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3,4-Dimethylbenzophenone

    • Product Name 3,4-Dimethylbenzophenone
    • Alias 3,4-Dimethylbenzanilide
    • Einecs 214-604-0
    • 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

    291998

    Chemicalname 3,4-Dimethylbenzophenone
    Casnumber 2434-58-6
    Molecularformula C15H14O
    Molecularweight 210.27 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 77-80°C
    Boilingpoint 331.7°C at 760 mmHg
    Density 1.08 g/cm³
    Solubility Insoluble in water, soluble in organic solvents
    Flashpoint 163.5°C
    Smiles CC1=CC(=CC=C1)C(=O)C2=CC=CC=C2
    Inchi InChI=1S/C15H14O/c1-11-8-9-13(2)14(10-11)15(16)12-6-4-3-5-7-12/h3-10H,1-2H3

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

    Packing & Storage
    Packing 250g of 3,4-Dimethylbenzophenone is supplied in a tightly sealed amber glass bottle with a white label detailing product information.
    Shipping **Shipping Description for 3,4-Dimethylbenzophenone:** 3,4-Dimethylbenzophenone is typically shipped in tightly sealed containers to prevent contamination. Store and transport in a cool, dry, and well-ventilated area, away from incompatible substances. Handle with care, using appropriate personal protective equipment. Comply with local, national, and international transport regulations regarding chemical substances.
    Storage 3,4-Dimethylbenzophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep it out of moisture to prevent degradation. Ensure proper labeling and secure storage to prevent accidental exposure or spillage. Follow all relevant safety and chemical storage regulations.
    Application of 3,4-Dimethylbenzophenone

    Applications of 3,4-Dimethylbenzophenone in Industrial Manufacturing

    3,4-Dimethylbenzophenone serves as a specialized intermediate in multiple industrial sectors, contributing to performance and compliance across fine chemicals, photoinitiator synthesis, pigment manufacturing, and advanced coatings. Our production supports downstream manufacturers with consistently pure material in demanding applications where regulatory adherence, precise formulation, and robust supply are critical.

    1. Photoinitiator Synthesis for UV-Curable Coatings and Inks

    Downstream manufacturers use 3,4-dimethylbenzophenone as a core structural building block in the synthesis of specialized photoinitiators applied in UV-curable coatings and inks for packaging, electronics, and automotive finishes. The integration of this compound increases absorption efficiency of photoinitiator systems in the near-UV range, supporting fast polymerization and high surface hardness in demanding production settings.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing consistency
    • EuPIA Exclusion Policy for Printing Inks and Related Products
    • REACH Regulation (EC No 1907/2006) for chemical substances
    • GMP for Printing Inks (Swiss Ordinance SR 817.023.21)

    Typical usage ratio

    • 10–30% as a precursor within photoinitiator formulations, precise content depends on the target absorption spectrum and reactivity balance; chemists adjust levels for low-migration or high-reactivity UV resin recipes.

    Downstream process integration

    • The compound enters the photoinitiator synthesis step as a substituted benzophenone intermediate. Processers react it with functional agents under controlled condensation or acylation reactions to develop specialized photoinitiator molecules tailored for end-application performance.

    Final product types

    • UV-curable coatings for wood and plastic substrates
    • Offset and inkjet printing inks for packaging and labels
    • Protective automotive clearcoats
    • Electronics-grade conformal coatings

    2. Fine Chemical Intermediate for Pharmaceutical and Agrochemical Synthesis

    Our facility supplies 3,4-dimethylbenzophenone to downstream fine chemical producers as a core intermediate for synthesizing active pharmaceutical ingredient (API) fragments and agrochemical precursors. Its chemical structure enables selective derivatization during the multi-step synthesis of target compounds, particularly in aromatic ketone-based molecules and ligands, ensuring batch-to-batch reproducibility in regulated industries.

    Industry compliance standards

    • Good Manufacturing Practice (GMP; ICH Q7)
    • Pharmacopoeial requirements as per USP, Ph. Eur. (where intermediate registration needed)
    • ISO 22716 for process chemicals in regulated manufacturing
    • REACH and CLP Regulation compliance for chemical handling

    Typical usage ratio

    • Ranging from 5–18% as an intermediate substrate; chemists determine exact input based on the target molecule yield, step yield, and specificity of subsequent derivatizations.

