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HS Code |
450544 |
| Chemical Name | Alpha-Bromo-2-Chlorophenylacetic Acid |
| Cas Number | 21404-07-5 |
| Molecular Formula | C8H6BrClO2 |
| Molecular Weight | 249.49 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 110-112 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.75 g/cm³ (approximate) |
| Storage Conditions | Store at 2-8 °C, keep container tightly closed |
| Smiles | C1=CC=C(C(=C1)Cl)C(C(=O)O)Br |
| Ec Number | 629-552-7 |
| Synonyms | 2-Chloro-alpha-bromophenylacetic acid |
As an accredited Alpha-Bromo-2-Chlorophenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Opaque amber glass bottle, 25 grams, screw cap, tamper-evident seal, chemical label with hazard pictograms and product details. |
| Shipping | Alpha-Bromo-2-Chlorophenylacetic Acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is handled as a hazardous material, requiring proper labeling and documentation. The package must be protected from moisture and heat, and transit complies with relevant local, national, and international chemical shipping regulations. |
| Storage | Alpha-Bromo-2-Chlorophenylacetic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it separate from incompatible substances such as strong bases and oxidizers. Store at room temperature, and avoid exposure to moisture to prevent decomposition. Ensure proper labeling and restrict access to trained personnel only. |
Applications of Alpha-Bromo-2-Chlorophenylacetic Acid in Industrial ManufacturingAs a direct manufacturer of Alpha-Bromo-2-Chlorophenylacetic Acid, we supply this specialty intermediate to regulated downstream sectors that require exacting control over formulation, process, and finished product quality. Below, we outline its key industrial applications, providing practical integration details for professional formulators and process engineers. 1. Pharmaceutical API Intermediate for CNS DrugsThis compound serves as a critical building block in the synthesis route for select central nervous system (CNS) active pharmaceutical ingredients, notably in the manufacture of active moieties with antipsychotic or anxiolytic effects. Production plants utilize its halogen substitution pattern to facilitate controlled aromatic substitution reactions, forming key linkages in multi-step synthetic API libraries designed for generic and patent-based drugs. Industry compliance standards
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2. Agrochemical Synthesis: Pyridine/Pyrimidine Derivative PipelineAgrochemical formulators in crop protection leverage this intermediate for nucleophilic aromatic substitutions that introduce functionalized acetic acid side chains into pyridine or pyrimidine scaffolds. This reactivity facilitates scalable synthesis of key herbicide and fungicide precursors – typically proceeding through further ring-closing, esterification, or amidation reactions essential to modern agricultural chemistry. Industry compliance standards
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3. Fine Chemical Intermediate for Specialty Dye ManufacturingManufacturers of high-persistence specialty dyes incorporate this molecule to introduce halogenated acetic acid motifs, influencing dye bath stability and chromatophore binding performance. Its use centers on targeted azo and anthraquinone dye synthesis where precise molecular modification is required for robust color fastness in industrial textiles and high-performance coatings. Industry compliance standards
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4. Chemical Intermediate in Advanced Photoinitiator SynthesisProducers in the photochemical sector employ this acid-derived moiety during the synthesis of specialty photoinitiators for UV-curable inks, coatings, and adhesives. Its bromo and chloro substitutions provide essential sites for nucleophilic displacement or further functionalization, critical for achieving controlled reactivity in radical-initiated polymerization systems. Industry compliance standards
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In the chemical industry, not every intermediate stands out from the crowd, but Alpha-Bromo-2-Chlorophenylacetic Acid earns its keep in the workspace. Its CAS number 26282-70-4 pops up often in pharmaceutical syntheses, and its distinct makeup—a bromine atom across from a chlorine on the ring, both flanking the acetic acid side chain—gives it some unique advantages in the toolkit for creating active molecules. We’ve spent plenty of hours in the plant scaling reactions just to form this one compound with the right balance between purity and yield. Years of production runs taught us that this step forms the backbone for specialty medicine building blocks, dye compounds, and even some agrochemical research.
Making Alpha-Bromo-2-Chlorophenylacetic Acid in our plant means managing tight controls at each stage. It starts with a 2-chlorophenylacetic acid core, which forms the foundation. Once production begins, bromination requires cool temperatures, strict stoichiometry, and constant testing. Even a slight variation from the setpoint shifts the purity or the reaction byproducts. Over years of batch records, we’ve seen yields lift from 70% into the 90% range after implementing inline sampling and better phase separation.
