gum flavor formulations
    • Ready-to-use food flavor syrups and emulsions

    2. Pharmaceutical Intermediate Synthesis

    API and generics manufacturers employ p-Anisaldehyde as a fine chemicals intermediate, participating in side-chain modification, condensation, and protective-group transformations. It serves as a controlled reactant in the preparation of several pharmacologically active benzaldehyde derivatives. This usage requires thorough documentation, impurity profiling, and validation under cGMP systems to comply with national pharmacopoeial directives and marketing authorization dossiers.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF Monograph Standards (where applicable)
    • Ph. Eur. (European Pharmacopoeia)
    • Local authority GMP certification (e.g., CFDA, US FDA)

    Typical usage ratio

    • Stoichiometric to ~5% molar excess relative to main reactant, based on specific API intermediate processes; excess minimized to control costs and facilitate purification in subsequent crystallization or distillation steps.

    Downstream process integration

    • Fed as a neat liquid or dissolved in a suitable organic solvent (e.g., ethanol, acetonitrile) at the condensation or reductive amination stage; main integration points include batch reactors under reflux, with in-process checks for aldehyde conversion and residuality.

    Final product types

    • Intermediate compounds for cough suppressants (e.g., antitussives based on anisyl derivatives)
    • Building blocks for antihistamine APIs
    • Precursor units for certain vasodilators and antifungal agents
    • Pharmaceutical grade bulk intermediates

    3. Fine Fragrance and Aromachemical Formulation

    Aromachemical manufacturers rely on p-Anisaldehyde for its distinctive sweet, spicy, and anisic top notes. It forms a persistent basis for premium perfumery accords and is widely used as a core modifier in the formulation of floral, fougère, and oriental fragrances. Processing requires adherence to global cosmetic and fragrance safety mandates, with meticulous dosing to achieve olfactory performance and avoid regulatory exceedances in finished consumer goods.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards & Amendments
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001:2015 (Quality Management Systems for aromatic compounds)
    • REACH Registration (where required in EU)

    Typical usage ratio

    • 0.1% to 3% by weight of total fragrance compound depending on target intensity, accord balance, and product class (e.g., eau de toilette, parfum); higher loading in soap bars and homecare fragrances when allowed by IFRA guidelines.

    Downstream process integration

    • Charged directly into the aromatic blending tank, often late in the compounding cycle due to its moderate volatility; undergoes QC sample evaluation for stability and batch-to-batch sensory profile prior to filtration and packaging.

    Final product types

    • Alcohol-based fine fragrances (eau de parfum, eau de toilette)
    • Fragrance oils for luxury candles and home diffusers
    • Soap fragrances (anise, herbal, powdery blends)
    • Personal care product scents (creams, body oils, shampoos)

    4. Agricultural Fungicide Synthesis

    Crop protection formulators include p-Anisaldehyde as a key intermediate in the synthesis of certain fungicide molecules, notably those with aromatic aldehyde structural motifs. This application line requires careful compliance with agrochemical registration protocols and environmental impact evaluation. Manufacturers must precisely dose and monitor its addition during closed-system reactions due to the strict impurity profile and efficacy requirements in registered plant protection products.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals – Pesticide Residues
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001/14001 (Agrochemical manufacturing and stewardship)
    • Country-specific pesticide registration regulations (such as US EPA FIFRA or China MARA)

    Typical usage ratio

    • Typically 1.5–8% by weight of reaction mixture, calculated according to the stoichiometric conversion required in individual active ingredient synthesis; proportion adjusted based on targeted fungicidal activity and purification yield requirements.

    Downstream process integration

    • Introduced during the initial charge phase of the active ingredient synthesis—commonly added to reaction mixtures containing other aromatic aldehydes, with monitored conversion and downstream neutralization/extraction steps to control residual aromatics.

    Final product types

    • Technical grade fungicidal actives (benzaldehyde-structured derivatives)
    • Wettable powder and suspension concentrate agrochemical formulations
    • Systemic protectant fungicides for cereals, fruits, and vegetable crops
    • Registered crop protection products for international agricultural markets

    5. Industrial Dye and Speciality Pigment Manufacturing

    Producers of specialty dyes integrate p-Anisaldehyde as a functionalized aldehyde in the synthesis of azo and xanthene dyes. Its electron-donating methoxy group yields desirable color intensity and shifting in chromophore frameworks. Dosing and process control respond to the target hue, application substrate, and dye purity required by the textile, paper, or ink end-use certifications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Safety)
    • EN 71-3 (Safety of Toys – Migration of certain elements for inks)
    • ISO 9001 for pigment/dye manufacturing
    • EU REACH regulation (for industrial colorants)

    Typical usage ratio

    • Between 2% and 12% of dye batch, precisely determined by desired molar chromophore substitutions and required color fastness; adjusted for batch volume and end-use performance targets (e.g., shade depth, wash resistance).

    Downstream process integration

    • Charged into the reaction vessel during diazotization or coupling steps, usually under inert atmosphere and controlled temperature, followed by neutralization and precipitation to isolate the constructed pigment structure; monitored with in-process spectrophotometry.

    Final product types

    • Specialty azo dyes for textiles and leather finishing
    • Xanthene-structured colorants for printing inks
    • High-purity pigments for artist and industrial paints
    • Paper colorants for premium grades
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