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HS Code |
797948 |
| Chemical Name | 3-Bromo-2-Hydroxybenzaldehyde |
| Molecular Formula | C7H5BrO2 |
| Molecular Weight | 201.02 g/mol |
| Cas Number | 6945-79-1 |
| Appearance | Light yellow to beige solid |
| Melting Point | 109-112 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as ethanol, DMSO, and acetone |
| Density | 1.78 g/cm³ (estimated) |
| Structural Formula | BrC6H3(OH)CHO |
| Iupac Name | 3-bromo-2-hydroxybenzaldehyde |
| Storage Conditions | Store at 2-8 °C, protected from light and moisture |
| Synonyms | 2-Hydroxy-3-bromobenzaldehyde |
As an accredited 3-Bromo-2-Hydroxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with screw cap; white label displaying chemical name, CAS number, hazard symbols, and handling instructions. |
| Shipping | 3-Bromo-2-Hydroxybenzaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. The packaging complies with applicable regulations for hazardous chemicals. During transport, it is protected from extreme temperatures, physical damage, and direct sunlight. Accurate documentation and labeling ensure safe handling and swift delivery to the destination. |
| Storage | 3-Bromo-2-Hydroxybenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat, ignition, and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Store under inert atmosphere if possible to prevent degradation, and always ensure proper labeling and secondary containment to avoid accidental exposure or spills. |
Applications of 3-Bromo-2-Hydroxybenzaldehyde in Industrial ManufacturingOur 3-Bromo-2-Hydroxybenzaldehyde plays a vital upstream role in multiple fine chemical manufacturing chains. As an original producer, we supply this compound to specialized sectors where precise reactivity and validated quality support downstream synthesis, formulation, and commercialization workflows. Below we present detailed application insights from key downstream segments. 1. Pharmaceutical Intermediates for API SynthesisPharmaceutical manufacturers use 3-Bromo-2-Hydroxybenzaldehyde as a core building block in the synthesis of certain heterocyclic drug intermediates, especially benzoxazole and benzothiazole derivatives. These reactions often require careful purification and traceability from entry into the reactor to isolation of the intermediate. Accurate batch records and contaminant control ensure seamless compliance and downstream pharmacological safety. Our on-site analytical release supports API manufacturers from laboratory scale to validated commercial production. Industry compliance standards
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2. Agrochemical Synthetic IntermediatesLeading crop protection formulators use this material as a mono-bromo functionalized precursor in the design of selective fungicide and herbicide actives. Its aromatic substitution pattern enables efficient stepwise synthesis of triazole and imidazole-based agrochemical molecules. Process control requires strong adherence to local and international safety standards for raw input evaluation, residue minimization, and trace impurity disclosure for downstream registration. Industry compliance standards
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3. Fine Chemical Production—Aromatic Blend ComponentsManufacturers of performance aromatics employ our product as a specialty additive in formulating high-purity benzaldehyde blends for fragrances and dye precursors. Its ortho-bromo and hydroxyl substituents provide a unique foundation for subsequent functional group manipulation, such as nucleophilic aromatic substitution and aldehyde extension. Continuous QC sampling and trace metal analysis support integrity during scale-up, allowing seamless integration into batch reactor or continuous flow operations. Industry compliance standards
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4. Specialty Polymer Chain ModifiersAdvanced polymer manufacturers utilize 3-Bromo-2-Hydroxybenzaldehyde for selective copolymerization or as an end-group modifier in engineering plastics production. The molecule’s dual functional groups allow controlled cross-linking or introduction of bromine-labeled sites for further surface modification. Raw material traceability, batch homogeneity, and bromine residual testing support customer demands for consistent downstream reactivity in thermoplastic or thermoset manufacture. Industry compliance standards
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Every chemical we produce tells a story grounded in real-life problem-solving. As a manufacturer with years of hands-on experience in fine organic synthesis, we'd like to introduce 3-Bromo-2-Hydroxybenzaldehyde. Our journey with this compound springs from its core role in pharmaceutical research and advanced material development. It's not just another aromatic intermediate; this molecule signifies both reliability and adaptability.
This compound, also referred to as 3-bromo-salicylaldehyde, carries the molecular formula C7H5BrO2 and boasts a purity routinely above 99%. Our proprietary process foregoes unnecessary step-ups often seen in older protocols, keeping side impurities below trace levels. The result—off-white to pale yellow crystalline solid—offers exceptional reproducibility batch-to-batch, providing peace of mind for both synthesis scale-up and research labs.
