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3,4'-Dimethylbenzophenone

    • Product Name 3,4'-Dimethylbenzophenone
    • Einecs 215-891-1
    • 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

    307837

    Cas Number 1806-28-4
    Molecular Formula C15H14O
    Molecular Weight 210.27 g/mol
    Appearance White to off-white solid
    Melting Point 70-73 °C
    Boiling Point 347.7 °C at 760 mmHg
    Density 1.06 g/cm3
    Solubility In Water Insoluble
    Refractive Index 1.589
    Flash Point 163.3 °C
    Smiles CC1=CC=CC=C1C(=O)C2=CC=C(C)C=C2
    Pubchem Cid 222926

    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 A 25-gram sample of 3,4'-Dimethylbenzophenone is supplied in an amber glass bottle with a tightly sealed cap, labeled for laboratory use.
    Shipping **Shipping Description for 3,4'-Dimethylbenzophenone:** Ships in a well-sealed, chemical-resistant container, compliant with all applicable regulations. Package is clearly labeled with substance name, CAS number (1741-09-1), and hazard information if applicable. Protect from moisture and light. Store and transport at room temperature. Handle in accordance with standard chemical safety guidelines.
    Storage Store **3,4'-Dimethylbenzophenone** in a tightly sealed container, placed in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizing agents, acids, and bases. Ensure appropriate labeling and avoid moisture exposure. Use secondary containment to prevent spills and regularly check for container integrity and chemical leaks.
    Application of 3,4'-Dimethylbenzophenone

    Applications of 3,4'-Dimethylbenzophenone in Industrial Manufacturing

    Manufacturers in the chemical sector utilize 3,4'-Dimethylbenzophenone as a functional intermediate across several distinct downstream industries. Its molecular structure and reactivity profile support specialized roles in advanced organic synthesis, photoactive chemistry, polymer modification, and specialty coatings. The following sections outline core industrial applications, detailing compliance requirements, integration points, and typical product types for each market segment.

    1. Photoinitiators for UV-Curable Coatings

    Producers of UV-curable coatings or inks utilize 3,4'-Dimethylbenzophenone as a builder block in synthesizing Type I and Type II photoinitiators. The compound’s methyl-substituted backbone delivers effective energy transfer under UV exposure, directly affecting polymerization speed and cure depth in applications such as wood coatings, industrial printing, or electronics varnishing. Raw material intake occurs predominantly in the early synthesis of benzophenone-based photoinitiators designed for high-activity inks and clear coatings.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (EC) No 1907/2006 compliance for use in coatings
    • Specific migration limits (SML) under EU Regulation (EU) 10/2011 for packaging inks
    • RoHS (Directive 2011/65/EU) for electronics applications

    Typical usage ratio

    • 5–20% as a weighed intermediate during photoinitiator synthesis. The final addition to coating formulations is typically 1–4% total photoinitiator package by resin weight, tunable based on film thickness and desired cure speed.

    Downstream process integration

    • Integration begins with precursor blending in organic solvent reactors during photoinitiator manufacturing. Downstream users incorporate synthesized photoinitiators into the resin blend before coating formulation, just prior to the pigment or additive mixer stage.

    Final product types

    • UV-curable industrial wood varnishes
    • Inkjet and conventional printing inks for labels and packaging
    • Electronics conformal coatings
    • Protective coatings for automotive plastic components

    2. Intermediate for Advanced Agrochemical Synthesis

    Chemical manufacturers process 3,4'-Dimethylbenzophenone as a key intermediate when building certain selective herbicide and pesticide molecules. Its reactive sites enable tailored Friedel–Crafts alkylation and acylation, guiding the construction of active benzophenone skeletons in molecules targeting weed or insect resistance profiles. Industrial integration typically occurs in multi-step batch processes under controlled temperature and pressure, with strict traceability of starting materials.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015
    • Globally Harmonized System (GHS) SDS for agrochemical intermediates
    • Regulatory technical dossiers for EU (EC Regulation 1107/2009) and US EPA FIFRA
    • Control of Substances Hazardous to Health (COSHH, UK) compliance during manufacture

    Typical usage ratio

    • 10–30% input by mass in agrochemical intermediate synthesis runs. The exact charge adjusted to molar equivalence per herbicide or pesticide target scaffold.

