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HS Code |
260514 |
| Cas Number | 99734-09-5 |
| Molecular Formula | C4H7BrO2 |
| Molecular Weight | 167.01 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 67-69°C at 7 mmHg |
| Density | 1.624 g/cm³ at 25°C |
| Refractive Index | 1.446-1.448 |
| Flash Point | 80°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as ether and chloroform |
As an accredited 2-Bromomethyl-1,3-Dioxolane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 g of 2-Bromomethyl-1,3-dioxolane is supplied in a clear, tightly sealed amber glass bottle with safety labeling. |
| Shipping | 2-Bromomethyl-1,3-Dioxolane is shipped in tightly sealed containers, protected from moisture and light, and packed according to hazardous material regulations. It is classified as a flammable liquid, requiring UN-approved packaging and appropriate labeling. Transport is conducted by qualified carriers, ensuring compliance with local and international chemical shipping standards. |
| Storage | 2-Bromomethyl-1,3-dioxolane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible materials such as strong oxidizers and bases. Protect from light and direct sunlight. Use secondary containment to prevent leaks or spills and label storage clearly. Always follow chemical safety protocols and local regulations. |
Applications of 2-Bromomethyl-1,3-Dioxolane in Industrial Manufacturing2-Bromomethyl-1,3-Dioxolane serves as a key intermediate in several chemical manufacturing processes. Designed for regulated industrial environments, it enables the precise synthesis of specialty compounds required for pharmaceuticals, agrochemicals, and advanced material applications. Below, we share verified downstream application scenarios with technical integration insights. 1. Pharmaceutical Intermediate SynthesisPharmaceutical producers use 2-Bromomethyl-1,3-Dioxolane as an alkylating agent for the targeted protection and functionalization of hydroxyl groups in complex molecule synthesis. This material supports multi-step API production, specifically for regulated synthesis of antiretroviral and cephalosporin derivatives. Customers incorporate it at the protective group stage to achieve high yields and process control in line with cGMP manufacturing. Industry compliance standards
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2. Agrochemical Building Block PreparationLeading agrochemical formulators deploy this material for the controlled alkylation of precursors involved in pesticide and herbicide actives construction. It supports the synthesis of protected glycol derivatives and specific acetal functions, which are then deprotected, allowing downstream production of selective crop protection actives. Manufacturers select this raw material for its reproducible performance in pilot and commercial batch production. Industry compliance standards
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3. Specialty Polymer Monomer FunctionalizationMajor polymer plants utilize this specialty brominated acetal to introduce reactive sites for subsequent polymerization or functional modification. Used as a protected difunctional monomer or chain transfer agent precursor, it permits custom tailoring of polymer backbone properties, such as solubility or degradability. Production employs stringent QC for residual monomer removal due to application in specialty plastics and controlled-release matrices. Industry compliance standards
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4. Fine Chemical Synthesis for Analytical ReagentsCertified reagent manufacturers employ this intermediate for protected aldehyde synthesis essential in trace-level analytical standards and calibration mixtures. Its controlled reactivity and selectivity enable precise preparation of reference compounds used in high-performance liquid chromatography (HPLC) and gas chromatography (GC) method development, where batch reproducibility is mandatory for accreditation. Industry compliance standards
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From the manufacturing floor, the purpose of each batch of 2-Bromomethyl-1,3-dioxolane pushes far beyond the drum. We do not package abstractions; we provide a building block refined for real-world chemical challenges. This compound has earned its place as a favored intermediate among those who work hands-on with fine chemicals, flavors & fragrances synthesis, and agrochemical research. Years of continuous production have taught us more than what goes into technical data: the rigor needed to meet consistency requirements, the discipline in each distillation, and the skilled attention that separates pure chemistry from guesswork.
Each operator and lab technician who handles 2-Bromomethyl-1,3-dioxolane in our plant understands the stakes involved. Pristine, colorless liquid matters just as much as the aligned purity levels expected by experienced organic chemists. We have set an in-house standard for not less than 98% purity (by gas chromatography), with strict controls on the water content and color index. This level of attention reduces the risk of errors downstream, whether the customer focuses on pharmaceutical R&D or custom molecule development for electronics.
