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HS Code |
965947 |
| Chemical Name | 2-Bromobenzaldehyde Oxime |
| Cas Number | 53121-48-1 |
| Molecular Formula | C7H6BrNO |
| Molecular Weight | 200.04 |
| Appearance | Light yellow solid |
| Melting Point | 105-108°C |
| Boiling Point | No data available |
| Density | No data available |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC=CC(=C1Br)C=NO |
| Inchi | InChI=1S/C7H6BrNO/c8-7-4-2-1-3-6(7)5-9-10/h1-5,10H |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2-Bromobenzaldehyde Oxime factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed with a secure screw cap, labeled clearly with chemical name, purity, hazard, and supplier details. |
| Shipping | **2-Bromobenzaldehyde Oxime** is shipped in tightly sealed containers to prevent moisture and air exposure. It should be handled as a hazardous chemical, following all relevant transportation regulations. The packaging includes proper labeling, cushioning, and secondary containment to ensure safety during transit and to prevent leaks or accidental release. |
| Storage | 2-Bromobenzaldehyde oxime should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong acids and oxidizers. The chemical should be kept tightly sealed in a labeled container to avoid moisture absorption and contamination. Use chemical-resistant shelving and secondary containment to prevent accidental spills or leaks. |
Applications of 2-Bromobenzaldehyde Oxime in Industrial Manufacturing2-Bromobenzaldehyde oxime is a key intermediate in the fine chemicals industry, providing specialized molecular functionality to enable precise transformations in targeted downstream sectors. As an established manufacturer, we directly supply this raw material to diverse segments where its unique chemical reactivity and compatibility with advanced production processes play a critical role. Below we detail several leading industrial application areas, specifying compliance, usage levels, manufacturing integrations, and final product types relevant to each segment. 1. Active Pharmaceutical Ingredient Synthesis (API Intermediate)Pharmaceutical process chemists use this oxime as a pivotal intermediate during multi-step synthesis for complex heterocyclic APIs. The aromatic bromine and oxime moieties permit regioselective transformations such as cyclizations, condensations, and reductive aminations under controlled manufacturing conditions. GMP production facilities employ batch or semi-batch reactors with stringent impurity monitoring. Process validation ensures all starting materials, including this intermediate, meet regulatory and pharmacopoeial specifications for human use APIs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate ManufactureAgricultural chemical manufacturers employ 2-bromobenzaldehyde oxime for the synthesis of selective herbicides and fungicides, particularly those requiring substituted benzoxazoles or related nitrogen heterocycles. Chemical process units typically generate the benzoxazole ring via a cyclodehydration or condensation step with this oxime as a starting point. Production runs are monitored for controlled by-product formation, with routine QC to guarantee formulation performance and regulatory acceptance for field use. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dyestuff and Pigment Intermediate ProductionIn pigment and dye manufacturing, the oxime functions as a nucleophile or condensation partner for the synthesis of high-purity azo and anthraquinone dyes. Utilized specifically in controlled-stage couplings, it imparts improved light fastness and customized chromophore properties. Quality departments implement strict raw material traceability under ISO systems, and batch formulation must reference specific color index requirements depending on the intended textile, ink, or plastic application. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis for Electronic MaterialsProducers of organic semiconductors and advanced functional materials utilize this oxime for synthesizing molecular precursors to liquid crystal and OLED device layers. Its stable brominated aromatic core enables lithiation, cross-coupling, or directed ortho-metalation protocols under anhydrous, oxygen-free conditions. Analytical and production workflows demand close monitoring of metallic impurities and trace byproducts, with batch certification tied to IEC and electronics-specific purity norms. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Specialized Analytical Reagent ManufactureLaboratory chemical suppliers and diagnostic kit producers source this oxime as a reagent or derivatization agent for trace analytics or molecular detection. In particular, chromatographic workflows integrate the compound as a derivatizing agent for benzaldehyde and related analytes, improving GC or LC selectivity and yield of stable detection products. Packing and QC teams comply with international reference material procedures and chemical traceability audits for analytical reliability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Coming from years in the specialty chemical manufacturing field, I’ve seen both the challenges and the demand for materials that support the pharmaceutical and agrochemical industries. Among the versatile intermediates, 2-Bromobenzaldehyde Oxime stands out for its performance in complex syntheses. By bringing this compound to our catalog, we've focused on producing consistent, high-quality batches that serve advanced research and industrial production alike.
Our facility uses a fine-tuned route for synthesizing 2-Bromobenzaldehyde Oxime that gives excellent yield and purity. This has grown from our experience running reactions under tight quality controls. In this line of work, small differences in process control show up in the consistency and physical characteristics of every batch. Chemists in our plant monitor reaction stages, purity checks, and moisture content, not just at the final step but throughout the entire workflow. This approach minimizes byproducts and ensures that downstream formulations remain as predictable as possible.
