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2,3-Dimethoxybenzaldehyde

    • Product Name 2,3-Dimethoxybenzaldehyde
    • Alias o-Vanillin
    • Einecs 219-993-5
    • 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

    624622

    Chemical Name 2,3-Dimethoxybenzaldehyde
    Molecular Formula C9H10O3
    Molecular Weight 166.18 g/mol
    Cas Number 86-51-1
    Appearance White to pale yellow crystalline solid
    Boiling Point 304 °C
    Melting Point 53-56 °C
    Density 1.14 g/cm³
    Solubility In Water Slightly soluble
    Smiles COC1=CC=CC(=C1OC)C=O
    Pubchem Cid 69818
    Refractive Index 1.553
    Flash Point 146.8 °C
    Inchi InChI=1S/C9H10O3/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-6H,1-2H3

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, white screw cap, chemical label displaying "2,3-Dimethoxybenzaldehyde," hazard symbols, lot and expiry details.
    Shipping 2,3-Dimethoxybenzaldehyde is shipped in secure, leak-proof containers compliant with chemical safety regulations. The packaging protects from moisture, light, and physical damage during transit. Shipments include appropriate labeling and documentation as required for hazardous materials. Handle and store in a cool, dry place away from incompatible substances during transport and storage.
    Storage 2,3-Dimethoxybenzaldehyde should be stored in a tightly closed container, kept in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Protect from moisture and light. Ensure storage area is equipped with proper spill containment and fire suppression systems. Always label containers clearly and follow institutional safety protocols.
    Application of 2,3-Dimethoxybenzaldehyde

    Applications of 2,3-Dimethoxybenzaldehyde in Industrial Manufacturing

    As a direct producer of 2,3-Dimethoxybenzaldehyde, we support specialized applications across several industrial sectors. This intermediate serves roles in targeted organic syntheses, regulated aroma compound production, pharmaceutical ingredient building, and advanced material development. The following real-world downstream uses elaborate on typical process practices, compliance requirements, dosage guidelines, workflow positioning, and final manufactured goods.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies employ 2,3-Dimethoxybenzaldehyde for constructing active pharmaceutical ingredient (API) scaffolds, specifically in benzylisoquinoline and phenethylamine derivatives. Process chemists typically condense the aldehyde with amines or phenols under controlled pH and temperature to facilitate C–N or C–C bond formation. Consistent supply and defined purity grades ensure reproducibility in GMP-compliant synthesis runs, which directly relate to the quality of finished drug substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monographs (for related intermediates and excipients)
    • EU EudraLex Volume 4 Part II GMP
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.15–0.35 molar equivalents in condensation and reductive amination stages, adjusted per target molecule's stoichiometry

    Downstream process integration

    • Early-stage step for benzyl and isoquinoline framework formation in multi-step batch synthesis
    • Direct charge to reactor after dissolution in compatible solvent (e.g., ethanol, toluene)
    • Purification via recrystallization or chromatographic methods post-reaction
    • Stringent in-process analytical control using HPLC and NMR at critical stages

    Final product types

    • API precursors for antihypertensive agents
    • Alkaloid-based drug substances
    • CNS-active pharmaceutical molecules
    • Custom synthetic intermediates for clinical trial supply

    2. Fine Fragrance and Aroma Chemical Manufacture

    Aroma chemical producers utilize 2,3-Dimethoxybenzaldehyde for synthesis of high-value perfumery aldehydes and masking agents. The aldehyde undergoes specific reactions like acetalization, reduction, or etherification, transforming its aromatic character suitable for bulk and niche fragrance ingredients. Rigorous adherence to IFRA and REACH guidelines oversees impurity profiles and safe-use levels in formulation labs and commercial blending facilities.

