Bromoacetone

    • Product Name: Bromoacetone
    • Alias: BA
    • Einecs: 209-795-0
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    411030

    Chemicalname Bromoacetone
    Casnumber 598-31-2
    Molecularformula C3H5BrO
    Molarmass 136.98 g/mol
    Appearance Colorless to yellow liquid
    Boilingpoint 137 °C (279 °F)
    Meltingpoint -56 °C (-68.8 °F)
    Density 1.616 g/cm³ at 20 °C
    Solubilityinwater Slightly soluble
    Odor Pungent, irritating
    Flashpoint 40 °C (104 °F)
    Vaporpressure 2.5 mmHg at 20 °C

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

    Packing & Storage
    Packing Bromoacetone is packaged in a 100 mL amber glass bottle, sealed with a secure cap, and labeled with hazard warnings.
    Shipping Bromoacetone should be shipped in tightly sealed containers, protected from light, heat, and moisture. It is transported as a hazardous material due to its toxic and lachrymatory properties, following strict regulatory guidelines (such as DOT and IATA). Ensure proper labeling, documentation, and use of spill-proof, compatible packaging during shipping.
    Storage Bromoacetone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and heat sources. It must be kept separately from acids, bases, oxidizing agents, and reducing agents. Use secondary containment and store in a designated poison cabinet with appropriate hazard labeling. Access should be restricted to trained personnel only.
    Application of Bromoacetone

    Applications of Bromoacetone in Industrial Manufacturing

    As a direct manufacturer of bromoacetone, we supply this raw material to established industrial end-users focused on synthesis, fine chemicals, and specialty intermediates. Below we outline specific application scenarios, each reflecting genuine, large-scale down-chain usage, formulation parameters, and requirements recognized across global production standards.

    1. Pharmaceutical Intermediate Synthesis (Ketone Derivative APIs)

    Bromoacetone serves as a key alkylating agent in the production of narcotic antagonists and anti-infective drug intermediates, where selectivity and impurity control are critical. Chemical synthesis routes involving this compound focus on introducing bromoacetyl moieties for the further elaboration of active pharmaceutical ingredients, such as certain opioid antagonists and cephalosporin precursors. All process steps require validated contamination controls to ensure compliance with regional and international drug quality standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <797> Sterile Compounding
    • EU GMP Part II APIs
    • Chinese Pharmacopoeia (where applicable to downstream product)

    Typical usage ratio

    • 0.4 – 1.2 molar equivalents, based on specific active molecule synthesis pathways and the reactivity of corresponding amine or sulfa substrates

    Downstream process integration

    • Used during key alkylation and acylation steps post-activation of the substrate, often under controlled temperature and inert atmosphere to prevent side-reactions and over-alkylation

    Final product types

    • API intermediates for opioid antagonists (e.g., naloxone derivatives)
    • Intermediates for β-lactam antibiotics
    • Cephalosporin antibiotic precursors
    • Specialized custom small-molecule probes

    2. Agrochemical Active Ingredient Building Block

    Bromoacetone contributes as a functionalized building block in the production of select herbicide intermediates and fungistatic compounds where mono- and di-substituted ketones are sought for their reactive sites. Formulators employ this intermediate, capitalizing on its nucleophilic substitution potential to introduce functional groups crucial to the final agrochemical's efficacy and selectivity, always considering worker safety and downstream ecotoxicological guidelines.

    Industry compliance standards

    • REACH (EC) No 1907/2006 Registration, Evaluation and Authorization of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management in Agrochemical Manufacturing
    • Local pesticide registration and labeling regulations (e.g., EPA, CCCMHPIE China)

    Typical usage ratio

    • 5 – 18% by weight relative to total reactants (formulation adjusted to downstream yield and process efficiency requirements)

    Downstream process integration

    • Commonly introduced at the second or third chemical transformation during the construction of heterocyclic or aromatic ring systems in pre-emergent herbicide preparations

    Final product types

    • Triazole-based fungicide intermediates
    • Precursor hydrazone herbicides
    • Sulfonylurea herbicide intermediates
    • Other non-selective weed control agents