Process safety takes a front seat. Small changes in agitation or feed can push the endpoint too far, so we keep the human element close. Each reactor operator knows how to spot trouble—color shifts, transient foaming, or phase inversion call for rapid response. Electronic monitoring goes hand-in-hand with hands-on skill: controlling exotherms so that we get high-purity, crystalline product after quench and filtration.
You’ll find Alpha-Bromo-2-Chlorophenylacetic Acid in both industrial and research settings, but our customers tell us what matters most is the reliability in each drum or bottle. Our typical product specification clocks in at greater than 98% purity, white to off-white crystalline solid, true to form, with minimal impurities and a melting point in the 95-99°C range. Our lot analysis rarely strays outside this window because we test incoming raw materials for trace contaminants—bromide impurities found early can cascade into later stages, so controlling the process from step one keeps downstream steps manageable.
The team carefully monitors chloride and bromide residues. Residual solvent, if left unchecked, tanks customer yields during scale-up or GMP validation. We routinely vacuum-dry the product and run Karl Fischer moisture checks before packing. It’s not glamorous work, but it keeps manufacturing headaches at bay for everybody down the supply chain.
We’ve handled other bromo- and chloro-acetic acid derivatives, but few combine the same reactivity and selectivity as this one. The bromine at the alpha position adds strong leaving group ability—essential for nucleophilic substitution or coupling reactions—while the ortho-chloro on the aromatic ring changes its electronics, offering options in further halogen exchange or Suzuki coupling. In side-by-side tests, beta-bromo isomers lose stability and can hydrolyze, and mono-halogen variants miss the mark in forming tight, regioselective bonds later in a synthesis.
Chemists in our client base lean on this intermediate for peptidomimetic drugs or specialty dye precursors. We’ve run collaborative projects where swapping out the bromine or shifting the chloro group drastically altered the active properties of the end-product. Our staff worked through the solubility differences too—alpha-bromo-2-chlorophenylacetic acid dissolves uniformly in a range of polar aprotic solvents, which simplifies in-process handling and downstream crystallization.
Alpha-Bromo-2-Chlorophenylacetic Acid steps into the spotlight during the construction of new pharmaceutical scaffolds. In our company’s pilot plant, we’ve seen its value in the key couplings of non-steroidal anti-inflammatory drug candidates, and in the extension of aryl glycine-based building blocks. The bromine serves as the drop-in handle for further functionalization—SN2 reactions with nitrogen, oxygen, or sulfur nucleophiles work under mild conditions, saving on energy costs and simplifying purification downstream.
For agrochemical innovation, we’ve supplied development-scale batches to research outfits aiming to design herbicidal compounds with higher selectivity. In situations demanding the formation of complex heterocycles, our intermediate made it possible to set the regiochemistry cleanly, avoiding positional isomers that cause headaches at registration stage.
We keep open lines of communication between our process and R&D teams. During one pilot campaign, our partners flagged inconsistent downstream reactivity. Our joint troubleshooting uncovered a minor solvent impurity from local purification steps—which only appeared at larger scale. A process tweak and a new solvent drying regime closed the gap. This sort of feedback loop comes standard, and we update our production SOPs to catch and fix new issues as soon as they surface.
Customers who synthesize high-value APIs or scale advanced materials often insist on the consistent behavior of substrates like Alpha-Bromo-2-Chlorophenylacetic Acid. One year, a client ran into trouble when impurities in raw material batches triggered off-cycle Vilsmeier–Haack formylation. Their troubleshooting traced the fault to minor but persistent bromoacetophenone formation stemming from a supplier’s rushed workup. After analysis, we supplied a consistently pure compound, restoring the reaction’s performance and timelines.
On our floor, every batch comes with a detailed COA, but our team expects more than paperwork. We run follow-up HPLC and NMR to confirm nothing slips through the cracks. Missed trace metals or solvent carryover can add steps or require repurification—so we stake our reputation on batch reliability as much as the paperwork trail.
Brominated aromatics have a reputation for reactivity, but experienced hands shape safety protocols. Bromine evolution during manufacture means operators work with fume hoods, air monitoring, and PPE. We maintain proper neutralization tanks for any acidic byproducts, using sodium thiosulfate to quench excess elemental halogen before discharge.
