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2-Acetoxy-2-Methylpropionyl Bromide

    • Product Name 2-Acetoxy-2-Methylpropionyl Bromide
    • Alias Bromoisobutyryl bromide
    • Einecs 251-871-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    929567

    Chemical Name 2-Acetoxy-2-Methylpropionyl Bromide
    Molecular Formula C6H9BrO3
    Molecular Weight 209.04 g/mol
    Cas Number 63042-16-8
    Appearance Colorless to pale yellow liquid
    Density 1.474 g/cm3
    Boiling Point 80-82°C at 8 mmHg
    Solubility Hydrolyzes in water
    Refractive Index 1.470 - 1.480
    Storage Conditions Store under inert gas, in a cool, dry place
    Smiles CC(=O)OC(C)(C)C(=O)Br
    Inchi Key FGVPKAYESCRAHK-UHFFFAOYSA-N

    As an accredited 2-Acetoxy-2-Methylpropionyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package features a sealed amber glass bottle, labeled with hazard symbols, chemical name, and handling instructions, inside protective cushioning.
    Shipping 2-Acetoxy-2-Methylpropionyl Bromide should be shipped in tightly sealed containers, protected from moisture and incompatible materials. It requires cool, dry storage, and must comply with hazardous material regulations due to its corrosive and reactive properties. Shipping must use appropriate labeling and documentation, and handlers must wear protective equipment.
    Storage 2-Acetoxy-2-methylpropionyl bromide should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protected from light. Store under an inert atmosphere, such as nitrogen, if recommended. Handle with proper personal protective equipment, as the chemical is corrosive and potentially harmful.
    Application of 2-Acetoxy-2-Methylpropionyl Bromide

    Applications of 2-Acetoxy-2-Methylpropionyl Bromide in Industrial Manufacturing

    As a direct manufacturer, we supply 2-Acetoxy-2-methylpropionyl bromide to industrial partners integrating advanced acylation and bromination chemistry. Below, we highlight key downstream application tracks, detailing compliance, process, formulation, and end products to match the operational needs of formulators and chemical processors.

    1. Pharmaceutical Intermediate Synthesis

    Downstream pharmaceutical manufacturers leverage this material as a building block for synthesizing complex active pharmaceutical ingredients (APIs), specifically for introducing acetoxy and bromoacetyl functionalities. The reagent participates in multi-step routes for antivirals, cephalosporin derivatives, and selective anticancer intermediates, with process parameters strictly controlled to limit residual bromide and define impurity profiles. Customer QC teams require traceability, batch consistency, and oversight on solvent and catalyst compatibility based on route selection.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • EDQM (Ph. Eur. GMP guidelines for starting materials)
    • Chinese Pharmacopoeia/JP/EU DMF filing support documentation

    Typical usage ratio

    • Typically dosed at 0.7 – 1.3 equivalents relative to nucleophile or amino-alcohol substrate in the formation step, with adjustment based on process scale, expected yield, and target purity of downstream intermediate.

    Downstream process integration

    • Added during the acylation or bromoacetylation stage under controlled temperature (<8°C scheduled additions) and inert atmosphere, fed via jacketed glass-lined reactors equipped with local exhaust and scrubber setups.

    Final product types

    • Cephalosporin side-chain intermediates
    • Antiviral nucleoside precursors
    • Pyrimidine or purine acyl derivatives for customized APIs
    • Bromoacetylated building blocks for oncology compound synthesis

    2. Agrochemical Synthesis (Herbicide & Fungicide Intermediates)

    This acyl bromide serves as a key chlorinating and acetoxy transfer agent in the multi-stage preparation of complex agrochemical skeletons. Chemical producers employ it for selective blocking or activation during construction of heterocyclic herbicide scaffolds and bromoacetylated fungicidal amide linkages. Strict effluent controls and by-product monitoring are implemented at plants using halogenated intermediates.