    3. Fine Chemical Synthesis: Dye and Pigment Intermediates

    Industry utilizes bromoacetone in the formulation and customization of advanced organic dyes and pigments, especially where controlled bromination supports chromophore extension and colorfastness. Process engineers and chemists prefer it for introducing functional bromo groups that later dictate the dye’s final shade, binding ability, and stability against UV and chemical bleaching agents. Integration must comply with strict effluent and byproduct control due to regulatory scrutiny of halogenated by-products.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for non-toxic dye ingredients)
    • GHS for classification, labeling, and handling of hazardous substances
    • ISO 14001 for environmental management relating to halogenated intermediates
    • Global colorant directive (e.g., REACH Annex XVII entry for aromatic amines bound to colorants)

    Typical usage ratio

    • Varies from 2 – 9% by mass of the target chromophoric molecule, depending on molecular weight and substitution pattern needed

    Downstream process integration

    • Added in the nucleophilic bromination step, with rigorous process control to avoid over-bromination and unwanted color shifts during dye precursor synthesis

    Final product types

    • Azo dye intermediates
    • Reactive dye compounds for cellulose fibers
    • Colorfast synthetic pigment bases
    • Inkjet printer dye components

    4. Laboratory Reagent Formulation (Chemical Research and Analytical Standards)

    In fine chemical laboratories and accredited analytical testing facilities, bromoacetone offers a functionalized reference point for validating nucleophilic addition reactions, especially under controlled research synthesis where traceable, well-characterized chemicals are required. Facilities handling this compound must follow laboratory safety regulations and chemical traceability for reference standards, ensuring suitability for academic and industrial research applications, including analyte calibration or reaction mechanism exploration.

    Industry compliance standards

    • ISO/IEC 17025:2017 for testing and calibration laboratories
    • GLP (Good Laboratory Practice) as per OECD Principles
    • Chemical Hygiene Plan (US Occupational Safety and Health Administration - OSHA 1910.1450)
    • Local hazardous material storage and transport codes

    Typical usage ratio

    • 0.05 – 1.0 mmol per experimental batch, scaled for analytical runs or synthesis, based on the nature of the investigated reaction or the calibration procedure

    Downstream process integration

    • Used directly as an analytical or synthetic reagent in controlled, small-scale setups; commonly integrated during calibration runs or as a spiking standard to validate techniques such as HPLC or GC-MS

    Final product types

    • Certified analytical reagents
    • Reference material kits for chemical analysis
    • Research laboratory synthesis stock
    • Standard solutions for chemical education and kinetic studies
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    Certification & Compliance
    More Introduction

    Bromoacetone: Precision Chemistry from the Source

    True Manufacturer’s Approach to Bromoacetone

    In our daily work, producing Bromoacetone takes a careful balance of chemistry and plant operations. The compound carries the formula C3H5BrO and is known across several industries for its specialized reactivity. Each batch we make starts out with a focus on purity, reliability, and safety. From process control inside the reactor, right down to the packed drum or flask, consistency flows from every stage. This isn’t magic—it’s just what happens after years of refining the underlying bromination route.

    What Makes Our Bromoacetone Different

    Bromoacetone isn’t something we pull off the shelf and send out as a commodity. The produce-and-pack routine doesn’t cut it for applications that demand tightly-defined specifications. Most users want material at purity levels upwards of 99%. Every contaminant and trace impurity affects downstream chemistry—so we run gas chromatography and water tests at several points. If you’ve ever worked up a Grignard reagent or prepared a pharmaceutical intermediate, you know that a little moisture or an off-ratio byproduct sets the whole sequence off course. So we do the basic things many overlook: flush the lines, dry the plant environment, and occasionally swap out contact parts.

    Model, Purity, and Handling

    We label our shipments by batch number and certificate of analysis, not just grade. Most requests focus on technical or laboratory grades; some groups require advanced research grade material. Our standard bromoacetone typically clocks in above 99 % GC purity, and we include water content and color data for transparency. The liquid itself comes in clear to pale yellow, easy to identify from the sulfurous or musty odor unique to bromoacetone. In comparison with solvent-grade acetone or lower halogenated acetones, our product resists air-oxidation when held in amber glass or metal drums, under nitrogen atmosphere.

    Due to the lacrimatory (tear-inducing) properties, trained handling always gets top priority. We supply bromoacetone under strict containment, with properly vented, sealed drums and distinct hazard labeling. This not only keeps the workplace safe but reduces waste from degraded or off-spec material. Over the years, we’ve fielded dozens of requests for customized packaging—from sub-liter glass, to nailed PFA bottles for specialty research.

