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HS Code |
461533 |
| Chemical Name | Methyl 2,5-Dichlorobenzoate |
| Cas Number | 2163-58-0 |
| Molecular Formula | C8H6Cl2O2 |
| Molecular Weight | 205.04 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 54-57 °C |
| Boiling Point | 284 °C |
| Density | 1.38 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC(=O)C1=CC(=C(C=C1)Cl)Cl |
| Inchi | InChI=1S/C8H6Cl2O2/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4H,1H3 |
| Refractive Index | 1.574 |
As an accredited Methyl 2,5-Dichlorobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 2,5-Dichlorobenzoate is supplied in a sealed, amber glass bottle, 100 grams, with hazard labeling and tamper-evident cap. |
| Shipping | Methyl 2,5-Dichlorobenzoate is typically shipped in sealed, chemical-resistant containers that prevent leakage and contamination. The packaging complies with relevant regulations for hazardous materials. During transport, the product should be kept cool and dry, away from incompatible substances, with clear labeling to ensure safe handling and proper identification upon receipt. |
| Storage | Methyl 2,5-Dichlorobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat, sparks, or open flames. Protect from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the chemical container clearly labeled and out of reach of unauthorized personnel. Store at ambient temperature unless otherwise specified by the manufacturer. |
Applications of Methyl 2,5-Dichlorobenzoate in Industrial ManufacturingMethyl 2,5-Dichlorobenzoate serves as a specialty intermediate across several tightly focused, process-driven manufacturing sectors. As the original producer, we supply formulators and large-scale plants that require strict adherence to industry protocols and detailed processing knowledge. Below, you will find key downstream application tracks, detailing integration, compliance, dosage guidance, workflow steps, and representative finished products. 1. Synthesis of Agrochemical Active IngredientsProducers of selective herbicides and insecticides employ our compound as a core building block during multi-step synthesis of diverse chlorinated benzoyl derivatives. It typically acts as an intermediate reactant in Friedel-Crafts acylation and nucleophilic substitution stages, enabling manufacturers to access target molecules with precise halogen placements for advanced crop protection formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate ManufacturingPharmaceutical ingredient producers leverage this material in multi-step synthesis routes when constructing complex aromatic scaffolds required for APIs such as anti-infectives and CNS candidates. Specific substitution patterns on methyl 2,5-dichlorobenzoate allow for precision-controlled downstream halogenation, hydrolysis, or coupling with amines using robust cGMP-compliant processes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer Additives and ModifiersManufacturers of high-performance engineering plastics and custom polymer blends include methyl 2,5-dichlorobenzoate as a nucleating or chain-modifying agent. Its controlled reactivity to aromatic electrophilic substitution enables tuning of thermal and mechanical properties in final resins such as polyesters and aromatic copolymers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical and Fragrance Intermediate SynthesisProducers in the fine chemical and specialty fragrance sector utilize this material as a halogenated aromatic intermediate for constructing key aromatic esters and aldehydes. Combined with selective reduction or further esterification, it paves the way for keynotes and modifiers in fragrance compositions and high-value intermediates for flavor and aroma chemicals. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Our teams work hands-on with Methyl 2,5-Dichlorobenzoate (also called 2,5-dichlorobenzoic acid methyl ester) year-round, and over the past decade, we’ve learned a few things about manufacturing, handling, and supplying this useful compound. The finished product comes out as a pale crystalline solid, offering strong stability and consistent purity. It’s typically processed in batch reactors equipped with glass lining to prevent any inside wall corrosion, since both raw materials and finished ester need reliable containment. With a melting point often in the mid-40s Celsius and a boiling point above 270°C, our teams appreciate the manageable handling window – it rarely clumps or degrades during storage or transport, either on-site or for longer-distance shipping.
Our main focus in production sits with the reaction between 2,5-dichlorobenzoic acid and methanol under acidic conditions, followed by careful purification. Several years of experimentation dialed in parameters that guide methanol feed rates, agitation, and temperature holding, all to avoid by-product formation and keep residual acid minimal. High-quality output starts from feedstock selection. Substituted benzoic acid quality varies by supplier, and we screen every lot for iron, sodium, moisture, and color before it enters our reactors. A common complaint among end-users comes from trace metal content, which can cause instability in downstream syntheses. Our standard monitoring methods always catch out-of-spec lots before they affect our final product.
Unlike straight methyl benzoate and unsubstituted methyl chlorobenzoates, this compound’s two chlorine substituents at the 2 and 5 positions shift its reactivity. These electron-withdrawing groups change how the molecule participates in further chemical modification, like nucleophilic substitutions or reductions. For those working in crop protection intermediates, pharmaceutical syntheses, or specialty dyes, this difference matters. Other methyl dichlorobenzoate products, particularly those substituted at 3,4 or 2,4, deliver distinctly different reaction outcomes as precursors. Our regular clients in fine chemicals and agrochemical research have tested all major isomers and turned to 2,5- substitution when seeking a starting material with lower para reactivity and specific halogen migration patterns.
