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HS Code |
643560 |
| Product Name | O-Bromotoluene |
| Chemical Formula | C7H7Br |
| Molecular Weight | 171.04 g/mol |
| Cas Number | 95-46-5 |
| Boiling Point | 183-185°C |
| Melting Point | -24°C |
| Density | 1.48 g/cm³ |
| Appearance | Colorless to pale yellow liquid |
| Flash Point | 72°C |
| Solubility In Water | Insoluble |
| Refractive Index | 1.565 |
| Pubchem Cid | 7295 |
As an accredited O-Bromotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | O-Bromotoluene is packaged in a 500 mL amber glass bottle, tightly sealed with a screw cap, and labeled with safety information. |
| Shipping | O-Bromotoluene should be shipped in tightly sealed containers, away from heat, flames, and incompatible substances. It is classified as a hazardous material and must comply with applicable transport regulations (e.g., DOT, IATA, IMDG). Ensure proper labeling and use secondary containment to prevent leaks or spills during transit. Handle with appropriate personal protective equipment. |
| Storage | O-Bromotoluene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light. Use chemical-resistant containers, clearly labeled, and avoid exposure to heat or direct sunlight. Store at room temperature, and ensure proper spill containment measures are in place. |
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Purity 99%: O-Bromotoluene with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 7°C: O-Bromotoluene with a melting point of 7°C is used in agrochemical manufacturing, where it provides reliable phase control during formulation. Molecular Weight 171.03 g/mol: O-Bromotoluene with a molecular weight of 171.03 g/mol is used in specialty dye production, where it enables precise stoichiometric calculations for batch processing. Low Moisture Content: O-Bromotoluene with low moisture content is used in Grignard reaction setups, where it minimizes side reactions and by-product formation. High Chemical Stability: O-Bromotoluene with high chemical stability is used in polymer additive synthesis, where it maintains reactivity without decomposition under process conditions. Refractive Index 1.564: O-Bromotoluene with a refractive index of 1.564 is used in fine chemical development, where it assists in accurate process monitoring and compound identification. Boiling Point 183°C: O-Bromotoluene with a boiling point of 183°C is used in organic synthesis, where it provides controlled evaporation for solvent removal techniques. Assay ≥98%: O-Bromotoluene with assay ≥98% is used in bromination reactions, where it delivers reliable halogen introduction for advanced intermediates. |
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O-Bromotoluene might not sound familiar unless you spend your days around lab benches, but this simple aromatic compound quietly shapes significant pieces of the chemical industry. Often carrying the label of 1-Bromo-2-methylbenzene, o-bromotoluene walks into labs as a clear, colorless to pale-yellow liquid, all ready for demanding applications. Knowing exactly what o-bromotoluene offers and how it differs from similar compounds helps both seasoned chemists and those just entering the world of specialty chemicals make smarter decisions.
O-bromotoluene doesn’t show up in the headlines, but it finds its way into several important reactions. This compound is a cornerstone in synthesis work, especially for pharmaceuticals and agricultural chemicals. Its structure—a benzene ring with a methyl group and a bromine atom on adjacent carbons—sets the stage as a versatile building block. Manufacturers rely on o-bromotoluene for Grignard reactions, which give birth to new carbon-carbon bonds. If you’ve ever wondered how chemists create novel drugs or pesticides, you’ll often find compounds like o-bromotoluene at the very beginning of that journey.
The appeal lies in the way the methyl and bromo groups sit next to each other on the ring. This setup makes substitution chemistry far more targeted than on its cousins—like p-bromotoluene, where groups sit across from each other, or m-bromotoluene, where they sit with a one-carbon gap. Here, reactions can push incoming groups right into the ortho position, carving out new options for downstream chemistry. Products like specific dye precursors, complex antioxidants, and fine-tuned polymers often start with this molecule.
Anyone who has worked with o-bromotoluene recognizes its distinct aroma and gentle viscosity. There’s a physical presence to it—a certain weight in the bottle, almost like holding a legacy. As with many aromatic bromides, safety counts for plenty. You want proper gloves, real ventilation, and rows of chromatography tubes ready, since o-bromotoluene can head into a dozen directions during a day's prep. In the lab, you measure it by density and boiling point, but in the field, you measure it by how reliably it performs as a precursor.
