|
HS Code |
417293 |
| Iupac Name | 2-Chloro-6-tert-butylphenol |
| Molecular Formula | C10H13ClO |
| Molecular Weight | 184.66 g/mol |
| Cas Number | 3964-56-5 |
| Appearance | White to off-white crystalline solid |
| Boiling Point | 260-262 °C |
| Melting Point | 68-71 °C |
| Density | 1.16 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 160 °C |
| Refractive Index | 1.553 (20 °C) |
| Synonyms | 2-Chloro-6-tert-butylphenol, PCNB, 6-tert-butyl-2-chlorophenol |
| Smiles | CC(C)(C)c1cccc(c1Cl)O |
As an accredited Phenol, 2-Chloro-6- (1,1-Dimethylethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 500g amber glass bottle with a secure screw cap and clear hazard labeling for safe handling. |
| Shipping | Phenol, 2-Chloro-6-(1,1-dimethylethyl)- should be shipped in tightly sealed containers, away from sources of heat, ignition, and incompatible materials. It is classified as a hazardous material and requires appropriate labeling and documentation according to transport regulations. Ensure secondary containment and proper ventilation during transit to prevent leaks and exposure. |
| Storage | Store **Phenol, 2-Chloro-6-(1,1-Dimethylethyl)-** in a tightly closed container in a cool, dry, and well-ventilated area away from direct sunlight, heat, and incompatible substances such as strong oxidizers and acids. Keep away from ignition sources and moisture. Use in a chemical fume hood, and avoid prolonged exposure or inhalation. Label storage clearly and ensure proper spill containment. |
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Days in a chemical manufacturer’s workshop don’t roll by in abstract terminology. From the moment the first raw drum lands in the facility, the reality of chemical production emerges in the details—the smell, the color, the trace behavior during processing. 2-Chloro-6-(1,1-Dimethylethyl)phenol, long known for its value in specialty synthesis, earns respect in the shop for its clean, crisp profile and reliability, both in production and downstream usage.
Most customers know this compound for its chemical mouthful of a name, though in practice, the science comes down to a straightforward tri-substituted phenol carrying a chlorine at the 2-position and a tert-butyl at the 6-position. We often see it written as 2-chloro-6-tert-butylphenol. Our crew has worked this material for years. Its melting and boiling points shape how we plan storeroom heating and how we time batch runs. From experience, its moderate volatility makes it safer and less prone to loss during transfer than its lighter cousins, and the tert-butyl group keeps its structure stable against oxidation.
Chemicals that travel through reactors and holding tanks do not all behave the same, even with similar chemical frameworks. The tert-butyl group on this phenol adds bulk, which influences both reactivity and handling. Our batch workers never quite handle it the same way as parent phenol or lighter chlorophenols. Phenol by itself—a chemistry staple for decades—gives off a sharp scent and flashes its volatility right at room air. 2-Chloro-6-(1,1-Dimethylethyl)phenol, on the other hand, has more body. Every production line adjustment traces back to that molecular scaffold. Storage calls for attention: this compound demands closed systems, not only to preserve purity but to protect batch yields and maintain workplace air quality. The chlorine and tert-butyl functions each change the way the material interacts with glass, steel, packing, and sealants. Ten years ago, early runs in older lines forced emergency gasket swaps; the memory still shapes our maintenance routines.
Buyers ask for purity. Batches here rarely dip below 99% by GC. For applications in agricultural intermediates, fine chemicals, or specialized resins, off-standard material makes headaches, not just for us but for those down the value chain. Customers in the antiseptics field, who value both the phenolic group’s reactivity and the shield against further oxidation from the tert-butyl moiety, have told us that batch-to-batch consistency reduces requalification costs and lets them predict downstream product shelf-life.
In our work, purity does not simply translate to numbers on paper. Low impurities reflect real operational discipline—controlled distillation, inert-atmosphere handling, and precise charging to limit over-chlorination or side-reactions. Even trace differences in by-product profile can impact how the compound works in sensitive syntheses. Years of method tweaks, from column packing materials to condenser temperature profiles, come to bear on every finished drum.
Chemists often ask: what sets this phenolic compound apart? The answer runs deeper than just having two substitutions on the ring. In our shop, after years of running chlorophenolic structures, several key aspects mark this one out.
The tert-butyl group at the 6-position brings significant steric hindrance. It's not marketing fluff—on the reactor floor, this changes reaction rates, product purity, and even physical handling. You can wash standard chlorophenol residues off glass and hoses with ease, but this bulkier phenol sticks less, resists oxidative fouling, and gives a tighter boil-up curve during distillation.
At the finished goods bay, users in polymer modification and the dye industry comment on the compound’s consistent melting behavior and storage stability. Unlike unsubstituted chlorophenols, which often require stabilizers to avoid slow decomposition, our product keeps well, so long as it’s sealed from moisture and direct sunlight.
Another difference lies in the compound’s electrophilic properties. Compared to plain chlorophenols, the tert-butyl ring substitution pulls electron density in a way that modulates reactivity without losing phenolic character. Formulators who blend it into antimicrobial products and polymer additives rely on this—to them, it’s more selective, less prone to unwanted side reactivity, and, from experience, better at holding its color and clarity through manufacturing cycles.
Questions about usage always surface in customer calls: Where does it fit best? How does it hold up alongside similar molecules?
In agrochemical synthesis, chlorinated phenols function as key intermediates, and 2-chloro-6-tert-butylphenol finds its way into robust herbicide and fungicide frameworks. Its bulky tert-butyl makes downstream molecules more resistant to biological breakdown. This translates to real-life durability in field treatments—an insight that’s passed between technical directors and procurement offices, not just scientists.