    Downstream process integration

    • Material feeds into the first or second synthetic step of complex molecule assembly. Its role typically precedes halogenation, sulfonation, or alkoxy-group additions, depending on final crop protection molecule design.

    Final product types

    • Selective post-emergence herbicides
    • Insecticidal active ingredients
    • Agrochemical formulation intermediates for crop resistance
    • Plant growth regulatory compounds

    3. Modifier in High-Performance Polymer Backbones

    Advanced materials plants use this compound as a reactive modifier in the synthesis of specialty high-performance polymers, including liquid crystal polymers (LCPs) and engineering thermoplastics. Its methylated aromatic structure confers dimensional stability, thermal resistance, and ultraviolet stability to final polymers, meeting specifications for demanding end-uses in automotive, aerospace, and consumer electronics.

    Industry compliance standards

    • UL 94 flammability standards (for plastics and polymers)
    • ISO 14001:2015 Environmental Management
    • ASTM D638 (tensile properties of plastics) and D256 (impact resistance)
    • RoHS and REACH for electronic and automotive part qualification

    Typical usage ratio

    • 3–8% by monomer batch mass, adjusted for mechanical and optical property targets. Higher loading may apply for color stability or UV resistance improvements.

    Downstream process integration

    • Material enters during initial monomer mixing before polymerization. Labs test compounded batches for molecular weight consistency and dispersion prior to extrusion or molding.

    Final product types

    • Thin-wall LCP components for telecommunications
    • High-heat automotive plug housings
    • Display panel backplates and bezels
    • Wear-resistant gears and mechanical parts

    4. Precursor for Liquid Crystal Material Synthesis

    Manufacturers producing liquid crystal (LC) compounds for flat-panel display or optical device applications utilize this raw material as a tailored core intermediate. The ortho and para-methyl functionalities enable synthesis of advanced mesogenic benzophenone derivatives, controlling phase transition temperatures and birefringent properties essential for dynamic display performance. Precision control over purity levels and trace contaminant removal remains critical during manufacture to meet strict display industry standards.

    Industry compliance standards

    • ISO 9001:2015 for display component intermediates
    • IEC 61249-2-21:2017 (halogen-free certification for electronic assemblies)
    • RoHS 3 (Directive 2015/863) for display materials
    • QC080000 (IECQ HSPM Hazardous Substance Process Management) for electronic materials

    Typical usage ratio

    • 2–7% of the total synthesis mass for single-component LC mixtures, scaled depending on the desired molecular weight and birefringence range.

    Downstream process integration

    • Raw feedstock enters the nucleation stage of mesogen assembly, typically combined with flexible chain spacers and cyano groups before purification for blending into liquid crystal mixtures.

    Final product types

    • Twisted nematic liquid crystal mixtures for LCDs
    • In-plane switching (IPS) display panel materials
    • Optical routing films
    • LC-based light modulating elements

    5. Synthesis of Specialty Fragrance and Flavor Intermediates

    In aromatic chemicals manufacturing, 3,4'-Dimethylbenzophenone stands as a reactive precursor for the synthesis of complex ketones and aldehydes used in niche fragrance and flavor compositions. Its methylated structure allows precise Friedel–Crafts acylation to deliver nuanced olfactory compounds tailored for high-value perfume and specialty food ingredient markets. Strict control over byproduct removal and residual solvent levels is maintained to conform to consumer safety and product stability demands.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 9235:2013 for natural and synthetic aromatic raw materials
    • FDA 21 CFR Part 172 (food additive regulations, where flavor ingredients apply)
    • Good Manufacturing Practice (GMP) standards (EC No 2023/2006)

    Typical usage ratio

    • 1–10% of starting material charge depending on synthesis target. Lower fraction for top-note compounds, higher for fixatives and supporting aromatics.

    Downstream process integration

    • Material enters at the initial acylation or condensation stage for fragrance molecule assembly. Finished intermediates are then further processed into fragrance oils or flavor bases.

