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HS Code |
869330 |
| Chemicalname | 4-Chlorobenzoic Acid |
| Casnumber | 74-11-3 |
| Molecularformula | C7H5ClO2 |
| Molecularweight | 156.57 g/mol |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 241-243 °C |
| Boilingpoint | 313.6 °C at 760 mmHg |
| Solubilityinwater | Slightly soluble |
| Density | 1.55 g/cm³ |
| Pka | 3.98 |
| Flashpoint | 154.7 °C |
| Smiles | C1=CC(=CC=C1C(=O)O)Cl |
| Refractiveindex | 1.581 |
As an accredited 4-Chlorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle, labeled "4-Chlorobenzoic Acid," features a white screw cap and hazard warnings, securely sealed for laboratory use. |
| Shipping | 4-Chlorobenzoic Acid is shipped in tightly sealed containers, typically made of glass or HDPE, to prevent contamination and moisture ingress. Packages are labeled according to chemical safety regulations and transported in compliance with relevant hazardous goods protocols. Protective measures ensure stability during transit and safeguard handlers from potential exposure. |
| Storage | 4-Chlorobenzoic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Protect the chemical from moisture and direct sunlight. Properly label the storage container and keep it away from food and drinking water. Use appropriate personal protective equipment (PPE) when handling. |
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Purity 99%: 4-Chlorobenzoic Acid with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity content in final products. Melting Point 242°C: 4-Chlorobenzoic Acid with a melting point of 242°C is used in the production of high-performance polymers, where it provides thermal stability and precise processing temperatures. Particle Size <50 µm: 4-Chlorobenzoic Acid with particle size less than 50 µm is applied in specialty coatings manufacturing, where it facilitates uniform dispersion and improved coating smoothness. Moisture Content <0.2%: 4-Chlorobenzoic Acid with moisture content below 0.2% is utilized in agrochemical formulation, where it prevents clumping and enhances shelf-life stability. Molecular Weight 156.57 g/mol: 4-Chlorobenzoic Acid with a molecular weight of 156.57 g/mol is employed in organic synthesis, where it offers precise stoichiometric control for reproducible reactions. Stability Temperature 180°C: 4-Chlorobenzoic Acid with a stability temperature of 180°C is used in electronics chemical processing, where it maintains consistent performance under elevated thermal conditions. Assay ≥99%: 4-Chlorobenzoic Acid with assay greater than or equal to 99% is used in laboratory research applications, where it guarantees reproducible experimental outcomes and data integrity. |
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Ask anyone who’s spent time in a laboratory, and they’ll tell you that what sets certain chemicals apart isn’t just what’s on the label, but how they fit into the daily rhythm of research and manufacturing. 4-Chlorobenzoic acid, known among chemists for its stable crystalline structure and sharp, almost medicinal aroma, carves out its place in the chemical world thanks to its unique properties and diverse applications. Anyone handling organic synthesis, pharmaceutical research, or specialty polymers has probably crossed paths with it, whether they recognize the name or not. Over the years, my own run-ins with 4-chlorobenzoic acid have shown just how valuable this molecule can become—not just for its chemical usefulness, but for the kinds of solutions it unlocks.
Chemists often describe benzoic acid derivatives as building blocks, but the subtle difference of a single chlorine atom transforms the 4-position product into something distinct. This tweak shapes its chemical reactivity and physical characteristics, which shows up in both lab results and real-world performance. The white, powdery substance dissolves in ethanol or ether but resists water, a balance that influences how companies choose to use and store it. The model offered by most suppliers aligns with expectations: high purity percentages, clear labeling, and batch traceability. But there are differences from the sea of alternatives—parabenzoic acid and other chlorinated analogues often can't match its precise melting point or offer the same reactivity profiles that synthetic chemists need.
My first real use of this compound came during a project on active pharmaceutical ingredients. Doctors and patients alike rely on products whose ingredients can be made consistently, with exacting attention to detail. 4-Chlorobenzoic acid’s predictable behavior in both esterification and amidation reactions makes it a real ally. Manufacturers look for that type of dependability; the right intermediates make it possible to create not just drugs, but inks, dyes, and even custom polymers. Because it’s well known among those who work in fine chemicals, 4-chlorobenzoic acid has become a kind of gold standard for intermediates where precision matters.
