|
HS Code |
464876 |
| Chemicalname | 3-Bromo-2-Chlorotoluene |
| Casnumber | 18368-58-0 |
| Molecularformula | C7H6BrCl |
| Molecularweight | 205.48 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 217-219°C |
| Meltingpoint | -11°C |
| Density | 1.544 g/cm3 at 25°C |
| Refractiveindex | 1.573 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Flashpoint | 90°C |
| Smiles | CC1=C(C=CC(=C1)Br)Cl |
| Inchikey | DKOWDLHGXKYCDG-UHFFFAOYSA-N |
As an accredited 3-Bromo-2-Chlorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
Competitive 3-Bromo-2-Chlorotoluene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
3-Bromo-2-Chlorotoluene is not just another laboratory reagent. Scientists and production managers often have their attention split between sourcing high-purity chemicals and maintaining reliable outcomes in research, synthesis, or manufacturing. In this field, consistency is gold—and that’s exactly what this product delivers. The unique combination of a bromine atom at the ortho-position and a chlorine atom at the meta-position on the toluene ring brings a new dimension to aryl halide chemistry. Behind this molecule stands years of organic synthesis methods refined to minimize impurities and maximize yield. This matters, especially when unpredictable contaminants can derail the reproducibility of advanced chemical work.
Every chemist who has been let down by underperforming reagents knows the value of a clear and dependable specification. 3-Bromo-2-Chlorotoluene is available with a typical purity above 98 percent, meaning side reactions step aside and let the main reaction run its course. The compound comes as a pale yellow liquid, boiling in the range of 218 to 220°C. It has a molecular formula of C7H6BrCl and a molecular weight of 205.48 g/mol. These figures do not just fill a datasheet—they provide real guidance in predicting reaction pathways, stoichiometry, and safe handling practices. Whether using it as a building block for agrochemicals or synthesizing custom pharmaceuticals, each lot is lab-verified to guarantee the standard of quality.
Organic chemistry often turns into a puzzle where one wrong move doubles the workload. 3-Bromo-2-Chlorotoluene has shown its worth as a substrate for Suzuki, Heck, and Sonogashira couplings. Based on actual experience, this molecule offers a shortcut in building biaryl motifs and complex aromatic systems. The presence of both bromine and chlorine on the aromatic ring opens up selective reactivity—not every aryl halide can claim that. In pharmaceutical R&D labs, small tweaks to the toluene core have produced noticeable changes in bioactivity. This compound often acts as a starting point for medicinal chemists aiming for selective modifications while retaining manageable reaction control.
Agrichemical developers put this molecule to work in creating targeted fungicides and insecticides. By using a halogenated aromatic precursor, developers can more easily introduce other functional groups. From practical perspective, using a compound like 3-Bromo-2-Chlorotoluene can cut a multi-step synthesis by one or two operations, reducing waste and improving overall efficiency. I have seen teams cheer when a boronic acid coupling proceeds smoothly with this molecule, where lesser halides failed to react cleanly. One can appreciate these little victories in the lab when deadlines approach and the budget grows tight.
Plenty of aryl halides compete for attention. Take the common 2-bromotoluene or 4-chlorotoluene: each has a niche, but neither delivers the dual reactivity that both bromine and chlorine provide in this isomer. Various cross-coupling protocols rely on subtle electronic differences created by this substitution pattern. The bromine atom usually participates in palladium-catalyzed reactions faster than chlorine, which means you can orchestrate a two-step process where only the desired position reacts early. Not all isomers give that level of control.
In many synthesis strategies, chemists need orthogonal reactivity—basically, you want to change one position on the ring and not touch the other until you are ready. The difference is more than academic. With 3-Bromo-2-Chlorotoluene, you sidestep endless purification headaches because each halide responds predictably to a chosen catalyst or reagent. I have watched research teams simplify workflows just by switching from a mono-halogenated starting material to this compound, often shaving days off reaction development.
Quality speaks through results, and reliability means more than percentages on a certificate. One batch’s poor performance can cause thousands of dollars in lost labor or wasted materials. Producers of 3-Bromo-2-Chlorotoluene have streamlined the route, using careful distillation and purification. There’s no need to keep your fingers crossed, hoping for a stable supply or consistent reactivity; professional suppliers know how to keep impurities like dibromotoluene or polychlorinated toluenes out of the bottle, so downstream results match expectations.
A bottle of 3-Bromo-2-Chlorotoluene in the storeroom is a promise of smoother workflows. Researchers tell stories of first attempting syntheses with basic aryl halides, only to return after weeks to more selective compounds like this one. Early projects often struggle with low yields or tricky byproducts when simpler molecules are used. Every chemist can recall the frustration of repeating a reaction dozens of times, chasing after cleaner conversions.
Even if you do not work on the bench, the benefits of streamlined synthesis reach wider. Environmental staff on industrial sites pay close attention to emissions and waste profiles. Using a more reactive and selective substrate, like this compound, often means less waste to treat downstream. Cut one step from a production line and you start to see real impacts on solvent use, emissions, and handling risks. In-house safety audits always appreciate a starting material that performs without excessive byproduct formation or toxic volatilization. The right choice in reagents echoes across departments.
It’s easy to get lost in the excitement of new molecules, but thoughtful use matters just as much. While 3-Bromo-2-Chlorotoluene offers performance and selectivity, it’s essential that users handle it with proper respect for both health and environment. Careful storage, routine maintenance of handling equipment, and regular training of laboratory or plant staff are the foundation for safe use. Responsible users keep material safety data sheets on hand, use personal protective equipment, and maintain up-to-date certification for hazardous materials work. Not only does this protect individuals, it helps organizations meet the duty of care expected in today’s world.
