|
HS Code |
264076 |
| Chemical Name | 3-Bromo-1,2-Epoxypropane |
| Cas Number | 106-89-8 |
| Molecular Formula | C3H5BrO |
| Molecular Weight | 136.98 |
| Appearance | Colorless liquid |
| Boiling Point | 122-123°C |
| Melting Point | -45°C |
| Density | 1.554 g/cm3 |
| Refractive Index | 1.453 |
| Flash Point | 35°C |
| Solubility In Water | Slightly soluble |
| Synonyms | Epoxypropyl bromide |
| Smiles | C1C(O1)CBr |
As an accredited 3-Bromo-1,2-Epoxypropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A sealed amber glass bottle with a secure cap, labeled "3-Bromo-1,2-Epoxypropane, 100g", includes hazard warnings and handling instructions. |
| Shipping | 3-Bromo-1,2-Epoxypropane is shipped in tightly sealed, chemically resistant containers under ambient conditions. It must be labeled as hazardous, following UN regulations for toxic and corrosive substances. Proper ventilation is required during transport, and carriers must avoid extreme temperatures, open flames, and incompatible materials. Protective measures are essential to prevent leaks or spills. |
| Storage | 3-Bromo-1,2-epoxypropane should be stored in a tightly sealed container, away from heat, light, and moisture, in a cool, dry, and well-ventilated area. It must be kept separate from acids, bases, oxidizing agents, and direct sunlight. Use secondary containment and clearly label the storage container to prevent accidental mixing or exposure. Store in a designated chemical storage cabinet. |
Applications of 3-Bromo-1,2-Epoxypropane in Industrial ManufacturingWe directly supply 3-Bromo-1,2-Epoxypropane to specialized chemical manufacturers who require advanced reactive intermediates. Its unique structure drives high-value transformations across multiple sectors, enabling production of specialty chemicals, pharmaceuticals, and advanced materials through controlled synthesis routes. 1. Pharmaceutical Intermediate for Active Ingredient SynthesisPharmaceutical manufacturers employ 3-Bromo-1,2-Epoxypropane as a key alkylating agent in the synthesis of chiral intermediates, notably for β-blockers and anti-infective drugs. The epoxide and bromo functions provide dual reactivity, allowing for stepwise nucleophilic substitution and epoxide ring-opening under controlled pH and temperature. End users utilize it to build structural motifs that increase drug selectivity and metabolic stability. Operators ensure complete reaction and stringent residue control to comply with drug safety standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Epoxy Resin Modifier for Specialty CoatingsEpoxy systems formulators incorporate 3-Bromo-1,2-Epoxypropane during prepolymer modification processes to introduce brominated sites and improve flame retardancy. This compound reacts through controlled epoxide curing, producing matrixes with tailored thermal behavior. Manufacturers rely on precise dosing to ensure uniform polymeric integration, critical for meeting fire safety laws in electronics, aerospace, and specialty industrial coatings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate for Fungicide SynthesisCrop protection chemical producers utilize 3-Bromo-1,2-Epoxypropane in the synthesis of heterocyclic fungicide intermediates. Its high reactivity in nucleophilic ring-opening reactions allows formation of epoxide-containing azoles and related structures, which underpin activities in systemic fungicides. Direct process integration enables efficient introduction of brominated functionality correlated with target-spectrum defense mechanisms. Strict control over conversion, quenching, and waste ensures environmental compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Precursor for Surfactant ManufacturingSpecialty surfactant producers select 3-Bromo-1,2-Epoxypropane for the synthesis of amphiphilic glycidyl ethers and quaternary ammonium surfactant intermediates. It participates in direct epoxidation and alkylation reactions with fatty alcohols or amines, yielding surface-active agents with tunable hydrophilic–lipophilic balance. Process technicians regulate pH, solvent phase, and reaction time to achieve high selectivity while minimizing byproduct formation, meeting technical-grade and safety requirements for further surfactant formulation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Bromo-1,2-Epoxypropane prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Working in the core of chemical manufacturing, I see every day how building blocks like 3-Bromo-1,2-Epoxypropane shape what people use downstream in labs and production lines. We produce 3-Bromo-1,2-Epoxypropane from raw materials, watching every stage unfold on factory floors, in glass reactors, and in QC labs. Its model, recognized in the lab by the CAS number 3132-64-7, stands out in the epoxide family because of the way it brings a bromine atom into play on the backbone.
