The chemical industry grew out of curiosity and necessity, wrestling with how to re-shape the world’s building blocks into reliable tools. Aromatic bromides like 1-Bromo-4-butylbenzene found their purpose in the 20th century as researchers dug into electrophilic aromatic substitution. This compound, with a butyl chain sitting planted para to a bromine on a benzene ring, made a niche for itself during the surge in organic synthesis that followed the development of bench-scale halogenation techniques. As the pharmaceutical boom rose, the simplicity, directness, and robust reactivity of para-substituted aryl bromides put them in the spotlight. Today, I see the lineage: beginnings in dusty, glassware-filled research labs, then scaling up for a new era of custom molecules and specialty materials.
1-Bromo-4-butylbenzene stands out for its role as a reliable synthetic intermediate. Its structure, with a benzene ring holding a bromine atom on one end and a straight four-carbon butyl chain on the other, makes it a candidate for diverse modifications. Labs and industries alike have leaned on its ease of handling and predictable reactivity. Researchers have reached for it to build advanced ligands, pharmaceuticals, and novel polymers. From my own time working in a synthetic lab, nothing beats the practical value of a chemical that does what you expect every single time—no surprises, just clean, consistent results.
This compound comes as a colorless to pale yellow liquid, speaking to its relatively low volatility and manageable viscosity. With a boiling point around 255-257°C, it holds its own during heated reactions and distillation routines. Its density clocks in near 1.16 g/cm³, typical for aryl bromides. The benzene core, buttressed by the bromine atom, gives it distinct reactivity in cross-coupling and substitution. Immiscible with water, soluble in most organic solvents—this profile fits right into the workflow of anyone who has ever worked on carbon-carbon bond formation or precursor halogenation. The slightly sweet smell brings back memories of late nights in the lab, a subtle reminder of classic organics.
Producers usually source 1-Bromo-4-butylbenzene to meet high-purity standards, suitable for research and production alike. Each container gets clear labeling: chemical name, batch number, CAS: 104-65-4, purity level often exceeding 97%, and hazard statements based on current GHS guidelines. There’s something reassuring about seeing a bottle with tightly regulated specs sitting beside the NMR spectrometer; any deviation in purity or labeling could derail a project and waste valuable resources. Barcode tracking and tamper-proof packaging have become increasingly standard as regulatory scrutiny grows, supporting the safe use and traceability of every drop.
Synthetically, 1-Bromo-4-butylbenzene comes from straightforward routes. The classic method kicks off with 4-butylbenzene, and an electrophilic bromination with bromine in the presence of a Lewis acid—often iron(III) bromide—drives the reaction. This method tends to favor substitution at the para position, minimizing unwanted byproducts. Sometimes, aryl lithium intermediates step in as part of a Grignard sequence for fine control. In factories, process engineers keep a close eye on temperature, stoichiometry, and work-up conditions to keep the yield high and the waste low. I remember the staining, distinctive red of bromine vapors creeping through the fume hood, highlighting the practical importance of containment and ventilation.
The bromo position on this molecule opens doors to endless chemistry. 1-Bromo-4-butylbenzene thrives as a starting point for Suzuki, Heck, and Negishi coupling reactions, key moves for linking aromatic systems together. That bromine atom becomes a site for replacement, allowing synthesis of more complex derivatives or direct installation of versatile groups like amines, alcohols, or under palladium catalysis, even more exotic chains. Building blocks like these have fueled both the creation of patent-protected drugs and the next generation of advanced materials. In my own work, bromoarenes stood out as reliable “handles,” giving reliable reactivity and straightforward separations, streamlining benchwork.
Marketplaces and chemical catalogs recognize 1-Bromo-4-butylbenzene under multiple names: para-Butylbromobenzene, 1-Bromo-p-butylbenzene, and 4-butylphenyl bromide. CAS: 104-65-4 ties together the regional preferences and naming conventions from labs across the globe. Keeping synonyms straight helps chemists avoid costly order errors and keeps supply chains moving, especially where regulatory languages differ.
