Products

3,5-Dimethylbenzoyl Chloride

    • Product Name: 3,5-Dimethylbenzoyl Chloride
    • Alias: m-Xylene α-chloride
    • Einecs: 221-911-1
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 636467
    Chemical Name 3,5-Dimethylbenzoyl Chloride
    Cas Number 1711-03-1
    Molecular Formula C9H9ClO
    Molecular Weight 168.62 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 246-248 °C
    Melting Point 13-15 °C
    Density 1.14 g/cm³
    Flash Point 110 °C
    Solubility Reacts with water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms M-Xylylcarbonyl chloride
    Smiles CC1=CC(=CC(=C1)C)C(=O)Cl
    Refractive Index 1.561
    Storage Conditions Store in a cool, dry place; tightly closed container; away from moisture

    As an accredited 3,5-Dimethylbenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 3,5-Dimethylbenzoyl Chloride is supplied in a sealed amber glass bottle with a secure screw cap for protection.
    Shipping 3,5-Dimethylbenzoyl Chloride is shipped in tightly sealed, corrosion-resistant containers to prevent moisture and air exposure. Classified as a hazardous material, it requires appropriate labeling, accompanied by safety documentation. Transport occurs via ground or air freight under controlled temperature conditions, adhering to national and international regulations for hazardous chemicals.
    Storage **3,5-Dimethylbenzoyl chloride** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat sources, and direct sunlight. It must be kept away from incompatible substances such as water, alcohols, bases, and oxidizing agents. Proper labeling and secondary containment are recommended to prevent accidental release or reaction.
    Application of 3,5-Dimethylbenzoyl Chloride
    Purity 98%: 3,5-Dimethylbenzoyl Chloride with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Molecular Weight 168.63 g/mol: 3,5-Dimethylbenzoyl Chloride with molecular weight 168.63 g/mol is used in agrochemical production, where precise stoichiometry improves formulation accuracy. Melting Point 33-36°C: 3,5-Dimethylbenzoyl Chloride with melting point 33-36°C is used in temperature-sensitive organic syntheses, where controlled melting enhances process safety. Boiling Point 244°C: 3,5-Dimethylbenzoyl Chloride with boiling point 244°C is used in polymer additive manufacturing, where thermal stability supports high-temperature processing. Stability Temperature up to 40°C: 3,5-Dimethylbenzoyl Chloride with stability temperature up to 40°C is used in chemical storage applications, where it retains reactivity without decomposition. Color Index APHA ≤ 30: 3,5-Dimethylbenzoyl Chloride with color index APHA ≤ 30 is used in fine chemical synthesis, where low color index ensures product purity and visual clarity. Acid Chloride Functionality: 3,5-Dimethylbenzoyl Chloride with strong acid chloride functionality is used in acylation reactions, where it delivers high conversion efficiency for aromatic compounds. Reactivity Grade High: 3,5-Dimethylbenzoyl Chloride with high reactivity grade is used in custom organic intermediate preparation, where fast reaction kinetics reduce process time.
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    Certification & Compliance
    More Introduction

    3,5-Dimethylbenzoyl Chloride: Reliability from the Source

    Real Insights from the Manufacturer’s Line

    Every batch of 3,5-dimethylbenzoyl chloride that leaves our plant carries decades of hands-on experience with specialty chlorinated aromatics. Colleagues on our production floor can spot subtle shifts—color, clarity, even how quickly it reacts during synthesis—which means we never trust simply a spec sheet to tell us quality. Over the years, we’ve spent time streamlining the synthesis route for C9H9ClO, always looking for better ways to minimize trace contaminants and maximize reliability during downstream reactions. Direct feedback from labs and process chemists drives our adjustments, refining what ends up in your flask.

    What keeps this compound in steady demand? In our world, 3,5-dimethylbenzoyl chloride stands out for offering consistent chlorinating power for benzophenone synthesis, UV absorber manufacturing, and agrochemical advances. The pattern of methyl groups on the ring helps block side reactions that tend to plague similar reagents, like meta-chlorination or oxidative degradation. Our team intentionally tailors its purity profile above 99%, keeping hydrolysis and benzoic acid byproducts well below detection—something that, from experience, matters when you’re scaling up from pilot to full commercial runs.

    Every Bag Tells a Story

    We’ve seen all sorts of approaches from traders trying to move random stocks, often mixing grades from multiple origins. In our process, the story behind each lot is consistent—core starting materials sourced under long-term chemical supply agreements, continuous flow chlorination monitored by in-line analytics, and precise temperature control. These steps lead to a product our own operators are comfortable staking their name on. Between initial crude separation and final vacuum fractionation, every lot reflects why hands-on process control beats any spec sheet alone.