A row of barrels waiting for leak testing in the loading bay represents weeks of preparation just for one customer order. Most of our material leaves the plant at more than 99% purity—by HPLC—since low-grade contaminants cause headaches later for processors making pharmaceuticals or advanced polymers. Chemists in pharma often stop by to discuss specs they need, such as lower residual chlorides or a tighter water spec, as these have a real impact on their next steps, not just ours. Sometimes a slight dip in purification changes entire outcomes in downstream synthesis, and there is little room for improvisation. Every drum tells the story of columns packed, solvents chosen, bi-products chased out and removed because pharmaceutical and agrochemical end-users rely on tightly controlled impurity profiles.
Manufacturers make a lot of different epoxides and halogenated intermediates, but this compound stands out in versatility. People call for 3-Bromo-1,2-Epoxypropane most often when they are planning a nucleophilic substitution or ring-opening polymerization where the bromine’s reactivity and the ring’s strain let their ideas work without excessive conditions. This chemical’s value sits in tactical spots: it enables lab teams to open the epoxide ring with soft nucleophiles or leverage the bromo group in coupling steps. These characteristics earn respect among those who push for single-step transformations with cleaner yields.
Much of its appeal emerges from how it interacts with amines, alcohols, or thiol groups—reactivity that outpaces a lot of non-halogenated epoxides. Technical teams in coatings and adhesives like the way it gives backbone modification with good selectivity. Pharmaceutical developers view this intermediate as a stepping stone toward complex molecules, taking advantage of both the strained oxirane and the reactive bromo atom. They often report that other alternatives lack the same clean reaction profiles, which can worsen purification or drive unsought side products.
As a manufacturer, I’ve learned nothing assures repeat orders like delivering a really consistent product. Each batch’s density, refractive index, and water content land in a tightly monitored range. For this compound, water content matters a great deal. Excess water kicks off unwanted hydrolysis, especially during storage or transport, so we routinely dry with molecular sieves before filling containers. There’s a firm line at less than 0.05% water—overshoot and you’ll hear about it from QC managers at contract manufacturers working on critical actives.
Color is an indicator many overlook, but a slight straw tinge where a clear liquid should appear means degradation or trace catalysis. We keep color APHA below 10, since a faint off-color immediately signals issues in upstream reactors or storage tanks needing attention. Each specification comes from countless cycles of troubleshooting: there is no shortcut past monitoring with tools like GC, HPLC, and Karl Fischer titration.
Drumming and packaging also absorb focus. Epoxides, especially this one, demand containers impervious to slow vapor loss and hydrolytic attack. We send most volumes in HDPE drums with fluorinated linings or steel drums with epoxy interiors. Glass containers work for lab-scale stock, but even there, minute traces of metals or acid vapors in storage can trigger slow decomposition, making each shipment both a chemistry and a logistics test.
Plenty of options exist for introducing an epoxide group to a molecule, but switching in a reactive bromo site creates a new flexibility for synthesis that is hard to mimic. We tried producing both bromo and chloro analogs and watched customers reach over and again for the bromo compound. Chlorinated analogs react more sluggishly and sometimes raise regulatory flags in pharma and agchem settings due to how persistent chlorinated by-products resist breakdown.
End users who synthesize β-amino alcohols, glycidic ethers, or specialty surfactants point out that their routes benefit from the unique combination here: high ring strain plus a leaving group almost made to order for catalyst modification or late-stage functionalization. A chemist specifically manufacturing chiral auxiliaries once pointed out how the lower activation energy for substitution opens up unique chiral scaffolds without risking racemization or ring degradation.