    Industry compliance standards

    • IFRA Standards and Guidelines
    • EC Regulation No 1223/2009 (Cosmetics Regulation)
    • REACH Registration for industrial use
    • ISO 9001:2015 for process consistency

    Typical usage ratio

    • 1–5% in pre-blend formulations; further diluted post-synthesis depending on performance evaluation and regulatory thresholds

    Downstream process integration

    • Initial synthetic step for specialty aldehyde or ether aroma compounds
    • Integrated into continuous or semi-batch reactors for scale-up runs
    • Fractional distillation and odor note evaluation performed in QC labs
    • Bulk and pre-packaged transfer to contract fragrance houses/globals under trace documentation

    Final product types

    • Specialty aroma ingredients (e.g., methoxy-benzaldehyde derivatives)
    • Complex perfume compositions
    • Personal care masking agents
    • Odor modulators for air care formulations

    3. Agrochemical Synthesis: Pesticide and Herbicide Intermediates

    Leading agrochemical formulation plants use 2,3-Dimethoxybenzaldehyde as a core building block for selective herbicide and fungicide intermediates, particularly in the synthesis of diaryl ether and substituted benzaldehyde analogues. Synthesis protocols demand precise ratio control and extended reflux or high-pressure conditions, emphasizing minimization of process impurities to remain compliant with international agriculture safety standards and pesticide residue requirements.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 17025 Testing Laboratory Accreditation
    • EU Regulation 1107/2009 on Plant Protection Products
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.2–0.5 molar equivalents, fine-tuned for targeted yield and purity in catalyst-assisted syntheses

    Downstream process integration

    • Charged into condensation reaction vessels with phenoxy or other aromatic partners
    • Mid-stage intermediate isolation for stepwise assembly of bioactive agents
    • Analytical monitoring using GC-MS and titration for contaminant control
    • Protocol development for scale-up and batch validation

    Final product types

    • Diarylether herbicide intermediates
    • Fungicide precursor compounds
    • Synergist additive molecules for crop protection
    • Registered technical active ingredient intermediates

    4. Dye and Pigment Intermediate Supply

    Industrial colorant manufacturers formulate synthetic dyes and performance pigments by leveraging 2,3-Dimethoxybenzaldehyde in azo and anthraquinone dye molecular constructs. This intermediate enters the early diazotization or coupling stages, supporting tight control of ligand orientation and chromophore intensity. Compliance with support documentation for heavy metal absence and trace solvent residues confirms usability for textiles and coatings, given pivotal customer acceptance criteria in global coloration supply chains.

    Industry compliance standards

    • Oeko-Tex Standard 100
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • ISO 14001 Environmental Management
    • REACH Regulation for dye and pigment registration

    Typical usage ratio

    • 0.05–0.15 molar equivalents, determined by targeted dye/pigment molecular structure and color depth requirements

    Downstream process integration

    • Charged at the start of synthetic batch for diazotization with aromatic amines
    • Undergoes coupling and subsequent ring closure reactions
    • In-line NMR and UV-Vis absorbance monitored during reaction progress
    • Feeds purified intermediates into granulation or dispersion lines for final pigments

    Final product types

    • Textile disperse dyes
    • Synthetic pigment dispersions
    • Solvent-based specialty colorants for plastics
    • Industrial paint and ink pigment bases

    5. Advanced Materials: Organic Electronic Components

    Research and semi-commercial production units in the material science sector use 2,3-Dimethoxybenzaldehyde as an intermediate for synthesizing charge transport materials, specifically in organic semiconductors and photonic dyes. The molecule contributes to step-growth polymerizations and core modifications of pi-conjugated systems. Documentation ensuring residual solvent and ionic contaminant controls underpins material purity critical to functional performance within OLEDs and photovoltaic layers.

    Industry compliance standards

    • ISO 9001:2015 Quality Assurance for Specialty Chemicals
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 62321 Chemical Analysis of Electronic Components
    • Material Safety Data Sheets (SDS) requirements for laboratory handling

    Typical usage ratio

    • 0.02–0.10 equivalents in final step polymerizations; ratio selected based on target molecular weight and film-forming properties

    Downstream process integration

    • Monomer charge point for solution or melt-phase polymerizations
    • Enters batch or flow reactors with ancillary conjugation agents, base catalysts, and inhibitors
    • Intermediate isolation and material purification under inert atmosphere
    • Transfer to device fabrication units for layer formation or inkjet printing

    Final product types

    • OLED charge transport layers
    • Organic photodetector sensitisers
    • Electrochromic display materials
    • Polymer-based photovoltaic active layers
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