    Users in UV curable resin fields tell us stories about discoloration or slow curing with lower-grade material they tried elsewhere. It’s always the same root cause—trace less than 0.5% benzoic acid or faulty HPLC step-down that traders miss because they don’t see the reaction environment. We pull composite samples from random containers in every shipment and physically verify results—no exceptions for “big” or “small” orders. Only then does a pallet get loaded for departure.

    What Sets 3,5-Dimethylbenzoyl Chloride Apart

    Anyone running benzoyl chloride derivatives knows the distinct grassy odor and its strong, clean acylating punch. With 3,5-dimethylbenzoyl chloride, the methyl substituents on the ring add bulk and electron-donating effects, which change its reactivity compared to simple benzoyl chloride. This alters selectivity in peptide coupling and fine polymerizations. We’ve walked the line with researchers who swapped in cheaper isomers, reporting tedious purification cycles or off-smell in final material. Most aren’t aware that, during large-scale reactions, small differences in impurity levels amplify as you multiply throughput—a lesson only direct experience reveals.

    Technical teams come to us after finding moisture-sensitive byproducts creeping into their polymers, particularly during humid summer months. In our plant, air moisture stays under tight control throughout all open-container transfers. Standard lab packs come in nitrogen-flushed glass rather than poly, holding off hydrolysis for longer storage. Production drums receive foil-sealed liners to contain any free acid formation, especially vital for high-purity optical or electronic intermediates. Over time, we’ve found that only strict discipline through the packaging stage holds back trouble down the line—a practice we never cut corners on, even for “commodity” shipments.

    Models and Grades Backed by Real-Life Results

    Our standard product rolls out at technical, fine chemical, and high-purity research grades. Technical-grade works for run-of-the-mill industrial endpoints where trace contamination won’t cripple complex downstream syntheses—though as the manufacturer, we never encourage stretching spec limits just for price. Fine chemical and research grades get full chromatographic profiles, confirming the near absence of positional isomers, residual chlorinated tars, and volatile water content.

    Feedback often comes from process scale-ups that hit a wall with inferior supply. For instance, a recent client running UV initiator synthesis in a 10 m3 reactor hit unexpected foaming due to unrecognized hydrolysis byproducts in competitor material. Our direct communication let them trace the issue to too-long dwell times during competitor chlorination. Because our reactors are built for continuous flow—not batch—these problems stay out of our pipeline. Adapting gear and fine-tuning residence intervals took us years, but the result is a product that shows predictable performance even at commercial scales.

    Applications That Prove Themselves

    You’ll spot 3,5-dimethylbenzoyl chloride at the heart of many advances. Producers of photoinitiators for UV-cured adhesives credit the compound for delivering clean, rapid bond strength. From inside our plant, we see how small structure tweaks in a benzoyl chloride analog shape final material properties and end-user process safety. Our compound shines in custom synthesis of substituted benzophenones, where high selectivity and minimal tar byproduct make purification less of a chore. Some of the custom molecules now enabling next-generation sunscreens or advanced resin systems rely on uninterrupted quality, batch after batch.

    Medchem teams working with benzamide structures value the dialkyl effect of our material, noting how it improves steric profile without blocking conventional coupling sites. A few of our partners point out that switching to other isomers, especially with 2,4- or 2,6-dimethyl substitution, means fighting much higher levels of isomeric impurities and dealing with unreliable melting point profiles. We’ve sat down over plenty of tech calls helping clients avoid those detours, always emphasizing which grade, model, and packaging fit their application based on what really happens inside their flasks—not just theoretical specs.

    Supporting Data, Not Just Claims

    Across more than two decades, we’ve watched the market fill with fly-by-night offers claiming 99.5% purity at too-good-to-be-true prices, only for disappointed users to find their downstream reactions suffer. Rather than make empty promises, we regularly update batch COAs, include packed column GC traces, and invite audits from long-term partners. We host client labs in-plant so teams can see—step by step—how we keep hydrolysis and cross-contamination under control. What’s more, we routinely test residue on packaging, providing clients with traceability that survives any audit.

    The more transparent we make the process, the more our end users come to value working straight from the source. Several partners who once worked with resellers now send their own chemists for in-person batch sampling in our QC line, comparing our product against others. Time after time, results align with what we report—backed by our willingness to run control reactions side by side using real production samples.

    Safety in Manufacture and Use: From Operator to Customer

    Chlorinated acyls present handling challenges that only become apparent after repeat exposure—not just to dust and fumes, but also minor leaks during warm storage. In our facility, workers dress out in full PPE, double-glove for every drum changeover, and run all ventilation through multistage acid scrubbers. We trained our staff through first-hand incident reviews and system upgrades; over several years of refinement, lost-time accidents dropped sharply and we passed all safety audits on first inspection.