We run our reactors at tightly regulated temperatures to restrain side reactions. Stray by-products drain yield and increase waste treatment costs, so we monitor every kettle batch and purification pass. Each detection step is not just protocol—it’s a defense for your work, reinforced by years of in-process adjustments guided by production experience rather than armchair speculation.
Chemical manufacturers of fine intermediates navigate challenging territory. The promise of 2-Bromomethyl-1,3-dioxolane sits in its role as a versatile alkylating agent. In our process, raw feedstocks enter a multi-stage reaction sequence where bromination must occur in a manner that does not sacrifice the stability of the dioxolane ring. The bromomethyl group reacts efficiently with a variety of nucleophiles. Its selective reactivity gives rise to a diverse set of target compounds and unlocks synthetic options for those working on pharmaceutical scaffolds, specialty polymers, and agrochemical candidates.
Those synthesizing protected aldehydes or ketones often rely on the dioxolane group as a protecting agent, but with the bromomethyl functionality, the chemist can further explore C–C or C–heteroatom bond formation. Our approach maintains rigorous control of batch-to-batch uniformity. Customers have pointed out that higher impurity levels in dioxolane intermediates can catalyze unwanted side reactions that complicate downstream purification. Years in the plant have provided a front-row seat to the troubleshooting needed when raw material inconsistencies spill over into R&D slowdowns or regulatory tests.
Anyone relying on similar bromoalkyl reagents—such as bromomethyl ethers or halomethyl-substituted aromatics—soon discovers what makes 2-Bromomethyl-1,3-dioxolane stand apart. Its five-membered ring structure brings more than just stability. It introduces a predictable reactivity profile that stands up to both strong and weak nucleophiles without collapsing or fragmenting under routine conditions. This difference translates to better yields and more straightforward scale-up, which does not go unnoticed by anyone who faces the cost and timeline pressure that comes with pilot-plant or kilo-lab runs.
In real-world operations, product removal after reaction means everything. Unlike chloro- or iodo- methyl dioxolanes, the bromo analog balances good leaving group ability with more manageable safety considerations compared to its iodine cousin, and fewer regulatory red flags attached to chlorinated solvents or residues. The ether-based alternatives, while sometimes cheaper, have a higher tendency to form peroxides or present volatility management risks not seen with the dioxolane backbone. The difference reveals itself not just in the yield calculation but in the handling steps faced by lab teams who must clean, distill, and transport reactive intermediates.
Across years of large-scale production, feedback from users has shaped our manufacturing priorities. Many of our largest consumers turn to 2-Bromomethyl-1,3-dioxolane to build ethers and esters that ultimately end up in high-value product streams. The importance of purity and consistent reactivity is most obvious during key transformations like O-alkylation—where introducing the bromomethyl group shields aldehydes and ketones for subsequent reactions. Small variances in water or unreacted starting materials can derail selectivity and force rework.
Lab teams often comment on its low melting and boiling point, which allows for simple isolation, handling, and addition protocols. But there are realities to face: under prolonged storage or in the presence of moisture, hydrolysis can sneak in. Every operator in our filling lines recognizes the need for moisture-free drums, verified seals, and sound packaging to prevent costly loss of material or drop-off in reactivity. These aren’t industry platitudes; they are solutions that emerged from solving customer headaches and shipping container failures that once risked expensive project timelines.
We don’t compromise with excipients or fillers because the market for dioxolane intermediates rarely forgives raw material drift. Instead, we choose high-purity raw stocks and double-walled jacketed reactors to keep thermal excursions in check. Logistic teams on our loading docks know the handling codes by heart and spot condensation on containers during seasonal shifts—sometimes before a supervisor realizes. Rapid batch turnaround demands clear communication from lab analysts who communicate directly with production foremen.
Quality control is not just an internal affair. Auditors from overseas clients have stopped by the plant floor. They ask about traceability, not because regulations dictate it but because one off-spec shipment can delay a whole drug registration docket. In response, over several production cycles, we have adjusted parameters—tightening drying steps, fine-tuning distillation cuts, and ironing out packaging improvements. The result: feedback loops where the user’s experience shapes production priorities, not just the language in a datasheet.
