|
HS Code |
960076 |
| Cas Number | 2519-85-3 |
| Molecular Formula | C7H2Cl4O2 |
| Molecular Weight | 259.90 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 226-230 °C |
| Boiling Point | Decomposes before boiling |
| Density | 1.8 g/cm³ (approximate) |
| Solubility In Water | Slightly soluble |
| Pka | 2.1 (carboxylic acid group) |
| Synonyms | 2,3,4,5-Tetrachloro-1-benzoic acid |
| Ec Number | 219-784-2 |
| Pubchem Cid | 17816 |
As an accredited 2,3,4,5-Tetrachlorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g 2,3,4,5-Tetrachlorobenzoic Acid comes in a sealed, amber glass bottle with a screw cap and safety labeling. |
| Shipping | 2,3,4,5-Tetrachlorobenzoic Acid is shipped in tightly sealed containers to prevent moisture exposure. It is packaged according to regulatory guidelines for hazardous chemicals. During transit, proper labeling and documentation are provided to ensure safe handling. The substance should be stored in a cool, dry place away from incompatible materials. |
| Storage | 2,3,4,5-Tetrachlorobenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Keep it away from direct sunlight and sources of ignition. Use secondary containment to prevent spills and store at room temperature. Handle with appropriate personal protective equipment. |
Applications of 2,3,4,5-Tetrachlorobenzoic Acid in Industrial Manufacturing2,3,4,5-Tetrachlorobenzoic acid serves as a critical intermediate across several specialized chemical industry chains. Its chlorinated aromatic structure enables targeted reactivity, positioning it as a foundation for downstream formulations in advanced polymers, crop protection actives, specialty pigment synthesis, and electronic materials. The following scenarios outline the precise integration of this material in certified manufacturing processes, guided by regulatory requirements, validated process methodologies, and defined end product specifications. 1. Synthesis of Chlorinated Polyimide Resins for Electrical InsulationWithin high-performance polymer production, 2,3,4,5-tetrachlorobenzoic acid is a strategic monomer for developing polyimides used as electrical insulators in industrial and consumer electronics. Its defined chlorination pattern enhances thermal stability and flame retardance, making it essential for insulation components where operating temperatures and fire safety are paramount. Manufacturers incorporate this acid at prepolymer or dianhydride stages in closed reactor systems with real-time in-process verification. Industry compliance standards
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2. Intermediate for Agrochemical Active Ingredient ManufacturingThe molecular structure of 2,3,4,5-tetrachlorobenzoic acid allows its use as a building block in synthesizing specific chlorinated herbicides and fungicides. Agrochemical manufacturers use it as a substituent ring precursor in multi-step organic synthesis, leveraging its selective chlorination for downstream coupling and halogen-exchange reactions. All processes utilize closed handling systems with traceable batch protocols to eliminate residual contamination. Industry compliance standards
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3. Specialty Pigment & Dye ManufacturingThis compound introduces critical halogenated moieties during the manufacture of specialized organic pigments, especially for high-durability coatings and inks. Its well-defined substitution pattern enables bright, solvent- and light-stable pigment structures when integrated into azo and phthalocyanine pigment synthesis routes. Industrial pigment lines use it as a selectivity agent to improve chroma and weatherfastness, supporting regulated product certification. Industry compliance standards
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4. Advanced Electronic and Semiconductor ChemicalsProducers of certain microelectronic chemicals and photoresist additives utilize this acid as an intermediate in the synthesis of halogenated aromatic compounds tailored for wafer fabrication and etching processes. Its use supports the development of molecules with precisely controlled electron-withdrawing characteristics, granting enhanced etch resistance and patternability within microcircuit manufacturing. Industry compliance standards
Typical usage ratio
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In our work as a long-standing producer of chlorinated aromatics, 2,3,4,5-Tetrachlorobenzoic Acid stands out as a specialized intermediate. Its structure, carrying four chlorine atoms on the benzene ring and anchored by a carboxylic acid group, gives this molecule a distinct chemical profile that’s found high value in agrochemical and fine chemical routes. Years of refining and scaling up production taught us a few things about quality, handling, and who exactly benefits from a batch done right.
We manufacture 2,3,4,5-Tetrachlorobenzoic Acid using controlled chlorination processes and high-efficiency purification. Exchange at the plant level or with our technical team usually centers on the product’s purity—experiments and downstream reaction consistency both hang on this detail. Typical purity by HPLC tests runs above 98%, a figure that’s not achieved by accident, but by real back-and-forth on parameters. What looks like a white to faintly off-white crystalline powder might sound interchangeable with other benzoic acids, but subtle differences in handling, filtration and washing make a world of difference in scaling up to full batches.