    Clients consult with us about safe storage and transfer because they value lessons learned from operators, not just regulator checklists. We explain why quick transfer from drum to reactor at site minimizes hydrolysis, and why storing under nitrogen or dry argon preserves purity for long-haul storage. By design, we avoid old-style blow-off vents that release trace vapors to warehouse air. Our plant shift leaders build those safety habits into every outbound shipment, not as a box-ticking exercise, but with the same attention they use at their own stations.

    Ever-Evolving Quality Control

    No two batches start exactly the same. Sometimes upstream feedstock variation, sometimes ambient weather shifts, sometimes tweaks in chlorination quenching—all affect the final output. Our team learned long ago that lab-scale protocols can’t always capture the full complexity of industrial runs. We maintain a deep logbook capturing every tweak, every odd result, and each time a new trace impurity appeared in a packed column GC trace. Instead of brushing over outlying data, our lab chiefs dig back to root causes, often catching process drift before customers notice any change.

    We recheck final bottles for even faint signs of color change, residue, or odor shift. This isn’t some ritual; a customer’s failed batch can cost as much as a month’s profit for us. Our bottling line supervisors, most with more than a decade on the job, do not hesitate to block a lot if something doesn’t look, smell, or weigh right. They have the authority, not just the paperwork, to intervene; that’s how family-owned plants like ours thrive where faceless players fall down.

    Distinction from Other Chlorinated Benzoyls

    Anyone who’s run a separation on a panel of benzoyl chlorides knows the practical headaches of working with similar structures. With 3,5-dimethylbenzoyl chloride, the dual methyl pattern adds not only steric control to limit ortho chlorination, but real-world stability in both cold and mild heat storage. Colleagues using o-toluoyl or 4-methylbenzoyl analogs face higher losses from ring chlorination and more byproduct tar, which gums up reactors and fouls downstream columns. Early in our manufacturing life, we received enough “rescue” requests to see how the differences between these compounds play out not on paper, but in plant bottlenecks, purification headaches, and rising costs down the line.

    Our technical conversations with end users go deep—not just on number-based comparisons, but on living with these products every day. Peers mention how switching to bulk Chinese-supplied technical benzoyl chloride packs led to repeated C13 NMR “ghost peaks,” revealing unpredictable minor contaminants. Our team’s strict process conditions mean users routinely see sharper, easier-to-interpret spectra, with less polishing needed for downstream products. These are not hypothetical advantages; our full-time chemists walk through each spectrum, knowing which one-off impurity comes from a brief power hiccup on the line, rather than a persistent site contamination.

    Troubleshooting and Working with Chemists

    We spend time on the phone, in the lab, and—when needed—on the road working through problems with users who run large-scale reactors or scientific syntheses. Most issues fall into a few realities: trace hydrolysis from too much storage exposure, temperature swing-induced impurity formation, or unexpected cross-reactions in multi-step syntheses. We don’t just drop a technical data sheet in your inbox; we walk users through each checkpoint, using operational field notes, past incident logs, and documented spectra comparisons.

    Those who have run into trouble switching suppliers quickly learn the value of open communication. One common call involves demystifying why a batch from another source ruins a key photoinitiator synthesis, only to discover that thermal ramp rates exceeded typical laboratory profiles. In our plant, we repeat real-use protocols to replicate those outcomes, then tweak reaction parameters until side products drop below the client’s detection threshold. There’s no shortcut to this—years of collaboration with customers teaches you what truly matters beyond the purity number on the bottle.

    Sustainability and Forward Outlook

    We don’t simply watch regulations shift from the sidelines. Chlorinated aromatics face growing scrutiny in wastewater, in solids handling, and in compliance inspections. Our facility engineers new effluent controls, upgrades solvent handling lines to close new leaks, and sacks all production residues for outside incineration not just to meet rules, but because we live beside the communities we serve. We update clients frankly about changing waste handling laws, helping them design recycling systems and containment protocols that actually work. The future of this product line depends on balancing quality, safety, and environmental discipline—no shortcuts, no promises that don’t align with the ground truth.

    Our operators, most of whom have families living near the plant, bring their best every day not just to manufacture a chemical, but to protect the long-term promise of specialty chlorinated benzoyls. As standards increase, we make improvements not only to impress auditors, but because everyone here wants the work to last for the next generation of chemists, operators, and clients.

    Closing Thoughts from the Production Floor

    Every bottle of 3,5-dimethylbenzoyl chloride tells the story of care, grit, and expertise. Our team doesn’t take shortcuts, because we understand both the complexity of the compound and the high stakes for our customers. Over repeated cycles, from small-lot custom syntheses to fifty-ton reactors, we adjust and perfect both the chemistry and the delivery. It’s the hands-on experience, shared between production and user teams, that keeps bringing real results: fewer headaches, cleaner outcomes, and more innovation downstream. That’s the true difference you can expect directly from our line.

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