|
HS Code |
337031 |
| Chemical Name | 3-Bromopropionyl Bromide |
| Cas Number | 597-87-1 |
| Molecular Formula | C3H4Br2O |
| Molecular Weight | 215.87 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 173-174 °C |
| Density | 2.073 g/mL at 25 °C |
| Melting Point | -48 °C |
| Refractive Index | 1.536 |
| Flash Point | 80 °C |
| Solubility | Reacts with water |
| Odor | Pungent, irritating |
As an accredited 3-Bromopropionyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Bromopropionyl Bromide is packaged in a tightly sealed, amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 3-Bromopropionyl Bromide is shipped as a hazardous material, requiring secure, leak-proof packaging and proper labeling in compliance with international regulations. It should be transported under cool conditions, away from moisture and incompatible substances. Ensure documentation includes relevant safety data, and only trained personnel should handle shipping and receipt. |
| Storage | **3-Bromopropionyl bromide** should be stored in a tightly sealed, corrosion-resistant container under inert gas, such as nitrogen or argon, to prevent moisture ingress. Store it in a cool, dry, well-ventilated area away from heat, direct sunlight, water, bases, and oxidizers. Use secondary containment to avoid leaks. Follow all local regulations regarding the storage of corrosive and lachrymatory chemicals. |
Applications of 3-Bromopropionyl Bromide in Industrial ManufacturingAs a specialized producer of fine chemicals, we supply 3-Bromopropionyl Bromide for integration in advanced downstream value chains. Below, we outline its established roles in certified industrial sectors, highlighting practical formulation ratios, entry points into production lines, applicable compliance protocols, and the specific finished products manufactured with it. All scenarios listed reflect real, validated applications in accordance with regional and international regulatory standards. 1. Pharmaceutical Active Ingredient IntermediatesPharmaceutical manufacturers rely on 3-Bromopropionyl Bromide for the acylation of amines and synthesis of intermediates used in the production of beta-lactam antibiotics, anti-cancer compounds, and certain anticonvulsants. This compound enters the synthetic scheme as a key acylating agent, facilitating efficient introduction of bromopropionyl groups which are crucial for subsequent cyclization and coupling reactions. R&D and scale production both must conform to stringent regulatory controls, with in-process monitoring critical to ensure product integrity and downstream purity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis (Herbicides & Fungicides)The crop protection sector incorporates 3-Bromopropionyl Bromide for the construction of bromoacyl moieties in specialized herbicide and fungicide molecules. Manufacturers use its high reactivity for introducing sidechains critical for binding to target enzymes in weeds and fungal pathogens. Particular attention is given to process control and cleaning validation to preempt any risk of cross-contamination in dedicated agrochemical synthesis trains. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer ModificationAdvanced polymer manufacturers use 3-Bromopropionyl Bromide as a functional group introducer to modify backbone or pendant chain structures. Its use is especially prominent in the synthesis of specialty copolymers that demand sites for further nucleophilic substitution or controlled crosslinking. Operations require rigorous control of residual by-product management and off-gas scrubbing, subject to both chemical and environmental compliance audits. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Organic Synthesis of Imaging and Diagnostic AgentsProducers serving medical imaging, contrast agents, and diagnostic reagent markets utilize this brominated compound to build complex, bromoacyl-derivatized precursor frameworks for both MRI and radiolabeled imaging molecules. These routes demand meticulous process isolation and batch-traceable production under full documentation to meet quality assurance and regulatory protocols, especially when intended for clinical or pre-clinical environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Bromopropionyl Bromide 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!
In our years of manufacturing 3-Bromopropionyl Bromide, we’ve come to appreciate both its technical demands and its role in new synthetic chemistry. Our facility produces this product at high purity levels, with true batch-to-batch consistency. Chemists in our plant maintain vigilant raw material screening for contaminants such as trace halides and moisture, which not only influence final purity but can trigger unwanted side reactions downstream for users. Raw propionyl bromide and elemental bromine each undergo multi-step purification before introduction to tightly controlled reaction vessels. We insist on real-time analytics at each stage — not just for compliance, but because insufficient process control tends to create persistent off-color byproducts. Rather than framing production only by compliance and throughput, our team reviews every single batch record as if we were the ones using this material at the bench.
