|
HS Code |
336172 |
| Chemical Name | 2-Benzyl-3-Chlorophenol |
| Molecular Formula | C13H11ClO |
| Molecular Weight | 218.68 g/mol |
| Cas Number | 4563-31-3 |
| Appearance | White to off-white solid |
| Melting Point | 52-55°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Smiles | c1ccccc1CC2=C(C=CC(=C2)Cl)O |
| Inchi | InChI=1S/C13H11ClO/c14-12-7-6-10(15)13(9-12)8-11-4-2-1-3-5-11/h1-7,9,15H,8H2 |
As an accredited 2-Benzyl-3-Chlorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-Benzyl-3-Chlorophenol, sealed in an amber glass bottle with a tamper-evident cap and clear hazard labeling. |
| Shipping | 2-Benzyl-3-Chlorophenol is shipped in secure, tightly sealed containers to prevent leakage and contamination. Packaging complies with relevant chemical and hazardous goods regulations. The shipment is accompanied by a safety data sheet (SDS) and appropriate hazard labeling. Handle and store in a cool, well-ventilated area, away from incompatible materials. |
| Storage | 2-Benzyl-3-Chlorophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep the chemical away from heat sources and ignition points. Clearly label the container and ensure access is restricted to trained personnel. Handle with appropriate safety precautions, including the use of gloves and eye protection. |
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Every batch of 2-Benzyl-3-Chlorophenol produced in our facilities reflects years of experience handling aromatic chemicals, particularly those with challenging chlorinated substituents. We build this compound with careful attention to purity and consistency, because downstream applications demand that level of reliability. Our 2-Benzyl-3-Chlorophenol (C13H11ClO, CAS 13319-61-6), known for its unique structure—where a benzyl group anchors itself to a chlorinated phenol nucleus—serves as a critical intermediate in several specialty chemical lines.
The core difference in 2-Benzyl-3-Chlorophenol lies in its dual-substituted aromatic profile. The para position on the phenol ring isn’t left untouched like in simpler cresols or phenols. Instead, it captures a benzyl moiety next to the chlorine atom, creating a molecule with steric bulk and electronic properties well-suited for selective coupling and tailored reactivity. Our plant lines run this synthetic step with genuine care for moisture control and reaction selectivity; even minor impurities, such as unreacted monochlorophenols or dibenzylated byproducts, can complicate downstream purification. So, every kilo leaving our reactors meets the standard needed for fine chemical and pharmaceutical intermediate synthesis.
Typical output presents as a pale-to-light tan crystalline powder. Solubility characteristics sit between those of more hydrophobic biphenyl derivatives and the family of simple phenols—it dissolves well in alcohol, ether, and many organic solvents, but holds limited water solubility. Melting points consistently land within a tightly held range, an important marker reflecting careful temperature monitoring and consistent raw material screening. Impurity control benefits from decades spent learning the quirks of chlorinated aromatic chemistry. Our analytical teams don’t just check boxes—they keep batch histories on nearly every output so trends in chloride handling or raw benzyl reagent variability don’t slip past unnoticed.
Working in the manufacturing space, we see a constant push away from commodity phenolics toward higher-value custom intermediates. 2-Benzyl-3-Chlorophenol doesn’t fall into the pool of ‘general disinfectants’ or basic organic synthons. Its true value shows up in those chemical transformations where alternative chlorophenols fall short: in controlled oxidative couplings, in fine tuning ring activation for Friedel-Crafts, or in preparing specialty ethers for agrochemical actives. From our experience, laboratories needing robust, predictable reactivity—without unpredictable side chemistry from multi-substituted ring systems—consistently come back to this molecule.
Many formulators ask us how this product compares with standard options like 3-chlorophenol, 4-benzylphenol, or simple phenolic building blocks. We’ve run those same reactions side by side on our kilo-scale arrays. The results rarely surprise us anymore: 3-chlorophenol often brings too much reactivity at the wrong site, leading to unwanted isomers. 4-benzylphenol usually misses the subtle electron-pulling effect of the ortho-chloro group and struggles controlling regioselectivity in substitution reactions. Pure phenol might look simpler, but it offers little versatility in modern fine-chemical syntheses. By fixing both groups—benzyl and chloro—in just the right positions, 2-Benzyl-3-Chlorophenol strikes the balance needed for selective reactions and fewer side products. Synthetic chemists chasing difficult intermediates or aiming to build complex aryl structures appreciate those advantages in their workflow.