    Industry compliance standards

    • FAO/WHO specifications for technical pesticide actives
    • ISO 9001:2015 (applicable to process QC)
    • China National Standard GB/T 1604-2012 (Agrochemical production)
    • MARPOL Annex III (hazardous chemical transport regulations)

    Typical usage ratio

    • Dosed between 0.6 – 1.5 equivalents versus amine, amide, or hydroxy precursor, with stoichiometry modified according to desired bromoacetyl conversion and residual free bromide minimization for downstream crystallization yield.

    Downstream process integration

    • Added directly into the acylation reactor at the intermediate stage following initial heterocycle assembly, typically prior to ring-closing or alkylation steps, under automated dosing control with halide recovery modules in place.

    Final product types

    • Bromoacetylated triazole herbicides
    • Acetoxy-based amide fungicides
    • Intermediates for chloroacetamide/Pyridine herbicide production
    • Halogenated urea derivatives for crop protection

    3. Custom Monomer Preparation for Specialty Polymers

    Advanced polymer producers select this reagent as an acyl-bromide source during custom monomer manufacturing, specifically where acetoxy or bromo-functional groups require installation onto acrylate or methacrylate frameworks. It enables the precise engineering of reactivity and side-chain incorporation, essential for specialty coatings, high-performance resins, and electronics-grade polymers. Batch documentation and process residue minimization remain priority during scale-up.

    Industry compliance standards

    • ISO 14001 (Environmental management in chemical production)
    • REACH Regulation (EC No 1907/2006)
    • RoHS 3 (EU Directive 2015/863 for electronics polymer components)
    • EPA TSCA (US polymer reporting for new chemical substances)

    Typical usage ratio

    • Ranges from 0.9 – 1.2 equivalents per hydroxyl-terminated monomer or initiator compound, with process engineers monitoring excess minimization and downstream removal of unreacted material by vacuum stripping and washing.

    Downstream process integration

    • Charged during monomer functionalization step in solvent (e.g., chlorinated or aromatic hydrocarbons) in closed-loop reactors equipped with continuous mixing and thermal feedback control, prior to chain extension or copolymerization stages.

    Final product types

    • UV-cure acrylate monomers for adhesives
    • Acetoxy-functionalized resins for electronic encapsulation
    • Bromoacyl copolymer building blocks for high-refractive-index films
    • Cross-linkable additives for automotive coatings

    4. Fine Chemical Synthesis of Specialty Esters and Ketones

    Producers in the flavors, fragrance, and advanced surfactant sectors use the acyl bromide for creating highly pure esters and bromo-ketones with defined branching or acetoxy capping. It participates as a reactant in condensation and transesterification routes under strictly anhydrous conditions. End use relies on oxidative or reductive downstream steps; tight impurity controls are observed to prevent odor or color defects in finished materials.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards
    • EU Food Flavoring Regulation (EC) No 1334/2008
    • HACCP risk management documentation
    • Halal / Kosher process segregation when required

    Typical usage ratio

    • 0.8 – 1.3 equivalents when reacting with primary or secondary alcohols, adjusted to optimize ester purity and minimize by-product formation; parameters are fine-tuned by analytical QC feedback.

    Downstream process integration

    • Reagent introduced via jacketed reactor addition under dry nitrogen with in situ monitoring of exotherm and phase separation; process includes staged neutralization and brine washing before downstream distillation or crystallization.

    Final product types

    • Branched-chain aroma esters for perfume blending
    • Key intermediates for surfactant alcohols
    • Specialty ketone ingredients for flavors
    • Custom acetoxy derivatives for personal care formulas
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    Certification & Compliance
    More Introduction

    2-Acetoxy-2-Methylpropionyl Bromide: A Behind-the-Scenes Look From the Manufacturer’s Perspective

    Understanding What Sets This Reactive Intermediate Apart

    Few chemicals in our line-up see the kind of steady, purposeful demand as 2-Acetoxy-2-Methylpropionyl Bromide. In over fifteen years of handling synthetic intermediates for pharmaceutical and specialty applications, we have worked with many acylating and brominating reagents, but few deliver the same narrow, tailored reactivity. As a manufacturer, you become deeply aware of both the advantages and watchpoints with each compound you handle—not just the listed properties, but also how those properties actually show up batch after batch, on the shop floor and in your customers’ reactors.

