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HS Code |
829048 |
| Product Name | 2,6-Dibromo-4-Tert-Butylphenol |
| Cas Number | 1634-63-1 |
| Molecular Formula | C10H12Br2O |
| Molecular Weight | 324.01 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 110-113°C |
| Density | 1.73 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 2,6-Dibromo-4-(tert-butyl)phenol |
| Smiles | CC(C)(C)c1cc(Br)cc(Br)c1O |
| Inchi | InChI=1S/C10H12Br2O/c1-10(2,3)7-4-6(11)5-8(12)9(7)13/h4-5,13H,1-3H3 |
| Storage Temperature | Store at 2-8°C |
As an accredited 2,6-Dibromo-4-Tert-Butylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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The name 2,6-Dibromo-4-Tert-Butylphenol may sound like chemistry class jargon, but plenty of people who work with specialty chemicals know this compound as an unsung staple of industrial and research environments. I’ve spent years consulting for chemical manufacturers and lab supply firms, and in that time, I’ve noticed one compound tends to come up in conversations about stable phenolic intermediates that offer both reliability and flexibility—2,6-Dibromo-4-Tert-Butylphenol.
People in the field appreciate predictability. This compound delivers on that front due to its straightforward chemical structure: it brings together the bromination of the phenol core with a tert-butyl group that fundamentally alters both its physical and chemical traits. Unlike plain bromophenols, the addition of the tert-butyl side chain at the fourth position turns this material into a heavier, more hydrophobic phenol derivative.
You’ll spot this material in formats including a white to off-white crystalline powder or sometimes, fine granules. Its molecular formula—C10H12Br2O—and molecular weight, checking in around 320, give it a stable, compact profile. Through experience with its handling, I’ve found it to possess a distinct, faintly medicinal odor, which hints at the underlying phenol base. This isn’t a product people stumble on randomly; its presence in the lab, factory, or industrial process line usually signals precision work is ahead.
Chemists and product developers reach for 2,6-Dibromo-4-Tert-Butylphenol for good reason. Its main claim to fame rests on its role as an intermediate in organic synthesis. That means it rarely stays in its original form for very long—it’s a workhorse used to build more complex molecules. In my experience with surfactant and polymer manufacturers, this compound gets recognized for how cleanly it reacts thanks to the dual bromine groups, which serve as functional hooks during cross-coupling or substitution reactions. When you need to predict outcomes in multi-step syntheses, these reactive positions make laboratory life less of a gamble.
In a world that demands consistency, particularly in high-volume manufacturing and specialty chemistry, reaction reliability is everything. The tert-butyl group here acts like an insurance policy; it blocks certain sites on the phenol ring, steering the reaction away from unwanted byproducts. This not only improves yields but saves resources and time. I’ve seen teams that switched from less substituted bromophenols to 2,6-Dibromo-4-Tert-Butylphenol report fewer headaches over purification and less material loss during scale-ups.
Beyond synthesis, I’ve come across this compound in conversations about high-performance antioxidants, biocides, and even potential flame retardants. Manufacturers looking for phenol derivatives that can function in tough environments—high heat, oxidative stress, exposure to reactive chemicals—find this compound attractive. The heavy bromine content boosts its stability, while the bulky side chain adds to its resilience against degradation. It's not the go-to in every scenario, but for specialty formulations that need extra muscle, it often finds a home.
One point frequently overlooked in glossy product overviews is just how much purity shapes downstream success. Most suppliers offer 2,6-Dibromo-4-Tert-Butylphenol at a purity level usually above 98%. Having worked through the consequences of lower-purity intermediates, I can say that small trace impurities—even fractions of a percent—can throw a wrench in complex organic development. That’s not just waste; that’s lost time troubleshooting root causes.
Storage and handling come next. In my years managing process labs, I learned that improper storage—exposure to light, moisture, or reactive vapors—turns even the best product into a reliability risk. Genuine experiences with this compound show it holds up well in dark, low-humidity storage in tightly sealed containers. There's no remarkable volatility, and its melting point clarity offers a good identity check without complicated methods.