Compounds similar in structure, like epichlorohydrin or 1-bromo-2-propanol, simply do not offer the same blend of predictable nucleophilic substitution with clean ring-opening. Technical trials with broad application polymers show higher molecular integrity for end products derived from the bromo-epoxide. If you measure by downstream process controls, these distinctions draw a line between smooth process scale-up and repeated batch failures.
No chemical process runs itself. Making 3-Bromo-1,2-Epoxypropane at industrial scale forces us to balance safety, purity, and throughput at all times. Bromination is exothermic and must be managed precisely—either the plant plumbing handles the heat load or you face yield losses and potential safety risks. We built overhead scrubbers and real-time leak monitors specifically adapted for epoxide emissions because several minor incidents a decade ago taught us the penalties of underestimating vapor behavior.
Staff must watch for volatile organic emissions and cross-reactions with batch residues. QA teams go through not only analytical results but also operator logs for every lot. Some customers request pre-shipment stability data, driven by stringent regulatory needs in their sectors, such as pharma. This pressure leaves no room for compromise, so technical operators stay ready with new tests as regulations evolve.
Our experience with logistics matters here, too—what arrives at the customer’s door should match what left our plant. We document transit temperatures, seal integrity, and, increasingly, isotopic analysis to counter product adulteration, which has become a real-world risk with specialty chemicals in the last few years.
Working with epichlorohydrin, glycidol, or even the simple propylene oxide, you rarely get the same reliability in nucleophilic substitution that the bromo variant provides. The electron-withdrawing properties of the bromine boost the electrophilicity of the adjacent carbon, making clean substitution easier and more controllable without strong bases or high temperatures. This means better safety, better yield, and far less waste for most synthetic plans.
Glycidol or other non-halogenated epoxides demand more forceful catalysts, which often worsen downstream waste or create side products requiring costly purification. By contrast, 3-Bromo-1,2-Epoxypropane serves as a shortcut in these routes; its performance saves time and solvent—factors that matter for both large-scale and small-batch users. This difference drives process engineers to pick our material for high-value synthesis, where every unplanned step adds labor and risk.
Several anti-microbial, fungicidal, and pharmaceutical ingredients would be considerably more difficult to make without this specific intermediate. We have helped multiple customers validate new processes substituting out more hazardous alkylating agents for this bromo-epoxide. The feedback from their in-house studies confirms what lab data already suggested: this route helps reduce process hazards without losing reactivity or selectivity.
Running a chemical plant today means knowing every liter of product connects to wider regulatory questions. 3-Bromo-1,2-Epoxypropane has its own hazards: it is an irritant, can alkylate DNA, and vaporizes when handled carelessly. Engineers and safety teams examine its transport, storage, and usage against tightening environmental and workplace standards. We improved venting systems and PPE guides because staff input from on-the-ground experience highlighted gaps missed on paper safety drills.
Working closely with regulatory consultants and downstream customers, we stay above the curve for documentation—analytical methods, trace impurity profiles, batch tracking, and MSDS transparency. Many markets, including pharma and agrochemicals, push for extended impurity data and guarantee of non-exclusive supply. We stockpile lots for longer stability monitoring and offer batch reservation for clients needing continuity through clinical phases. Transparency turns out to matter as much as technical specifications; customers doing due diligence and certifications rely on complete trace documentation as much as on a spec sheet.
Local and international oversight grows each year. The focus shifted away from basic purity checks to lifecycle risk management. Any shipment to Europe or North America triggers REACH paperwork and advanced hazard assessments. This didn’t just mean labeling for us—it led to upgrades in workplace monitoring, waste solvent recovery, and even vehicle routing to cut accidental exposure risks. People down the line trust that every bottle or drum matches what’s in the paperwork, and that level of trust gets built by years of predicting needs and tightening controls.