In the world of fine chemicals, not every oxime delivers the same performance. Our production focuses on the model with a molecular formula C7H6BrNO and a typical melting point range of 80–84°C. While most commercial grades target basic purity, we routinely secure 98% minimum purity as a standard, based on feedback from our clients engaged in both bench-scale and pilot plant synthesis. Each lot undergoes GC and NMR validation to verify structure and exclude unwanted side products like regioisomers or hydrolysis derivatives.
One misunderstood area comes from believing all benzaldehyde oximes can slot into the same reactions. The true impact of the bromine atom on the ortho-position of the aromatic ring changes reactivity in subtle but crucial ways. For instance, it alters electron density, influencing both nucleophilic and electrophilic substitutions. In pharmaceutical R&D, this subtle tweak can affect both the yield and the ease of downstream conversions into active pharmaceutical ingredients or crop protection leads. Over the years, our teams have received requests from medicinal chemistry groups looking for reliable supply with tight impurity control, recognizing that even minor process contaminants may influence biological screening outcomes.
As a chemical manufacturer, we talk directly with process chemists, research scientists, and formulation engineers. Most of our demand for 2-Bromobenzaldehyde Oxime comes from custom synthesis houses and contract manufacturing clients working on pharmaceutical discovery. The oxime motif is frequently a precursor route for converting aromatic aldehydes into amide bonds or nitriles. Bromine’s ortho substitution supports further modifications, such as Suzuki or Buchwald couplings, and enables rapid library development in combinatorial chemistry.
Another advantage centers on regioselectivity during transformation steps. In laboratory settings, some chemists choose other substituted benzaldehyde oximes, only to find the resulting side reactions lower their final yield or complicate purification. Our clients have reported smoother workflows by starting with our 2-Bromobenzaldehyde Oxime, reducing the need for troubleshooting later.
Pharmaceutical R&D teams rely on reagents that don’t surprise them batch-to-batch. Water content, particle size, and impurity profile all influence homogeneity in larger-scale reactions, especially when working toward kilo or ton quantities of a finished compound. In the years we’ve manufactured this oxime, we have received requests to adjust specifications for unique synthesis pathways. Sometimes this means drying the product more thoroughly or producing a fine powder rather than a crystalline solid for specific dissolution requirements. We have designed our workflow to accommodate these shifts based on customer discussion, implementing adjustments without compromising material integrity.
Over the past decade, the use of aromatic oximes as directing groups or intermediates in C–H activation chemistry has taken off. Academic labs and start-ups exploring new patentable compounds benefit from halogen-substituted oximes, which provide both blocking and activating effects in functional group transformations. In countless talks with researchers, we spot a need for intermediates that no catalog supplier has thoughtfully tailored. Our response: direct feedback into our process controls, aiming for reproducible batches and clear lot-specific data sheets that matter in a regulatory or patent-support context.
People sometimes expect benzaldehyde oximes to substitute for one another in synthetic plans. The bromine substituent at the ortho position delivers a significantly different outcome from the para-substituted or unsubstituted forms. In our hands, ortho-bromine provides improved selectivity in further halogen-based couplings, while meta and para versions perform differently when it comes to rates of transformation or compatibility with certain catalysts.
Another common comparison shows up between 2-Bromobenzaldehyde Oxime and its chloro or iodo analogues. Although iodine offers greater activation toward metal-catalyzed coupling, bromine gives a good balance of reactivity and cost. Our clients tell us this is a decisive factor when translating small scale discovery to cost-sensitive larger-scale manufacturing. Chlorinated analogues tend to resist certain transitions, leading to longer reaction times or harsher conditions, which many try to avoid.
Because we produce at source, we guarantee fresher shipments than many secondary suppliers, and we can offer lot-specific technical support for troubleshooting. Every run faces its own practical twists—reaction temperature shifts, stirrer speeds, trace moisture, or input solvents—each influencing the degree of isomerization or byproduct formation. Our engineers track these factors on every batch, supporting not just order fulfillment but the overall project goals of our customers.
A lot of confusion in specialty chemicals comes from hand-offs and unknown provenance. Buying direct from the factory mattered even more during global shortages and supply chain unpredictability recently. By manufacturing 2-Bromobenzaldehyde Oxime at our own facility, we can immediately address stability questions, shelf life, or optimal storage recommendations based on how the batch was processed. This has solved several real-world problems for our partners, such as resolving questions about color changes, clumping, or air sensitivity. Whenever a customer needs technical data, we’re able to reference original batch records and QC logs, sparing the frustration and time waste seen with untraceable third-party material.
Our approach emphasizes traceability by coding every batch and archiving process-specific documentation. This practice fulfills not just our own internal quality goals, but matches GMP or ISO-compliance standards sought in regulated markets. Laboratories and scaling facilities achieve more reliable results because they know exactly what went into their process. This approach has become a baseline expectation, not a marketing claim.
In chemical manufacturing, every step matters for environmental impact. The synthesis of 2-Bromobenzaldehyde Oxime involves hazardous intermediates, but our plant staff has refined the work-up and waste handling to sharply reduce solvent emissions and minimize halogenated byproducts. Early on, we saw the challenge of solvent recycling and moved to in-house recovery systems for commonly used solvents in the oximation step.