    Final product types

    • Specialty fragrance base ketones
    • Fine perfume fixative intermediates
    • Food-grade aroma compounds
    • Fragrance modifiers for personal care and cosmetics
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    Certification & Compliance
    More Introduction

    Introducing 3,4'-Dimethylbenzophenone: A Trusted Choice for Specialized Synthesis

    Real-World Manufacturing Experience with 3,4'-Dimethylbenzophenone

    In manufacturing chemicals for the past twenty years, I have come to appreciate how a single molecule can influence both downstream processes and end-user results. Among the aromatic ketones that cross our production lines, 3,4'-Dimethylbenzophenone has maintained a steady presence. Chemists recognize it for its unique substitution pattern, which leads to reliable performance where subtlety in molecular structure actually matters. We start every batch with carefully sourced raw materials, using control methods that track purity and consistency across multiple scales—gram to tonne. For researchers and formulators, this offers confidence in reproducibility, a trait demanded by both R&D and commercial production teams.

    Understanding the Model and Specifications

    Our 3,4'-Dimethylbenzophenone, with the molecular formula C15H14O, sits apart from many ketones you find on the open market. Its structure includes methyl groups located on the 3 and 4' positions of the benzophenone skeleton. This feature brings several advantages over simpler analogs. We check each lot for physical characteristics—white crystalline powder or off-white flakes, melting point, HPLC purity (minimum 99.5%), residual solvents, and specific trace impurities. These details affect downstream chemistry, so if you are running a process that needs consistent UV absorption, high selectivity in photo-initiated reactions, or cleaner crystallizations, these differences are not minor technicalities—they are decisive variables.

    Our GC and HPLC systems are calibrated daily. Every melting point test draws samples from different zones of the production kettle. If a customer wants a full impurity profile, our QA staff can provide it; if moisture is a concern, we deliver Karl Fischer titration data. Technical staff from both resin and pharmaceutical labs ask about single-batch, multi-kg runs for development phases, and we address these with the same scrutiny applied to our highest-grade lots. We also keep full records on traceability—including all reaction conditions, timelines, batch documentation, and operator logs. This comes from years spent answering audits and requests from major industry players.

    Applications Driving Today’s Demand

    3,4'-Dimethylbenzophenone has found a variety of supporters in industries ranging from photoinitiators and specialty polymer additives to fine chemicals and crop protection intermediates. Our own facility first began routine production to serve photochemistry researchers in Asia who demanded ketones that could offer more defined triplet-state behavior. Methyl groups on the 3,4'-positions shift the absorption properties, opening the door for bespoke UV-curable systems, particularly in clear coatings and printing inks.

    Manufacturers of advanced resins see the advantage, especially where small modifications in additive chemistry impact color stability or cure speed. Technicians running pilot polymerizations have remarked that switching from unsubstituted benzophenone to this dimethyl analog changed both reactivity and the clarity of their product. In our experience, formulators who move toward higher brightness standards in clear coatings are drawn to 3,4'-Dimethylbenzophenone for this reason. It performs with reduced risk of yellowing—an issue chronic in lower-cost benzophenones, which can contain trace impurities that catalyze side reactions or produce colored byproducts over time.

    The pharmaceutical world also leverages this molecule. 3,4'-Dimethylbenzophenone serves as an intermediate for certain APIs and advanced intermediates, thanks to its clean reactivity and low residual contamination. Process chemists tell us that unnecessary side products in an intermediate stage often translate to increased purification steps, greater solvent consumption, and more waste. Our batches offer purity levels that keep chromatography runs short and manageable.

    A Clear View on the Differences with Other Benzophenones

    Experience has taught me that not all benzophenones bring the same value to a synthesis bench or production plant. 3,4'-Dimethylbenzophenone, with its targeted methyl substitutions, develops unique chemical and photophysical properties. The meta and para methyl groups shield certain positions on the aromatic rings, providing increased steric hindrance compared to the parent benzophenone. This difference circumvents issues associated with uncontrolled polymerization, especially in UV-curing environments, where unmodified benzophenone can act either too aggressively or insufficiently as a photoinitiator.