In practical settings, I’ve watched junior chemists switch from p-bromotoluene to o-bromotoluene mid-project, frustrated by the lack of reactivity or by poor regioselectivity in their reactions. The ortho isomer solves many of those headaches. It takes well to substitution under mild conditions. In synthesis where reaction temperature and product yield make or break the process, o-bromotoluene often edges out its peers by showing more predictable behavior.
Compared to other brominated toluene isomers, o-bromotoluene sits in a sweet spot for making intermediates. The ortho position allows for direct transformation into all sorts of biaryls, key flavors, and specialty polymers. The methyl group draws in electron density, creating a perfect launch pad for further reactions. Even in everyday manufacturing, this edge means less wasted material and better control over where each atom ends up.
For anyone invested in green chemistry, O-bromotoluene presents some challenges but also unique opportunities. Its reactivity reduces the need for harsh reagents or prolonged heating, which in turn lessens energy use and side-product generation. Many process engineers have shifted synthesis steps away from older, less selective halides and towards o-bromotoluene for both economic and environmental reasons. Also, it aligns well with modern catalytic methods, including palladium-catalyzed cross-coupling reactions, without the stubborn issues of some meta- or para-isomers.
Those who purchase and use o-bromotoluene learn quickly that quality isn’t just a buzzword. Impurities can act like sand in the gears, especially in sensitive reactions. Manufacturers and bulk consumers look for clear, traceable documentation and purity levels that can be independently verified. Technology for purifying and testing aromatic halides keeps improving, thanks to modern chromatography and sophisticated spectroscopy techniques.
In my own work sourcing chemical feedstocks for specialized reactions, o-bromotoluene stands out as a model for how attention to purity translates directly to outcome. A minor impurity—say, a trace of catalytic poison—can drop yields and send days of work down the drain. Those spending on advanced synthesis know that upstream quality trumps almost any downstream fix. When you open an amber bottle and see clear, pale liquid without suspended matter, it’s not just an aesthetic point; it signals process integrity before you even weigh out the first grams.
Market access to o-bromotoluene continues to grow, but not every supplier treats quality, packaging, or documentation the same. Seasoned purchasers watch out for differences in storage recommendations and shelf life. Bulk packaging might cost less per liter, yet in practice, lab-scale users often lose material to evaporation or contamination if storage is subpar.
The rise of e-commerce in the chemical sector has made it easier to compare sources and read reviews from actual users. During the past few years, uncertainty around global supply chains drove up prices for some halogenated aromatics. The more reliable suppliers won greater loyalty by keeping customers up to date about lead times and shipment tracking. Nothing shakes trust faster than opening a shipment only to find the seals broken or the paperwork inconsistent. It pays to vet suppliers not just on price, but also on their transparency about sourcing, shipping processes, and after-sale support.
Those pushing the boundaries of modern chemistry keep finding new uses for o-bromotoluene. Among researchers chasing the next blockbuster drug or more effective agrochemical, this molecule provides starting points for Suzuki-Miyaura coupling and similar reactions. Sometimes, these are processes never dreamed of a decade ago, where precision and efficiency matter more than ever. The position of the bromine and methyl groups allows for cleaner pathways to multiply substituted benzenes—scaffolds that play starring roles in pharmaceutical innovation.
On the technology side, better catalysts, more intelligent reaction planning software, and deeper knowledge about reactivity have shifted thinking about what o-bromotoluene can do. Labs that a decade ago handled only tens of grams now scale up to kilograms, using automated reactors. Downstream, specialty chemical manufacturers lean on its unique properties to make colorants, UV absorbers, and advanced polymers that show up in everything from electronics to solar panels. The cycle of innovation, testing, and product launch depends on building block chemicals that don’t compromise consistency or performance. O-bromotoluene is one of those quietly reliable partners at nearly every step.
The conversation around chemical safety grows each year. O-bromotoluene isn’t acutely toxic at minuscule levels, but responsible use still means paying attention to workplace exposure and environmental stewardship. Occupational standards and recordkeeping around aromatic halides have tightened, mostly due to regulators tracking potential environmental impact and worker exposure. Recent years have seen more rigorous tracking of imports and material safety data.
