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Bromochloroacetic Acid

    • Product Name Bromochloroacetic Acid
    • Alias BCAA
    • Einecs 204-059-8
    • 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
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    Specifications

    HS Code

    615797

    Chemical Name Bromochloroacetic Acid
    Cas Number 558-13-4
    Molecular Formula C2H2BrClO2
    Molecular Weight 171.39 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 72-76°C
    Density 2.039 g/cm3
    Solubility In Water Soluble
    Pka 1.59
    Storage Conditions Store in a cool, dry, well-ventilated place, tightly closed
    Hazard Class Corrosive
    Smiles C(C(=O)O)(Br)Cl
    Inchi InChI=1S/C2H2BrClO2/c3-1(4)2(5)6/h1H,(H,5,6)

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

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    Application of Bromochloroacetic Acid

    Applications of Bromochloroacetic Acid in Industrial Manufacturing

    Our advanced production of Bromochloroacetic Acid supports downstream industrial manufacturers seeking high-purity, specification-compliant raw materials for synthesis and specialty chemical processing. The following application scenarios illustrate dedicated use cases developed in close cooperation with customers in core chemical industries, outlining the relevant regulatory frameworks, precise usage parameters, and process integration methods for commercial-scale manufacturing.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (API)

    Bromochloroacetic Acid plays an established role as a key building block in the multi-step synthesis of pharmaceutical intermediates, especially for APIs requiring halogenated acetic acid derivatives. GMP-compliant batch operations utilize the molecule for functional group transformations, such as α-halogenation and carboxyl activation, providing a controlled route to next-generation active components. The introduction of this raw material directly impacts downstream substance purity and regulatory acceptance, where reliable supply and trace-level impurity control remain essential.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs relating to ingredient purity and residual solvents
    • US FDA CFR Title 21, Part 211 (for finished drug quality control)
    • Chinese Pharmacopoeia specifications on pharmaceutical intermediates

    Typical usage ratio

    • Applied at molar equivalence levels of 0.8–1.2 equivalents for halogenation steps; adjusted based on substrate reactivity and downstream purity targets

    Downstream process integration

    • Charged into reaction vessels after initial solvent charging and base addition; used in closed, batch-controlled environments under nitrogen protection to ensure precise conversion and minimized byproduct formation

    Final product types

    • API intermediates containing haloacetic ester or amide functionalities, including selected beta-lactam and cephalosporin derivatives
    • Specialty n-heterocyclic compounds used in oncology and antimicrobial candidates
    • Contract-manufactured intermediate blocks for export-oriented synthesis

    2. Agrochemical Intermediate Production

    In the agrochemical sector, this material forms the cornerstone for preparing selective herbicides and insecticides where the dual halogen atom profile supports unique reactivity in constructing target molecules. Strategic addition during synthesis enables the formation of haloacetate substructures critical for biological activity modulation. Safeguarding worker safety and residue limits, downstream manufacturers leverage tight specification controls for consistency in high-volume campaigns.

    Industry compliance standards

    • FAO/WHO Guidelines on pesticide technical material quality (FAO specification manual)
    • REACH Regulation (EC) No 1907/2006 for import and use in the EU
    • ISO 9001:2015 for process and quality management in agrochemical plants
    • China GB 2763 for maximum residue limits in agricultural commodities

    Typical usage ratio

    • Variable, typically 3–7% by weight as halogen source or chain extender, with adjustments dictated by desired end-group incorporation and crop selectivity

    Downstream process integration

    • Introduced post-initial reactants during core coupling or cyclization stages, often under controlled temperature and pH to steer product profiles and minimize side reaction formation; reactor configuration usually includes ambient or chilled water jackets

    Final product types

    • Acid herbicide intermediates for triazine and pyridine-based actives
    • Halogenated insecticidal esters for seed treatment or foliar application
    • Processed bulk intermediates for formulation into exportable pesticide technical concentrates

    3. Fine Chemical Building Block in Special Polymer Additives

    This specialty acid serves as a functional monomer unit in synthesizing tailored polymer additives, imparting flame retardant and surface-active properties to high-performance plastics and elastomers. Precise dosing ensures optimal incorporation of halogen functionalities, which in turn enable downstream flame-resistance or tailored dielectric profiles in engineered resins for automotive or electronic components. Strict process monitoring ensures complete reaction to avoid free acid impurities in final polymers.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastic Materials for Parts in Devices and Appliances)
    • RoHS Directive (2011/65/EU) regarding restriction of hazardous substances
    • ISO 14001 for environmental management in polymer production
    • ASTM D5630 for halogen content in polymers