Our standard offering features purity above 99% by GC, organobromide content closely monitored, and limited acid impurities, which are common in many low-cost processes. We use only HDPE packaging to prevent chemical attack from leaching metals, which, as any synthetic chemist knows, can catalyze unwanted side chemistry if the drum liner fails. Shelf life tracks closely with air exposure, so we keep pack-downs small to ensure customers don’t open a drum unless they intend to use the product soon. There’s plenty of chemistry in this, but also plain experience: any chemist who’s opened a bromine-based acyl halide after it’s sat in a steel drum understands how much trouble a few weeks of moisture ingress can cause.
What reaches customers reflects everything we’ve learned from decades of process improvement. The product itself is a clear to pale yellow liquid at normal room temperature, with a highly reactive acyl bromide functionality. Each drum includes a certificate of analysis detailing GC content, water content by Karl Fischer, and acidity, because in brominated reagents, even tiny changes in these parameters affect downstream yields. Chemical workers expect a certain level of reliability — not only that the reagent performs as specified, but that it won’t introduce wildcards into a synthesis route. We routinely cross-check our standard batch against customer reference lots and, rarely, adjust our purification if synthetic outcomes start to shift — especially for pharmaceutical and agrochemical clients, where trace variances change everything.
Every chlorinated or brominated acyl halide has quirks, but 3-Bromopropionyl Bromide stands out for the unique way it couples its propionyl moiety and reactivity profile with the bromo marker on the three-position. In downstream organic synthesis, that extra bromo atom precisely positions reactive sites in a way you don’t get with traditional propionyl or acetyl halides. We see this used heavily in the development of specialty intermediates and building blocks for pharmaceuticals and crop protection molecules. Modifying the backbone with a three-position bromine lets chemists target specific reactivity, exploiting both the acylation reactivity and the option for downstream substitution or elimination. This opens up routes otherwise unavailable with classic propionyl bromide or even propionyl chloride.
With more standard acyl halides, such as acetyl or propionyl chloride, workers run into selectivity issues. Acid chlorides can be more aggressive, sometimes leading to multiple unwanted side reactions or difficulties in purifying end products due to the higher nucleophilicity. In contrast, the bromo group in 3-Bromopropionyl Bromide tempers direct reactivity, tuning selectivity and, in some cases, facilitating transformation steps with milder conditions. This isn’t just chemical theory; our technical staff has worked alongside small molecule research groups and witnessed firsthand the way a well-placed bromo group helps prevent over-acylation or branching. The trade-off: greater care must go into handling, since organobromide products tend toward higher toxicity and require better containment. But the benefits, for the intended chemistries, outweigh the handling demands.
In our work with clients, both academic labs and industry producers have detailed how this reagent supports library synthesis for early drug discovery and advanced development. Route scouting often involves small starts, with several structural analogs made in parallel. That’s where 3-Bromopropionyl Bromide’s unique reactivity gives the greatest return: the bromo functionality allows later downstream activation — Suzuki couplings, nucleophilic aromatic substitutions, or Grignard extensions — with the first acyl step simply locking in the key three-carbon scaffold. Synthesis teams report that using the bromo-propionyl route can slash weeks from analog generation, giving medicinal chemists better SAR (structure–activity relationship) data faster.
Customers in the agrochemical space also highlight the role this intermediate plays. Active ingredient backbones for herbicides, fungicides, and insecticides increasingly demand selective derivatization. Recent crop protection trends include highly specific brominated and fluorinated moieties for targeted pest control with lower non-target toxicity. 3-Bromopropionyl Bromide allows for a fine-tuned introduction of a propionyl chain that can undergo further functionalization in fewer synthetic steps than older approaches allowed. We observed, over several projects, that this method consistently achieves higher conversion with fewer byproducts, reducing the time and solvent needed for purification. As environmental limits on waste grow ever more tight, this kind of improvement is more than good housekeeping — it’s essential for regulatory compliance.
Anyone working with brominated acyl halides recognizes their hazards: strong lachrymators, prone to react violently with water, and not forgiving of careless handling. In our own experience, even small leaks or failures in containment can foul a laboratory or plant floor for hours. We work with quality drums featuring fluoropolymer gaskets and lined closures, plus heavy-duty liners for all outbound shipments. Our safety systems mandate both static and dynamic containment, with coordinated spill response.