    We have compared plenty of substituted benzophenones—2,4-dimethyl, 4-methyl, 2,2',4,4'-tetramethyl, to name a few. Customers notice the differences in melting points, solubility in monomers, and volatility. Some need more hydrophobicity, and here the methyl substitutions help. They also introduce a slight tuning of both electronic and steric effects, impacting the reactivity profile. Lab trials at our customer’s site have found that impurities in other substituted forms often linger through workup, complicating crystallization and leading to inconsistent batch appearance or yields. We document and share these findings so formulation teams can match the right product to their process, cutting time and cost on troubleshooting.

    On the packaging front, our product resists caking and clumping better than more hygroscopic benzophenone derivatives. Technicians saving room in their climate-controlled storerooms appreciate this. We store drums in dry, shaded warehouses, and we test random packs for water content before shipments are released. From a technical coordination perspective, this level of care proves essential for customers running automated dosing systems.

    Real Stories from Manufacturing and Downstream Application

    A few years ago, a large-scale ink producer approached us, unsatisfied with the inhomogeneity and yellowing produced by their earlier supplier’s benzophenone. Their lines deal with massive daily throughput, and any production hiccup trickles down to packaging and shipping. Our team provided a direct swap—3,4'-Dimethylbenzophenone—along with a full run of physical property data. After two weeks, the ink plant reported less sediment and lower rejection rates for high-speed printing. Maintenance frequency dropped, and the plant saw a tangible reduction in cleaning overhead.

    Material scientists in powder coating development often explore new compositions. One partner company integrated our product in a novel, low-temperature cure powder formula, seeking better balance of UV stability and process economy. The result: sharper cure profiles with lower emissions and greater shelf life, credited in part to the reduced interaction between the dimethyl groups and ambient moisture. This came not from guesswork, but from repeated trials and data exchanged openly between our labs and the user’s pilot line.

    We have also seen positive results with custom synthesis shops that use 3,4'-Dimethylbenzophenone as a building block for more complex molecules. These are not bulk scale, but small to medium-sized operations where yield and consistent performance matter. Proprietary active compounds made from our product have made it to launch without surprises during scale-up—a big relief for project managers with tight timelines.

    There are lessons here for anyone considering a switch in aromatic ketone suppliers. Consistency cannot be measured by a single purity number on a certificate of analysis. Instead, it grows out of engaged communication, coordinated logistics, and a willingness to fine-tune process parameters. We often get called into conference calls or lab visits, where we review not only analytical sheets, but also talk through physical handling, dosage points, and any unanticipated outcomes.

    Technical Challenges: Manufacturing and Quality Perspectives

    Producing 3,4'-Dimethylbenzophenone at industrial scale brings its own set of technical challenges. The Friedel–Crafts acylation that forms the core of the process is sensitive to excesses in both temperature and catalyst. We run multiple pilot batches annually to push yield boundaries and lower residual chlorides, keeping in mind that even trace metals or acid remnants can create headaches for downstream users. Our batch documentation grows thicker with each season, as we layer in more real-time analytics and corrective actions.

    Supply chain fluctuations can disrupt precursor chemicals. When that happens, we quickly verify alternatives and test them under simulated full-plant conditions before rolling out any change. We retain reserve samples for every production run, allowing us to track historical profiles if customers query results months down the line. No two chemical plants face exactly the same solvent recovery or waste management standards; our in-house environmental team regularly reviews emissions and waste output, balancing regulatory needs with customer expectations for responsible production.

    Lab technicians in multiple regions have sent feedback regarding color drift, odor, or inconsistent melting point among alternative suppliers. We tackle this with small adjustments in purification—switching columns, modifying washing solutions, or revising recrystallization protocols as needed. Quality is cumulative, coming from a thousand daily steps that might never make it onto a finished specification sheet, but that make a difference at the point of use. For users who value real reliability, our logs are an open book.

    Customer Collaboration Drives Continuous Improvement

    Over the years, many of our product’s refinements grew from direct conversations with partners. Whether developing better drum liners to prevent sticking, rearranging logistics to minimize transit time, or customizing packaging for facility automation, these aren’t standard responses from a faceless supply chain. Engineers and purchasing staff on the receiving end see benefits not just in yield, but in workflow simplification—a difference noticed most during critical launches or periods of rapid scale-up.