Handling aromatic bromides brings real hazards. Contact with skin or inhalation may lead to irritation or, in rare cases, sensitization. Labs stress the use of gloves, goggles, and solid ventilation as common sense. Storage containers stay sealed, cool, and away from light to prevent decomposition. Larger operations go further, implementing local exhaust and systematic waste treatment to stop accidental releases or chronic exposure. The safety data sheet lays it out: risks include acute toxicity and environmental harm if spills reach waterways. Inspection routines and regular training serve as frontline defense, habits I picked up through close calls and watching more experienced hands work meticulously.
1-Bromo-4-butylbenzene has cemented its status as a go-to intermediate for pharmaceuticals, specialty chemicals, and crop protectants. Medicinal chemists use this template to stitch together heterocycles, kinase inhibitors, and next-generation analgesics. In materials research, the butyl tail adds flexibility to polymers, helps tweak surface properties, and improves solubility profiles for coatings and adhesives. The petrochemical industry explores such compounds for their role as precursors in fuel additives or complex lubricants. Its predictability and wide reach mean almost every industrial chemist has relied on it—sometimes without even realizing it’s there, buried inside a longer synthetic sequence.
Current research efforts target new, greener synthetic methods, using milder reagents, catalytic bromination, or solvent recovery systems to shrink the environmental footprint. There’s genuine excitement about leveraging biocatalysts or recyclable supports in the late-stage functionalization of aromatics, which could push efficiency while reducing waste. As regulations tighten, companies seek safer alternatives to conventional bromination—pushing both academic labs and manufacturers into a collaborative race for improved processes. These efforts unlock new derivatives with optimized pharmacokinetics, stronger electronic properties, or bespoke activity, broadening the playground for discovery.
Lab and industrial safety demand a close understanding of how 1-Bromo-4-butylbenzene interacts with living systems. Acute toxicity looks moderate by the numbers, but its lipophilicity lets it slip across cellular barriers, so long-term studies dig into potential impacts on reproduction, carcinogenicity, and chronic organ effects. Regulatory watchdogs flag its persistence in the environment and danger to aquatic species, especially since few breakdown pathways exist in natural settings. I’ve seen firsthand how environmental, health, and safety teams work hard to contain every gram, knowing that accidental releases can shape the fate of both workers and the watershed down the street. Vigilance remains non-negotiable.
Looking ahead, 1-Bromo-4-butylbenzene shows every sign of staying relevant. The push toward all-things-sustainable will force suppliers to rethink sourcing, purification, and scale-up methods. Chemists working at the interface of green chemistry and pharmaceuticals look at aromatic bromides as templates worth upgrading, deploying renewable feedstocks or non-hazardous reagents. Emerging research into machine-assisted retrosynthesis, improved catalyst systems, and automation promises a world where intermediates like this one flow through compact, recyclable reactors with low energy footprints. As science grows more interdisciplinary, the demand for simple, reliable building blocks will only rise. By staying flexible and responsive to new challenges, everyone from bench scientist to production engineer keeps 1-Bromo-4-butylbenzene not just on the shelf, but at the heart of the next wave of innovation.
Chemistry speaks its own language, but you don’t need a lab coat to get a grip on something as specific as 1-Bromo-4-butylbenzene. Its name might sound like jargon, but it breaks down to a set of simple moves. You have a benzene ring—the classic hexagon that people know from basic science class stories—with a bromine atom attached to the number one carbon, and a butyl group hanging off the fourth spot. That full skeleton gives it a formula of C10H13Br. This isn’t just trivia for a chemist; every atom in that lineup shapes what the molecule does, how it reacts, and where it goes.
Having a formula like C10H13Br in hand isn’t just an exercise for a classroom quiz. In practical terms, people in research, manufacturing, and even safety oversight rely on that identity to predict risks and benefits. If you’ve ever watched a team in a pharmaceutical lab, you’ll see them trace the roadmap of atoms through every step before they scale up a reaction. They look for stability, for unwanted byproducts, and always for red flags around reactivity. 1-Bromo-4-butylbenzene steps into the ring as a building block for more complex compounds—folks use it when they want to tack a butyl tail and a bromine onto something larger. It serves as a precursor, a sort of gateway, in routes that cook up fragrances, bioactive molecules, or specialty materials.
