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2',4'-Dimethylacetophenone

    • Product Name 2',4'-Dimethylacetophenone
    • Alias DMA
    • Einecs 242-515-7
    • 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

    109311

    Iupac Name 1-(2,4-dimethylphenyl)ethan-1-one
    Cas Number 15944-65-9
    Molecular Formula C10H12O
    Molecular Weight 148.20
    Appearance Colorless to pale yellow liquid
    Boiling Point C 255-257
    Density G Per Cm3 1.008
    Refractive Index N20d 1.531
    Flash Point C 98
    Solubility In Water Insoluble
    Smiles CC1=CC(=C(C=C1)C)C(=O)C
    Pubchem Cid 89248

    As an accredited 2',4'-Dimethylacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2',4'-Dimethylacetophenone, sealed with a screw cap and labeled with hazard information.
    Shipping 2',4'-Dimethylacetophenone is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a flammable organic compound and transported according to local and international regulations for hazardous chemicals. Ensure proper labeling and use secondary containment to prevent leakage during transit. Store in a cool, ventilated area upon arrival.
    Storage 2',4'-Dimethylacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and direct sunlight. It should be kept separate from strong oxidizers and acids to prevent hazardous reactions. Proper chemical labeling and secure placement are essential to avoid accidental spills or exposure. Always follow local and institutional safety regulations.
    Application of 2',4'-Dimethylacetophenone

    Applications of 2',4'-Dimethylacetophenone in Industrial Manufacturing

    2',4'-Dimethylacetophenone is a specialty aromatic ketone widely adopted by manufacturers in the organic chemicals sector for its selective reactivity and structural benefits. Its performance contributes to demanding applications in aroma chemicals, pharmaceuticals, specialty coatings, agro-intermediates, and fine chemicals. As a direct producer, we ensure that our supply meets the rigorous expectations of established industries globally.

    1. Fragrance Intermediates for Fine Aroma Chemicals

    Downstream manufacturers use 2',4'-Dimethylacetophenone as a key intermediate in synthesizing musky and floral aromatic compounds. Its methylated structure allows for precise transformation within controlled Friedel–Crafts alkylation or acylation steps, supporting the development of stable, long-lasting fragrance bases for high-end perfumery. Formulators closely monitor impurity levels to comply with regulatory directives for human contact materials and target consistent olfactory profiles in finished aromas.

    Industry compliance standards

    • International Fragrance Association (IFRA) Guidelines
    • REACH Registration (EU)
    • ISO 9235:2013 (Aromatic Natural Raw Materials and Derivatives)
    • Good Manufacturing Practice (GMP) for Aroma Ingredients

    Typical usage ratio

    • 3%–7% weight-by-weight in core reaction feeds; adjusted depending on desired yield and olfactory intensity target

    Downstream process integration

    • Enters the organic synthesis stage as a precursor in batch or continuous stirred-tank reactors; post-reaction purification involves fractional distillation and crystallization to achieve fragrance-grade purity

    Final product types

    • Musky ketone intermediates
    • Complex fragrance bases for perfumes
    • Functional scent additives for fine soaps and detergents
    • Aroma concentrates for flavor and fragrance formulators

    2. Pharmaceutical Intermediate in Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis

    Pharmaceutical manufacturers utilize this substance as a critical starting material in the multi-step synthesis of certain non-steroidal anti-inflammatory drug scaffolds, thanks to its clean methyl substitution and acetyl group. Its high assay supports downstream halogenation, reduction, or amination processes under GMP. Stringent impurity profiling and documentation ensure safety and regulatory acceptance in APIs and intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • 21 CFR Part 210/211 (US FDA cGMP)
    • European Pharmacopoeia (Ph. Eur.) intermediate requirements
    • USP-NF Monographs for Ketone Precursors (where applicable)

    Typical usage ratio

    • 15%–22% molar ratio in initial condensation steps; adjusted based on target batch scale and final purity yield

    Downstream process integration

    • Loaded directly into reactor for Grignard or Suzuki coupling reactions; followed by extraction, isolation of intermediates, and conversion to active drug substances through multi-step synthetic protocols

    Final product types

    • API intermediates for analgesic and anti-inflammatory agents
    • Bulk pharmaceutical ingredients (BPI) synthesis intermediates
    • Building blocks for custom organic synthesis in drug discovery projects

    3. UV-Curable Coatings and Industrial Surface Treatments

    Within the advanced coatings sector, 2',4'-Dimethylacetophenone serves as an intermediate in the formulation of UV-curable monomers and oligomers. Its structural properties impart improved surface hardness and chemical resistance after photochemical curing. Coating formulators precisely control the material feed and subsequent polymerization to comply with application-specific durability and environmental regulations.