Standard methyl benzoate barely reacts with potassium hydroxide in fusion, nor with amines at moderate temperatures. In contrast, our 2,5-dichloro-methyl ester allows more selective substitution at the 4-position, guided by the neighboring duo of chlorines. This saves both time and cost in multi-step synthesis. Demand for meta-oriented chlorine esters stayed strong even during raw materials disruptions because specialty syntheses depend on the right substitution map. Unlike single-chlorine derivatives, which sometimes fit generic applications, the 2,5-dichloro version stands alone for certain laddered intermediates in fungicide and herbicide manufacturing. Lab teams developing next-generation active ingredients often try alternative isomers first, only to return to this compound after running pilot reactions.
Another point, while some may look at cost or shelf life, we’ve seen customers come back again and again because our in-house manufacturing gives better control over trace impurity patterns. A batch bought from mass traders with unknown provenance often holds residual solvents or odd UV-absorbing contaminants that show up downstream. Our own standards keep total organics and metal traces low, and we always give clients access to analytical files on each batch. We find that a little extra transparency and the discipline of routine checks reduce problems for those running HPLC or high-yield syntheses.
Within our production unit, operators check for methyl 2,5-dichlorobenzoate by both melting point and GC purity. We operate at purity levels above 99%, and every shift includes both interim samples and end-of-batch certificates checked by senior staff. One area that often catches less-experienced manufacturers out comes from incomplete drying post-esterification; any leftover water dulls reactivity and can cause odd spots in TLC for folks synthesizing downstream products. We switched to pressure filtration and vacuum rotary evaporation several years ago, which cut typical water residues to less than 0.1%.
Material moves from reaction vessel through deep-bed filtration, then over to drying under mild heat and vacuum. Visual checks for clumping or discoloration can sometimes pick up iron contamination before more advanced analysis. Every couple of months, we audit each line for potential leaching from glove fittings, glassware, or valves. If any deviation from spec is found, material won’t make its way to customers. Tracking this much detail may sound over-the-top to those who only trade or re-pack chemical inventory, but producing a specialty ester like methyl 2,5-dichlorobenzoate demands this kind of care.
Storing and packing the finished solid requires ambient warehouse conditions. The material does not tend to deliquesce or degrade with short exposure to light or air, but we use opaque containers and inert bag lining for longer storage. Every drum leaves our facility with a full traceability barcode and batch certificate that links back through the whole process. Our logistics managers stick to clean, dry transport, and we rarely hear about material arriving with caked lumps or leaks from careless handling.
In our years manufacturing methyl 2,5-dichlorobenzoate, the dominant demand comes from the specialty chemicals market, particularly as a stepping stone to more complex benzoic acid derivatives. Many projects in pharmaceutical research rely on this ester as a stable stock for custom synthesis, since its melting and boiling points allow easy manipulation on standard lab and plant scale. Medicinal chemists value the electron-deficient aromatic ring, which can accept different nucleophiles or undergo further halogenation. Rarely do they find such versatility in related methyl esters or other dichlorobenzoic compounds.
Formulators in agrochemicals also buy our product to generate selective herbicide and fungicide intermediates. The dual chlorine substitution at the 2 and 5 positions makes it a good candidate for further etherification, amide formation, or reductive cleavage. Compared to its 3,4-substituted cousins, this isomer resists unwanted side-reactions under high-pressure or catalytic hydrogenation steps. Lab teams confirm that yields run higher and purification steps take less time when starting from our 2,5-dichloro methyl ester.
Smaller markets use our material as a foundation block for certain UV-absorbing dyes, specialty polymers, and in custom scent molecule development in the flavors and fragrance sector. Traceability and purity take on special importance for these customers, since unexpected by-products or off-odors can derail an entire run. Our experience says this: reliable starting material makes development smoother.
Every isomer in the methyl dichlorobenzoate family holds its own quirks, but from our production and client feedback, the 2,5 isomer’s main strength lies in predictable chemistry downstream. For example, methyl 3,4-dichlorobenzoate may look similar on a spec sheet, but its reactivity profile fits fewer syntheses and the pattern of electron withdrawal only rarely matches the needs of custom pharmaceutical intermediates. Our labs processed several tons of both 2,4- and 2,5-dichloro methyl esters, side by side, and discovered that the 2,4 version often creates more side products in substitution reactions, requiring longer purification and tighter control of conditions.
