|
HS Code |
321932 |
| Productname | 2-Bromo-5-(Tert-Butyl)Phenol |
| Casnumber | 61659-08-1 |
| Molecularformula | C10H13BrO |
| Molecularweight | 229.12 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 80-84°C |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Synonyms | 4-(Tert-butyl)-2-bromophenol |
| Smiles | CC(C)(C)C1=CC(Br)=C(O)C=C1 |
| Inchikey | KCRKQSRUJONIQG-UHFFFAOYSA-N |
| Storagetemperature | Store at 2-8°C |
| Hazardclass | Irritant |
As an accredited 2-Bromo-5-(Tert-Butyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g quantity; sealed cap, white label with product name, CAS number, and hazard symbols, manufacturer branding included. |
| Shipping | 2-Bromo-5-(tert-butyl)phenol is shipped in tightly sealed containers, protected from light and moisture, and in accordance with regulations for handling hazardous materials. Packaging ensures no leakage, with suitable labeling for chemical identification and hazard classification. It is transported by certified carriers specializing in chemical shipments, complying with local and international safety guidelines. |
| Storage | 2-Bromo-5-(tert-butyl)phenol should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizing agents. Store in a cool, dry, well-ventilated area, ideally in a chemical storage cabinet designated for hazardous or organic compounds. Ensure containers are clearly labeled. Avoid exposure to heat and sources of ignition. Follow all relevant safety guidelines. |
Competitive 2-Bromo-5-(Tert-Butyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
At our plant, the daily routine revolves around meeting a global demand for specialty chemicals that never rests. Making 2-Bromo-5-(tert-butyl)phenol, or simply 2-BTBP for those of us working with it every day, is about precision, vigilance, and continuous improvement. Unlike standard phenols, this molecule brings together a bromine atom and a tert-butyl group, each carefully positioned on the aromatic ring. Every shift, I see our chemists double-checking purity and lot histories. Consistency in our batches helps researchers and downstream manufacturers trust that what they order this month will match what they used last year.
Nobody orders 2-BTBP on a whim. Most of our customers contact us with exacting requirements for their research or production lines. From synthesis labs working on new pharmaceuticals to agrochemical innovation teams, people want molecules tailored for particular reactions. 2-BTBP’s layout—bromine at the second position and tert-butyl at the fifth—affects both its reactivity and solubility choices. In some cases, our partners rely on this compound as an intermediate where a standard bromophenol just won’t do. The tert-butyl group brings extra steric hindrance, while the bromine gives room for further functionalization through cross-coupling. The molecule’s particular substitution pattern steers selectivity and performance in catalytic environments.
Walk out onto our shop floor and you won’t mistake 2-BTBP synthesis for that of basic, commodity phenols. Chemicals enter the reactor in a specific order. The aromatic ring receives a tert-butyl group in a controlled alkylation step—timing and temperature set by years of process optimization campaigns. Bromination comes next. This isn’t a matter of tossing in a halogen and waiting; the position-selectivity stems from how well we balance kinetic and thermodynamic pathways. Overbromination and other by-products pop up if controls slip. Tight analytics let our QC teams keep the specifications right where end-users expect them.
As yields vary from batch to batch in any chemical process, we track our conversion rates and adjust parameters to drive toward both optimal output and reduced waste. Solvent choices matter. Early on, we learned that a swap from one solvent to another could cut purification time by a third while improving the product’s overall brightness. Each adjustment flows into our production log, not just for compliance but for our own learning curve. A handful of operators bring decades of collective experience to the craft, balancing the art and science of running a fine chemicals plant.
Every flask, reactor, and drum tells a story about development. The model our facility produces carries a purity of 98% most days, measured by gas chromatography, and occasionally hitting even tighter windows for bespoke requests. Melting point sits right around the expected range for this molecule, signaling correct substitution without excess isomers. Color, moisture, and even part-per-million levels of byproducts get checked using IR and NMR.
Some of our partners ask for custom particle sizes, whether for expedient dissolution or to satisfy requirements in solid formulations. Rather than holding to a one-size-fits-all model, experienced operators oversee everything from drying profiles to sieving steps. Nothing happens without considering how someone on the receiving end will use what we ship.
Our regular specification addresses:
Chemists and buyers who know their way around the periodic table spot the difference between various halogenated, alkylated phenols at a glance. The real test comes during application. Compare 2-BTBP with similar molecules like 2-bromo-4-methylphenol or 4-tert-butylphenol and you’ll notice changes in reactivity, solubility, and even odor. The larger tert-butyl group in the 5-position blocks unwanted reactions at nearby sites. This tweak makes the molecule more selective in certain cross-coupling chemistry and reduces off-target effects where position-specific activation matters, such as in polymer synthesis or fine-tuning catalysts for pharmaceutical research.
We’ve shipped drums to R&D departments experimenting with new agrochemical scaffolds. Teams have told us that standard alkylphenols failed at key selectivity points, but swapping in 2-BTBP unlocked new regioselectivity pathways. The bromine facilitates coupling reactions—Suzuki, Heck, and Ullmann all turn more efficient with the right leaving group in the right spot. A smaller bromophenol doesn’t offer the same robustness in high-temperature catalysis. The tert-butyl group adds both physical and chemical bulk, repelling unwanted side reactions and stabilizing the molecule in some aggressive synthetic conditions.