We see 2-Benzyl-3-Chlorophenol headed most often to facilities focused on advanced synthesis. Its largest adoption comes in the manufacture of high-value pharmaceutical intermediates, where two-step and three-step reaction reliability wins out over cheaper alternatives. Routine users in our customer base operate pilot and manufacturing lines—these aren’t just academic chemists mixing beakers. We hear regular reports of teams using our material as the building block for novel anti-infectives, herbicide analogs, and high-purity specialty resins. Some clients look for the compound as a coupling partner in microwave-assisted syntheses, others target precise etherification where both the chloro- and benzyl groups must remain intact until the final deprotection step.
Sugar-coating the reality doesn’t help production managers planning real-world process campaigns. 2-Benzyl-3-Chlorophenol, with its extended aromatic system, demands tight control of exposure to oxidants during storage. Light and air can encourage slight off-coloration or, worse, slow formation of quinones—so we pack and store under inert conditions based on lessons learned in early pilot batches. Odor reminds us of the parent chlorophenols, but proper ventilation keeps the workspaces healthy. We mark lots with analytical grade details and regularly retest any inventory held beyond standard timeframes, avoiding surprises mid-campaign or inconsistent reaction profiles for long-term partners. Much of this protocol—labeling, sampling, tracking—grew out of responding directly to what users flagged: slight functional group drift or erroneous melting points only became known after barrel-scale storage in one specific climate. Forgetting those hard lessons means risking the next batch, so we put them into our regular training.
The road to improving safety and consistency for 2-Benzyl-3-Chlorophenol echoed paths we walked with other chlorinated aromatic intermediates. On the production floor, the conversation turned from generalized safe handling to specifics: filtration steps with antistatic protocols, carefully calibrated temperature ramps to avoid exothermic events, and strict documentation of each filtration cycle. We trust structured process hazard analyses—not just regulatory checklists—because minor uncontrolled variables can multiply in aromatic halide chemistry. Plant operators know firsthand the difference between running a well-behaved batch and chasing unplanned hot spots in the reactor.
Our R&D colleagues take feedback from chemists working at the front lines seriously. Some of the improvements made to our process—smarter drying cycles, more efficient mother liquor recovery—happened because someone took a moment to explain a recurring bottleneck in their own pilot run. The confidence that teams put in a consistent lot of 2-Benzyl-3-Chlorophenol often rests not on salesmanship, but on consecutive years of reproducible outcomes. We answer direct questions about reaction compatibility, not just because it builds loyalty, but because unexplained reactivity or strange impurities almost always signal something to fix upstream.
The drive for repeatability never comes from regulatory demands alone. Customers who rely on kilogram-to-ton lots learn quickly that only consistent batches let them scale up without troubleshooting every time. Every plant manager here has tackled a batch that ran flawlessly in one cycle but threw off a new impurity after a barely noticeable temperature dip or solvent variation in the next. Our internal guidelines focus on minimizing batch-to-batch variation even at raw material sourcing—testing chlorinated feedstocks for trace acidic residues, qualifying benzyl sources for trace polymeric contamination, and policing water content at all stages.
Line workers and operators handling overheads, crystallizations, and packaging come up with most of the practical innovation. From choosing better filter media that minimize cross-contamination, to flagging a subtle shift in powder color through months of visual inspection logs, these small observations keep our quality on point. Junior chemists on the plant floor may be the first to catch a hint of an off-odor, often a sign of degradation in a drum left unsealed for a few hours in humid conditions. Supervisors tie such clues directly to storage and packaging changes—double-layer drum liners, switched-out gasket types, small cycle time tweaks at the cooling stage. No algorithm could capture these insights without engaged teams taking ownership of the day-to-day process.