    Typical usage ratio

    • Dosage typically ranges from 0.5–5% by resin mass, depending on the target level of halogenation and end-product performance requirements; optimal concentration validated through bench-scale extrusion trials

    Downstream process integration

    • Added during bulk resin blending phase or as a reactive co-monomer in melt-phase polycondensation, often following catalyst addition to maximize incorporation and minimize chain defects; monitored via in-line spectrophotometric analysis

    Final product types

    • Flame-retardant epoxy and polyester resin additives
    • Halogenated elastomeric coatings for wire and cable insulation
    • Masterbatch concentrates for thermoplastic compounding

    4. Intermediate for Dye and Pigment Synthesis

    Manufacturers in the dye and pigment industries rely on the reactivity of this molecule to introduce halogen substituents in chromophoric groups, enhancing color-fastness and environmental stability in organic colorants. The controlled addition ensures the successful preparation of β-halo carboxylic acid motifs, serving as essential handles for further cross-coupling or diazo reactions that define pigment structure and longevity. Sourcing high-purity grades helps attain consistent shade and conformance with regulatory migration requirements in end-use textiles or coatings.

    Industry compliance standards

    • EN 71-3 for migration of certain elements (safety of toys, relevant for colored articles)
    • OEKO-TEX Standard 100 for restricted substance content in textiles
    • ISO 9001:2015 for specialty colorant batch production
    • REACH Substances of Very High Concern (SVHC) guidance for aromatic amine content

    Typical usage ratio

    • 1–6% by reactive precursor mass; adjusted according to desired halogen content in final pigment or dye molecule, as well as downstream purity requirements

    Downstream process integration

    • Introduced at the nucleophilic substitution or diazotization step, following primary aromatic substitution reactions; operations conducted under strict pH and temperature conditions to control formation of desired chromophores and pigment structures

    Final product types

    • Halogenated azo and anthraquinone dye intermediates
    • Color-fast pigments for industrial coatings and artist colors
    • Textile dye components for high-end garment finishing

    5. Derivative Preparation in Specialty Organic Synthesis

    Chemical process developers and contract manufacturing organizations incorporate this raw material as a selective electrophile in the targeted preparation of custom organic molecules. Its use enables sophisticated structure modification—particularly α-halogenation of carboxyl groups or generation of mixed anhydrides and esters—supporting rapid analog synthesis and method development for downstream pharmaceutical, agrochemical, and material science applications. The process demands precise charge order, temperature control, and reaction monitoring to maintain sample integrity through scale-up.

    Industry compliance standards

    • ISO 17025 for analytical quality control in contract synthesis
    • GMP or ISO 9001 certification for custom synthesis operations
    • Globally Harmonized System (GHS) for labeling and safety data in intermediates supply
    • Local environmental discharge regulations governing halogenated waste

    Typical usage ratio

    • Ranges from 5–20 mol% relative to primary substrate, optimized through pilot batch trials for purity and target conversion

    Downstream process integration

    • Dosed into reaction vessels as a first or second charge, following in situ base/acid activation, often under chilled solvent to moderate reaction exotherm; downstream neutralization and phase separation protocols applied prior to isolation of target derivatives

    Final product types

    • Functionalized carboxylic acids and esters for pharmaceutical screening
    • Intermediate compounds for ligand and catalyst development
    • Custom multi-halogenated building blocks for research and development projects
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    More Introduction

    Bromochloroacetic Acid: Understanding Its Role in Modern Chemistry and Production

    Bromochloroacetic acid stands out as a specialty chemical combining bromine, chlorine, and acetic acid structures. Its formula, C2H2BrClO2, indicates the unique way it merges halogen atoms with a simple carboxylic group. Over the years, chemists found value in bromochloroacetic acid for tasks where selectivity, reactivity, and clear performance matter. Its model—often presented as high-purity, reagent-grade crystals—caters to both industrial and research needs, with specifications that include purity levels above 98 percent, minimal water content, and packaging in amber glass bottles to reduce degradation.

    I see the importance of such chemicals not only in their reactivity but also in the experience of working with highly controlled substances in the lab. Handling bromochloroacetic acid brings back memories of synthesizing rare intermediates for pharmaceutical projects, where a precise outcome required strict attention to purity and consistency.

    Intended Uses: Why Bromochloroacetic Acid Matters

    Bromochloroacetic acid serves as an acylating agent and intermediate in organic synthesis. Its dual halogen content makes it more reactive than compounds with only a single halogen, like monochloroacetic acid. This quality lets chemists achieve transformations on molecules that might resist change with other reagents. It finds use in agricultural chemical development, specialty polymers, optoelectronic materials, and, above all, the synthesis of complex pharmaceutical molecules. In these areas, reaction predictability saves weeks of troubleshooting.