    Downstream process integration

    • The compound is charged in early to mid-stage synthesis steps—often during Friedel-Crafts acylation, alkylation, or functionalization—enabling the introduction of methyl-substituted benzophenone skeletons into key pharma or agro templates.

    Final product types

    • Pharmaceutical intermediate building blocks
    • Precursor molecules for selective herbicides or fungicides
    • Custom aromatic ketone derivatives for clinical research
    • Specialty ligands for chiral synthesis or catalytic applications

    3. Pigment and Dye Intermediate for High-Performance Colorants

    3,4-dimethylbenzophenone functions as a key substrate in the synthesis of high-purity pigments and dyes, including certain specialty azo and anthraquinone colorants. Downstream pigment manufacturers value its dual methyl groups for introducing color-fastness and extended stability to pigments used in plastics, textiles, and industrial paints, with robust traceability and consistency maintained through process controls.

    Industry compliance standards

    • EN 71-3:2019 for toy safety (migration of certain elements)
    • ISO 18451-1:2019 for pigment identification and purity
    • REACH authorization for use in colorant production
    • OEKO-TEX Standard 100 for textile chemicals (input level)

    Typical usage ratio

    • 8–22% based on pigment molecule design; variations depend on desired chromatic intensity, fastness performance, and downstream product matrices.

    Downstream process integration

    • The raw material enters the pigment manufacturing process during the diazotization and coupling or condensation synthesis steps. Its methyl substitutions allow downstream chemists to tailor molecular properties of colorants for application-specific thermal and light stability.

    Final product types

    • Engineering plastics colorants for automotive interior parts
    • Textile disperse dyes for polyester fabrics
    • Industrial paint pigments for metal coatings
    • Masterbatch concentrates for film and fiber extrusion

    4. Additive Intermediate for UV-Absorbing Polymeric Materials

    Downstream polymer engineering sectors incorporate 3,4-dimethylbenzophenone during formulation of UV-absorbing additives, particularly for high-performance plastics such as polycarbonate, acrylic, and polyolefin systems requiring long-term stability and color retention under sunlight exposure. The molecule’s structure provides a backbone for modifying and optimizing UV attenuation, supporting compliance with end-use safety and durability mandates.

    Industry compliance standards

    • ISO 4892-2 for accelerated weathering of plastics
    • UL 94 for material flammability (end-use context)
    • REACH authorization and registration (Annex XIV and XVII)
    • FDA 21 CFR 177.1580 (polymers in contact with food, if applicable)

    Typical usage ratio

    • 0.2–2.5% as a precursor for UV-absorbing agents in masterbatch or compounded resin; manufacturers adjust the input according to polymer matrix and service life specifications.

    Downstream process integration

    • The material is introduced in the synthesis of UV-stabilizing monomers, then incorporated into polymerization or compounding processes for plastics manufacturers, ensuring uniform dispersion in the final matrix.

    Final product types

    • Architectural polycarbonate panels for greenhouses
    • Outdoor signage films and advertising sheets
    • Clear packaging films sensitive to UV degradation
    • UV-stabilized automotive interior plastic components
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 3,4-Dimethylbenzophenone: Direct from the Manufacturer

    Knowledge Earned Through Hands-On Chemical Synthesis

    Crafting 3,4-Dimethylbenzophenone demands patience, careful control, and keen attention to consistency. Over decades in the lab, our technicians have learned what separates reliable products from mediocre or uncertain outcomes. Building every batch, we work directly with premium methyl and benzophenone feedstocks, paying close attention to reaction timing, temperature regulation, and purification to keep impurities out and maintain colorless, crystalline output. Our own technicians monitor each step, confirming specs both visually and with chromatography and melting point tests, so every kilogram matches structural expectations again and again.

    What Sets 3,4-Dimethylbenzophenone Apart

    Within the benzophenone family, subtle changes in molecular structure significantly impact both processing and downstream applications. Adding methyl groups at the 3- and 4- positions creates unique steric and electronic effects. This structural shift influences everything from melting point and solubility to its behavior in photoinitiator and pharmaceutical development. Our material exhibits a reliably sharp melting point in the expected range, along with low volatility and easy filtration. High-purity output allows synthetic chemists and industrial formulators to trust their reaction outcomes, without unpredictable by-products interfering or requiring extra purification steps.