Keeping field chemists safe means everything. We’ve provided client-site training, walking through not only best practices for decanting and dilution but also rapid neutralization, environmental containment, and decontamination. Most users opt for single-use, sealed ampules for small-scale work, especially in R&D. For larger campaigns, we’ve engineered vessel transfer systems with nitrogen inerting and negative-pressure pump lines, so operators never have to handle open containers. These are investments, but any time lost to an exposure event isn’t recoverable. A simple lesson: better equipment and proactive safety pay for themselves many times over.
Through customer feedback and analytical review, we’ve learned that even top-shelf material shows degradation when stored too long, especially if exposed to atmospheric moisture. 3-Bromopropionyl Bromide readily hydrolyzes to release HBr and related acid traces. In extreme cases, even a partially compromised seal or temperature cycling during storage can cause yellowing, exotherm, or crystal formation around lid seals — signs of imminent loss of performance. Because of this, we rigorously monitor warehouse turnover, delivering only freshly packed product from climate-controlled environments, and working closely with supply chain teams to minimize on-site storage times. There’s no workaround: fresh, airtight product always performs best, especially for critical, late-stage synthesis.
We avoid offering bulk “storage deals” that may encourage long storage times in non-climate-controlled settings. From experience, clients facing unexpected delays will contact us, asking for advice when older drums don’t react as expected or generate excessive acidic byproduct. Our lab support team routinely runs side-by-side studies to confirm activity loss in aged material, underscoring the risk of stocking excess reagent in unsuitable conditions.
Experience teaches that quality matters most at the margins. While some may substitute with regular propionyl bromide or chlorinated analogs, we have seen key differences in outcome. 3-Bromopropionyl Bromide, especially when made under strict anhydrous and contamination-free protocols, gives higher coupling selectivity, improved conversion rates, and cleaner separations during workup. Acyl chlorides tend to be too reactive, leading to lower yield due to overacylation and formation of polyacylated side-products, especially on more nucleophilic starting materials. Competing products from generic producers sometimes save on cost per kilogram, but our records on complaint returns prove: most problems arise from trace impurities that were missed during manufacturing. We see this effect consistently, leading us to invest in finer filtration, vacuum lines, and in-process analytics instead of simply tightening inspection at the end.
In more complex syntheses — for example, those with late-stage Suzuki coupling or Stille reactions — the presence of trace chlorides or oxidizing residues can completely derail product outcomes. We’ve supported scale-up projects where switching to our high-purity drum shaved two weeks off a kilo production campaign, due to more reliable product recovery and less time spent fixing problematic chromatography fractions. These aren’t abstract wins; they translate directly to real cost savings for the customer and to smoother operations for the production teams.
A few years back, a pharma client piloting a series of bromoalkylated heterocycles reported unexpected side-residues. We conducted a root cause analysis, including reanalysis of sample lots, and found that a minor impurity from trace acetone in an earlier batch had carried through to their final API, generating a chromophoric contaminant. We altered our drying protocol with additional vacuum purging, then triple-tested outgoing lots; contaminants dropped below detection, and their product advanced to scale-up without repeat issues. Our investment in this level of trace impurity control emerged from just such real-world headaches. It fueled the case for adding new analytical lanes to our QC program, specifically targeted at volatile losses and non-brominated residue tracking.
Another long-term client in the agrochemical sector moved to 3-Bromopropionyl Bromide in a key precursor step for postemergence herbicide synthesis. They reported that clean bromo functionality allowed an improved regioselective substitution, while traditional routes using acyl chlorides produced more byproducts and created challenging waste stream issues from excess acid and salts. Using our drum-packed supply, their team reduced the number of purification cycles and cut solvent costs by nearly 40 percent, simply by starting with a higher-purity, more suitable intermediate.
We support university research groups probing new reactions with our product, as genuine partners, not just suppliers. Those collaborations have revealed subtle advantages and drawbacks in various reaction types. For instance, certain Pd-catalyzed couplings respond unpredictably to trace halide content, so we keep our product line free from extraneous halides. We have also seen how hydrogenolysis steps progress more cleanly using our 3-Bromopropionyl Bromide, thanks largely to the controlled acidity and minimal peroxide residue from our purification system.