Our customers’ chemists almost daily use 2-Benzyl-3-Chlorophenol as a tactical building block, not a simple additive or excipient. The irreplaceable value comes in chemical routes where failure at a single step can mean losing weeks of development time or hundreds of thousands of euros in lost pilot batches. Variability between lots can throw off product yields, disrupt coupling efficiency, or force time-consuming purification just when a regulatory deadline looms. Open discussions about our real-world process controls—solvent grade, filtration steps, or small drying tweaks—are not just box-ticking; they’re part of the relationship that gives buyers more than a drum and a label.
Many customers reach out long before their scale-up begins. We keep a technical onboarding process that involves not just sending certificates of analysis, but connecting process chemists, reviewing application notes, and (with permission) setting up trial batches with their own feedstocks. Sometimes those trials reveal a small difference in impurity tolerance based on their target molecule. Such instances often prompt us to adjust filtration protocols, modify crystallization time, or make other practical changes before the full batch ships. By maintaining an open channel, both teams save months of troubleshooting and gain shared lessons that benefit the next project in line.
Commoditization threatens much of the fine chemical sector, but we’ve resisted pressure to treat specialty intermediates like screenable line items. Our team follows every shipment with regular review, tracking shipment and usage data where possible (subject to privacy and legal rules) to refine our service. Reports from long-term partners trigger plant-side reviews: If a client notes subtle changes in dissolution rate or mentions an unexpected tint, we dive into the data and compare with other recent campaigns. That discipline has more than once caught a catalyst drift or incremental contamination at the solvent-heat exchanger—long before any regulatory or QC audit flagged the change.
Ethical manufacturing for specialty chemicals can’t just be a slogan. Early in our production history, we faced the pitfalls of aromatic effluent management. Waste treatment for 2-Benzyl-3-Chlorophenol residuals, especially those with persistent halogenation, demanded investment in better scrubbing and advanced oxidation units. Teams now run regular reviews of each system, always keeping sight of emission limits and best practices. We learned from challenging moments where the cost of retroactive fixes far exceeded the up-front investment in containment and process refinement. By handling those responsibilities head-on, we safeguard both the communities around us and the continuity of our global supply chain.
Every safety incident or near-miss, no matter how minor, gets reviewed down to the root causes. Operators see their input reflected in the next update to protocols—from new PPE guidance during drum handling to changes in transfer methods for solvents. Senior engineers translate those findings into revised batch guidelines so each new campaign of 2-Benzyl-3-Chlorophenol runs with a lower risk profile. Case reviews circulate internally, with teams dissecting everything from false alarms on gas detectors to small leaks in gasket seating. Our aim is always the same: make sure the next generation of plant workers—and the chemists relying on each shipment—find a safer, more transparent workflow than the last.
No amount of marketing replaces first-hand user trust. The best relationships with procurement teams and research chemists started from open, honest communication about what our product can and cannot do. It’s tempting to trumpet only the wins—a streamlined batch, reaction conditions met on the first try, fewer purification cycles. But we’ve also seen value come from sharing the lessons of lots that drifted in purity or minor packaging hiccups that led to evaporation risk. Our sales staff, drawn from the labs themselves, prefer to speak plainly. They’ll disclose a shift in synthetic strategy or address a challenging impurity head-on, because those small admissions lead to joint solutions.
Manufacturing a specialty like 2-Benzyl-3-Chlorophenol means rarely running on autopilot. Every improvement in analysis, each tweak to a workup sequence, and every user report ripple through our workflows. Some of the most substantial technical partnerships have grown where initial hiccups revealed major insights—cases where, after shared troubleshooting, both sides found a new reaction pathway or an impurity that became a useful marker for downstream analytics. Over the years, this process of continuous feedback and practical problem solving has created genuine value, surpassing what could be found in a technical data sheet or catalog order.
Real-world manufacturing of 2-Benzyl-3-Chlorophenol is as much about respecting the complexity faced by downstream chemists as it is about technical prowess. Every drum shipped, every sample released for pilot work, every analytical certificate shared reflects the ongoing conversation between our production lines and the problem-solvers in labs and plants worldwide. By learning from feedback, anticipating potential stumbling blocks, and adapting practices in real time, we anchor our reliability not just in written specifications but in shared, hard-earned trust. For teams that need an aromatic intermediate that performs as expected—batch after batch—the difference comes not just from our reactors or clean-in-place systems, but from the practical knowledge gathered and acted upon by hands-on experts.