    Many buyers find themselves comparing this compound to alternatives such as 2,4-Dimethylbenzophenone or unsubstituted benzophenone. Experience in catalytic oxidation and condensation reactions shows that even minor placement of methyl groups changes kinetics, yields, and product stability. Customers working in organic electronics, light-absorbing polymers, or pharmaceutical intermediates see clear benefits in using the 3,4-substitution pattern when reliable results are essential — whether due to absorption spectra, reactivity with amines or acids, or ease of isolation. We've handled both regular and custom synthesis; the differences between these positional isomers show clearly in both lab work and final performance.

    Product Characteristics: What We Deliver

    Our 3,4-Dimethylbenzophenone appears as a colorless to pale yellow crystalline solid, depending on storage and batch size. Material passes through sieved drying and filtration lines, reducing dust and preventing clumping. Typical melting points match literature values, often clustering around 58–62°C, reflecting purity rather than contamination. Dissolving easily in common organic solvents, this ketone supports quick preparation for further reactions, as well as straightforward incorporation into more complex syntheses. From our own experience, properly made product maintains stability both sealed in drums or spread thinly on glass plates under typical light conditions.

    Packaged in tight-sealing, chemical-resistant containers, each shipment includes batch lot and test data. Our operators wash, dry, and label every package by hand as part of our process, with random batch sampling sent to an independent testing center for extra assurance. This hands-on approach, run entirely in-house, stems from lessons learned through years of supply contracts with academic labs and major manufacturers alike: chemical buyers remember quality, and they never appreciate surprises that risk production downtime.

    Industrial and Research Uses: Insight from Field Experience

    Consistent batches of 3,4-Dimethylbenzophenone have proven themselves as key precursors in a range of industrial projects. We regularly field calls from formulators in coatings, adhesives, agricultural chemicals, advanced resins, and emerging electronics, all seeking molecules that respond predictably during formulation and end-use. The unique combination of substituted aromatic rings and ketone reactivity allows this compound to anchor synthetic pathways — whether the goal is creating UV-cured polymers or custom ligands for catalysts.

    Years of production have shown that this particular isomer stands out for its photo-activity profile. In photoinitiator chemistry, the electron-donating methyl groups at the 3 and 4 positions alter the absorption and charge separation behavior, which proves essential for fine-tuning polymerization speeds and the stability of finished materials. Recent research into organic semiconductors and advanced optical coatings points toward increased adoption of such molecules, with OEMs valuing reliable melting range and clean UV signature.

    In pharmaceutical custom synthesis, fine distinctions between benzophenone derivatives directly affect the yield and selectivity of target molecules. We have supported pilot runs and regular production of small-molecule intermediates, with chemists returning year after year to reorder from the same validated lot because their synthetic protocols depend on narrow purity windows. For research or scale-up, having transparent, single-source information about the actual batch gives peace of mind and avoids scaleup headaches.

    Direct Access to Support and Customization

    As an actual manufacturer, we respond to operational feedback and work hands-on with scientists at both the bench and production scale. If a customer notices color drift, particle sizing trouble, or solvent pickup, we trace upstream issues in our own equipment. In one instance, an irregular cooling rate led to stubborn clumping, and our shift operators immediately adjusted jacket settings and retested the batch — shipping a new lot in days, not weeks. That kind of direct accountability allows rapid troubleshooting and prompt correction.

    Requests for custom particle size or specialized blending to match automated feeders have led to process improvements benefiting every buyer. Sometimes, a specific application in powder coatings or tablet formulation required us to adapt drying steps or implement tighter sieving routines. Years of tweaking purging, crystallization, and packaging steps have honed a routine that meets both typical uses and rare edge cases.

    Compliance, Traceability, and Safety Knowledge

    Direct handling and bottling bring complete transparency on compliance and quality. Every lot comes from the same audited reactors, and we keep a full record of solvents, process aids, and all analytical checks from receipt of raw inputs to shipment of finished product. Our team participates in chemical safety training, not because regulators require it, but because years in the industry have taught us about the real hazards facing production workers, warehouse teams, and downstream users.

    Material is made in a facility registered under national and local chemical safety codes, and audited by both internal EH&S staff and third-party inspectors. Our quality control group conducts all compliance tests — chemical analysis, purity confirmation, residual solvent screening — using both in-house equipment and outside labs for cross-verification if any anomaly arises. Many downstream users ask about REACH registration, RoHS compliance, or compatibility with specific food-contact or electronics standards. We openly share assay results and processing detail, so no one is left guessing about potential contamination or hidden impurities.