Chemists coming from a trader or distributor background might underestimate the logistical quirks that come up with 2,3,4,5-Tetrachlorobenzoic Acid. In-house, we focus hard on avoiding caking and clumping in storage. Our experience says: don’t assume a high-melting aromatic acid behaves “like the others.” With a melting range about 255–260°C, thermal stability sets this material apart from some lighter chlorinated benzoic types, making it practical for recycling from reaction filtrates or precise thermal processing. The physical structure after drying—free-flowing versus compacted—carries implications for dosing, weighing, and scaling in both pilot and full commercial runs.
Handling chlorinated acids isn’t just about what’s in the drum. Downstream, the way material is manufactured drives safety performance on multiple levels. Our operation practices rigorous control on fugitive emissions during production; it hasn’t just protected worker health, it’s cut regulatory headaches. Unlike some benzoic acid variants, residual unreacted chlorine and process mother liquors demand special treatment and tight monitoring to avoid off-gassing or persistent trace contamination in effluent. Years of developing in-plant loop capture systems have cut our waste loads and improved the carbon footprint significantly.
Commercial partners and direct consumers in our experience put a premium on consistency batch-to-batch. In laboratory synthesis, a few points of purity drift get flagged, but in plant operations, they translate to hours of troubleshooting. Because the tetra-chloro pattern of the molecule can attract trace metals or bind solvent residues more tightly than lower chlorinated benzoic acids, we’ve honed a two-stage crystallization practice that directly yields the preferred physicochemical form for most downstream applications. This specific morphology, and the ability to predict it, saves headaches for formulators, blenders, and analytical chemists taken by surprise by polymorphic mismatch or erratic dissolution.
Fine organic synthesis circles know that chlorinated benzoic acids serve as stepping stones into active pharmaceutical ingredients, herbicides, and advanced materials. The tetra-chloro layout found here gives it reactivity distinct from the mono- and di-chloro analogues widely produced elsewhere. Where some acids see use in food preservation, our product’s profile lends itself to more targeted, specialty work—alkaline hydrolysis, nucleophilic aromatic substitution, or building more heavily functionalized aromatics for complex synthetic targets. The chlorine-rich backbone tunes the acid for resilience under harsher synthesis conditions, letting it serve as a formidable intermediate where lighter analogues falter.
The big difference between 2,3,4,5-Tetrachlorobenzoic Acid and other isomers lies not only in reactivity, but in how they are handled during high-volume manufacture. Lower-chlorinated benzoic acids, like the mono- or di-chloro types, tend toward less thermal stability and a slightly increased risk of oxidation or color body development over time. From years of filling, re-crystallizing, and analyzing the final shipments, we know that the tetra-chloro variant holds up better in long-term storage, exhibits less degradation under typical warehouse conditions, and offers greater predictability for downstream chlorination or amide-formation steps.
For end users that need tougher intermediates that don’t break down or drift in purity during storage, the tetra-chloro acid offers a higher-performance option. Not every application will call for it—price and reactivity considerations drive choices in commodity synthesis, but customers working in agrochemicals, certain colorant lines, and research formulations find it pays off. The expected purity range and strict control on trace byproducts also set it apart from bulk supplier material, which often shows minute impurities that lead to unwanted side reactions or color fouling.
It’s easy to overlook the importance of optimized process design when discussing specialty chemicals, but the difference is real in day-to-day running. Early runs making 2,3,4,5-Tetrachlorobenzoic Acid taught us the hard way about solvent carryover in final product, especially when aiming for less than 0.2% by weight for residuals. Tweaks in drying temperatures, longer filtration times, and carefully selected filter aids changed the consistency of every lot shipped since. These are not academic changes; they cut down off-spec returns and improved customer confidence in our readiness to meet the next spec increase.
Solubility tuning also came up often. The higher chlorinated benzoic acids can show stubborn behavior in organic solvents, affecting dissolution rates during downstream synthesis. Working with formulators directly, our team tested modified drying and micronization strategies that yield powders with an improved particle size profile—leading to faster, more complete dissolution in standard solvents. Over the past decade, feedback cycles with our partners directly influenced every major process upgrade, with real-world cases driving change rather than lab theory alone.
Our plant has supplied 2,3,4,5-Tetrachlorobenzoic Acid chiefly as a building block in the synthesis of agrochemicals, dyestuffs, and high-end research reagents. Researchers gravitate toward it for building dense aromatic rings or as a starting point for complex carboxylic acid derivatives. Few alternatives can reliably stand up to the same reaction environments or deliver on byproduct control. The acid’s chemical features enable select transformations, such as directed ortho-lithiation, nucleophilic substitution, or controlled reduction, making it a preferred choice in programs requiring dense core modifications in multi-ring systems.