Those who handle 2-Bromomethyl-1,3-dioxolane daily know the importance of real-life storage protocols. Bulk storage demands climate-controlled rooms and careful stacking. Open drums picked for sampling are never left uncapped, and lines are always purged with inert gas before and after filling cycles. Field experience proves that even minor lapses in sealing can allow moisture ingress, triggering gradual hydrolysis. Such challenges prompted us to redesign our drum liners and work with suppliers on more resilient gasket materials.
Across repeated pilot-scale synthesis campaigns, product shelf life has demanded continual improvement. Customers who received material stored too long under sub-optimal conditions reported sluggish alkylation and trace impurities that crept into their analytical screens. These production stories have guided us away from speculative packing methods toward vacuum-sealed, desiccant-supported containment solutions. Material picked up by freight partners leaves our gate with a clear stamp of production date and strict rotation records, reflecting lessons learned rather than textbook practice.
Our QA technicians calibrate their instruments not just by the book but by pattern recognition developed from thousands of HPLC and GC runs. Each lot of 2-Bromomethyl-1,3-dioxolane receives parallel testing—chromatograms checked for even minor trace by-products. Years of production have identified what regular paperwork misses: common impurity peaks from unreacted starting material, traces of over-bromination products, or unexpected high boiler residues. Every corrective action initiated after seeing a trend in off-gassing or sample color turns into a process tweak downstream.
Long-term customers may not always read batch sheets in detail, but our analysts document everything. Where earlier generations of the product struggled with color instability or haze formation during long sea transits, adjustments in the post-synthesis filtration and pre-loading quality snapshot have improved clarity and color index. The proof emerges with fewer customer complaints and shorter turnaround for cleared invoices, not just in-domain expertise claimed without follow-through.
Routine support calls with chemists and process engineers often open our eyes to new uses for 2-Bromomethyl-1,3-dioxolane. From protecting groups in total synthesis to transition-metal-catalyzed routes, the stories shared by users feed our cycle of process reinforcement and risk management. Customers exploring organometallic additions find the dioxolane ring confers resistance to certain conditions where other protecting groups fail, and feedback from these trials influences tweaks in our dehydration procedure.
Manufacturing this product is not just about batch yield. Operators must react quickly when an exothermic spike warns of runaway reaction potential. Quality teams collaborate closely with production when a shipment is flagged for higher moisture, jumping in to rework or re-distill as needed. For us, process development draws on advice from those at the hood and those routing tankers—combining technical reports with the day-to-day vigilance that arises only from living with a substance over years, not just passing through on a project basis.
As manufacturers, we remain accountable, not only to regulations but to the researchers relying on our product for timeline-sensitive syntheses. Questions from process development chemists or regulatory reviewers push us to pursue new analytical techniques, explore greener synthesis routes, and evaluate packaging that survives both short-haul and overseas transit. More recently, a growing number of inquiries have come from startups in sustainable materials and custom biocatalysis, seeking cleaner, more transparent supply lines. These relationships draw us toward high-integrity sourcing and ever-tighter QC documentation standards.
Our operators understand the impact of by-product drag and contamination—all it takes is one phone call about a stopped pilot plant or a rejected GMP batch to drive home the cost of error. Such realities led to our transition away from legacy halogen sources and towards cleaner, less waste-generating reagents. Waste treatment personnel contribute practical adjustments, closing the loop between synthesis and environmental stewardship in a way that would not emerge from planning meetings alone.
Decades of manufacturing 2-Bromomethyl-1,3-dioxolane for a demanding, global market have taught us to value partnership over platitudes. Our technical decisions flow from practical incidents—material compatibility, batch failure types, operator feedback, repeat client audits—not from marketing brochures or website templates. Each production run benefits from collective expertise drawn from both the old hands and the younger, tech-driven analysts who see details and demand proof at every hand-off.
The value brought by our 2-Bromomethyl-1,3-dioxolane lies not only in high purity and a repeatable analytical profile but in the responsiveness to user realities and the willingness to adapt, adjust, and recalibrate. No shortcut replaces first-hand problem-solving, and each improvement reflects another layer of operational wisdom. Such an approach might not sound glamorous, but over years, this steady, direct engagement with both molecule and customer shapes the product—and the team—into a source others trust for their most critical synthesis needs.