    Model and Specifications: Clarity in What We Provide

    Our product is manufactured to a consistent, high-purity profile. Experience has shown us that for 2-Acetoxy-2-Methylpropionyl Bromide, trace-level moisture, residual acid impurities, and slight differences in batch yield may mean the difference between a clean downstream transformation and a sluggish, problematic process. We see to it that every batch meets a minimum 98% assay by GC, with moisture below 0.2% and residual acid below 0.1%. These are not arbitrary numbers—these standards were born from real-world synthetic results, and from conversations with process chemists at pilot and commercial scales.

    While the chemical world often focuses on theoretical reactivity, practical work tells us that lot-to-lot consistency matters just as much. Over years of manufacture, we have learned where the process tolerances lie, and we keep our specifications exactly at the level needed for reliability. Chromatographic purity, color, and Br-content are all measured for every lot, not just during validation but all through full-scale runs.

    Real-World Usage: Why Chemists Keep Coming Back

    You don’t pick 2-Acetoxy-2-Methylpropionyl Bromide if you’re after a general bromination reagent. You choose it for the tightness of its reactivity—especially in acylation steps, where the acetoxy and methylpropionyl moieties give access to intermediates that plain acyl bromides or mixed anhydrides can struggle with. We’ve watched it become the reagent of choice for constructing building blocks in the synthesis of several active pharmaceutical ingredients and advanced materials. Our own history with the compound really begins with a challenging step in the production route for a new cardiovascular compound more than a decade ago. Our client’s process only reached acceptable cleanliness after we tuned the crystallization profile of this bromide to avoid byproduct entrapment. That story illustrates what makes it different—it comes down to selective reactivity and the unique combination of functional groups.

    Unlike more generic brominating agents, this material delivers both the required specificity and a cleaner workup. Saponification rates are more controlled than with straight-up acetyl bromide. The methyl substitution cuts down on off-target alkylations often seen with less hindered acylating agents. If your downstream step needs a functional group that remains untouched by strong acid or base, this molecule wins over alternatives, because the acetoxy acts as a ready leaving group under nearly neutral conditions. This is not a theoretical advantage; we can point to dozens of multi-step syntheses where a swap to this intermediate cut down overall impurity loads and allowed higher yields of the final API.

    Differences from Other Intermediate Bromides and Acylators

    In practice, we manufacture and supply a whole family of reactive bromides. Side-by-side, 2-Acetoxy-2-Methylpropionyl Bromide shows clear distinctions. Take bromoacetic acid derivatives, for instance: those materials react more violently, can hydrolyze with a speed that erodes batch reliability, and frequently give byproducts that are a pain to separate from the desired intermediate. Meanwhile, derivatives like acetyl bromide or isobutyryl bromide lack the same selectivity; they either react too fast, too broadly, or else introduce unwanted groups.

    We don’t just watch these differences on paper. On every manufacturing run, batch journals record thermal stability, exotherm profiles, and handling characteristics. We run validation batches alongside alternate reagents for custom synthesis partners. Over time, we’ve signed off on numerous process reports confirming that where you use 2-Acetoxy-2-Methylpropionyl Bromide, you get more predictable exotherms, smaller impurity profiles, and fewer end-of-line headaches during workup—even for kilogram-scale runs. Anyone with production experience knows the relief that brings.

