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HS Code |
522416 |
| Product Name | 2-Bromide Butyrate |
| Cas Number | 2032-11-9 |
| Molecular Formula | C4H7BrO2 |
| Molecular Weight | 167.00 g/mol |
| Appearance | Colorless to yellowish liquid |
| Boiling Point | 191-193°C |
| Density | 1.569 g/cm³ at 20°C |
| Melting Point | -53°C |
| Refractive Index | 1.449 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Flash Point | 70°C (closed cup) |
| Smiles | CCC(Br)C(=O)O |
| Iupac Name | 2-bromobutanoic acid |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
As an accredited 2-Bromide Butyrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Today’s science-driven industries don’t just run on breakthroughs, but on the steady pulse of chemicals that quietly get things done. 2-Bromide Butyrate, though not a household name, earns respect where reliability in synthesis means everything. With the model designation of C4H7BrO2, this compound stands out for both its chemical versatility and its dependable performance in a toolkit full of specialty reagents.
2-Bromide Butyrate packs structural integrity that makes it useful for a range of lab and industrial applications. With a butyric acid backbone and a bromine atom attached to the second carbon, this molecule falls in the category of bromo-carboxylic acids. The backbone gives it a predictable reactivity, and the bromo group opens doors for substitution and coupling reactions. What people often notice in practice is its stable liquid state under standard conditions, its clear or pale yellow appearance, and its signature odor. The boiling point tends to hover between 180°C and 200°C, marking it as manageable for distillation and separation steps.
Attention to purity sits at the center of successful experiments. Commercial sources usually offer 2-Bromide Butyrate in grades above 98%, with trace impurities like dibromides or unsaturated byproducts screened out through rigorous filtration and quality control. Density hovers around 1.5 g/cm³, higher than most simple butyrates, a direct result of the heavier bromine. Such details matter because subtle changes in density or composition can alter rates of reaction or the efficiency of downstream processing.
Over the years, many of us working in pharmaceutical research and fine chemical production have run across 2-Bromide Butyrate during key steps in synthesis. Its true strength becomes clear during alkylation reactions, especially for introducing butyryloxy groups into target molecules. In my work, I've leaned on it as a reagent for esterification, converting alcohols into butyrate esters with a bromine 'hook' left for further substitution. The presence of the bromine atom allows for easy nucleophilic displacement, so chemists can introduce a wide range of substituents, tailoring molecular properties to meet a specific goal.
In companies that build molecules for pharmaceuticals, fragrances, and agrochemicals, 2-Bromide Butyrate bridges the gap between raw feedstock and finished goods. Its role in the functionalization of aromatic compounds, for instance, often simplifies steps that would otherwise require clunky, less selective reagents. The molecule’s consistent reactivity also saves troubleshooting time during scale-up, where surprises can turn into expensive detours.
Beyond the bench, safety and storage matter. 2-Bromide Butyrate isn’t as volatile as light ethers or simple chlorides, yet it’s not free from hazards either. Careful storage in a cool, well-ventilated area away from strong bases keeps accidental releases under control. Unlike some of the old-generation halogenated acids, it tends to cause fewer headaches related to corrosion or environmental persistence. Nevertheless, a good fume hood and protective gloves aren’t negotiable.
The butyrate family has grown with the arrival of various halogen-substituted versions, but not all bring the same balance of performance and manageability. In the lab, it’s common to see requests for both 2- and 4-bromide isomers. The 2-bromide structure, with the reactive site closer to the carboxylic acid, gives you more control over regioselectivity in complex syntheses. In contrast, 4-bromobutyrate tends to deliver cleaner results when long alkyl chains are essential, but it doesn’t provide as much leverage in activating aromatic rings or optimizing sterics.
Chlorinated analogues always seem to get compared as well. While 2-chlorobutyrate can perform many of the same substitutions, the lower atomic weight of chlorine translates to less dramatic reactivity shifts. Bromine’s size and polarizability often help drive reactions at milder conditions, which matters if you’re working with sensitive substrates. I've experimented with both, and the brominated version stands out by cutting reaction times and boosting yields in cases where aldehydes or amines are prone to degradation.