During packaging, we uncovered issues with electrostatic buildup in early years. Brominated fine powders generate static cling that leads to sticking on fillers and transfer loss, which adds cost and slows production. Switching to conductive polymer liners and grounded loading systems put an end to spillage and variability. These challenges teach us the value of everyday vigilance in plant safety—not just meeting a checklist.
Many intermediates break down over time, especially under varying humidity and heat. Experience shows Alpha-Bromo-2-Chlorophenylacetic Acid holds up well if sealed in airtight, light-protected packaging. We fill nitrogen-flushed HDPE drums or glass bottles for lab samples, storing them in cool, dry areas to avoid hydrolysis or unwanted discoloration. When mixed or reused frequently, we encourage clients to return opened containers to storage after each transfer to avoid long-term exposure.
While the alpha-bromo group gives reactivity for intended reactions, it also means the compound can react in the presence of nucleophilic contaminants—even small amounts of water or amines. We stress the importance of clean, dry tools during handling for maximum shelf life and consistent reactivity.
Handling halogenated intermediates, we see the environmental impact firsthand. Waste management policies grow tighter year by year, and disposing of spent solvents or halogen residues now calls for detailed tracking and staged treatment rather than simple neutralization. Our internal procedures include segregated waste streams and batch tracking for end-of-life disposal. Local authorities demand records for each shipment of waste, so we run regular audits and retrain staff to stay in compliance.
REACH and other global regulations highlight the need for supply chain transparency. We disclose process chemicals to approved auditors and provide detailed impurity profiles, supporting customers navigating their own compliance audits. Certification for transport—as a hazardous chemical—adds effort, but it’s built into our documentation and CRM systems for traceability.
Our portfolio covers a spectrum of arylacetic acid derivatives, including alpha-chloro, plain phenylacetic acid, and various ring-substituted acids. Alpha-chloro-phenylacetic acids fail to match the reaction speed and selectivity the bromo analog enables; even with similar synthetic steps, their leaving group efficiency trails behind, often forcing the use of stronger conditions and risking unwanted byproducts.
Within the world of bromo-derivatives, some clients try mono-halogenated or meta-substituted analogs, chasing cost savings or novel reactivity. We’ve seen reactions stutter or stop with the wrong positional isomer—yield drops, impurities creep up, and recrystallization can become a non-starter. Chemists come back to this specific structure for these very reasons: reliability and balanced reactivity at scale.
The presence of both bromo and chloro groups translates into more reaction options, and these small differences often spell the line between a routine synthesis and one beset by troubleshooting. Our decades of real-world feedback support these claims—trial with similar analogs often leads labs right back to this original intermediate.
Shipping hazardous chemicals doesn’t finish at the packing bay. We select vapor-tight, rigid containers sized for the client’s use-case. In our experience, bulk users in fine chemicals rely on 25 kg drums, while R&D partners order small bottles. When out-of-gauge requests arise—urgent 5 kg shipments or specialized FIFO protocols—we collaborate directly with logistics to meet sometimes challenging timelines. Our in-house documentation ensures packages meet both DOT and IATA guidelines.
Clients share feedback with us after their campaign runs—sometimes raw on detail. One major pharmaceutical user once flagged a recurring trace impurity from a non-metallic gasket leaching organics into their product, undetectable by routine analysis. Plant review pinpointed the origin, and gasket material switched on the next cycle. Another team flagged that sample caking occurred in repeatedly opened containers. We updated drying procedures and issued modified sample protocols.
The chemical industry rewards those with attention to detail and problem-solving rooted in experience. Alpha-Bromo-2-Chlorophenylacetic Acid became a staple of our line through repeated trials—initial learning curves with plant bromination, setbacks with purity drift, and the practicalities of working with hazardous, high-value intermediates. Today, our plant runs dedicate time and space to ensure new lots match the expectation set by every returning customer. Each drum or bottle sent out draws on years of improvements made by real people, chasing better, repeatable chemistry—not just in the lab, but in the day-to-day of the factory and the feedback flows that tie it all together.
For chemists chasing efficiency, new synthesis, or reliability with each new campaign, we deliver a product forged by hands-on know-how and a long view formed by decades of practical work. We know what’s on the line in your plant because it’s what we face in ours—steady product, safe handling, and honest feedback on every order. Alpha-Bromo-2-Chlorophenylacetic Acid stands as a testament to that ongoing effort.