We ship 2-BTBP not just in high-purity batches, but with accompanying batch records so end-users get transparency down to the starting materials and cleaning logs. Auditors—internal and external—drop by unannounced. They walk the aisles, reviewing not only how we work, but why we do things a certain way. Our documents reflect years of lessons, from revised filtration steps to adjustments in quenching reagents, all with risk management and operator safety in mind.
The conversation rarely ends at a sale. Customers will call and ask about trace solvents, appearance, or even storage temperature over the long term. We don’t wait for those questions; we test stability across storage conditions so labs get data, not surprises. In one instance, a warehouse flagged clumping after opening a drum in high humidity. We worked through the issue—reworking our packaging protocol and shifting to nitrogen headspace for sensitive orders. By acting on feedback, we eliminate future risks and build trust across our user base.
Researchers buying 2-BTBP usually don’t treat it like a bench reagent. This molecule plays a role in crafting novel ligands or acting as a coupling partner in modern C–C bond formation. The bromine handles oxidative addition and leaves cleanly, a bonus compared to less reactive halogens. The tert-butyl group’s bulk steers reactions away from less desirable sites. Some users blend 2-BTBP into formulations that end up in specialty polymers—especially those needing thermal resistance or precise molecular weights.
It’s not just about the reactions. Some partners find that the specific substitution makes downstream purification easier. Distillation and crystallization steps flow smoother because impurities tied to alternative substitution models just don’t show up. We designed our workflow so products stay pure across the supply chain, turning what could be an operational headache into a smooth process.
Factories like ours face scrutiny for everything from solvent handling to emissions. Producing 2-BTBP safely shaped our investments. Modern fume extraction, closed system alkylation, and secondary containment lines cut down on fugitive emissions. Bromination carries well-known environmental risks, so our strategy starts with minimizing overuse and recycling off-gasses whenever we can. Each kilogram sent off as hazardous waste costs twice as much as what could be recovered, purified, and reused. These details aren’t marketing lines—they underpin long-term supply stability and pricing consistency.
Handling tert-butyl reagents demands respect—flammable, volatile, and, if handled poorly, a source of costly downtime. Our team completed site-wide safety upgrades after an early-days incident taught us about polymeric fouling in exhaust lines. Since then, operator training covers both technical and practical troubleshooting scenarios. Each tank, valve, and monitor sees regular tests, catching problems long before they reach a drum. These real-world choices come through in our specifications and, ultimately, in the reliability we deliver batch after batch.
We rely on regular calls with formulation scientists, scale-up engineers, and quality leads. Some use 2-BTBP as a bridge molecule toward larger, more complex aromatic systems. Others value it for the selective introduction of new functional groups via palladium-catalyzed reactions. Their feedback lands directly on the production floor: changes in labeling, requests for extra analytical documentation, or slight shifts in product drying curves. We hear about challenges too—losses tied to minor impurities, chromatography difficulties, or unexpected color changes. Because we’ve run hundreds of batches, we compare notes, run parallel syntheses, and suggest tweaks that minimize these hitches.
Having a tight relationship with buyers matters. It lets us spot demand surges long before the market moves. In one surge, polymer catalysts using 2-BTBP suddenly jumped, straining supply on many intermediates. Early warning from customers helped us adjust, scaling up safely, without the inefficiencies that come from rushed production. Long-term partnerships help everyone stay ahead of sudden regulatory changes too, which show up more in specialty organics than in base chemicals.
If you spend years in production, you see cycles. Molecules once considered niche can become critical as new technologies emerge. The biotech sector has increasingly explored 2-BTBP as a building block for functional ligands in enzyme mimics. Downstream applications broaden every year, driven by what researchers discover in lab-scale reactions and then work into production. Some users push us for ever-lower impurity levels. Others need fresh ideas for recycling solvent waste or reusing packaging.
We approach all these expectations not just as rules to follow but as the next frontier for process innovation. Upgrading purification, bringing new in-line analytics, trying new catalyst systems to boost yield—these aren’t abstract goals. They grow from everyday observations about what worked and what could be better. Our expertise doesn’t just come from textbooks or regulatory documents. It’s forged through the realities of scale, the challenge of a missed spec, and the satisfaction of a customer returning time after time for a product that just works.
We don’t make every substituted phenol on the market, but we work closely with customers who use a wide range of them. For many, simple bromophenols offer a lower-cost option, yet the lack of bulky substituents limits their applications when selectivity or resistance to side reactions is key. Meanwhile, other providers focus on lighter or heavier alkyl groups, but these often come with decreased solubility or higher steric clash in some high-precision applications.
Feedback often centers on the reliability of downstream chemistry using our product compared to generics. Whether in the formation of aryl ethers, advanced pharmaceuticals, or agrochemical scaffolds, 2-BTBP’s structure means reactions complete with fewer unwanted byproducts. This reduces both cost and complexity in purification. In cases where users try to swap in 4-tert-butylphenol or similar structures, they report increased off-target alkylation or polymerization. Those insights come from real-world failures and corrections—mistakes engineers and chemists like us learn from deeply.
Manufacturing 2-bromo-5-(tert-butyl)phenol depends on care, technical know-how, and a willingness to respond to what’s really happening at each link in the supply chain. Each kilogram signals a commitment—not just to meet specifications, but to deliver a product whose consistency, safety, and performance can be counted on. We track market shifts, speak honestly about our process, and look for places to improve by working together with the chemists, scientists, and engineers who shape what comes next. In a business where trace impurities or a missed shipment can turn opportunity into risk, our experience stands as the difference-maker. With each batch, we build on the lessons of the last, always improving, and staying ready for new challenges wherever chemical innovation moves next.