    Industry compliance standards

    • ISO 12944-6 (Protective Paint Systems)
    • RoHS Directive (2011/65/EU)
    • ASTM D6862 (Cured Coatings)
    • REACH Regulation for downstream user safety

    Typical usage ratio

    • 1.5%–4% in prepolymer synthesis blends; used as a specialty intermediate with the ratio tailored to end-use hardness and optical clarity targets

    Downstream process integration

    • Introduced during the prepolymer synthesis stage, followed by mixing, polymer chain extension, and final UV curing to crosslink and set the film's mechanical properties

    Final product types

    • UV-curable floor coatings
    • Industrial metal surface treatments
    • Scratch-resistant automotive component coatings
    • Optical-grade polymer films

    4. Agrochemical Synthesis—Herbicide and Pesticide Intermediate

    Producers of crop protection chemicals integrate 2',4'-Dimethylacetophenone as a building block in multi-step processes to generate selective herbicide and pesticide molecules with specific substituent patterns. Its defined reactivity supports halogenation, nitration, and further functionalizations required for achieving potent biological activity and formulation stability under field conditions.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 158 (US)
    • Regulation (EC) No 1107/2009 for Plant Protection Products (EU)
    • ISO 9001:2015 in agrochemical manufacturing environments

    Typical usage ratio

    • 6%–12% based on active ingredient formation requirements; proportion varies according to target molecule and activity spectrum

    Downstream process integration

    • Input in condensation or cyclization stages; undergoes subsequent functional group interconversion, extraction, and formulation with stabilizers or carriers before packaging as crop-protection agents

    Final product types

    • Selective pre-emergent herbicides
    • Synthetic pyrethroid insecticide intermediates
    • Active substances for formulated field-ready agrochemicals

    5. Fine Chemicals for Photoinitiator Production

    Manufacturers of photoinitiators for UV-cured inks and adhesives source 2',4'-Dimethylacetophenone as a crucial core for downstream construction of benzoin-type or acetophenone photoinitiator molecules. Its methyl substituents enhance absorption and photoreactivity, meeting strict light stability and performance criteria in specialty printing and electronics processing.

    Industry compliance standards

    • ISO 2846-1:2017 (Graphic Technology—Inks for UV Printing)
    • EN 71-3 (Toy Safety for Printed Plastics)
    • Swiss Ordinance on Materials & Articles (SR 817.023.21 Appendix 10)
    • Quality system certification (ISO 9001:2015)

    Typical usage ratio

    • 2%–5% in photoinitiator synthesis batches; final proportion set by target absorption wavelength and ink formulation compatibility

    Downstream process integration

    • Submitted to acylation and nucleophilic substitution reactions, isolated, then purified photoinitiator integrated into pre-ink or adhesive masterbatch blends

    Final product types

    • UV-curing photoinitiators for printing inks
    • Adhesive formulation photoinitiators
    • Coating specialties for microelectronics substrates
    Free Quote

    Competitive 2',4'-Dimethylacetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 2',4'-Dimethylacetophenone: A Closer Look at Our Process and Its Capabilities

    A Manufacturer’s Hands-On Perspective

    Developing fine organic chemicals involves more than combining ingredients and expecting a reliable outcome. Every batch we make at our facility reflects real production experience with materials like 2',4'-Dimethylacetophenone. Over the years, we’ve watched how changes in input quality or subtle tweaks in technical conditions shape the final product and its consistency. 2',4'-Dimethylacetophenone, also known by its CAS number 41030-93-9, represents one of those specialty aromatic ketones where technical skill truly matters.

    Our team works daily with aromatic building blocks—an area that requires attention to both raw material selection and careful control of process parameters. 2',4'-Dimethylacetophenone stands out for its unique reactivity among methyl-substituted acetophenones. By positioning both methyl groups at the 2′ and 4′ positions on the phenyl ring, the molecule’s reactivity, solubility, and even odor profile shift, influencing how end users employ it in downstream synthesis or product formulations. The structure drives subtle differences. In our plant, we keep a close eye on the distillation stage to achieve the expected boiling range and limit unwanted side products. Purity, in this case, matters; trace impurities can compromise yield or interfere with performance in further reactions.