    We have observed supply chain managers move away from spot buying on open commodity platforms. Instead, more procurement staff now seek transparent sourcing and traceability, pushing for collaborative relationships with real manufacturers. By keeping production records, shipping manifests, and QC checkpoints fully available, we empower users to satisfy not just their own regulatory auditors, but also their internal standards teams. The days of counting solely on a third-party trader’s word are fading fast; direct dialog with the factory now drives both trust and future project planning.

    Meeting Regulatory and Environmental Expectations

    Most of our high-volume partners operate in regulated environments where product stewardship matters. Our facility undergoes frequent audits, and we prioritize not just product consistency but safe, responsible practices. Internal teams routinely track emissions, monitor waste profiles, and implement process upgrades in anticipation of both local and export market requirements.

    Customers from Europe and North America often ask us for full reach and hazard profile data, as well as annual trend analyses of trace contaminants. This isn’t just a check-box exercise; it reveals small drifts in process stability, guiding us toward even tighter controls. Newer clients in emerging markets increasingly echo these requests, showing how regulatory convergence is pushing chemical producers to operate with global transparency.

    Onsite staff has participated in cross-industry discussions about circular economy and more sustainable chemical production. We have piloted small-scale heat recovery units, solvent recapture methods, and safer catalyst systems based on real-world feedback. By documenting each upgrade and outcome—positive and negative—we stay accountable, both to customers and to our own standard of care.

    Developments in Downstream Performance

    Recent years have seen new uses for 3,4'-Dimethylbenzophenone, thanks to advances in photochemistry and specialty polymer chemistry. Teams experimenting with digital imaging technologies have reported reduced fogging in photoresist layers. Coating formulators invested in automotive and outdoor applications have remarked on improved UV resistance and surface finish consistency. In these environments, upstream trace impurities—even at low levels—can skew results. By narrowing our process tolerances and improving contaminant tracking, we keep end-user surprises to a minimum.

    Some R&D groups working in light-curable adhesives found that using the dimethyl analog versus common benzophenone delivered more robust shelf stability for their products. These anecdotal reports, backed by side-by-side stability trials and cure rate measurements, support industry trends toward higher-purity specialty additives built around targeted structural modifications.

    Looking Ahead: Innovation Guided by Direct Experience

    The specialty chemicals landscape rewards teams that keep close contact with both suppliers and customers. Our ongoing conversations often blend technical insight with shared problem-solving, whether tuning the crystallization step for scale-up or troubleshooting a batch that didn’t deliver on gloss expectations. The product's role as a dependable intermediate—cleaner, more predictable in its behavior than lesser-tracked alternatives—makes it one of the first choices for those who run projects on accelerated schedules or with strict compliance standards.

    Our team keeps learning from every batch, every feedback form, every escalation from a partner site. This openness to ongoing improvement, paired with the ability to scale changes smoothly, underpins the trust that long-term users place in our product. We keep labs and plants in the loop, avoid shortcuts, and back every lot with precise, reproducible documentation.

    Why 3,4'-Dimethylbenzophenone Continues to Deliver Value

    In the world of specialty intermediates, consistent chemistry means less downtime at the receiving plant, fewer repeat tests, and savings that multiply with scale. We have seen how minute details, invisible to those who never step onto the production floor, can translate into major impact when volumes rise or standards tighten. Methyl substitutions may seem a small tweak, but their knock-on effect across performance incentives, waste management, and final product integrity proves substantial.

    Direct supply relationships eliminate confusion and guarantee flow. By answering technical queries in real time, sharing manufacturing insights without hiding behind brokers, and responding rapidly to changing specifications, the manufacturer-user partnership grows into an engine for innovation. Whether your team is targeting a cleaner photoinitiator, a more stable polymer additive, or a reliable building block for pharmaceutical synthesis, the reality is clear: the subtle differences in molecules, protected by process and people, make all the difference downstream.

    Over time, it’s not the specification alone that delivers value—it is a transparent relationship, a shared understanding of risk, and the combined knowledge of factory floor and lab bench. In the journey to develop, refine, and deliver 3,4'-Dimethylbenzophenone at its best, we welcome every new challenge, every troubleshooting call, and every project where chemistry meets real-world outcomes.