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3,4-Dimethylbenzamide

    • Product Name 3,4-Dimethylbenzamide
    • Alias m-Xylene amide
    • Einecs 214-552-5
    • 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

    818990

    Chemicalname 3,4-Dimethylbenzamide
    Molecularformula C9H11NO
    Molecularweight 149.19 g/mol
    Casnumber 25331-76-4
    Appearance White to off-white crystalline powder
    Meltingpoint 98-101°C
    Boilingpoint 319.3°C at 760 mmHg
    Density 1.07 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CC1=CC(=C(C=C1)C)C(=O)N
    Pubchemcid 254597
    Flashpoint 146.8°C
    Inchi InChI=1S/C9H11NO/c1-6-3-4-8(7(2)5-6)9(10)11/h3-5H,1-2H3,(H2,10,11)

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

    Packing & Storage
    Packing The 100g package of 3,4-Dimethylbenzamide comes in a sealed amber glass bottle with a secure screw cap and warning label.
    Shipping 3,4-Dimethylbenzamide is shipped in sealed, chemical-resistant containers, clearly labeled and compliant with relevant hazardous materials regulations. During transit, it is protected from moisture, excessive heat, and incompatible substances. Appropriate safety data and handling instructions accompany each shipment to ensure safe and secure delivery to laboratories or industrial facilities.
    Storage 3,4-Dimethylbenzamide should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers. Keep it away from direct sunlight and sources of ignition. Ensure the storage area is clearly labeled and restrict access to trained personnel. Follow all local, state, and federal regulations for chemical storage.
    Application of 3,4-Dimethylbenzamide

    Applications of 3,4-Dimethylbenzamide in Industrial Manufacturing

    3,4-Dimethylbenzamide serves as a key intermediate in several specialized chemical industries, where precision and compliance drive formulation and synthesis processes. The following sections detail specific downstream application scenarios, reflecting authentic industrial practices, regulatory requirements, and technical integration.

    1. Agrochemical Synthesis: Herbicide and Pesticide Intermediates

    Agrochemical companies use 3,4-Dimethylbenzamide as a carbonyl-containing intermediate to build complex amide and aromatic structures needed in selective herbicide and pesticide actives, such as substituted benzamides. Manufacturers typically introduce the material into condensation or amidation steps following catalytic hydrogenation or chlorination, determining its ratio according to the desired molecular architecture and residue requirements. Finished products must comply with residue, purity, and toxicology controls for crop protection compounds as set by global authorities.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization specifications for pesticide formulations
    • US EPA regulations (40 CFR Part 180) for pesticide residues
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • ISO 17025 laboratory accreditation for quality control

    Typical usage ratio

    • 10–25% w/w in multi-step aromatic amide frameworks; the ratio adjusts for molecular design and solubility
    • Concentration increases in synthesis of active ingredients with high benzamide load

    Downstream process integration

    • Added post-nitration, pre-condensation stage in main synthetic route
    • Participates in batch-wise addition to reaction vessels under inert atmosphere
    • Introduced with controlled dosing for catalytic conversion
    • Acts as coupling agent in amidation before downstream purification

    Final product types

    • Phenyl-substituted herbicide actives (e.g., acetanilide and related benzamide herbicides)
    • Pesticide intermediates for formulation
    • Custom active compounds for soy, maize, and wheat crop protection
    • Post-emergence weed control agents

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers employ 3,4-Dimethylbenzamide as a chemical intermediate in the controlled synthesis of specific APIs, especially where orthogonal benzamide rings confer selective receptor affinity or metabolic stability. Production environments document all handling and integration steps in GMP-certified facilities, adjusting input ratios based on molecule-specific synthesis routes. The compound enters multi-step organic syntheses right after halogenation or acylation, with close temperature and impurity monitoring.

    Industry compliance standards

    • ICH Q7A Guidelines for GMP active pharmaceutical ingredient manufacturing
    • US FDA 21 CFR Part 211 for drug production
    • EU EudraLex Volume 4 GMP for API processing
    • USP and Ph. Eur monograph references for API purity

    Typical usage ratio

    • 5–18% of total reactant mass, depending on synthesis complexity
    • Low-excess use, typically stoichiometric or slight molar extra for complete conversion

    Downstream process integration

    • Introduced following halogen substitution to build amide moiety
    • Added under nitrogen with controlled agitation to reduce by-product formation
    • Blended with co-reactants in pilot or commercial glass-lined reactors
    • Monitored via in-process HPLC for reaction completion before further derivatization

    Final product types

    • Analgesic and antipyretic API intermediates
    • Pharmaceutical grade aromatic benzamide derivatives
    • Small molecule oncology research compounds
    • Custom-developed therapeutic candidates for clinical trials

    3. Dye and Pigment Intermediate: High-Performance Colorant Manufacture

    In the manufacture of high-performance dyes and organic pigments, 3,4-Dimethylbenzamide functions as a key aromatic amide precursor. Pigment producers add this compound during the synthesis of complex azo or anthraquinone colorant molecules, enabling precise chromophore tuning and structural control for specialty textile and plastic applications. Careful management of feed ratio ensures optimal color strength and light fastness, while all production batches follow dedicated chemical safety and environmental standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile colorants
    • EN 71-3 Toy Safety for pigment use in plastic and coatings
    • REACH Annex XVII for aromatic amide intermediates in dyes
    • ISO 105-J01:1997 for color fastness assessment

    Typical usage ratio

    • Between 8–16% in pigment intermediate blends, modulated as required for hue intensity
    • Higher input for deep-shade or technical pigments for industrial coatings

    Downstream process integration

    • Added after sulfonation or nitration as an amide group donor
    • Co-charged with diazo or coupling agents in closed reaction systems
    • Dosed into aqueous or solvent-based synthesis lines under full dust control
    • Blended for specific chromogenic reactions before isolation and grinding

    Final product types

    • Reactive textile dyes
    • Organic pigments for plastics and engineering polymers
    • Inks for technical printing and packaging
    • Color masterbatches for fiber and film extrusion

    4. Fine Chemical Building Block for Custom Synthesis

    Specialty fine chemical producers adopt 3,4-Dimethylbenzamide as a building block when assembling tailored molecules for advanced materials, specialty additives, or contract research purposes. Synthesis labs adjust dosage and purity requirements per project, controlling each process step under ISO-certified quality and consistent documentation. The material integrates with halogenations, alkylations, and ring-closing reactions to introduce methylated benzamide groups into molecular scaffolds where steric or electronic properties drive performance.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management Systems
    • Responsible Care® performance standards for chemical producers
    • Registration under REACH for manufacturing and downstream use
    • National Chemical Inventory listings (TSCA, IECSC, DSL, PICCS)

    Typical usage ratio

    • Ranges from 2–15% w/w in custom processes; dose adjusted for end-use purity targets and molecular complexity
    • Higher ratios for direct methylamide incorporation; lower for multistep transformations

    Downstream process integration

    • Charged with other aromatics post-activation in synthesis sequence
    • Injected in controlled portions under inert gas to minimize side reactions
    • Participates in ring closure or heterocycle formation as a methyl donor
    • Processed in stepwise flow or batch reactors with real-time inline analysis

    Final product types

    • Advanced performance additives for lubricants and coatings
    • Functionalized monomers for polymer synthesis
    • Cross-linking agents for resin chemistry
    • Custom-organic molecules for R&D and material science applications
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