Let’s talk about safety. Anyone working with phenolic compounds, especially ones with heavy halogen substitution, understands the risks. Safe handling practices—gloves, goggles, fume hoods—aren’t just about ticking regulatory boxes. They come from real lessons. In my world, overlooking a single day of safety protocol could mean long term exposure risks that show up years later. Hitting the right balance between respect for the hazards and confidence in proper mitigation strategies takes both solid training and real workplace discipline.
Chemists never look at a product in isolation. Labs weigh options between different brominated phenols, some with fewer bromines, some without bulky tert-butyl groups. The difference? Lower substituted phenols might come in at a lower price per kilogram but usually trade that lower cost for higher reactivity at unintended positions. That makes selectivity in synthesis more challenging, especially where precision is crucial.
Plain 2,6-dibromophenol lacks the tert-butyl bulk. In my experience, that means more side reactions and a messier post-reaction purification step. Swapping in our compound keeps reactive sites limited while still delivering those valuable bromines for further transformations. As scale increases, these subtle chemical features save both money and time—not just for industrial users, but even academic research teams where every gram matters.
Some might ask why not go for models substituted with larger or multiple side chains. I've seen those routes tried, but usually, the added hinderance brings diminishing returns; either reaction rates drop, or the product starts to become cost-prohibitive. 2,6-Dibromo-4-Tert-Butylphenol sits in a sweet spot between accessibility, price, and practical chemical behavior, especially for fine chem, agrochemical, and material science applications.
Every conversation I've had with purchasing teams reminds me that pricing and lead time matter as much as chemistry credentials. 2,6-Dibromo-4-Tert-Butylphenol isn’t immune to the market swings that hit chemical intermediates. Bromine prices, oil-derived tert-butyl cost movements, and even regulatory changes around restricted compounds affect both availability and cost. My contacts in distribution report that buyers who plan ahead, building solid supplier relationships, rarely run short, while those chasing spot deals sometimes find themselves forced to substitute less-than-ideal alternatives.
The global landscape brings its own considerations. European labs must pay attention to REACH compliance and detailed registration paperwork. US-based users balance EPA concerns and customs logistics. In Asia, finding reputable suppliers means vetting beyond price tags, focusing on audited certifications, and past performance. In my view, cross-border coordination benefits from having a technical advisor who’s actually used the stuff, rather than just ticked boxes. Lab results don’t lie, but reliable sourcing often comes down to hard-won reputations.
I often hear questions about the long-term implications of using halogenated organics, especially in light of tightening environmental rules. The very features that make 2,6-Dibromo-4-Tert-Butylphenol appealing—its persistence, chemical stability, resistance to breakdown—also mean it sticks around in waste streams. Disposal presents real challenges. A lot of waste destruction facilities are wary about halogenated phenolics because traditional incineration produces problematic byproducts.
Some forward-thinking firms have begun evaluating greener synthesis routes and more thorough capture of waste streams before they leave the site. I’ve witnessed some success with improved reaction selectivity, designed to minimize offcuts and reduce total waste. Others opt for advanced oxidation processes, using photocatalysis or hydrogen peroxide to decompose any wash residues before effluent hits the drain. These investments cost real money, so for small and mid-size labs, collaborative efforts with local treatment partners often deliver better environmental stewardship without blowing the budget.
One real opportunity I’ve noticed is the move toward closed-loop manufacturing. By recovering solvents and integrating waste management up front, companies can cut both disposal liabilities and raw material purchases. This helps satisfy an increasingly sustainability-focused market—customers, investors, and regulators alike. But change rarely comes quickly in the chemicals game, so the savvy teams get started early.
Working with phenolic intermediates for a decade has shown me that not all batches behave the same, even from the most reputable suppliers. Minor differences in crystalline habit, color, or even odor flag up variations that can impact final product quality. One time, a subtle yellow tint in a batch ended up signaling the presence of trace oxidized impurities, which wouldn’t have passed unnoticed in a tightly-run QA lab. It forced the whole team to recheck protocols and reach out to the supplier. That experience hammered home the lesson that buying the same product name year in, year out, isn’t the same as getting identical performance.