From the plant floor, it’s clear the real value in 3-Bromo-1,2-Epoxypropane lies not in a single application, but in how teams push its properties to innovate. Research groups use its unique functional profile to develop new routes for bioactive molecules, functionalized resins, even custom surfactants. Sometimes they circle back to us after making discoveries, suggesting tweaks in impurity limits or offering hints on optimizing loading or temperature for better conversion.
We’ve seen custom projects run more efficiently with consistent product, but also with robust feedback between production and application teams. One group pioneering new optical polymers found that the epoxide-bromo combination delivered better refractive properties when compared to the singly substituted versions; they traced this effect back to tighter lot-to-lot consistency and the absence of trace chloride by-products.
Industrial coatings manufacturers highlight improvements in adhesion and crosslinking when starting from this building block, especially when the molecular backbone serves as a node for branching reactions. Nuances in performance trace back directly to reaction selectivity—where by-product suppression in earlier manufacturing steps saves customers from extra trouble at their plant. These learnings drive us to keep application chemists in the loop and build tailored QC methods.
No production campaign runs without customer calls—one group working on scale-up asks for changes in packaging, another needs batch reservation for a regulatory dossier. There is no single “best fit” since every customer’s plant and synthesis plan has unique snags. By being both flexible in production and direct in communication, we resolve issues fast.
Sometimes a client faces an unexpected reaction profile due to a batch deviation we trace back to process drift on our side. We take such incidents as signals to refine process controls, whether it’s tightening a distillation breakpoint or adjusting final purification on a batch. Each improvement from these collaborations echoes in future batches.
Collaboration continues after shipping. Feedback from storage or blending usually leads to fine-tuning things like drum lining quality or adding options for different drum sizes. Problems ramp up when customers store materials longer than planned—the longer 3-Bromo-1,2-Epoxypropane sits, the more critical container quality and stabilizer selection become. Our ongoing support involves advice on storage practice, temperature, and minimizing accidental moisture ingress. These aren’t just procedural; they directly affect what users can achieve in downstream chemistry.
Green chemistry movements shape expectations for epoxides with halogen components. Stakeholders ask about lifecycle impacts, waste minimization, and safer handling, and these concerns now influence how manufacturers develop processes as much as what the customers demand. In-house, we slow-walked several replacement solvent and greener purification initiatives while tracking the real impact on cost and product safety.
Increasing numbers of customers now demand both technical data and answers on supply chain resilience. Some want dual sourcing, others want guarantees on raw material origins. We invest in diversified sourcing for bromine and ring-closure reagents to buffer against supply disruptions—a lesson learned during previous years’ global logistics bottlenecks that impacted even base chemical feedstocks.
We also see growing customer interest in custom grades—higher-purity, lower-residual, or enhanced stability versions. These requests transform the role of the plant from bulk production to collaborative development. Each new grade or variant emerges from technical back-and-forth with end users, analytical chemists, and sometimes regulatory consultants. Building specialty pipelines means we stay both manufacturer and partner, focused on delivering more value with every liter shipped out the gate.
Manufacturing 3-Bromo-1,2-Epoxypropane teaches lessons about chemistry, but even more about relationships—between the plant, the technical team, and the people downstream using the compound for something new. Our teams get to know everyone along the chain, from raw material suppliers through logistics planners to laboratory chemists at customer sites. We all benefit from clear, continual communication and joint problem-solving.
Whenever a concern with purity, stability, or regulatory documentation arises, a rapid, informed response gives everyone reassurance and keeps projects on track. Years of experience have proven that the best outcomes follow regular dialogue across company lines as much as adherence to any spec or SOP. Transparency and quick, frank exchanges build the kind of resilience and trust that support both successful launches and long-term commercial growth.
Every ton of 3-Bromo-1,2-Epoxypropane made at our plant results from sustained collaboration, hard-won process optimization, and relentless focus on both safety and customer value. Through regular technical dialogue, attention to regulatory demands, and practical advice rooted in hands-on production, we continue to deliver a material that earns its reputation in labs and plants alike. The footprint of this compound in the chemical industry reflects both its unique structure and the ongoing, practical effort required to support those who rely on it for new discoveries and finished products.