    Manufacturing Insights: What We Have Learned

    The time in the plant tells you the real characteristics of a material. 2-Acetoxy-2-Methylpropionyl Bromide reacts with atmospheric water, though it gives a slower rise in acidity than other acyl bromides. That difference—meaning a couple hours’ window of safe handling under inert gas—has meant the difference between a manageable workflow and a rush job for many operations teams. The distillation cut of pure product forms cleanly, lining up with boiling points measured decade after decade, and the crystalline product forms needle-like, not clumpy or tarry. Bulk storage, transport, and repacking have each been streamlined so exposure to humidity and UV are minimized, further reducing hydrolytic degradation.

    Working with this product, plant teams quickly develop a sense for its odor threshold, its solubility quirks, and its temperature sensitivities. You notice that spills are easier to localize and neutralize, thanks to lower vapor pressure compared with lighter halogenated acylators. Glove and goggle protocols remain strict—the reactivity is very real—but the physical form lends itself to safer handling than many comparable bromides. Our safety data sheets are written out of direct plant experience, not just regulatory copy.

    Customer Experience: Feedback Driving Our Approach

    Every year, we hear from development chemists trying to shave time off scale-up, or quality managers looking for consistent performance. What comes back most often is a thank-you for minimizing batch variability and providing application notes rooted in real experience. We log every question and complaint, mapping them to both our process controls and our packaged product. For example, about five years ago, a series of customer complaints about cloudy solutions led us to revamp our drying protocols. We traced the issue to micro-entrained water in one reactor train, which never showed up above spec, but which clearly altered reactivity in sensitive transformations. Fixing this single aspect drove a measurable drop in field complaints and, almost immediately, an uptick in repeat orders from two major clients.

    Some long-term customers have reported using this reagent to replace a two-step process involving both an anhydride and bromine in custom syntheses. Switching to our single-step intermediate saved not only time but reduced total bromine tonnage, lowering inherent hazard profiles. In the pharmaceutical world where every gram counts and every impurity manifests at scale, that means a lot. We regularly supply process support for customers who want to test our bromide against their traditional routes, sharing anonymized, real-world yield and impurity traces to help process development teams make informed decisions. Years of data point consistently to better mass balance and cleaner overall processes using 2-Acetoxy-2-Methylpropionyl Bromide, so much so that a handful of new synthesis protocols in peer-reviewed literature highlight its use by name.

    Supply Chain Reliability and Scalable Batch Sizes

    We don’t just sell to the biggest buyers; boutique formulation labs and major multinationals alike have their own requirements. Our production lines are designed to accommodate everything from pilot-scale (as little as 5 kg) up to multi-metric-ton contracts, without cost or schedule overruns. Tetra-pack drums and amber-glass bottles are both standard, based on experience with customer product loss during shipment. Our teams plan order volumes based on actual customer usage patterns, not just market forecasts, which means inventory on hand matches true demand—critical during supply squeezes or seasonal rushes.

    Through downturns and upswings, we have never missed delivery on a confirmed PO, because we keep buffer stock and flexible logistics, including dual suppliers on all consumables and key raw materials. This attention to supply chain reliability may not sound glamorous, but for a reactive, specialist intermediate like 2-Acetoxy-2-Methylpropionyl Bromide, any shipping delay or lot inconsistency has real-world consequences for customers running multi-million-dollar reactors. We have seen entire production campaigns build around the reliability of our product flow, and we take that responsibility seriously.

    Environmental and Regulatory Considerations

    Being in the chemistry business means a long-term commitment to responsible stewardship. For every kilogram of 2-Acetoxy-2-Methylpropionyl Bromide produced, we process and destroy all off-gas and spent solvents via in-house neutralization and contracted hazardous waste vendors who are audited annually. This is no side issue—local regulations get stricter with every passing year, and clients in the pharmaceutical sector now audit not just final batch records but cradle-to-grave process controls. Our plant has invested steadily in closed-loop scrubbers, and process upgrades regularly target yield increases not just for efficiency but as a route to lower overall waste per unit sold.