Working with research chemists and formulation teams, we know how frustrating variable purity can be. Slight yields of unwanted isomers or colored byproducts can plague sensitive syntheses downstream. Our hands-on purification approach came from years of collaborating with those whose research budgets hinge on efficiency. Instead of hoping a generalized purification step suffices, we tailor each production run with chromatography gradients and drying regimens proven to maintain low water and halide content. Any uptick in non-target impurities triggers process review on our end.
The close feedback from teams using our product in heterocyclic assembly, dye intermediates, and fragment-based library work has shaped how we manufacture. Chemists have mentioned reduced batch rejections and simpler NMR interpretation compared to alternative material sourced elsewhere. What sounds technical on a spec sheet boils down to less time troubleshooting and fewer wasted resources.
End users in medicinal chemistry point to the aldehyde’s steady performance in C–C coupling reactions and selective O-alkylations. These applications often demand that the ortho-hydroxy group and the meta-bromine remain unmodified throughout long synthesis sequences. Feedback has come from both exploratory and process chemists: single-digit milligram variations in impurity profiles were enough to change a project’s path. Our plant’s commitment to regular GC-MS and HPLC screenings takes these details seriously.
Material scientists have brought up the advantage of a stable, moisture-controlled product during storage and handling. Since we pack the aldehyde under inert atmosphere and monitor temperature swings during transport, there’s less chance for degradation before it lands at a bench. We continue to invest in packaging safeguards based on real-world transport conditions, not generic warehousing.
It’s easy to fall back on technical data or listing generic “high purity” as a main selling point. Our process relies on stepwise introduction of the bromine using freshly distilled electrophilic agents and controlled benchtop cooling. This minimizes formation of polybrominated contaminants that can overshadow the target compound in downstream analysis.
Older methods from certain suppliers have been known to tolerate minor overheating or rely solely on aqueous work-ups, introducing variable hydrolysis products. Based on direct reports from partner companies, those approaches can lead to more frequent need for repurification, with costs stacking up in wasted labor and materials. By contrast, we control our process using thermal imaging and batch analytics keyed to both colorimetric tests and modern analytical runs. As a result, the batch consistency stays high, and end users rarely report extraneous peaks on routine NMR or LC/MS monitoring.
Handling aromatic aldehydes comes with its fair share of technical hurdles. Over the years, our plant has developed protocols to guard against oxidation and photolysis, especially during purification stages. Advances like wrapping glassware in UV-blocking films and incorporating gentle inert gas blankets during filtration aren’t just best practices on paper—they stem from lessons learned the hard way when stray light or oxygen marred batches.
On the scale-up side, even minor changes in solvent dryness or batch agitation have revealed itself in crystalline morphology shifts. We keep experienced operators on every synthesis, not leaving to automated systems alone what judgment and a practiced eye can catch. There’s value in knowledge transfer between workers: the subtle color changes at endpoint, the feel of a slurry that’s just right for recrystallization—all these details matter more than any automated line reading.
Over time, we have sourced competitor samples, analyzed them, and spoken openly with users from different sectors. What stands out most is not simply differences in appearance or label claims, but in how products perform at the bench. Some imported samples, though labeled at 98–99% purity, present trace poly-brominated material and higher levels of brominated isophthalic acid byproducts. These translate to headaches during downstream syntheses, as even trace contaminants can disrupt catalytic steps or demand tedious extra purification.
By contrast, the material from our line rarely leaves users struggling with these byproducts. We approach product release conservatively, holding material that skews too far from our internal historic profile. Other suppliers, especially those working as jobbers or re-packers, often lack this rigorous quality tracking—pulling from a wider spread of original production lines and introducing batch-to-batch variation that doesn't show up until the compound interacts with scale-up conditions.
We work alongside synthetic chemists developing new molecules as much as we work with process experts aiming to translate results up to kilogram scale. Over the years, suggestions from users have prompted us to adjust solvent blends, drying conditions, even the type of scooping spatulas we recommend for lab techs collecting samples. Each change led to cleaner results and more predictable yields in real-world applications—including libraries built for screening and specialty dyes with minimal unwanted background fluorescence.
Research teams frequently mention that switching to our product cut their troubleshooting time. Rather than needing repeated column runs to remove stubborn byproducts, they spend more time advancing projects. That feedback speaks volumes to us. From hearing about how much cleaner the spectra look, to chemists sharing yield bumps in target transformations, these are the differences that build trust over transactional buying.
Producing brominated aromatics does involve environmental stewardship. Our factory recycles process solvents and strictly controls halogen emissions, working well below regional safety thresholds. Historically, bromine waste management proved challenging; lessons learned from earlier waste-processing errors shaped our investment in recovery columns and closed-cycle cooling. Each product run addresses ways to further reduce water and solvent usage.