    Learning from Experience: Issues and Their Solutions

    Through years of production and customer feedback, we have encountered — and solved — a range of practical challenges. Storage temperature and humidity, for instance, can affect crystal formation and product flow. Early batches sometimes developed unwanted yellow tint from oxidation or light exposure. After several returns, our technical group implemented new packaging to shield product from air and UV, alongside stricter nitrogen purging before filling.

    Another challenge occurred with international shipments, as long transit led to condensation or compaction in some climates. We responded by adapting procedures to include secondary moisture barriers, as well as pre-shipment conditioning to better match customer storage conditions. The learning curve involved costs, but regular feedback from partners provided clear motivation to refine our logistics as we grew.

    Occasionally, inquiries arise concerning the distinction between batches sourced from large trading companies and direct manufacturer supply. From what we have seen in practice, direct relationships reduce supply chain confusion and enhance both technical support and transparency. Orders handled in-house spare customers from vague answers or mislabeling — crucial if someone’s process depends on specific melting behavior or minimal side-products.

    Environmental and Sustainability Considerations

    Chemical manufacturing today cannot ignore resource use or waste generation. Our factory has faced pressure from local regulators and international clients alike to minimize environmental impact, so we invested in solvent recovery infrastructure and closed-loop water cooling. By optimizing batch sizes for demand, we cut down on residual organic waste and reduced emissions from off-gassing.

    Solid waste from filtration and unused side-product now routes to contracted disposal centers meeting current regulatory and landfill control standards. We remain open to customer audits, having learned that green credentials are not just marketing — they reflect the reality of chemical stewardship in a competitive industry. Over the years, actual feedback from material handlers, local auditors, and overseas partners has driven much of this improvement.

    Ongoing Development and Insights

    Being directly involved in both batch production and customer support brings continuous input on shifting specifications, emerging applications, and evolving standards. Ongoing collaboration with academics and manufacturing partners helps identify whether slight molecular tweaks could improve performance or solve persistent formulation headaches. This dialogue shapes not only changes in 3,4-Dimethylbenzophenone processing, but also ideas for new derivatives and related products.

    Sometimes, a customer will request documentation on previous impurity findings, or comparative data on related isomers such as 2,4- or 4,4'-dimethylbenzophenones. By maintaining a rich database of historical testing, we supply both current and trend information — more accurate than any uncertain secondary distributor. These records assist pharmaceutical chemists, resin formulators, and quality managers who must answer tough regulatory questions during audits or supply chain reviews.

    Educational outreach also plays a constant role in our operations. We bring research partners onsite to see equipment and process controls firsthand, regularly host technical seminars on safe handling, and support student internships who gain real-world training in modern chemical manufacturing. These investments have shaped both our community reputation and our internal skillset, delivering lasting benefits to staff and customers alike.

    Why Direct Manufacturing Matters for 3,4-Dimethylbenzophenone Buyers

    Direct supply guarantees clear traceability, along with immediate access to technical experts who understand both the theory and gritty details of production. Our experience highlights the risks associated with buying through chains of traders or platforms where batch origin, storage, or testing cannot be easily confirmed. In chemical synthesis and advanced manufacturing, small differences in purity, polymorph type, or contaminant level can cascade into significant process and product quality issues downstream.

    We have seen buyers miss deadlines due to poorly documented supply, non-homogeneous lots, or sudden changes in melting behavior traced back to muddled sourcing. Years managing production, and repairing mishaps from third-party batches, have convinced us that single-source, transparent, and thoroughly tested material stands out in both commercial and research applications. Clear communication and accessible batch records make all the difference for customers scaling up or troubleshooting new production routes.

    Looking Forward: Sharing Our Knowledge

    Our team recognizes that needs evolve, especially as chemistry advances and new applications for benzophenone derivatives emerge. Arms-length trading models rarely provide fast or meaningful feedback loops. By investing in tighter cooperation with buyers and directly supporting the research community, we keep standards high and anticipate tomorrow’s challenges before they create problems for the supply chain.

    As we look back on decades of learning and continuous improvement in 3,4-Dimethylbenzophenone synthesis, core values remain the same: unwavering quality, direct accountability, respect for technical accuracy, and sincere engagement with the chemists, engineers, and technologists who rely on us. Every batch shipped reflects the hands of our staff, the input of our partners, and the lessons only learned through direct action — not from a datasheet, but from years of commitment to the practical needs of science and industry.