The simple act of labeling a drum—“contains C10H13Br”—isn’t bureaucracy; it’s critical communication. That tells everyone what sort of caution signs belong in the workspace, whether there’s a flammability issue, or how to handle spills. Brominated chemicals can bump up toxicity, especially for those with prolonged exposure. Knowing exactly what’s inside each bottle keeps people safer—there’s no room for guesswork in a place where skin contact or inhalation could mean an emergency. The precise formula matters for regulators, too. They lean on chemical formulas to craft smart policies and set stringent workplace limits.
With chemistry, accuracy is justice. A mismatch, even by a single carbon or atom of bromine, can flip a safe lab day into disaster. But labels also help drive improvement. As society pushes for fewer hazardous byproducts, clearer chemical identities let manufacturers find greener ways to make and use something like 1-Bromo-4-butylbenzene. Modern labs now target reactions that leave less waste, slash the use of harsh solvents, and swap dangerous chemicals for safer substitutes whenever possible. Working with a clear formula translates to better choices throughout the supply chain—from raw materials to final products.
Too many headlines rush past the details, but the everyday use of chemical formulas gives everyone—from students in chemistry class to professionals in the plant—a solid footing. With C10H13Br, the code unlocks a catalog of information: how to handle it, what it can create, and how we all stay safe while keeping progress moving. For families living near a factory, the knowledge that materials get tracked and handled correctly means peace of mind. For firms seeking to modernize and cut hazards, specific formulas anchor smarter, leaner innovation.
1-Bromo-4-butylbenzene looks like just another specialty chemical, but people working in laboratories and factories know it as something more practical. Scientists count on this compound as a stepping stone. It brings a butyl chain to a benzene ring and attaches a bromine atom, and that combination unlocks new routes in organic synthesis. Forging these carbon-bromine bonds is no small detail—the chemical world runs on making and breaking these connections with precision. This compound enters the spotlight because it gives chemists exactly that kind of control for many core reactions.
Drug development often means assembling complicated molecules a piece at a time, with each fragment affecting the outcome. 1-Bromo-4-butylbenzene serves as a source of both the butyl group and the bromine, which makes it valuable for chemists piecing together new medicines. It acts as a trusted starting compound to build intermediates—the chemical “halfway points” on the path to the final drug. This process matters. Drug companies look for alternatives whenever a classic ingredient becomes expensive or hard to get. Adding a butyl group can improve a drug’s absorption, solubility, or even how long it stays active in the body. Researchers leverage this molecule to tweak those important properties and test their results.
Materials innovation can’t happen without custom chemical blocks. Polymer manufacturers use 1-Bromo-4-butylbenzene as a way to introduce butyl-armed phenyl groups into plastics. Small changes in the chemical structure can change a polymer’s flexibility, toughness, or electrical qualities. As someone who has seen material engineers at work, I know how a subtle tweak can mean the difference between a brittle plastic and something that bounces back from impact. The bromine here isn’t just for show; it provides a target for the next chemical step, allowing researchers to “grow” their material with careful additions. In coating technology, specific brominated compounds help create surfaces that resist corrosion or make paints that stick better and last longer. Fixing these old problems leads to products that cost less to maintain and waste fewer resources.
Manufacturers choose 1-Bromo-4-butylbenzene for more efficient assembly lines. It fits into Grignard reactions and similar metal-catalyzed processes, which have powered everything from flavorings to agrochemicals. Companies can get more predictable results with less waste, since the butyl and bromo groups attach where chemists need them most. Professional chemists know that cutting out a reaction step pays off in lower costs and smaller environmental footprints. Automation systems like the ones I’ve programmed thrive on consistency and reliability, and compounds like this support both.
Safe handling and responsible sourcing always factor into chemical selection. Bromine-based chemicals can hurt human health and ecosystems if released unmanaged. Companies follow strict protocols, not just for legal compliance, but also out of respect for their workers and local communities. Investing in better ventilation, improved containment, and robust waste treatment keeps risk in check and trust high. Developing greener alternatives or biodegradable derivatives remains an open field. Universities and companies work together to test replacements that keep useful properties but avoid the possible downsides of brominated compounds.