Routine use of IR spectroscopy, NMR, and GC-MS to verify identity and purity has become standard practice in advanced labs. This catches discrepancies before they reach a final process, saving a world of trouble downstream. Out in the field, small shops sometimes roll the dice with supplier-provided certificates alone. Based on what I’ve seen, the extra QC step always pays off, especially for higher-value syntheses where a single batch slip-up can ruin months of work.
The story of 2,6-Dibromo-4-Tert-Butylphenol today is not just about what happens inside the flask, but about responding to shifting rules and customer expectations. Demand for non-halogenated, greener alternatives has begun shaping R&D budgets and production planning even in traditional industries. Yet, conversations with industrial chemists and product managers show there’s reluctance to move away until newer options match the reliability, shelf life, and performance benchmarks that the current crop of halogenated phenolics set.
A few startups have started trialing bio-based antioxidants and synthetic intermediates meant to phase out legacy phenolic products. In practice, the data is still limited. My experience is that only when startups demonstrate actual head-to-head results under tough process conditions do mainstream buyers shift their loyalties. So 2,6-Dibromo-4-Tert-Butylphenol isn’t disappearing soon, but end users keep one eye on new data and regulatory bulletins, looking to anticipate change before it lands on their doorstep.
Choosing a source for any specialty chemical requires more legwork than skimming a catalog. Based on my years sourcing intermediates, the best outcomes come from dealing directly with established suppliers who provide both documentation and technical support. A responsive partner who can talk through a batch certificate, suggest process improvements, and back up claims with real technical data often makes a bigger impact than a fractionally better price. When it comes to 2,6-Dibromo-4-Tert-Butylphenol, I’ve repeatedly encountered situations where direct dialogue with a supplier's technical team unearthed better storage suggestions and even allowed for custom purification runs to suit a specific process.
Regular batch-to-batch sampling, on-site audits, and rigorous review of technical data sheets build in the trust required to avoid expensive surprises. In teams where I’ve set up supplier evaluations, I always recommend sending a test sample through your actual process rather than relying solely on spec sheets. The cost of a trial pays back quickly by preventing large-scale failures.
Ordering 2,6-Dibromo-4-Tert-Butylphenol only solves one challenge; safe storage and handling make up the next, and they’re often underestimated. Most shipments arrive in sealed fiber drums or durable HDPE containers—good for blocking moisture and light, which can otherwise cause clumping or slow degradation over time.
Based on direct storage experience, keeping the compound away from acidic or highly basic materials extends shelf life and prevents changes to the crystal profile. Overcrowding shelves or neglecting regular room ventilation can create unseen risks—especially in busy operations where a misstep gets magnified as volume scales up.
Few products are as forgiving as you’d hope. Investing in clear labeling, regular cycle checks, and employee training all boost both product safety and operational integrity. Anecdotes from peers confirm that facilities following strict packaging and storage protocols report fewer process breakdowns—an advantage that pays back in both safety and performance.
After tracking the specialty chemicals space for years, I see 2,6-Dibromo-4-Tert-Butylphenol continuing to serve as a dependable tool for both R&D and scaled manufacturing. Market surveys, conversations with buyers, and feedback from hands-on lab users all point to three realities. First, the push for better environmental performance is only getting stronger, so demand will likely pivot toward less hazardous, more biodegradable alternatives in coming years. Second, for applications where nothing else comes close in terms of chemical stability, yield, or cost-effectiveness, this compound will retain its foothold. Third, regulatory changes could reshape availability, especially as global rules harmonize.
The chemical industry adapts best with both roots and wings—respecting the old staples while investing in the new. Those who understand the true strengths and weaknesses of products like 2,6-Dibromo-4-Tert-Butylphenol can make smarter, safer, and more profitable decisions over time.
The story of 2,6-Dibromo-4-Tert-Butylphenol offers important lessons about balancing the needs of chemistry, business, and responsibility. Those who’ve worked both at the bench and in procurement see both the performance benefits and the broader obligations that come with using specialized chemicals. Pure technical details only go so far; lived experience and a willingness to adapt—whether in sourcing, handling, or disposal—make all the difference. In the end, smart choices about compounds like this enrich both the bottom line and the safety net for workers, communities, and the environment.