Over time, we’ve modified our intermediate purification streams to make reprocessing feasible, reducing residues requiring incineration or costly disposal. We encourage customers to discuss disposal options since many downstream users face strict regulatory limits. With every regular shipment, we offer updated handling suggestions based on the lot’s particular attributes. This commitment grew out of feedback from customers needing both reliable chemistry and confidence their materials don’t pose hidden environmental risks.
One challenge in our industry involves scaling reactions that work well in a flask but behave unpredictably at larger scale. Plant operators in our facility deal with batch-to-batch consistency, controlling each variable that matters—from raw material sourcing to blending and even packaging. Through direct conversations with end-users, we have adapted our delivery forms and adjusted packing materials to curb physical degradation or excessive static, especially important for oximes and their sensitivity to environmental factors.
Furthermore, we have developed logistics protocols so that sensitive intermediates arrive without extended transit times or temperature excursions. For 2-Bromobenzaldehyde Oxime, stability means more than shelf life—it influences batch release in customer downstream processes. If stored too warm or exposed to humidity, oxime compounds risk hydrolysis or browning, compromising both assay and appearance. By dispatching orders directly from our climate-controlled storage, we’ve sidestepped issues that resellers sometimes face with aged stock.
A story comes to mind about a customer pushing the boundaries of nickel-catalyzed couplings using our oxime as a starting point. Early trials showed variable yields until process details like water content and crystal habit were aligned. Our technical team jumped on multiple calls and reviewed lab production notes together. Adjustments in post-reaction drying, followed by customized particle size screening, ultimately brought the conversion to their target benchmarks. This sort of hand-in-glove cooperation isn’t always possible when sourcing through distant distributors or online catalogs.
Another example involves a partner start-up working on proprietary crop protection molecules. Their R&D depended on seamless adaptation between laboratory optimization and kilogram-level production. By keeping transparency at the center—sharing not only lot analysis but intermediate process results—they could adjust purification and isolation protocols midstream. That project taught us the value of treating every batch as a collaborative building block, not just an item number.
As requirements for documentation and traceability increase in pharmaceuticals and agrochemicals, vendors must provide more than just standard certificate of analysis documents. Over the years, we have helped clients draft necessary supporting documentation for filing new chemical entities or providing materials for GLP studies. From NMR spectra to chromatography trace files and detailed impurity profiles, our team supports the documentation trail necessary for proper regulatory submission.
Being able to provide full chain-of-custody records for every run matters for clients operating in tightly controlled markets. As more end-users require proof of source, audit trails, and cradle-to-gate sustainability metrics, our internal records—spanning everything from starting materials to shipping logs—have become a key support when entering regulated markets or foreign jurisdictions. This approach earns trust, but more importantly, it speeds up time-to-market for high stakes applications.
No chemical plant stands still. Improvements in process chemistry or plant safety come directly from lessons learned with every batch, and this real-world knowledge feeds back into each subsequent production run. Feedback loops—whether from a customer’s pilot plant run, a failed reaction in a medicinal chemistry setting, or an unexpected analytical pushback—drive incremental advances.
Over the years, we have gathered insights not just from internal analysis, but through site visits and customer sample evaluations. When quality issues arise, our teams don’t point fingers or shift responsibility; instead, they trace the challenge to its source, tackle process variables, and share discoveries across all customer-facing roles. This steady openness forms the backbone for our operational philosophy, and it’s reflected in the performance of our 2-Bromobenzaldehyde Oxime both in-house and out in the field.
The specialty chemical market is always evolving, with expanding complexity and tighter demands for documentation, purity, and environmental responsibility. Our team faces these head-on, leveraging decades of batch records, analytical troubleshooting, and international collaboration. In practical terms, it means maintaining a rigorous QC regime, routine method validation, and investing up front in process control tools.
Securing high-quality starting materials presents an ongoing challenge, but our sourcing team maintains relationships with primary producers and regularly runs checks to prevent contamination. On the analytical side, investments in instrument calibration and method development have elevated our technical deliverables, putting essential data in the hands of researchers fast.
Sustainable chemistry asks us all to look at waste, emissions, and solvent use with a critical eye. Instead of resting on the status quo, we continue to pilot greener alternatives in both upstream and downstream stages for 2-Bromobenzaldehyde Oxime, seeking improvements that pay off both in product quality and environmental impact.
Manufacturing 2-Bromobenzaldehyde Oxime offers more than a supply chain solution; it represents the cumulative experience of plant operators, chemists, and technical teams who understand the stakes for our customers. Through investment in quality control, batch traceability, collaborative support, and sustainability, every lot shipped is the result of collected know-how and continual improvement. Our focus remains clear: to deliver dependable intermediates that support breakthrough research and manufacturing for the next generation of pharmaceuticals and agrochemicals.