    Trying to get the right substitution pattern on a benzene ring or creating a chiral center with controlled stereochemistry tends to be a headache for organic chemists. Bromochloroacetic acid often acts as a shortcut, offering higher selectivity and fewer unwanted byproducts. Having spent days wrestling with unstable intermediates, I sometimes wish every reaction had a tool as straightforward as this one when demanding reactivity and targeting very specific molecular sites.

    Comparing with Other Halogenated Acetic Acids

    A closer look at bromochloroacetic acid’s family members, like monochloroacetic acid and dichloroacetic acid, reveals meaningful differences in chemical performance. Monochloroacetic acid brings basic halogenation to the table but seldom delivers the same level of chemical activation. Adding bromine changes the equation—this makes a world of difference when aiming for more challenging couplings or introducing halogens in a late synthetic step. Compared to dichloroacetic acid, bromochloroacetic acid packs a bigger punch in reactivity, due to the larger size and electron-withdrawing nature of bromine.

    I’ve used monochloroacetic acid for years to make basic esters and simple herbicide molecules. Plenty of times, the reaction stalled, or impurities showed up, driving home the fact that not all halogenated acids are made equal. Once bromochloroacetic acid came into play, speed picked up and so did conversion rates. Those lessons stuck with me—sometimes, paying more for a higher-functioning reagent pays off many times over.

    Specifications: What Sets It Apart

    Manufacturers often produce bromochloroacetic acid in crystalline, off-white form, stable at room temperature if shielded from light and moisture. The melting point hovers between 90 and 93 degrees Celsius, high enough for easy handling in standard laboratory conditions. Water content drops below 0.2 percent for top batches. Impurities, particularly unreacted starting materials and byproducts like dichloroacetic acid, need tight control to keep reactions reliable.

    High-purity grades are usually reserved for pharmaceutical or electronic applications, where a trace impurity can spell regulatory headaches or product recalls. Analytical chemists routinely deploy HPLC and GC-MS to verify composition and ensure compliance. I’ve reviewed batch certificates for bromochloroacetic acid batches declared “fit for synthesis,” scrutinizing every analysis report, knowing trace errors have cost more than a few labs time and money in failed scale-ups.

    Safety and Experience: Handling Reality in the Laboratory

    Bromochloroacetic acid isn’t a beginner’s material. Both the acid function and halogen atoms drive up toxicity and corrosivity. Skin contact leads to burns, and inhaling dust or vapor means immediate throat irritation. My earliest mistake with a halogenated acid wasn’t respecting the need for gloves and a fume hood—I learned from raw experience what a “minor spill” could mean for the day’s work.

    Standard practice in experienced labs keeps this material away from open benches. Working solutions remain capped, glass pipettes beat plastic, and cleaning after use becomes ritual. This isn’t about paranoia, just daily respect for something designed to react aggressively with a wide range of molecules.

    Quality Demands and the Reality of Sourcing

    High-stakes research and manufacturing put pressure on suppliers to deliver pure, defect-free bromochloroacetic acid. Oversights can lead to batch failures, poor yields, or damaged equipment. Reliable suppliers invest in analytical controls. They provide certificates of analysis with every shipment. Beyond purity, chemists look for full traceability, down to raw material lots and process documentation.

    Sourcing bromochloroacetic acid from unverified channels makes sense only until something goes wrong. Once a project falters on account of an off-profile reagent, trust in supply lines falls off sharply. In my experience, investing in a clear paper trail and validated suppliers doesn’t just buy peace of mind, it often shaves weeks off regulatory review on the back end.

    Scalability and Practical Production Challenges

    Lab-scale reactions with bromochloroacetic acid usually run smoothly, but scaling up exposes hidden headaches. As quantities increase, issues like exothermic behavior, reactor corrosion, and waste handling become more serious. During one multi-kilogram synthesis at a former employer, I learned that process parameters from a gram-scale pilot bore little resemblance to what surfaced on the factory floor. Reaction times lengthened, collation of product suffered, and halogenated waste became a disposal hurdle.

    Manufacturers focused on bulk production actively improve reaction monitoring, jacket cooling, and spend real money tackling emissions. The push for greener chemistry has made it clear that basic containment and neutralization steps aren’t enough. Ongoing dialogue between manufacturers and downstream users helps drive process improvements. Sometimes, even switching to a modified synthetic route makes sense if it halves the hazardous waste output.