    Reason for Bromoacetone’s Ongoing Role in Research and Synthesis

    Bromoacetone occupies a key role where other brominated compounds fall short. Its reactivity as an alkylating agent drives interest in both academic and commercial labs. Chemists working on heterocycle formation or novel small molecule ligands often request bromoacetone because it introduces the acetone backbone without flooding the reaction with side-products. Nucleophilic substitution and condensation work up reliably, and the product’s volatility allows for easy removal or purification after the reaction has run its course.

    Compared to bromoethane or similar reagents, the carbonyl function in bromoacetone supports more advanced transformations—especially for routes that demand a β-keto structure. Pharmaceuticals, crop science, and specialty materials research all benefit from this property. We’ve shipped to universities working on chromophore synthesis, to materials firms building specialty polymers, and to start-ups investigating enzyme-labeling probes.

    Industry Feedback and Lessons Learned

    Over the past ten years, user comments have shaped our workflow and decisions. Synthetic chemists told us that some batches, even at high purity, still caused migration or color change during storage. This problem traced back to a tiny residual of water and oxidative impurities, which didn’t always show up with simple titration or GC. So we swapped several filter elements, improved our in-line drying process, and changed the headspace gas from air to high-purity nitrogen during fill and sealing. Field complaints dropped sharply within months.

    On one large customer’s request, we ran a full stability series. We filled standard drums and small ampoules, then stored them at different temperatures and atmospheres for three months. After two weeks at ambient temperature, samples stored open to air showed browning and dropped below 98% purity. Sealed, inerted drums kept IC levels stable for the full duration. This didn’t seem surprising but reinforced a fact: without good sealing or air exclusion, bromoacetone won’t hold specification.

    Direct feedback also pointed toward label clarity. In earlier years, we saw confusion between bromoacetone and similar brominated solvents. Now, every drum, flask, and shipping document holds a batch-stamped product code and a summary of the GC report—no more confusion or unnecessary calls from receiving teams.

    Bromoacetone Differences From Other Halogenated Ketones

    Ask a handful of synthetic chemists to compare bromoacetone with other halogenated ketones, and the responses come fast. Chloroacetone, for example, may look similar on paper. Once tested in the lab, chloroacetone reacts slower, needs higher activation temperature, and leaves more persistent side odors. The C–Br bond in bromoacetone cracks much easier in substitution and condensation reactions, especially with weaker nucleophiles. Compared to iodoacetone, bromoacetone offers more stability and easier handling at ambient conditions; iodoacetone’s strong color and high reactivity often cause practical storage and isolation issues.

    Cost and availability also play a part. Iodoacetone production costs more due to the price and handling requirements of iodine feedstocks; chlorinated variants skirt cost but underperform in standard routes. This leaves bromoacetone as the “Goldilocks” option—right balance of reactivity, volatility, and affordability for bench chemistry and commercial-scale work. Our regular runs keep the price stable even during bromine market swings, since we’ve invested in long-term bromine supply contracts and solvent recycling.

    Environmental and regulatory concerns often dictate whether a plant or lab uses brominated or chlorinated ketones. Bromoacetone, unlike many persistent organic pollutants, decomposes fairly easily under the right neutralization and disposal steps. We keep abreast of changing chemical management laws in major markets to prevent shipment delays or customs hold-ups for our customers.

    User Cases and Application Methods

    In academic labs, a few grams of bromoacetone will kick-start the synthesis of a new pyridine derivative or act as a building block for antibiotic analogues. Its straightforward role as a β-bromoketone leaves little guesswork during reaction monitoring. For commercial groups scaling to pilot or plant runs, the product integrates into multi-step transformations targeting insecticides, vitamins, or specialty coatings. In a single-use process, the compound’s volatility makes for easy purging.

    Small biotech companies sometimes use bromoacetone in the synthesis of short peptides or derivatized nucleic acids, since the reagent cleanly installs a reactive handle. Material engineers blend bromoacetone into pre-polymers or specialty plastics, using it to introduce crosslinks or pendant groups. We still get questions from artists interested in old photographic processes—bromoacetone features in some vintage silver halide methods—although large-volume orders hover in chemical manufacturing, not art supplies.