Taste and odor sometimes matter to specialty fragrance houses. In head-to-head testing, our 2,5-dichloro product gave a lighter, more neutral aromatic profile compared to the heavier, sometimes resinous scent from ortho-substituted or 3,5 variants. The need for this subtle variability comes up whenever creative synthesis is involved, especially for formulators keen to avoid batch-to-batch variation.
Handling and storage also differentiate 2,5-dichloro methyl benzoate. While some esters with higher melting points clump at room temperatures, our customers find our product easy to weigh and dissolve with standard solvents like acetone, ethanol, or toluene. This translates into fewer technical complaints from both bench chemists and industrial operators.
Direct production poses a few hurdles, as anyone who’s tried to run an esterification using chlorinated benzoic acids knows. Yields can dip if either methanol purity or acidification runs off-target. Several years ago, we set up continuous methanol recycle and closed transfer for acid chlorides to reduce emissions and keep costs in check. Acid scavenging also keeps unwanted copper or nickel out of final batches.
Final purification sets the standard for usability. Trace dimers or over-chlorinated side products won’t always show until a reaction runs out at a customer’s pilot plant. We sample every drum at multiple points in the process and store retained samples for up to two production cycles. Customers tackling regulated syntheses or custom molecule syntheses trust that what’s declared on our analysis matches what lands on their site.
Over the years, we upgraded filter media and moved away from certain elastomer gaskets known to introduce contamination. Feedback from European and North American partners prompted tighter controls on trace metals, so we invested in new ICP-MS screening for every batch.
Buyers ask questions on each order: where did the base acid come from, what else was in the reaction, and who checked the batch. We maintain batch logs down to reagent lot, operator shift, and date. If a client in pharma R&D needs full documentation for regulatory submission, we have that archived and ready. Full transparency about raw materials and process changes makes audits go more smoothly and shortens customer validation time.
For customers blending this material as a feedstock into their own cleanrooms, every reduction in out-of-spec loads saves time and headache. Not every manufacturer can demonstrate they run incoming-raw stability holds or keep long-term retained samples, but we do. Our experience tells us customers with sensitive downstream HPLC or synthesis need this attention to detail.
Technical guidance forms part of our offering. If a client looks to scale a new reaction route, our lab shares historical reactor profiles, impurity tracking, and impurity mitigation advice. We swap tips through customer collaboration – for example, recent work with a dye house led to a different order-of-addition sequence, which cut their batch time by over 15%.
As pressure on environmental and global supply chain issues rises, we find more clients asking about not just quality, but supply resilience and waste reduction. Our choice to source dichlorobenzoic acids from domestic and vetted global partners means carbon footprint and lead times stay under control even as market volatility increases. Investments in solvent recycling and closed-loop system upgrades helped us cut process waste by 30% in the past three years.
Any production that reduces waste or minimizes emissions meets not only regulatory imperatives but also keeps customer cost in check. With most methyl 2,5-dichlorobenzoate made as an intermediate step, clients appreciate this up-front diligence since it lowers the environmental burden on their own reporting and certification.
We work closely with all major fine chemical, pharma, and crop science customers on customized solutions. Many of our long-standing partners started out purchasing raw material lots and have since shared their own process feedback, leading to tailored handling protocols. A straightforward, open channel for technical support goes a long way in preventing problems and fostering trust.
Beyond the technical, we honor customer timelines with clear lead times and backup stocks. If geopolitical shifts or raw material crunches hit, our early warning system flags possible interruptions, and we inform partners early. We don’t rely on stockpiling random inventory and hope for the best – the team forecasts, and shares inventory status openly.
Whether for small scale, gram amounts to support academic research or multi-ton lots for batch production in established plants, every single load matters to our manufacturing and logistics teams. Client feedback over the years encouraged us to dial in packaging, information support, and stability protocols. The result: less friction for all involved.
As applications for methyl 2,5-dichlorobenzoate grow with each year in agrochemicals, API synthesis, polymers, and dyes, we take lessons learned in daily production and pass these along to our partners. The most critical advantage, based on our experience, comes from consistent supply and tight specification control. That means not just flashy purity numbers, but reliable handling experience, minimal contamination, and full transparency in documentation.
We believe that steady improvement, constant feedback cycles, and attention to what really happens on customer production lines matter more than simple product sales. Customers running tight timelines, high-yield syntheses, or regulated processes depend on the trust built in how we run, pack, and deliver methyl 2,5-dichlorobenzoate.
As a chemical manufacturer, we take every batch seriously – not just as a product lot, but as a building block for someone else’s success. Through every stage, from raw acquisition to downstream feedback and application, our hands-on approach makes the difference that technical datasheets can’t always capture. That’s the story behind our methyl 2,5-dichlorobenzoate, and why year after year, customers rely on our supply for their next synthesis, innovation, or scale-up.