Some researchers ask about iodinated versions. Though possible to prepare, these are bulkier and much less common in commerce, mostly due to cost and less favorable safety profiles. In the plant or lab, bromide butyrates offer the sweet spot for folks seeking a balance between forcefulness in reaction and manageable hazards.
You can find textbook discussions about functionalized carboxylic acids, but hands-on users care more about what happens day in and day out. In practical terms, 2-Bromide Butyrate smooths over routine bottlenecks. Where free acids can fall short—showing limited solubility or mixing poorly with solvents—this compound often blends in with a wide range of organic or polar media. As someone who has spent hours troubleshooting solubility and reactivity issues, I've learned to appreciate the flexibility this brings. Unexpected precipitation or emulsions can zap hours from a tight project schedule, but this reagent’s predictable solubility prevents such headaches.
It shines in multi-step synthesis, where the choice of intermediate dictates the fate of the entire process. Specialty crop protection agents and APIs (active pharmaceutical ingredients) often require controlled and specific introduction of alkyl chains. Bromide butyrate offers chemists a reliable pathway to install those groups with fewer byproducts, leading to cleaner downstream profiles and easier final purification.
No chemical, no matter how versatile, works for every scenario. There have been occasions where an unexpected side reaction or incomplete conversion popped up when using 2-Bromide Butyrate. Examining the reaction setup, one key factor always came up—moisture sneaking in through glass joints or pipettes rushed from the stockroom. Bromides are notorious for hydrolysis, generating hydrobromic acid, which doesn’t play well with sensitive amines or acid-labile groups.
To counter that, a simple trick of oven-drying all glassware and flushing systems with inert gas has spared countless hours. In crowded labs where tools get recycled quickly, these habits are easy to forget. As a rule of thumb, personal vigilance is the surest defense. In teaching environments, passing on the lesson of “dry before you try” saves newcomers from avoidable setbacks with 2-Bromide Butyrate.
Scaling up brings its own lessons. Handling liters instead of milliliters amplifies minor issues. I remember one instance where inconsistent stirring rate during large-batch alkylation translated into hot spots and uneven yields. After re-fitting the reactor with a more robust overhead stirrer and rebalancing reagent addition rates, yields climbed, and the process could be transferred to pilot scale without fuss. Feedback from production and analytical teams proved the value of treating process transfer as a chance to refine, not just repeat, what worked at bench scale.
Awareness of the broader impact of chemical reagents has changed the way labs and plants operate. 2-Bromide Butyrate isn’t classified as environmentally persistent or bioaccumulative, which bodes well for its use in regulated settings. That said, safe handling releases and waste streams should always get top priority. In the companies I’ve worked with, dedicated waste disposal and spill response training have become standard, ensuring compliance and safety in everyday practice.
Compared to some older halogenated solvents and acids, this compound brings an advantage by breaking down more efficiently in properly managed waste treatment systems. Still, that loosens no one’s obligation. Routine use of secondary containment and periodic waste audits reinforce team accountability.
With global chemical regulations tightening—especially in regions following REACH and similar frameworks—supply chain documentation has improved. Certificates of analysis, batch traceability, and transport labels deliver peace of mind. They also allow rapid response if anything unusual happens.
Working at the bench, it’s natural to look for ways to push productivity higher. One opportunity comes from better process integration. In pharmaceutical chemistry, bringing together nucleophilic substitution with hydrolysis or esterification in a one-pot protocol often shaves hours off the schedule. By judiciously matching 2-Bromide Butyrate to the solvent system and catalyst, teams can avoid isolating unstable intermediates. The payoff isn’t just speed, but higher overall yield with less waste.