    Safety and Regulatory Practices from the Factory Floor

    Our production runs on strict process control, starting with isolated, ventilated synthesis areas and monitored reactor temperature. The lacrimatory effects from bromoacetone’s vapor require good containment. Operators wear full-face protection and lined butyl gloves. Make-up air in the plant runs through multiple scrubbers and carbon filtration to capture volatile losses. Any off-gas or spent reaction mass gets neutralized before exit. We track all releases and disposal in line with current waste regulations, with detailed logs to satisfy regulatory audits.

    Most countries control the supply and handling of bromoacetone; some designate it as a precursor. We track all shipments and keep granular records for traceability. Shipment documentation rides with the material, including hazard ID, lot trace, and test results. Experience tells us missing a step here holds up customs clearance or, worse, risks a compliance issue. Over time, even small lapses add up to big risks, so we double-check outgoing material and keep our compliance training up to date.

    Transport and Storage Tips for Users

    End-users benefit from storing bromoacetone in sealed, inerted containers away from heat or sunlight. We suggest steel or fluoropolymer drums with nitrogen backfill; glass suits small volumes. Our plant runs annual tests on our own packaged material, so users can match what we see—no surprises on the bench. Any sign of color change or strong odor shift signals the drum’s picked up air or found moisture—time to replace the container or, in rare cases, the material itself.

    Short moves within a site usually pose little risk, but for overland or international shipping, we only use certified carriers familiar with toxic and lachrymatory goods. Each container secures with obvious tamper seals and bold hazard labeling. Over the years, this approach spared several customers headaches with customs and local environmental inspections.

    Reducing Waste and Increasing Efficiency in Bromoacetone Manufacture

    We’ve learned that small tweaks in the process make the biggest impact on waste and resource use. In early years, our bromine usage efficiency lagged because temperature control wavered during the slow add phase. This produced off-spec product and required rework or disposal. With new reactor controls installed, selectivity shot up and off-spec runs nearly vanished. Bromine feed now runs closed-loop, and solvent recovery operates in real time, reusing acetone and cleaning up reactant streams. These shifts carved significant cost savings and made the process more sustainable.

    As environmental regulations tighten, especially in the European Union and North America, waste minimization isn’t just a matter for the sustainability report. We monitor process outputs for halogenated by-products and vapor phase loss, neutralizing waste with reputable destruction methods and reporting detailed numbers to authorities. Our lab continuously tests whether any new additives or process changes would let us drop even residual waste further.

    Fostering Trust with Permanent, Reliable Bromoacetone Supply

    Clients who order bromoacetone need predictability. Disrupted shipments or unannounced spec changes throw off production lines and R&D projects equally. Over the years, we established multiple bromination lines, kept deep reserves of acetone, and built redundancy with utility supply. Power flicker, reactive feedstock issues, or container shortages don’t often reach the customer-side.

    Trust comes from proactive communication. Anytime plant issues crop up or regulatory events push through last-minute changes, we send direct updates. We don’t overpromise and under-deliver. It’s better to spot potential delays early and share solutions or alternatives than leave end-users waiting for a shipment stuck at sea.

    Supporting Safer Chemistry: End-User Collaboration

    From active ingredient manufacturers to universities, most users appreciate hands-on support. Document packages ride out with each shipment and our technical team fields questions about application or scale-up issues. Field stories from customers drive many of our innovations—improved seals, clearer labels, advice on dosing and neutralization. We regularly crunch usage data and incident statistics, then bake those into yearly safety and training modules for both our own team and willing customers.

    Safer chemistry starts with honest assessment of material risk, robust containment, and readiness for the unexpected. It doesn’t end at our gate—so our team remains available before, during, and after the purchase.

    Looking Forward: Improvements on the Horizon

    Although bromoacetone is a mature product in chemistry, new uses continue to emerge each year. Advances in fine chemicals and pharma intermediates drive new requests for tighter specs, faster response times, and green chemistry options. Our R&D group pilots alternate routes—controlled photo-bromination, new continuous flow approaches, or energy-efficient plant heating. Some of these will yield greener footprints or faster cycle times; others might not pan out. But the goal stays constant: keep delivering the bromoacetone chemists can trust, with the data kept open and improvements ongoing.

    Where challenges arise—whether in logistics, regulation, or safety—being a direct maker brings a unique responsibility. By keeping feedback loops short, quality systems transparent, and investments tuned to both safety and output, the manufacturing side does more than fill a purchase order. We hand over a material with history behind it, experience stitched in, and care at every stage. That’s the ethos we bring to each shipment and every new collaboration.

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