Scaling up 3-Bromopropionyl Bromide for commercial campaigns taught us practical handling tips: the reagent’s volatility means rapid transfer times, well-balanced cooling, and nitrogen overlay all combine to minimize atmospheric contact. These methods, worked out through stressful long-haul shipping and process upsets, minimize batch loss and safety risks for the chemists who trust us. Companies that adopt similar strategies report better reproducibility and less downtime from leakage or spoilage. We regularly invite process engineers to visit and walk through our drum-packing and storage operations, because hands-on inspection and open feedback create better solutions than generic written instructions.
Manufacturing brominated organics comes with real stewardship responsibility. From the start, we launched recycling systems for offgas streams, vacuum pump catchpots, and neutralization reactors, not just to hit regulatory marks but because uncontrolled emissions can harm both our workers and the community around us. Any batch deviation or spill is investigated exhaustively, and our containment zones are designed for worst-case events, not just routine operation.
For customers generating acidic wash or spent reaction mass, we provide detailed waste neutralization protocols tailored to actual plant setups, not generic guides. High-capacity local neutralizers, recirculating scrubbers, and effluent monitoring all play a part in bringing down discharge volumes. As regulatory compliance grows more rigorous, and licensing for hazardous materials storage tightens, proactive design keeps both our plant and customer sites prepared. Service doesn’t end once the drum ships; we stay available to help with disposal or recycling schemes based on actual waste profiles.
Unpredictable conditions in the freight sector challenge high-purity reagent delivery. Delays and uncontrolled environments jeopardize moisture-sensitive products more than almost anything else. To counteract this, we introduced climate-controlled warehousing at regional depots and pre-treatment protocols when cross-border shipments take more than seven days in transit. This foresight grew from complaints over years past, when transit times led to off-color, sluggishly reacting product on the far end. By investing in logistics that prioritize chemical integrity, we bypass the old “ship and hope for the best” mentality and place confidence in our delivered material, wherever the end user may be.
We maintain relationships with forwarders accustomed to handling hazardous brominated cargo, with GPS-monitored deliveries for scale-up clients on schedule-critical timelines. These controls don’t just protect the material — they safeguard research, campaigns, and teams who depend on timely starts. Our container tracking flags shipment problems in real time, so corrective action can be taken long before anyone receives unusable or risky material. Our experience says: chemical reliability stems from investment up front, not repair on delivery.
No high-hazard chemical supports its user without support and real-time troubleshooting. Our technical teams field direct requests for troubleshooting at every hour, ranging from color changes in aging stocks to reaction outcome questions on novel substrates. We view every conversation as a chance to learn and improve. When a customer flags an issue — off-spec odor, emulsion after addition, appearance change post-dilution — our senior chemists get on the phone or visit in person, if needed.
We’ve provided in-lab training on everything from decanting to emergency spill response, hands-on and direct. In return, the field has offered us up-to-date insight on emerging synthetic methods, which we fold back into our improved process guidelines.
Regulatory frameworks around brominated chemicals move steadily toward tighter reporting, traceability, and emission limits. We stay ahead of new requirements by continually adjusting internal monitoring, chemical tracing, and documentation networks. The future also belongs to new synthetic methods that minimize hazardous intermediates: real-time analytics, microdose flow chemistry, and in situ quenching all gain ground year by year, sparking shifts in how 3-Bromopropionyl Bromide will be managed and consumed.
We invest in joint development work, aiming to help clients switch from batch to flow where appropriate, and support adoption of “greener” techniques wherever possible. These aren’t just slogans; companies using smaller reactors with rapid inline quenching report fewer operator incidents, improved batch reproducibility, and lower overall consumption. We listen to these field stories, adapting our technical materials and packing options to match — the end goal always remains the same: more efficient chemistry, less waste, and safer workplaces.
3-Bromopropionyl Bromide matters to us not just as a product but as a measure of what we stand for as chemical manufacturers. Every drum, ampule, and package carries the lessons of experience: respect for the user’s needs, attention to the realities of chemical handling, commitment to transparency, and dedication to continuous improvement. We’ve synthesized, packed, shipped, and stood with our customers in both routine use and difficult investigations. That’s the practical heritage that shapes science in the real world, and we intend to build on it with every lot we deliver.