No two batches come out exactly the same, but consistent high purity—often listed above 99%—sets apart the best sources of this acid. Impurities in industrial chemistry aren’t a minor annoyance; they can cause reactions to fail or lead to wasted product. That’s why the melting point, which typically falls between 241°C and 244°C for high-purity samples, often gets so much attention. Anyone who’s stood over a melting point apparatus knows that a drift of even a single degree can spell trouble for downstream reactions or cause quality audits to flag a shipment. Moisture content and trace solvent residues enter the conversation as well, since labs using advanced NMR or chromatography techniques watch for ghost peaks and trace contaminants. In my own experience with quality control, labs willing to pay a premium on key intermediates often end up saving money by solving fewer problems once production ramps up.
Other specifications target the specific needs of downstream users. Grain size isn’t just a talking point for dust collectors; it matters for handling, weighing, and dissolving. I’ve seen production lines grind to a halt over too many fines or a single stubborn clump that won’t dissolve. Batch records might include details on origin and analytical method, and nobody I’ve worked with laments the extra paperwork when it’s time for regulatory review. Each added detail builds a more complete picture of how the compound moves from bottle to finished product.
Walk into a pharmaceutical lab, and you’ll notice technical shelves filled with reagents ready for synthesis. 4-Chlorobenzoic acid earns its keep here, because its carboxylic group and para-chlorine configuration allow chemists to build complex structures efficiently. In practice, technicians convert it into esters, amides, and more specialized building blocks, bringing new drugs a step closer to reality. Research centers focused on developing safer or more effective painkillers, antifungals, and other treatments often use this acid to create molecular scaffolds that become part of their candidate drugs.
Outside medicine, this compound shows up in the plastics and coatings industries. Manufacturers who want precise control over polymer properties add 4-chlorobenzoic acid to tweak flexibility, resistance to heat, or color-fixing potential. I’ve toured plants where workers use large blending tanks and heating mantles; the acid, with its reliable response to heat and mixing, lets them hit their production targets without massive equipment overhauls. The same story plays out for certain dyes and specialty inks, where the acid’s chemical backbone helps control everything from solubility to lightfastness. Each factory, each product designer, finds a new reason to trust the balance of reactivity and stability.
Even as I write this, researchers around the world are exploring derivatives for electronics, where controlling impurity profiles and electrical properties matters more than ever. It’s easy for outsiders to undervalue these developments, but in my view, the steady flow of slightly improved benzoic acids underpins some of the most advanced material science happening today.
Plenty of benzoic acid derivatives line the shelves of chemical suppliers, each promising certain benefits. The para-chlorine atom isn’t just for show; it gives 4-chlorobenzoic acid a distinctive chemical fingerprint. Reactions that might stall with unsubstituted benzoic acid often move forward more smoothly on account of its electronic effects. Anyone familiar with organic mechanisms recognizes the difference a small shift in electron density makes, especially while planning multi-step syntheses where side products mean wasted time and money. I’ve seen teams choose this compound not because of marketing, but because actual reaction yields and purity numbers back up the decision every time.
4-Chlorobenzoic acid stands apart from related items like 2-chlorobenzoic or 3-chlorobenzoic acid, not just in catalog numbers but in the way these isomers behave. My own benchwork has shown that position matters: the para-chloro configuration keeps steric hindrance low and makes for easier downstream transformations. That subtle difference means researchers spend less time troubleshooting reactivity and more time building molecules that matter. It also enables companies to avoid problems with unwanted byproducts popping up in costlier downstream steps.
Compared to other halogenated acids—like 4-bromobenzoic acid—chlorine’s particular size and electronegativity seem to hit a sweet spot, enhancing reactivity but not introducing unnecessary hazards. Handling and storage remain more straightforward, with less concern about volatility or unexpected decomposition. These practical considerations take on real importance once you graduate from small lab samples to quarter-ton shipments destined for active manufacturing lines.
Storing and transporting reactive chemicals never turns entirely routine, no matter how experienced a team gets. 4-Chlorobenzoic acid, with its moderate hazard profile, still expects handlers to pay attention. It’s not the most hazardous benzoic acid derivative on the market, but that doesn’t mean teams can get careless. Eyes, gloves, and careful weighing remain part of regular practice. Runoff, dust, and accidental spills force conversations about containment, clean-up, and personal safety. In manufacturing settings I’ve visited, robust labeling, color-coded storage bins, and process documentation prevent minor mistakes from becoming major issues.