New discoveries often start with slight changes to established molecules. 1-Bromo-4-butylbenzene gives chemists a steady foundation for control and exploration. Whether building a molecule for the next breakthrough medication, shaping flexible plastics, or developing industrial coatings, it continues to play a practical role in solving real problems. People in science and manufacturing can expect more from this chemical as demand for specialized and sustainable solutions grows.
1-Bromo-4-butylbenzene won’t show much danger on the surface. Look deeper and it brings some clear risks to the table. I’ve seen colleagues develop skin rashes or headaches after ignoring safe handling guidelines. Ever get caught short by a chemical splash? Lessons learned fast. Safety isn’t about paranoia — it’s about making sure mistakes don’t ruin your well-being or your work environment.
Nitrile gloves are the material of choice here. Latex breaks down with organic solvents, so nitrile holds up where latex fails. For any risk of splashing, sturdy lab coats and chemical goggles matter even more. A standard dust mask isn’t enough; if fumes collect, a proper chemical cartridge respirator keeps you breathing safely. I once watched a small spill turn into an inhalation event — even with the fume hood on. PPE only does the job if it fits well and you’re actually wearing it the whole time.
Handling organics like this means good air flow is non-negotiable. Rely on a certified fume hood, not just an open window. If there’s ever an accident — and sooner or later, every lab sees one — absorb the spill with inert material, but don’t reach for paper towels. Commercial absorbent pads lock up the liquid without spreading vapors. Waste goes directly into a marked solvent waste container. Once, I saw someone mop up an aromatic spill with office rags and throw them in the trash — the room reeked for days and the risk stuck around just as long.
Description on the container must match what’s inside. Nobody wants to play chemical roulette. 1-Bromo-4-butylbenzene prefers a cool, dry place, away from open flames and oxidizers. Store it in tightly closed amber glass bottles, since light and heat speed up breakdown. Every lab fridge I’ve used runs into the same problem — too many liquids and not enough labeling discipline. One misplaced bottle can turn a routine day into a scramble to call the safety officer.
Direct skin contact leaves irritation. Eyes react fiercely even to small splashes, often needing an eye wash station. Prolonged exposure to vapors can spark headaches, dizziness, or nausea. Many ignore the slow buildup in a crowded lab until they start feeling sick. The risks grow even larger for those with sensitive skin or allergies.
Don’t pour leftovers down the drain. 1-Bromo-4-butylbenzene needs to join halogenated solvent waste in a sealed, properly labeled container. Waste management companies handle the rest, but without your discipline up front, everything downstream gets riskier — I’ve seen fines and shut-downs from sloppy disposal practices.
Every chemical task brings routine, but shortcuts turn small risks into hazards. Review the SDS every time a new bottle arrives. Keep spill kits stocked. Check ventilation before working. Safety only gets real once it becomes everyone’s habit — not just a checklist an intern fills out. Mindful handling means fewer surprises, tidier workflows, and healthier teams. That’s the mark of any well-run workplace, lab, or workshop.
Working in synthetic chemistry, one thing never changes—small impurities can ruin a big batch. 1-Bromo-4-butylbenzene, known in many labs as a reliable intermediate, isn’t special just because of its name. Purity defines how well it does the job. If a batch carries traces of similar compounds or leftover solvents, reactions start going sideways. So, chasing purity isn’t academic; it’s practical.
If you deal with aryl bromides, you know. Nobody likes unpleasant surprises when they analyze their product. Impure starting materials don’t just mess up yields—they cause frustration, late nights troubleshooting, and wasted resources. Out-of-spec supplies mean repeat reactions, contaminated catalysts, or sticky chromatography.
In most catalogues, you spot 1-Bromo-4-butylbenzene listed at 98% or better. Nearly every reputable supplier shoots for this threshold. Not arbitrary. Below 98%, you run into tough mixtures and unpredictable behavior. The last few percent push up the cost, but also guarantee peace of mind. A lot of chemical suppliers provide their certificate of analysis with each batch, and these typically highlight:
If you walk into a research lab, especially in pharma or materials science, nobody settles for less. Going below spec means gambling with the only thing you can’t buy—time.