    Because halogenated intermediates draw more scrutiny, our regulatory team stays close to all regional guidelines. We can provide run documentation for every batch, not just those shipping overseas. Transparency in this area is key—buyers want to know they get not just a reagent, but a supply chain partner ready to answer tough questions on compliance and documentation. The ability to trace our batches back to raw material lots, and auditor access to retention samples and analytical records, sets us apart from less disciplined suppliers.

    R&D and Ongoing Process Improvements

    The best aspect of manufacturing 2-Acetoxy-2-Methylpropionyl Bromide is the regular flow of suggestions and requests from our most technical clients. We are constantly being asked about new derivatives, tighter specs, or changes to isolation procedures to improve recovery or sustainability. These aren’t idle requests—they come from process development chemists and production engineers who are pushing the boundaries of what can be made from the core molecule. In response, we have piloted alternate synthetic routes to lower total waste and have implemented continuous-flow improvements for key reaction steps, all based on real operational feedback.

    Our team has also developed sample kits for academic and industrial researchers, including reference lots with full impurity profiles. This collaboration helps us understand which byproducts matter in advanced synthesis and allows us to improve not only primary quality metrics but also the trace impurity landscape that becomes critical in regulated API manufacture. Feedback loops like these ensure every batch we ship reflects not just today’s standards, but the evolving expectations of tomorrow’s chemistry.

    Potential Solutions to Common Handling and Application Challenges

    No chemical comes without risks or management hurdles, and 2-Acetoxy-2-Methylpropionyl Bromide is no exception. The primary challenge—reactivity with water and the need for inert conditions—is addressed by rigorous packaging standards and customer education. All customers receive detailed guidance tailored to their process needs, whether they source small bottles for bench work or large drums for plant-scale use. Shared experience suggests chilled storage and rapid sampling keep integrity high, so we provide insulated secondary containment and recommend best practices drawn from hundreds of batch-handling events.

    Our onsite technical service team is always available for troubleshooting. For instance, if a customer finds a higher than expected HBr content in a post-reaction mixture, we can consult on solvent, pH, and work-up protocols, since practical outcomes may hinge as much on the post-addition quench as on the main reaction time. Most process hiccups can be traced to simple missteps—sluicing an aliquot without nitrogen cover, for example, or using unconditioned glassware—so our chemists are available to walk through real-world workflows, not just send out generic MSDS sheets.

    Where end-users face scale-up from research to pilot or from kilo-lab to commercial runs, problem-solving shifts as well. We have worked with customers in adapting their reactor cleaning cycles and containment protocols, sharing plant-level engineering controls that cut costly downtime or cross-contamination risks. The two-way street of technical exchange has led to better results on both sides, which only deepens trust and mutual success.

    Looking Ahead: Industry Trends and Emerging Applications

    In the last few years, we have watched new uses for 2-Acetoxy-2-Methylpropionyl Bromide emerge—most notably in nimble, small-molecule pharmaceutical campaigns and certain advanced polymer applications where its unique reactivity profile cannot be matched. Methyl- and acetoxy-substituted building blocks have opened doors to faster, lower-cost synthesis of APIs for niche and orphan drugs, where every step economized translates directly to lives saved and production lines filled. We are proud to be more than raw material suppliers—we act as partners, advisers, and collaborators for each new use.

    As the industry leans further into sustainability, new pressure comes for both greener production and improved lifecycle management. Our team participates in pilot projects for solvent recovery and in research into alternate, less hazardous bromine sources. These projects promise incremental but real gains in both safety and cost competitiveness, and our ongoing role as a manufacturer gives us the hands-on data to test and adjust improvements quickly.

    With the pace of chemical innovation accelerating, clients expect technical flexibility, regulatory transparency, and process improvements—demands well matched to a dedicated manufacturer’s long-term commitment. For us, every lot shipped is more than a sale; it is a reflection of continuous improvement, technical pride, and a promise kept to our clients. Our experience with 2-Acetoxy-2-Methylpropionyl Bromide, from the first runs years ago up to today’s advanced process controls, shapes everything we do, both for this compound and for the family of intermediates we develop alongside it.