The disinfectant and preservative spaces value its dual attributes: broad-spectrum antibacterial power and chemical shielding. The compound’s role as a core in more complex molecules often raises the performance of the final product, and the stability ensures longer shelf life, especially for aqueous formulations prone to hydrolysis or oxidation.
On the shop floor, we have seen direct incorporation into resins where it acts as both a cross-linker and a stabilizer. Its ring structure and substitutions interact favorably in phenol-formaldehyde resin systems, creating polymers with improved resistance to yellowing and heat damage—a key requirement in laminate and insulation board manufacturing. Several high-performance adhesive formulators look for our specification for these very reasons.
Working in chemical manufacturing means constant comparison. At every shipment, buyers cross-compare models, specs, and outcomes. Against standard phenol, which is a sharp, volatile liquid, 2-chloro-6-(1,1-dimethylethyl)phenol feels like a more stable, less hazardous alternative for many applications. Its chlorine content makes it more reactive than tert-butylphenol alone, expanding its scope.
Standard phenol might break down or discolor under long-term heat or light. This chlorinated tert-butyl analog outperforms on storage stability, handling, and end-of-life properties. The difference stands out in downstream processes—reduced offgassing, less fouling of machinery, and a smoother run in continuous systems.
For chlorophenol blends, the tert-butyl group acts as a kind of built-in protection. Compared to 2,4- or 2,6-dichlorophenol, our compound resists dimerization and tar formation, both of which are notorious for causing process downtime and cleaning headaches. As a result, operations in dye, antiseptic, and plastics contexts have shifted procurement toward this option, favoring more predictable performance.
Our team packs the finished product in dedicated, lined drums, never recycled poly or single-use bags. After repeated trials, we’ve found that the material fares best with nitrogen-blanketed packaging, especially for export destinations with long transit times. Each drum’s seal tells a story; cut corners in storage or packaging show up at the next link in the supply chain, usually with rejection claims and wasted man-hours. We see every step—drumming, labeling, sealing—as a safeguard for both handlers and end users.
Handling protocols emerge from real lessons, not abstract guidance. Full PPE, well-ventilated decanting enclosures, strict exclusion of moisture and light, and equipment built with either stainless steel or glass-lining—these are living requirements rooted in decades of practical experience.
We’ve learned to avoid aluminum components, especially in transfer gear, because the chlorine atom, under certain conditions, can start corrosion cycles rarely seen with simpler phenols. Every batch record carries the legacy of troubleshooting, repairs, and hands-on fixes from previous runs.
Quality control isn’t a box-ticking exercise. Each laboratory run checks not just chemical purity, but also color, odor, and stability over time. We draw samples from every production lot and stress-test them for storage simulation, measuring changes in acid number, hue, and volatility. It’s only after meeting our own in-use standards—drawn from failures and fixes, not just regulatory necessity—that the product clears for sale.
Feedback loops from trusted end users drive our internal standards upward. In earlier years, one packaging flaw led to widespread clumping during an especially damp monsoon shipment—feedback led to complete overhaul of our sealing and drum selection, at significant cost, but better outcome for everyone. Sourcing of our raw inputs now includes in-house spot checks and external lab confirmation, ensuring no unwanted halogenated byproducts enter the plant.
Sustainability isn't just a buzzword—every drum returned, every emissions reading, every waste stream becomes a marker of manufacturing discipline. Chlorinated phenols demand real vigilance on the environmental front. Through regular engineering upgrades and tighter controls, our team has reduced vent stack emissions and improved solvent recycling rates year over year.
Real-world incidents shape our drive for safety. A minor spill in a tank farm several years ago led to revised containment and regular external audits. Risk-averse procedures are not cost-saving shortcuts but direct investments in worker health and community safety. As a team deeply invested in both production and the local environment, we push upstream and downstream partners for the same vigilance—closed-loop waste handling, proactive site monitoring, and clear communication of chemical handling hazards.
In the chemical field, recipe tweaks, regulatory shifts, and market changes never slow down. This compound’s distinct advantage—balancing reactivity with stability—has earned it a core place in several specialty applications. We continue to invest in refining our process, collaborating closely with R&D teams both inside and through customer partnerships.
Market feedback sometimes highlights regulatory hurdles, especially around transport and final product formulation. Our internal compliance teams continually track REACH, TSCA, and other regulatory regimes, adjusting documentation and batch controls as needed. Long-term customers value not just an invoice and a drum, but clear, factual transparency—how the product is made, tested, and moved.
Every year, innovations in process intensification and solvent reduction push us to rethink legacy practices. Recent pilot trials with greener chlorination systems, and reduction of off-stream waste, only happened because project teams—line workers, lab analysts, and logistics—brought direct experience to the table. User needs remain the final guide: performance on the ground defines what makes one batch, and one supplier, stand out from another.
2-Chloro-6-(1,1-Dimethylethyl)phenol represents both expertise and hands-on effort. It’s not just about chemical structure, but about each production run—raw inputs, plant conditions, and careful tweaks drawn from years in the field. From nuanced application advantages and live performance feedback to an unbroken chain of responsible handling, this compound stands as a signature of what disciplined, user-oriented chemical manufacturing can accomplish.
As we look forward, feedback and transparent exchange with users—R&D to plant floor—will keep refining the product edge and ensure that every batch moving through the warehouse stands up to the realities of modern industry.