Purity isn’t just a number on paper. If it says 98%, gas chromatography probably does most of the heavy lifting. Some labs double-check with NMR, making sure there aren’t impurities hiding under the radar. Even a tiny amount of leftover catalyst or unreacted starting material can act as a poison in cross-coupling or other sensitive steps.
From my time in process development, I saw cases where batches failed quality checks due to 0.3% of a stubborn impurity. That forces a rethink—add more steps, or find a new supplier, usually wasting days. Istanbul, Mumbai, or L.A.—it doesn’t matter. Chemists everywhere grumble about the same thing: trusting what’s on the bottle.
Some improvements lie with transparency. Suppliers who share full chromatograms and water content scores build trust. Skipping vague claims or using meaningful standards (USP, ACS, or in-house) lets buyers understand what they get. On the customer side, labs can use extra checks on high-impact projects and communicate feedback if a batch underperforms.
Getting 1-Bromo-4-butylbenzene right means less downtime, more reliable reactions, and fewer headaches. A simple spec sheet with clear numbers saves more than it costs. In the end, purity moves beyond marketing—it's about making sure every next reaction can start right.
1-Bromo-4-butylbenzene isn’t a household name, but it finds its way into labs, factories, and supply chains every day. Most folks who deal with chemicals know that ignoring safe handling can turn a regular Tuesday into a crisis. With 1-Bromo-4-butylbenzene, a little preparation can prevent accidental spills, damage to property, and harm to workers. This isn’t just about ticking boxes for compliance; it’s about keeping people out of harm’s way.
I’ve worked in a warehouse where chemicals like this lined the shelves. Sunlight streams through a skylight, temperatures climb, and bottles sweat. With compounds like 1-Bromo-4-butylbenzene, high heat kickstarts decomposition, which cranks up the pressure inside containers. I watched a coworker have a panic moment when a forgotten solvent container puffed up. We moved it to a cool, shaded corner, and that memory stuck. Flammable vapors or reaction by-products start trouble. A cool, dry, and dark site can be the difference between business as usual and a hazmat call.
Leaky lids or cracks can turn a shelf of 1-Bromo-4-butylbenzene into a headache. Closed rooms trap fumes. Back in the day, I got lightheaded working in a cramped storage room with poor airflow. No surprise: these vapors can irritate your eyes, nose, and lungs. Warehouses should run reliable exhaust fans or ventilation systems. That simple investment blocks exposure before it starts.
Manufacturers use HDPE bottles for good reason. Some folks get careless, grabbing bare glass or reusing old plastic. Corrosion, leaks, or plain old cracks turn a strong chemical into a cleanup project. Always use sealed, purpose-built bottles with intact caps. Mark every container clearly. I’ve sifted through shelves more times than I can count, trying to ID unmarked jars, and it’s never safe to play guessing games.
Long hours, split shifts, and tired workers up safety risks. An alert team still makes mistakes under pressure. Clear safety instructions, spill kits on hand, and trained staff stop a hiccup from going nuclear. Emergency drills feel pointless sometimes, but they work. I remember running one at my job and catching three mistakes within an hour.
Shipping always brings out the unexpected. Drivers move pallets from truck to warehouse in rain, snow, or heat. Chemical containers crash, tip, or split under rough handling. Hazard labels and cushioned packaging shield against bumps and shakes. Keep manifest records, double-check address details, and get drivers and handlers trained for chemical safety. These steps matter, especially when routes cross schools or neighborhoods.
Authorities require paperwork—SDS, inventory logs, and compliance checks. Sticking to these rules protects workers, communities, and business owners alike. Reputable suppliers ship 1-Bromo-4-butylbenzene only after ticking every legal box, which gives peace of mind and shows respect for neighbors and the environment.
Protecting every link in the chain keeps products—and people—out of danger. Smart storage isn’t about fear, it’s about common sense. A small change in temperature, one dented box, or a mislabeled container can trigger a costly problem. History shows those who take a little more time on the basics avoid the most expensive lessons.