    Sustainability, Regulations, and the Evolution of Practices

    Bromochloroacetic acid, like many halogenated chemicals, finds itself at the intersection of innovation and regulatory caution. Its utility in specialty chemical manufacture bumps against concerns about toxicity and environmental persistence. Regulatory authorities in the European Union and North America set strict guidelines for transportation, worker exposure, and waste handling. Inspections and standards get tougher over time, which serves as both challenge and opportunity for the industry.

    Newer processes often incorporate containment systems, automated monitoring, and sometimes switch from bulk solvent use to microreactor technology to limit emissions. I routinely noticed that companies investing in more sustainable practices requested not just the product, but also a complete dossier on environmental controls. In my work supporting environmental audits, the traceability of bromochloroacetic acid sources came under scrutiny, especially for exports and product registrations.

    Future Pathways: Meeting Market Demands and Addressing Concerns

    Looking at trends in research and manufacturing, the role of bromochloroacetic acid may evolve alongside green chemistry initiatives. Companies and academic groups experiment with alternatives that swap one halogen for another, but few substitutes match the unique profile of this compound for site-specific reactivity. Incremental improvements in purity, container technology, and safety measures continue to appear.

    Greater investment in process intensification—shorter reaction times, higher yields, and automated controls—offers a way forward. I see collaborations between research chemists and plant managers as key to effective adoption of new techniques. Tighter emission limits set by regulators often motivate innovation; chemists respond with improved catalysts or switch to continuous-flow reactors that cut waste. Over the years, experience has taught me that progress on these fronts doesn’t mean giving up powerful building blocks like bromochloroacetic acid—it means handling them more thoughtfully.

    Market Outlook: Demand, Competition, and Adaptation

    Specialty chemicals like bromochloroacetic acid may never headline the business section, but their impact on production cycles and product pipelines is undeniable. Demand shifts with trends in pharmaceuticals, pest control, and polymer electronics. While some alternatives knock at the door, switching away comes at a price—lost reaction selectivity, increased development time, or reduced performance in the finished product.

    Competing products, like monochloroacetic acid and mixed halogen precursors, often cost less but lag in the performance that matters for advanced synthesis. Long-term contracts and collaborative relationships between producer and user help weather market swings and insulate users from raw material price spikes. For end users, loyalty to a trustworthy supplier saves money over time, even if short-term pricing tilts toward lower-cost competitors.

    Practical Solutions: Improving Use and Limiting Downsides

    Safer and greener practices make using bromochloroacetic acid more sustainable. Smaller packaging reduces exposure risk during handling. New absorbent materials in spill kits cut clean-up time and cost. Shared best practices, once distributed as technical articles or word-of-mouth advice, now appear in digital safety platforms accessible to lab workers everywhere. My experience confirms that ongoing training and regular drills on spill response and personal protective equipment use keep accidents rare.

    On the production side, closing the loop—capturing emissions, recycling solvents, and neutralizing acid wastes—directly lowers costs and regulatory risk. For all the advanced theoretical work behind this chemical, practical, hands-on measures work best to address most real-world safety and sustainability issues. Once teams establish a culture of shared responsibility, accidents and compliance shortfalls tend to fall.

    Interdisciplinary Lessons and Broader Impacts

    Bromochloroacetic acid carries value beyond the simple act of synthesis. Its routine use catalyzes improvements in material science, medicinal chemistry, and analytical methods. New protocols for high-resolution separation, more selective catalysts, and on-the-fly impurity detection have roots in the ongoing need to handle and monitor reactive intermediates like this one. I often reflect on the experience of troubleshooting a failed batch; the lessons learned drive better tools and sharper oversight, which then lift standards for handling all reactive intermediates.

    While regulations sometimes feel like a barrier, they often become the framework by which safer labs and cleaner factories grow. Research teams spend less time troubleshooting and more time moving ideas up the pipeline to manufacturing. Everyone—from bench scientist to industrial chemist—benefits from working with a chemical that forces clear thinking, meticulous planning, and routine self-assessment.

    Conclusion: Moving Forward in a Changing Landscape

    Bromochloroacetic acid remains an anchor point in labs focused on challenging syntheses, new materials, and advanced pharmaceuticals. Its unique reactivity, tight specification profile, and predictable behavior continue to draw investment from companies eager to scale up or innovate. My experience shows that, with clear procedures, trusted sources, and rigorous controls, users get the most from this compound while limiting unwanted consequences. Every year, someone somewhere finds a new use or more efficient way to deploy bromochloroacetic acid—reminding the industry of the value in pushing for both performance and safety.