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Methyl 3,4-Dimethylbenzoate

    • Product Name Methyl 3,4-Dimethylbenzoate
    • Alias Methyl 3,4-xylylbenzoate
    • Einecs 223-604-8
    • 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

    334486

    Chemical Name Methyl 3,4-Dimethylbenzoate
    Molecular Formula C10H12O2
    Molar Mass 164.20 g/mol
    Cas Number 14368-95-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 252-254 °C
    Melting Point N/A
    Density 1.045 g/cm3
    Refractive Index 1.520
    Flash Point 112 °C
    Smiles CC1=CC(C)=CC=C1C(=O)OC
    Pubchem Cid 82303
    Solubility In Water Insoluble
    Synonyms Methyl m,p-xylene-3-carboxylate
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing 250g amber glass bottle with airtight screw cap, labeled “Methyl 3,4-Dimethylbenzoate” with hazard symbols, manufacturer and batch details.
    Shipping Methyl 3,4-Dimethylbenzoate should be shipped in tightly sealed containers, away from heat and ignition sources. Ensure compliance with local regulations for transporting chemicals. Use proper labeling, and package to prevent leaks or spills during transit. Typically transported as a non-hazardous material, but consult the SDS for specific shipping guidelines.
    Storage Methyl 3,4-Dimethylbenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Ensure all chemical containers are clearly labeled, and follow standard laboratory storage procedures to minimize risks of spills or contamination.
    Application of Methyl 3,4-Dimethylbenzoate

    Applications of Methyl 3,4-Dimethylbenzoate in Industrial Manufacturing

    Methyl 3,4-Dimethylbenzoate serves as a functional intermediate in multiple industrial sectors. Its chemical structure, reactivity, and solubility profile allow controlled incorporation during synthesis of specialty downstream chemicals.

    1. Agrochemical Synthesis Intermediates

    Agrochemical formulators incorporate this raw material during active ingredient synthesis, especially for selective herbicide or fungicide compounds that require ortho- or para-substituted aromatic esters. Synthesis processes leverage its methyl ester group for stepwise alkylation or condensation, contributing to yield stability and reproducibility. Downstream engineers monitor ester transformation and purification, ensuring compliance with strict thresholds for by-product and residual solvent content.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • EU REACH registration (EC No. 247-239-1)
    • China Pesticide Registration Regulation (ICAMA)
    • US EPA 40 CFR Parts 150–189: Pesticide Programs

    Typical usage ratio

    • 5–15% w/w in herbicide precursor syntheses, adjusted by targeted yield and molecular weight of active ingredients

    Downstream process integration

    • Add as a primary aromatic ester in the early condensation steps
    • Function as a chain-extender or blocking group for aromatic ring functionalization
    • Isolate by extraction and thin-film evaporation prior to active ingredient formulation

    Final product types

    • Triazole and pyridine-based systemic fungicides
    • Substituted benzoate herbicide actives
    • Plant growth regulator intermediates

    2. Pharmaceutical Intermediate Manufacturing

    Custom synthesis groups and contract manufacturing organizations use methyl 3,4-dimethylbenzoate as a building block for non-steroidal anti-inflammatory drugs and certain cardiovascular active pharmaceutical ingredients. Process chemists harness its methyl groups for directed ortho-metalation and carbamate formation. All production steps maintain validated procedures for trace impurity control, and batch-to-batch identity per applicable pharmacopoeias.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur. monographs for intermediates, where relevant)
    • United States Pharmacopeia (USP)–general chapter <795> (APIs)
    • 21 CFR Part 211: US cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 1–8% molar ratio, scoped per drug molecule scaffold and conversion efficiency in the key synthetic step

    Downstream process integration

    • Introduce as a Grignard or Friedel–Crafts substrate during the assembly of drug intermediate chains
    • Subject to ester hydrolysis or transesterification for carboxyl activation
    • Purge residual starting material in API crystallization and filtration stages

    Final product types

    • Analgesic pharmaceutical intermediates
    • Beta-blocker precursor compounds
    • Antipyretic formulation building blocks

    3. Flavor and Fragrance Ester Synthesis

    Within aroma chemical production, this compound functions as a precursor for higher-value esters imparting warm, musk-like notes in fragrances and fine flavors. Esterification reactors selectively modify its methyl groups, producing structurally consistent derivatives. Downstream formulation adheres to food safety and IFRA standards for stability, allergen levels, and compliance with usage restrictions specific to natural and artificial blends.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredients
    • US FDA 21 CFR 172: Food Additives Permitted for Direct Addition to Food for Human Consumption
    • EU Regulation (EC) No 1334/2008: Flavoring Substances in Food
    • ISO 9235: Aromatic Natural Raw Materials—Vocabulary