Disposal comes up regularly as well, both for sustainability and cost reasons. While the compound itself doesn’t create the most serious downstream threats, safe waste handling protocols remain essential. Compliance with local laws, careful record-keeping, and investments in on-site neutralization or collection distinguish companies committed to both worker safety and environmental responsibility. I’ve seen firsthand how the best companies carry these standards across their entire operation, not just the research department.
Lately, the topic of where and how intermediates like 4-chlorobenzoic acid are sourced stirs more debate than ever. Companies that once relied on a few traditional suppliers now confront a global web of pricing, regulations, and quality documentation. In practice, the best product doesn’t always come from the lowest bidder—my own experience tracking down reliable supply lines has shown me the value in building long-term relationships with vendors who prove themselves year after year. I’ve worked through audits where paperwork, certificates of analysis, and batch retests draw the line between trusted ingredient and reject pile. For pharmaceutical use or advanced electronics, the standards go up yet another notch. Buyers check not just for purity but for documented manufacturing practices, traceable raw materials, and transparent transport records. It’s not just bureaucracy; lives and critical equipment rely on these assurances.
Unexpected shipping delays or shortages test everyone’s patience. Forward-thinking firms keep reserved inventory, diversify sourcing partners, and maintain robust testing protocols for every incoming shipment. Good practice comes not only from regulatory pressure, but from knowing the cost of production interruptions. My most successful projects always benefited from open lines of communication between chemical buyers, warehouse staff, and end users, so gaps in the supply chain caused fewer headaches.
Chemistry’s role in society keeps evolving, and those of us who work in the field carry the responsibility to balance innovation with stewardship. 4-Chlorobenzoic acid, while not among the most notorious hazards, plays its part in ongoing conversations about sustainable sourcing, green chemistry, and transparent risk management. Progressive companies now go beyond minimum compliance, examining life-cycle impact and seeking out greener synthesis methods, reduced waste, and safer packaging solutions. Hands-on experience tells me that these investments typically pay off, both in terms of better worker morale and smoother regulatory reviews.
Many manufacturing facilities now invest in scrubbers and filtration systems to reduce emissions of dust and fumes, even where local laws fall short. Partnerships with reliable waste management services and increased attention to spill prevention protect not only nearby communities but also the long-term viability of company sites. Researchers watch for new developments in biodegradability and improved recovery methods, sometimes using their own push for safety as leverage in vendor negotiations.
On a personal note, the changing regulatory landscape sometimes feels overwhelming. Countries update their import and export controls, and certifying a new supplier can add months of paperwork. Yet, these requirements have a real purpose, and I’ve seen positive results when organizations rise to the challenge by improving standards and transparency. There’s an increasing push to digitize traceability, track batches throughout production, and share more with end customers about the origins and safety of critical ingredients.
The biggest opportunity comes from collaboration. I’ve watched chemical engineers, pharmacists, production teams, and environmental experts work together to improve not only yields but also workplace safety and environmental impact. Many solutions arrive on the scene when people share what works—not just in the lab, but in shipping, storage, documentation, and continuous training. It pays to invest in tools, equipment, and processes that turn these commitments into everyday practice. Stronger partnerships let companies handle shifting market forces, supply interruptions, or new regulatory hurdles without sacrificing either reliability or transparency.
Every time I open a bottle of 4-chlorobenzoic acid, I’m reminded that modern chemistry relies on more than the periodic table. Integrity, knowledge, and experience shape each batch and every application, just as much as atomic arrangement or melting point. Whether it’s the world’s next breakthrough medicine or a component in new-age plastics, this compound proves its worth through consistent performance, controllable properties, and robust safety protocols. Companies and labs who treat it as more than a commodity—who take time to understand its quirks and invest in responsible sourcing—set themselves up for success in a competitive, rapidly changing field.
The future doesn’t belong to any one molecule. Yet, for now, products like 4-chlorobenzoic acid sit at the crossroads of research, manufacturing, and careful stewardship. It’s up to all of us—chemists, engineers, buyers, regulators—to ensure that every step along the way reflects both knowledge and care, turning raw material into real progress.