    Purification remains central to our process. We do not stop at a single distillation. Instead, we combine distillation with other methods—crystallization or charcoal treatment where helpful—because we know that certain process contaminants can escape lighter purification. We regularly review product by GC and NMR analysis, not just relying on past data but tracking each lot ourselves. Our specification typically targets a purity above 98%, with moisture and volatile content kept low. Color, an often-overlooked quality factor, receives our attention as well; customers using this compound for fragrance intermediates or fine chemical synthesis have little patience for off-color batches.

    Users choose 2',4'-Dimethylacetophenone as a building block for synthesizing flavors, fragrances, pharmaceuticals, and advanced intermediates. On the factory floor, we receive queries from customers about the exact methylation pattern and its effects. It’s easy to confuse this isomer with 2′,6′-dimethylacetophenone or 3′,5′-dimethylacetophenone, but the chemical and physical properties show measurable differences in processability or odor threshold. Only through years of production do we appreciate how even a minor isomeric impurity shifts chromatograms or alters the performance in condensation reactions. So, we prioritize isomeric purity alongside chemical purity.

    We ship our product in a variety of packaging types, designed to prevent contamination or loss under common storage conditions. Over time, we’ve refined packaging not just to meet regulatory demands but to accommodate feedback from users handling the material in bulk or in smaller-scale R&D labs. Customers who process hundreds of kilograms have warned us about losses or caking in poorly chosen containers, so we’ve adapted, choosing proper liners and closures to keep the chemical stable right up to its last gram.

    Differentiating 2',4'-Dimethylacetophenone from Similar Compounds

    Among all methylated acetophenones, the 2',4' isomer occupies a distinct niche. The ortho and para methyl substitutions alter both electronic and steric factors on the aromatic ring—this changes its fit in reactions and its solubility in organic solvents. In our hands, this isomer reveals specific advantages in Friedel–Crafts acylations and other electrophilic aromatic substitutions, where reactivity and selectivity depend on precise substitution patterns. 2',6'-dimethylacetophenone, for example, tends toward different reaction outcomes, often requiring altered process conditions or more rigorous controls.

    We’ve worked on campaigns synthesizing both the 2',4' and other dimethylated variants. The 2',4'-Dimethylacetophenone produced in our plant exhibits more favorable melting behavior than its positional isomers, allowing for easier handling and a smoother purification process. Product yield and process cost benefit directly. Users in fragrance synthesis often report better performance from the 2',4' variant, particularly in downstream transformations to aldehydes or corresponding acids; this owes to the influence of the methyl groups’ positions on the reactivity of the carbonyl function.

    Color and odor differences, usually invisible on a datasheet, become quite real when working with relatively volatile ketones like this. Isomeric contaminants impact both and can give rise to unpleasant notes or unexpected coloration, especially in aromatic compounds destined for compounds where aesthetics and sensory properties matter. Our routine attention to fractionation and storage means less risk of off-quality lots, and customers with sensitive formulations benefit from that experience.

    Applications That Demand Reliable Quality

    We’ve seen the role of 2',4'-Dimethylacetophenone expand across several high-value sectors. In the fragrance industry, it serves as a core intermediate for musk aroma synthesis and special aldehydic bases. Fine chemicals manufacturers value its reactivity in building libraries of molecules by employing it in Mannich and aldol reactions. When pharmaceutical researchers come to us for grams-to-kilograms, it’s usually intended for unique active ingredients or advanced intermediates—places where a single impurity might derail research or require additional purification steps downstream.

    Our decades of production history give us a unique perspective on performance claims versus real-world outcomes in the lab or on a commercial scale. We have watched researchers and operators struggle with materials sourced from suppliers who cut corners or fail to disclose subtle manufacturing differences. Our process control measures guarantee predictable reaction outcomes—batch-to-batch reliability is not a marketing line, but the result of daily in-process checks, production training, and an insistence on tight analytical controls. It’s our experience that customers who begin with less consistent material eventually need additional purification or face failed syntheses, negating any initial cost savings.

    Batch records and signed analytical results travel with every shipment, and our technical team remains on call to discuss specific properties. Our plant runs several campaign sizes: small R&D lots, medium batches for specialty flavors, and larger runs for fragrance and pharma partners. We track how customer requirements evolve and adjust our process accordingly—sometimes shifting a stage to improve completeness of removal of side-products or adjusting input ratios to meet a customer’s particularly strict purity demands.