Digitalization and automation across labs have carved out another opportunity. With more data coming in faster—from reaction monitoring to chromatography—chemists can find optimal conditions sooner. For instance, high-throughput experiments can uncover where 2-Bromide Butyrate best matches reagents or substrates. Automation makes it easier to systematically address persistent bottlenecks, cutting down manual repetition and freeing up bandwidth for unexpected challenges.
Anyone who’s worked through supply chain turbulence will know the value of a compound that consistently arrives to spec on time. In the specialty chemicals market, 2-Bromide Butyrate occupies a niche with just enough global demand to support steady production, without the volatility that hits rare or highly regulated intermediates. Manufacturers supplying industries from pharmaceuticals to agrochemicals, and even specialty flavors and fragrances, have maintained reliable logistics channels, giving process managers peace of mind.
Economic pressures in recent years have tested the resilience of chemical supply on every continent. Companies sourcing 2-Bromide Butyrate have seen some increases in lead times during raw material disruptions. But its moderate production volume has kept it insulated from dramatic price swings. In my own experience shopping for unusual reagents, this stability lets teams plan research and scale-up projects with a clearer runway, knowing supplies won’t dry up unexpectedly.
Chemistry doesn’t stand still. As techniques evolve, more teams are using 2-Bromide Butyrate than ever before—not by rote, but with a deeper understanding of its quirks and strengths. In my years mentoring grad students and early-career chemists, I've seen how a solid introduction to this compound can save repeated troubleshooting. Demonstrations that walk through risk points—like hydrolysis, proper extraction, and safe neutralization—turn an unknown variable into a trusted part of the toolkit.
Conferences and workshops have played a useful role, too. Presentations on best practices for using brominated reagents—covering everything from waste mitigation to tougher topics like scale-sensitive exotherms—give teams real-world tools for smoother experimentation. Sharing near-misses and lab victories helps chemists on both sides of the bench, and makes working with 2-Bromide Butyrate less a matter of trial and error, more a matter of skillful routine.
More attention is falling on green chemistry, and that shines a new light on how intermediates like 2-Bromide Butyrate contribute to sustainability targets. Developing recyclable systems for halide recovery, designing closed-loop processes, and collaborating with upstream suppliers who use renewable feedstocks—it all weaves together into a responsible practice. Teams working at the intersection of academic research and industry have started trial runs using alternative solvents and catalysts, aiming to slice the carbon and halide footprint down even further.
The ongoing refinement of synthetic protocols, paired with continuous feedback between end-users and suppliers, keeps improvement on track. I’ve found that having an open channel to suppliers about batch composition, impurity profiles, and packaging options pays in the long run. Nobody wants to stall a process or re-validate a method due to an overlooked variable.
Working hands-on, 2-Bromide Butyrate stands out for three things—reliability, controllable reactivity, and a solid safety profile compared to less predictable alternatives. With enough data and anecdotal feedback stacked behind it, it’s earned a place in the workflow both for daily benchtop chemistry and for piloting the next big molecule. In a world where the difference between finished product and setback can hinge on the properties of a single reagent, it’s no exaggeration to say this compound earns trust with every successful batch.
It doesn’t promise miracles; nobody expects it to solve problems beyond its reach. But it does deliver the kind of confidence that comes only with consistent, predictable behavior—from one bottle to the next, from micromole-scale trials to industrial-scale syntheses. For professionals who deal with the realities of budgets, yield targets, regulatory scrutiny, and deadline pressure, that kind of reliability counts for a lot more than a flashy new label or a theoretical best-case scenario.
The next time you see a bottle labeled 2-Bromide Butyrate on your shelf, it’s worth a moment to reflect not just on what it is, but what it lets you do better. Backed by years of dependable service, and by a worldwide community of chemists refining their methods, it sits in the toolkit not because it’s the newest or flashiest, but because it just works. The drive to innovate responsibly, train colleagues well, and keep one step ahead of changing regulations will keep this modest molecule at the center of meaningful progress for years to come. With each new discovery and every improvement in responsible handling, it’s clear that real value in chemistry lies not in the wild claims, but in the steady, reliable progress of compounds like 2-Bromide Butyrate.