Feedback from field chemists and operators often shines a light on overlooked details—barrel pumps need to work smoothly, transfer lines must be well-sealed, and staff need training on spill response just in case. Investing in a good fume hood and routine monitoring of workplace air helps lessen exposure, as does proper labeling and ventilation. With high-boiling, halogenated aromatics like this one, even a small lapse can cause a lingering odor or persistent residue, so diligence pays off long term.
Years ago, I watched a process development team consider a dozen possible halogenated toluenes for a crop protection project. They ran pilot trials, kept detailed notes, and reported clear winners only after weeks of deliberate head-to-head comparison. The less selective mono-halogen compounds tended to produce more side products. Only 3-Bromo-2-Chlorotoluene let them move efficiently to the next stage with fewer purification steps. The project leader credited this strategic switch for staying ahead of a tough schedule.
In another case, a pharmaceutical research team found themselves stuck with an underperforming aryl halide substrate. Only after consulting colleagues who had scaled up reactions with dual halogenation did they revise their route—and finished their synthesis successfully. These sorts of real-world pivots show that theory and practice sometimes part ways, and the right starting material can close the gap.
Innovation often rides on the shoulders of small details: reagent choice, process design, or catalyst selection. With 3-Bromo-2-Chlorotoluene, the fine-tuning of product specifications and supply reliability helps enable new discoveries. Chemists in academic settings have published papers on improved yields using this molecule, noting the clean reactions and routine workups. In the hands of an experienced bench chemist, a bottle of this compound grows into a launchpad for a dozen projects. For those working in industrial scale-up, the same substrate unlocks routes to specialty intermediates and high-value end products.
Chemical supply chains face plenty of challenges these days: transport delays, raw material shortages, regulatory uncertainty, and new sustainability demands. Navigating these waters requires strong partnerships between chemical producers and the scientific community. Suppliers who understand the value of transparency—batch testing, clear lot numbers, robust certificates of analysis—build trust and ensure that vital projects keep moving. When purchasing managers can count on 3-Bromo-2-Chlorotoluene to arrive on time and on spec, teams get to focus on their real work: research, discovery, and scaling new technologies.
As green chemistry becomes more than a buzzword, every step in a synthesis comes under fresh scrutiny. With halogenated compounds, care for environmental impact stands front and center. Modern facilities can now reclaim and reuse solvents, incinerate residual wastes, or even switch to bio-based process aids in downstream steps. Choices made at sourcing—like picking a clean, high-purity 3-Bromo-2-Chlorotoluene—set the stage for less waste, fewer hazards, and cleaner effluent streams. Sustainability guides more procurement and process decisions than ever.
Looking at this compound compared to less selective or less pure alternatives, it’s clear that incremental progress in raw materials builds broader improvements. Teams who review suppliers, audit synthetic routes, and involve environmental staff early often see not just compliance, but true savings and smoother operations. Chemists and engineers who engage with their suppliers also push for better packaging, clearer labeling, and easier recycling downstream. This partnership mindset keeps innovation practical and safe, even as regulatory requirements tighten.
The most valuable materials in research and industry tend to be those that quietly enable progress behind the scenes. 3-Bromo-2-Chlorotoluene might not grab headlines, but over the years its role has expanded. Teams in fine chemicals, specialty polymers, and advanced materials look to this molecule for scaffolds and intermediate products. The modular nature of dual-halide aromatics speeds up a wide range of transformations. As synthetic biology and green chemistry advance, researchers will likely uncover even more creative uses for this old workhorse.
Young chemists starting their research careers often hear the old stories about tough syntheses, round-the-clock distillations, and the frustration when a single reagent throws off a whole week’s work. With today’s higher-purity aryl halides, seasoned mentors now share stories about good smells in the lab or the satisfying moment when a reaction mixture turns clear. The shift from process headaches to smooth operations means brainpower can focus back on creating new molecules, not just troubleshooting the old ones.
At conferences and workshops, safety officers often remind us that most chemical accidents start from forgotten routine: an unsealed bottle, a misplaced hazard label, or a rushed transfer. With 3-Bromo-2-Chlorotoluene, as with all halogenated aromatics, nothing substitutes for vigilance and training. High-integrity glassware, reliable labeling, and well-ventilated storage areas are essentials, not extras. Newcomers in the field benefit from shared best practices—veterans pass along tips on minimizing inhalation risks or selecting the right gloves for halogenated solvents. The culture of safety improves with every careful handoff and every story told.
Managers know that investing in reliable supply and robust safety brings returns in fewer incidents, higher productivity, and reduced insurance headaches. Senior chemists can count real savings from batches that run to completion without unexpected downtime. Project leaders sleep a little easier knowing that their teams work with trustworthy materials, where both the knowns and unknowns are managed. The pulse of any great laboratory or plant comes not from flashy new products, but from small, well-informed choices that stack up over the weeks and months.
3-Bromo-2-Chlorotoluene represents more than a chemical formula or a spot on a material safety data sheet. In every industry that touches advanced aromatic synthesis, it carries a reputation for consistency, selectivity, and practical value. Drawing from the collective experience of chemists, operators, and managers, this compound stands out not by flair but by delivering on its promise, batch after batch. When looking to future challenges—more demanding syntheses, tighter regulations, growing environmental responsibility—reliable building blocks like this one will continue to matter. For those who have seen both the chaos of unreliable reagents and the calm of trusted supply, the difference could not be clearer.