    Challenges in Manufacturing and Quality Assurance

    Manufacturing aromatic ketones like 2',4'-Dimethylacetophenone never runs as smoothly as theoretical yields might suggest. Real chemical production introduces variables—ambient temperature, input quality fluctuations, even equipment wear—that affect conversion and consistency. We have lived through many challenging batches: trace water in acetylating agents causing off-spec material, temperature drift in distillation columns requiring real-time adjustment, unexpected clogging from unrecognized byproducts. Each lesson shapes our prevention and intervention steps moving forward.

    Scale-up presents its own unique issues. What works smoothly on a two-liter flask can develop new headaches in a 1000-liter reactor. Mixing, heat transfer, and separation efficiencies change, and yields become sensitive to factors that never showed up at small scale. We invest time in process audits after each scale-up, tracing anomalies, fine-tuning parameters, and double-checking instrument calibrations to maintain product quality.

    Waste management must be considered right from synthesis planning. Spent acids, organic residues, and process solvents all require compliant handling and disposal. Over the years, we’ve moved toward increased recycling and recovery of solvents where feasible, both to reduce costs and to minimize environmental impact. Safety improvements aren’t taken lightly in our plant. Spills, pressure excursions, or equipment malfunctions during synthesis or packaging have occurred; thorough training, monitoring and contingency plans arose out of these lessons. Safe operation isn’t simply a matter of compliance for us—it’s based on lived experience and the desire to keep our team secure on the job.

    Why Consistent Production Matters in the Real World

    At first glance, minute impurity differences in a compound like 2',4'-Dimethylacetophenone might not seem significant, but downstream effects can be profound. We’ve witnessed customers run production lines with supplies from different sources, discovering yield loss and degraded product quality thanks to subtle contaminant profiles. Each molecule has its own behavior in target reactions; unchecked contaminants can serve as reaction poisons, color bodies, or off-odors that ruin entire lots.

    The habits we cultivated in our plant—routine process verification, ongoing worker education, and rapid response to customer feedback—stand behind the consistency of our product. Transparency also matters. Many customers approach us with technical concerns after struggling with off-spec goods from other manufacturers, and we supply both in-depth analytical reports and concrete batch history. Some of our best practices arose from troubleshooting support calls—adapting process steps to diminish recurring customer complaints or requests.

    This practical hands-on approach saves both us and our customers unnecessary troubleshooting and unexpected batch loss. We track every trend in test results, investigate any out-of-range result immediately, and revise our operation rituals as needed. End users who value methodological, reproducible chemistry over abstract guarantees notice these differences; they become long-term partners, returning for both product and honest technical advice.

    Continuous Improvement Based on Feedback and Evolving Demands

    Chemistry never stands still, and neither should production standards. Over time, we’ve worked closely with partners across industries to refine our process for 2',4'-Dimethylacetophenone, introducing improvements year after year. Whether it’s a change in feedstock sourcing to ensure long-term supply, process tweaks to reduce by-products, or filtration upgrades for clarity, customer collaboration drives our upgrades.

    Regulatory expectations and customer applications force us to examine not only purity but also trace contaminants, heavy metals, and environmental residue. Each year, new regulations or evolving analytical techniques drive us to audit our methods, sample more frequently, and invest in new instrumentation for deeper analysis. These upgrades aren’t just regulatory checkboxes; they often reveal hidden issues or unlock new performance benchmarks in our chemical outputs.

    We’ve adjusted packaging to meet customer needs. Bulk buyers managing pneumatic transfer systems needed sturdier containers. Smaller buyers working in labs requested more convenient, easy-pour bottles. We sourced and tested newer packaging options, trialed them in-house, and switched after confirming storage stability and safety in actual conditions. These changes come from real users, not theory.

    Safety also evolves. Early on, our focus leaned heavily toward process efficiency. Over time, as we experienced incidents and near-misses, we built in more systematic risk assessments, retrained the workforce, and hardened our processes. Both safety and reliability improved—in lockstep with customer confidence.

    Conclusion: Proven Manufacturing of 2',4'-Dimethylacetophenone

    Supplying a chemical like 2',4'-Dimethylacetophenone goes far beyond reaching an analytical specification. Behind every batch lies process knowledge, technical flexibility, and a long-term view of what real-world users need from their suppliers. Preparation, purification, and attention to consistency define our product as much as the chemical formula. Users demand a trustworthy supply and predictable quality—the only answer comes from experience, responsiveness, and a commitment to ongoing improvement. From our vantage point—right inside the plant—that’s the real story of 2',4'-Dimethylacetophenone manufacturing.