Those of us who have needed to adapt to changing rules know how much impact paperwork, labeling, and staff training can have on a business’s workflow. Larger organizations often have dedicated compliance staff, but in the academic or specialty manufacturing worlds, this burden falls to bench chemists or lab managers. Taking shortcuts on documentation or personal protective gear rarely ends well—mistakes here can cause headaches during audits or, much worse, during emergencies.
Regulation isn’t about making life hard for small users; it’s about creating common standards. Correct labeling, proper storage, and transparent sourcing let everyone in the supply chain work with confidence. Most importantly, it protects both workers and communities around production or research sites. It makes sense to respect these systems not as barriers but as tools for risk management. I’ve seen organizations that thrive on this—viewing regulatory milestones as a sign of professionalism and commitment rather than being another overhead cost.
In the ever-expanding world of halogenated aromatics, small differences between isomers often drive big gaps in performance and utility. While o-bromotoluene, m-bromotoluene, and p-bromotoluene share a basic formula, their real-world behavior underpins everything from reaction outcomes to cost-effectiveness.
O-bromotoluene stands apart due to its higher selectivity for metal-catalyzed coupling and electrophilic substitution. The adjacency of substituents opens doors for ortho-directing reactions and improved yield in certain syntheses. Those struggling with inefficient routes using p-bromotoluene find relief in o-bromotoluene’s cleaner conversions and higher tolerance to standard conditions.
In the pharmaceutical sector, for instance, isomer selection often relies on the final arrangement of functional groups in a drug candidate. Starting from o-bromotoluene allows for faster, more reliable access to critical intermediates. On the manufacturing side, processes leaning on o-bromotoluene often create fewer byproducts and improve atom economy, which matters both for profit margins and environmental sustainability. Even subtle shifts in storage stability, handling protocols, or regulatory classification can influence a chemist’s choice of precursor.
For all its advantages, o-bromotoluene also brings some stubborn challenges. Sourcing pure material during global supply chain hiccups keeps procurement teams busy. Storage in humid or warm environments can degrade quality, especially if containers aren’t perfectly sealed. Laboratory staff need to stay vigilant about minimizing exposure and ensuring good housekeeping to prevent unwanted contamination of more sensitive reagents.
Another challenge appears in the safe disposal of brominated organics. Where regulation requires heightened waste management, users find themselves tracking spent material with the same precision as raw stock. Small lapses in protocol can cause regulatory trouble or, worse, potential environmental impact. Development of greener disposal methods and better waste treatment protocols represents a growing focus among both industrial and academic users.
The movement toward green chemistry hasn’t skipped o-bromotoluene. Researchers and process engineers continue exploring routes that cut down on hazardous byproducts and minimize energy use. Modern synthetic planning often weighs the carbon footprint of starting materials, solvent use, and energy demands just as closely as chemical yield.
For o-bromotoluene, opportunities to improve come from moving to solvent-free reactions, reusable catalysts, and recycling process waste. Examples include continuous-flow reactors, where reaction control and heat management lead to both safer processes and lower emissions. Small, smart changes—like choosing more efficient packaging or sourcing from closer suppliers—also add up over time. Teams combining strategic sourcing, auditable waste protocols, and a commitment to staff training gain both regulatory compliance and a healthier balance sheet.
The chemical sector never stands still. As markets change and new technologies roll out, o-bromotoluene remains a smart choice for researchers and manufacturers seeking reliability in their feedstocks. Whether for a new generation of drugs, more effective crop treatments, or breakthroughs in material science, this compound supports ambitions without pushing volatility or unpredictability into the process. The measure of a foundational compound like o-bromotoluene lies not just in specs or purity, but in a track record built by thousands of successful syntheses around the world.
As someone who’s watched both failure and success ride on the choice of starting material, I’ve come to see the value in trusting molecules that quietly deliver. O-bromotoluene carries a weight of history in industry and research, yet its story is still unfolding. Whether resolving tight project deadlines or meeting stricter regulatory standards, it proves again and again that reliability beats novelty most days. Choosing the right chemical partner today lays the groundwork for tomorrow’s advances, and o-bromotoluene fits that role beyond expectation.