    Typical usage ratio

    • 0.1–5% of finished aroma concentrate; adjusted to target volatility and solubility in oil-based fragrance carriers

    Downstream process integration

    • Employ as the base aromatic structure in esterification or etherification with flavoring alcohols
    • Subject to molecular distillation prior to blend harmonization
    • Analyze with GC–MS to ensure trace residue control

    Final product types

    • Artificial musk esters in luxury perfumes
    • Flavor additives for fruit and spice profiles
    • Scenting agents in personal care lotions

    4. Polymer Additive Synthesis (Plasticizers and Modifiers)

    Producers of specialty polymers apply this material in the manufacture of custom plasticizers or as a co-monomer for resin modification. It participates in transesterification or copolymerization to impart flexibility, UV-resistance, and processability in end-use plastics. Analytical specialists verify purity, and adjust input ratios in real-time based on polymer matrix demands and process safety guidelines.

    Industry compliance standards

    • ASTM D638: Standard Test Method for Tensile Properties of Plastics
    • EU RoHS Directive 2011/65/EU for Restriction of Hazardous Substances
    • ISO 9001:2015 QMS for Polymer Additive Production
    • FDA 21 CFR 177.2420: Polyethylene Phthalate Polymers (for food contact)

    Typical usage ratio

    • 0.2–4% by total resin mass; levels controlled by flexibility, transparency, and thermal requirements of the target polymer product

    Downstream process integration

    • Incorporate through in-situ melt blending or reactive extrusion during resin production
    • Blend before pelletizing to ensure uniform dispersion
    • Analyze incorporation efficiency by FTIR and DSC before compounding

    Final product types

    • Modified polyester and PET resin grades
    • Low-migration specialty plasticizers for flexible films
    • UV-stable engineering thermoplastics
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    Certification & Compliance
    More Introduction

    Methyl 3,4-Dimethylbenzoate: Precision Chemistry From Direct Manufacturing

    Understanding the Value of Methyl 3,4-Dimethylbenzoate

    Working in chemical manufacturing for more than two decades has shown me the importance of knowing your raw materials on an intimate level—not just the technical details, but also the subtle differences that can shape an entire formulation or production run. Methyl 3,4-Dimethylbenzoate stands out among aromatic esters for a number of reasons. Unlike the more common methyl benzoate or methyl 2,4-dimethylbenzoate, this compound’s unique substitution pattern brings fresh possibilities to synthesis, especially for those pursuing reliable intermediates for active pharmaceutical ingredients, specialty agrochemicals, or flavors and fragrances.

    The route we use in-house for this product avoids unnecessary byproducts and keeps side reactions in check. Consistent methylation patterns matter: minor differences in the position of the methyl groups on the benzene ring can cause entirely different behaviors in subsequent reactions or change how a molecule bonds with catalysts, solvents, or target reactants. Many researchers who arrive at our plant are quick to point at the chemical formula, but only hands-on experience with the reactivity really brings home how much more stable and selective Methyl 3,4-Dimethylbenzoate behaves compared to its isomeric counterparts.

    Our Manufacturing Model: Bulk Quality, Reliable Specs

    Our process for producing Methyl 3,4-Dimethylbenzoate was developed specifically after repeated feedback from clients in the specialty chemical sector and in collaboration with university labs searching for non-linear alkylated aromatic esters. Each batch follows a strict batch-traceable route using high-purity starting materials; we don’t tolerate using recycled or downgraded intermediates for this ester. During every run, we target a purity specification—typically not less than 99 percent by GC analysis—that exceeds standardized benchmarks offered by many upstream suppliers. This isn’t only about laboratory numbers. Lower impurity levels mean easier downstream chemical separations and less risk when scaling up, especially for sensitive syntheses where side reactions eat away at your yield.

    Aside from color and miscibility, I’ve observed how subtle shifts in melting and boiling range can throw off an entire process. Lower-grade methyl esters, especially those cut with residual benzoic acids or inconsistent methylation, introduce unpredictability—something our reactors and glassware don’t forgive. Our technical team knows this product from the ground up. They don’t rely solely on datasheets but take a hands-on approach with every batch, paying close attention to esterification steps, moisture levels, and residual solvents. This attention to detail brings peace of mind to clients who have seen firsthand the impact of micro-scale impurities on catalysis or on the shelf life of blends.