Beyond classic chemical synthesis, some partners in surface chemistry or electronics pursue the acid for producing specialty resins or functionalized polymers, though technical hurdles remain in scale-up. The four chlorine groups open up pathways closed to lower-substituted acids, letting users push boundaries in molecular design. For these tasks, the clean shelf life and consistent particle form our team produces get called out repeatedly.
A host of storage and performance issues have shown up over our history. Though the product stands up better than most benzoic acids to warehouse conditions, improper packaging or unsealed bags can allow moisture pick-up and partial agglomeration—even in a low-humidity environment. These changes in physical consistency force users to rethink dosing or, worse, halt a crucial reaction for reprocessing. Our shift to multi-layer lined sacks and robust drum closures reduced these incidents sharply, a change pursued after seeing too many otherwise perfect lots become partially compromised in transit or months-long storage.
Analytical drift—caused by micro-contaminants or exposure to reactive vapors—also gets flagged on occasion, particularly in labs running highly sensitive analytical techniques. Continuous dialogue with advanced users prompted us to invest in cleaner, more filtered plant air supplies and improved in-process sampling, so every outgoing drum reflects the best we can do under scaled-up conditions. Our goal: give users confidence in every lot, not just the ones for headline research.
Most industrial users come to us looking for more than a bag or a drum. Needs are shaped by real projects—sometimes calling for a finer powder, sometimes for a particular residual moisture spec. Over time, we adopted flexible drying and milling schedules, making it possible to dial-in physical properties batch-by-batch. Our technical team also supports users launching new synthesis protocols, sharing processing experience that cuts down trial-and-error on their side. Unlike high-turnover, low-margin commodities, our business and reputation grow from keeping lines open to talk fast and solve small problems before they snowball.
This collaborative approach means some material gets adapted—for example, prepping smaller lot sizes for research institutions or working with pilot plants on tailored bulk shipment. The days when “one size fits all” worked are long gone. For advanced chemistries, the margin for error shrinks, and having a ready contact at the factory delivers more value than just another datasheet.
In choosing among chlorinated benzoic acids, plenty of chemists start with the easiest or cheapest route. Yet over the years, we found project timelines matter as much—or more—than up-front costs. Lower-chlorinated or mixed-isomer acids typically come with broader impurity profiles, and often don’t tolerate the oxidation or acidic cleaning conditions needed for more elaborate synthesis routes. With 2,3,4,5-Tetrachlorobenzoic Acid, users report fewer rework cycles and more predictable yields downstream.
Many who once tried switching among isomers or moving to “generic” sources encountered problems with unexpected byproducts or difficult color removal in later processing. What can look like a minor impurity at scale may catalyze complex, unwanted rearrangements. The tighter the control on the intermediate, the lower the chance of process shut-down. For us, this means returning customers who once tried trading off specification for price, only to return and ask for our high-purity, lot-traceable material.
Making and selling specialty chemicals like 2,3,4,5-Tetrachlorobenzoic Acid isn’t about hitting a purity number one time—it’s about building trust across teams and projects. Real factories experience real hiccups: operator turnover, equipment shifts, tighter government scrutiny, and evolving customer needs. Each production run adds to a data set that drives improvement—or flags problems fast. Sometimes, what matters to the user isn’t in the spec at all, but in response times, batch notes, or real-time troubleshooting support. Our role doesn’t end at shipment. Projects needing long-term, uninterrupted synthesis benefit from experienced manufacturers with a memory for past wrinkles and a willingness to share practical fix-it knowledge.
Through tighter in-plant analytics, upgraded packaging, and alive-to-risk logistics, we keep performance high. It’s not theory—it’s our direct answer to issues raised on the customer side and our own internal drive to do better each year. The goal: help users blend, react, develop, and analyze with maximum confidence, batch after batch.
Markets push for greener, more efficient, and safer processing routes. 2,3,4,5-Tetrachlorobenzoic Acid sits within a changing landscape. We field more questions about minimizing waste, cutting solvent footprints, and maximizing value across the product life cycle. By cooperating with end users and research partners, our plant adapts—upgrading chlorination efficiency, improving yield from recycled streams, and driving new purity or morphology standards as project partners ask for them. Shared experience and open feedback cycles shape what comes next.
We don’t view 2,3,4,5-Tetrachlorobenzoic Acid as a commodity filler but as a keystone for advanced, reliable, and responsible chemistry. Each kilogram carries real intention—on efficiency, consistency, and partnership. This may sound simple, but for anyone deep in specialty synthesis, the difference reveals itself, lot after lot and run after run.