Many customers in regulated industries want assurances on how raw materials and secondary streams are handled. We conduct annual external audits to support this commitment. Internal training covers not only safe material handling, but also routine checks for process leaks or off-spec discharge water. It’s in everyone’s best interest—manufacturer and customer alike—that chemical management closes the loop responsibly.
Controlling every step of the process matters, because subtle differences in handling and purification accumulate into tangible outcomes for users. As original producers, we take pride in not outsourcing critical synthesis or packaging steps. Every time our technical leads jump on a call with an end user, or troubleshoot a reported issue in person, that interaction informs decisions back at the plant. This hands-on history is not something that can be replicated by a warehouse or trader repackaging from a bulk source.
Each batch gets tracked from raw input chemicals—checked regularly for drifts in supplier quality—to the final sealed package. As a result, if a research team in Europe tells us about a small crystallization issue, we readily trace it back to process logs. Improvements get made, from adjusting drying times to swapping desiccant materials. These refinements eventually shape each new lot produced.
We’ve seen 3-Bromo-2-Hydroxybenzaldehyde prove its worth across several fields. In pharmaceutical intermediates, it provides a reliable anchor as a building block for coupling and condensation reactions. Analytical chemistry labs use it in custom ligand design, while pigment and dye manufacturers rely on it to maintain batch shade consistency. Each field brings its own set of hurdles: some demand pinpoint NMR clarity, others care most about storage life under humid conditions.
One team in peptide conjugation scale-up reported significant improvements using our material over parallel sources, specifically because our aldehyde stirred cleanly and did not leave residual bromine traces that complicated downstream purification. Another group in fluorescent material synthesis preferred our product because sample purity cut troubleshooting cycle time. In synthesis of fragments for medicinal chemistry screens, our consistency improved average yields on Suzuki couplings, making project progress more predictable.
Chemicals like this need thoughtful packaging. Thin-walled bottles or oversized drums create more problems than they solve—especially during international transit, where temperature swings and rough handling occur. We use robust, light-protective containers sized appropriately for laboratory use. High-barrier liners keep moisture and oxygen out, minimizing any aldehyde oxidation or yellowing, a frequent headache for chemists dealing with less carefully packed material.
From a user’s point of view, speed of access counts. We keep stock ready for both routine shipments and urgent last-minute requirements. Repeat users appreciate the minimal downtime between ordering and delivery, knowing they'll receive consistent material every shipment.
There’s a tendency to substitute with more readily available aromatic aldehydes, thinking little difference exists. Based on our observations, swapping out for 2-Hydroxybenzaldehyde or 3-Bromobenzaldehyde can shift both electronic properties and reactivity profiles, putting established procedures at risk. Even subtle ring electron density changes affect yields in complex multi-step syntheses. Our years of feedback suggest the specific positioning of both the hydroxy and bromo groups in the 3-Bromo-2-Hydroxybenzaldehyde structure unlocks reactivity patterns not achievable by mixing other building blocks.
We’ve helped resolve stuck reactions where alternative intermediates left users with stalled conversions or problematic side reactions. Detailed mechanism experiments have shown that the meta-bromine group offers selectivity in cross-coupling while the ortho-hydroxy group opens up pathways for directed metalation or further functionalization. These unique chemistry handles empower both academic and industrial labs to tackle challenging synthetic targets.
Staying ahead in fine chemicals manufacturing takes more than maintaining a static process. We keep engaging with researchers about their changing needs—whether for higher scale, new custom derivatives, or even modified packaging. Our process chemists run pilots with new greener solvents and lower-waste bromination routes, informed by the environmental standards clients expect. In every iteration, data from previous runs and real user feedback guide decision-making, letting us catch issues before they ever reach the end user.
Many of our improvements stem directly from open communication with chemists tackling diverse challenges. By keeping our production transparent—sharing batch analytics, explaining process shifts, welcoming plant visits—we build not just a business relationship but collaborative problem-solving. The end result: people can trust their most valuable research or manufacturing effort rests on foundation built with durable, well-made starting material.
Decades in the chemical business teaches a humility about what matters most in an intermediate like 3-Bromo-2-Hydroxybenzaldehyde. User experience comes down to consistency, transparency, and true collaboration between plant and bench. Each drum, every bottle we ship represents not just months of technical optimization, but the relationships we build across labs, universities, and factories. We stand by a simple promise—when synthetic chemists and research teams open our product, they get a tool they can count on.
For real advances to happen in chemistry, both traditional and cutting edge, the quality of raw building blocks can't be underestimated. Manufacturing is more than a business—it's an ongoing partnership with everyone working to discover new molecules and solve hard problems. That sense of responsibility shapes every batch, every improvement, and every conversation with those who rely on our compounds.