    Applications in Various Industries

    Methyl 3,4-Dimethylbenzoate finds its place in several industries, from pharmaceutical synthesis to designer monomers for advanced polymer projects. We’ve supported projects aiming for fine-tuned esters in the fragrance world—where small changes in structure open new olfactory notes or improve fixative properties. In agricultural chemistry, this compound often features in routes toward complex active ingredients that need consistent performance long-term under variable field conditions.

    Pharma manufacturers often start with our methyl ester when constructing larger molecular frameworks for CNS drugs or antivirals, using the 3,4-dimethyl pattern to orient further substitution with precision. After many years on the plant floor, I’ve seen how unpredictable results can be when suppliers deliver inconsistent isomer ratios, inadvertently introducing 2,4 or 2,5 dimethylbenzoate impurities. These impurities, even in trace amounts, shift downstream reaction rates and trigger unwanted side reactions. Avoiding the frustration of purifying out the wrong isomer saves time, waste, and money. It’s this real-world reliability that matters to those in scale-up and formulation, not just the numbers on a spec sheet.

    We don’t just focus on pharma and agchem. If you examine research journals in polymer and advanced materials, you’ll notice a growing trend toward using methylated aromatic esters as monomers or modifiers. Methyl 3,4-Dimethylbenzoate plays a part in these innovations, furnishing a consistent, high-purity aromatic backbone that integrates well in step-growth or chain-growth polymerizations, offering repeatability across small pilot runs and commercial operations alike.

    How 3,4-Dimethyl Matters: Differences from Similar Products

    It’s easy to group methylated benzoates together, but real lab and plant work quickly exposes the differences. The 3,4-dimethyl substitution pushes both methyl groups directly onto the central ring at neighboring positions. This creates an electron distribution distinct from the 2,4 or 2,5 forms. When you’re catalyzing Friedel-Crafts acylations or preparing cross-coupling partners, you notice a real impact: this substitution offers enhanced stability against nucleophilic attack on the methyl groups, and less activation toward unwanted side-chain reactions.

    Direct tests in our pilot lines have shown improved selectivity for the 3,4-isomer in reactions requiring ortho-para control. Chemists tuning reaction kinetics for amide or ether formation prefer this version for its cleaner separation profile—fewer overlapping byproducts, easier column clean-up, and less risk of co-eluted residuals. This pays off for large-scale operations where every minute of solvent recovery and column use weighs into your project’s budget and calendar.

    While methyl benzoate itself works as a common intermediate, the lack of methyl groups means it reacts less selectively in specific cross-coupling or electrophilic substitution reactions. On the other hand, the 2,4-dimethyl isomer can create steric clashes further along the synthetic process or complicate hydrogenation steps. We hear from customers who have wasted weeks untangling such issues. Going with the 3,4-form gets them back on track—higher yields, more predictable process design, and better performance in end-use formulations.

    Our Practical Experience: Avoiding the Pitfalls

    Factory-floor experience has taught my team and me the difference between a compound that behaves beautifully in the lab and one that holds up on the production line. With methyl 3,4-dimethylbenzoate, moisture and trace acid content can quickly throw off sensitive reactions. We’ve invested in multiple drying, purification, and inert handling stages. Cutting corners with less-controlled suppliers, as I’ve seen elsewhere, adds up in rework, batch loss, and QA headaches, especially when scaling up. Every lot is checked by well-trained staff, not just machines: you can’t replace the value of a trained chemist’s nose and eye, especially catching sub-visible haze, crystal formation, or faint off-odors.

    Transport and storage play a role as well. Unlike more volatile esters, this compound holds up well against evaporation losses, but poorly sealed drums or IBCs with unfiltered headspace can introduce contaminants. Each drum leaving our plant receives nitrogen purging, and we teach downstream partners the right handling routines to protect purity from dispatch to final use. Not every customer thinks about these logistics details until something goes wrong—we help smooth out those wrinkles before they become problems.

    Sometimes buyers chase bargains and end up with product materialized from non-dedicated facilities where cross-contamination from phthalates or even parabens lurks. We’ve engineered our lines for strict aromatic ester production. No risk of crossover with unrelated batches, meaning residual flavors or odors never jeopardize your formulation, and every analysis stays within trace background levels for organic and metal impurities.

    Troubleshooting and Tailoring Solutions

    Scale matters, and one of our core goals has always been bridging the gap between kilogram-scale trials and ton-scale commercial needs. On more than one occasion, we’ve fielded urgent calls from partners stuck with inconsistent lots from overextended suppliers. Reproducibility is not an abstract quality in this business. Any drift in methyl group position or tiny irregularity in color, viscosity, or odor at the plant can break months of development. We keep open lines of communication with technical teams on the client side, exchanging insights about how even a faintly darker color or a one-degree boiling range jump can indicate a production inconsistency. Addressing these real-world subtleties enables our end users to adapt quickly, order only what they need, and never hold excess risky inventory.

    Because our production line is flexible, custom runs aren’t out of reach for development labs or specialty projects. Adjusting purity thresholds, moisture content, or packaging sizes helps labs and commercial users focus on their process goals without compromise. Some customers request extra-low solvent carryover, especially for pharma and flavor applications, so we run extended purging and shorter transfer lines. Others need rapid turnaround for time-sensitive experiments—they get immediate batch-lot validation from our lab before goods leave the facility.

    Waste management and downstream life cycle planning matter in the modern regulatory climate. We’ve worked with clients adjusting process steps to enhance recoverability of spent esters, reducing both cost and environmental burden. Providing transparent information about origin, traceability, and our in-plant minimization of hazardous reagents gives regulatory teams peace of mind—our records and batch cards are always open for customer review.

    Personal experience dealing with formulation chemists and plant engineers taught us the benefit of flexible logistics. Some prefer smaller containers for bench-scale operations; others move entire batches to external blend tanks. We shape our production and delivery options to real project needs, not arbitrary shipping minimums.

    Product Reliability in Competitive Markets

    Every year brings new challenges: supply-chain shocks, evolving regulatory standards, shifting industry trends. Raw material costs and transport volatility hit all producers. In this environment, our ability to adapt batch size, packaging, documentation, and certification stands as our competitive edge. The 3,4-dimethylbenzoate segment may seem narrow to outsiders, but in the manufacturing trenches, slight cost savings or predictability improvements matter. Our partners—whether in specialty pharma, custom synthesis, or aroma chemical markets—keep returning because we keep our promises, not just in paperwork or in guarantees but through hands-on, transparent process audits and real troubleshooting support.

    Critical users focused on green chemistry prize predictable, high-quality intermediates that streamline their downstream processes. They also increasingly weigh environmental and operator safety metrics. Thanks to modernized equipment, disciplined water and energy usage in production, and safe handling procedures, our product leaves a smaller process footprint. We openly share process mass intensity data, solvent recovery rates, and waste stream profiles with any potential buyers or collaborators, supporting not just market needs but broader sustainability trends.

    Educating and Partnering for Applied Success

    No chemical exists in a vacuum. Year after year, we partner closely with buyers in applied research, pilot plants, and large-scale manufacturing to improve not only our process but also how our partners use methyl 3,4-dimethylbenzoate. Sharing real technical detail—not only marketing claims—lowers the risk of failed reactions and enables leaner, more responsive programs. A practical benefit of our direct manufacturing model lies in the transparency it offers. Users tap into both technical support and field-proven application tips gathered from years of close manufacturing collaboration. Whether you’re managing a one-off custom synthesis or responsible for a multi-ton, multi-year supply agreement, expertise in assessing subtle raw material differences leads to better overall process control and stronger business relationships.

    Questions about reactivity, downstream compatibility, or scale-up are welcome. Applying real production insights—about solubility in multicomponent blends, stability under different storage conditions, or potential for green solvent alternatives—gives users actionable tools to save time and reduce troubleshooting. We see our role as more than just a supplier: we’re genuine technical partners, invested in both our own and our customers’ long-term successes.

    Looking Forward: Continuous Improvement and Responsive Supply

    Real progress in specialty chemicals relies on both attention to detail and open-mindedness to new production trends or technical requirements. Our years of experience producing methyl 3,4-dimethylbenzoate inform continuing investments in process technology: moving toward continuous processing, sensor-driven quality control, and real-time process analytical technology (PAT). Adaptation isn’t a slogan but a day-to-day reality as customers revise requirements, regulators set tougher emissions or analytical standards, or new downstream applications emerge.

    Working at the source, we avoid the pitfalls of supply-chain opacity that plague resellers and commodity brokers. We trace every raw material, manage every batch, and keep communication lines open with all stakeholders. In doing so, we ensure each barrel or drum leaving our site reflects the same high standards that have built long-term partnerships across industries. Through this combination of technical rigor, practical experience, and shared know-how, we deliver not just product, but solutions that drive projects forward and keep innovation possible, even in the demanding world of specialty organic chemistry.