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HS Code |
933815 |
| Productname | 2-Hydroxy-5-Nitrobenzyl Bromide |
| Casnumber | 574-97-0 |
| Molecularformula | C7H6BrNO3 |
| Molecularweight | 232.03 |
| Appearance | Light yellow to brown crystalline powder |
| Meltingpoint | 106-109°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, ethanol |
| Synonyms | o-Hydroxy-p-nitrobenzyl bromide |
| Structuralformula | C1=C(C=C(C=C1Br)O)[N+](=O)[O-] |
| Smiles | C1=CC(=C(C=C1Br)O)[N+](=O)[O-] |
| Storagecondition | Store at 2-8°C, protect from light and moisture |
As an accredited 2-Hydroxy-5-Nitrobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g amber glass bottle has a tightly sealed cap, labeled "2-Hydroxy-5-Nitrobenzyl Bromide," includes hazard symbols and handling instructions. |
| Shipping | 2-Hydroxy-5-Nitrobenzyl Bromide is shipped in secure, chemical-resistant containers to ensure safety and product integrity. Packaging complies with standard hazardous materials regulations. Appropriate labeling and documentation are included. Shipping is typically via ground or air, depending on destination and regulatory requirements. Handle with care; store in a cool, dry place upon arrival. |
| Storage | 2-Hydroxy-5-Nitrobenzyl Bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect the chemical from light and moisture. Use secondary containment if possible and clearly label the storage area to prevent accidental exposure or mixing. |
Applications of 2-Hydroxy-5-Nitrobenzyl Bromide in Industrial ManufacturingAs a specialized producer, we supply 2-Hydroxy-5-Nitrobenzyl Bromide to manufacturers operating in select high-precision downstream fields. The following application scenarios reflect established industrial practices, strict regulatory adherence, and data-backed process integration from decades of on-site technical collaboration. Each sector utilizes this intermediate based on functionality, compliance obligations, and product-specific performance requirements. 1. Active Pharmaceutical Ingredient Intermediate for Anti-Infective AgentsPharmaceutical manufacturers incorporate this substance as a protected benzylating agent during multistep syntheses of complex anti-infective active pharmaceutical ingredients (APIs). The high-purity grade minimizes impurities and supports reaction step yields, particularly in cases requiring subsequent selective deprotection under mild conditions, thereby protecting sensitive heterocyclic systems. Industry compliance standards
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2. Photolabile Protecting Group Reagent in Custom Oligonucleotide SynthesisOligonucleotide manufacturers use this compound in solid-phase DNA and RNA synthesis protocols as a photoremovable protecting group reagent. Its unique structure enables the temporary masking of functional groups, followed by precise, light-triggered deprotection cycles, facilitating sequence assembly with high-fidelity on automated synthesizers. Industry compliance standards
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3. Intermediate for Functional Dyes and Optical MarkersProducers of specialty dyes employ this material in the formation of functional nitroaromatic derivatives with precise electronic properties for use in high-resolution imaging and analyte detection. Its stability as a brominated benzyl derivative supports complex aromatic coupling reactions, granting durability and targeted chromophore functionality in end-use pigments and markers. Industry compliance standards
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4. Building Block for Electronic Chemical Synthesis in OLED MaterialsCertain OLED compound developers integrate this substance as an activated benzyl bromide source during the synthesis of advanced aromatic frameworks. Its role is pivotal in introducing nitro-functionalities onto key molecules, enhancing charge transport or light emission profiles in next-generation organic semiconductors and emissive thin films. Industry compliance standards
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5. Precursor in Agrochemical Synthesis for Nitrophenolic Plant Growth RegulatorsAgrochemical formulators deploy this intermediate in multi-step synthesis pathways leading to selected nitrophenolic compounds utilized in regulated plant growth-control formulations. The precise nitro and hydroxyl placement confers enhanced bioactivity, while the bromide function supports substitution reactions under controlled, scalable conditions. Industry compliance standards
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Producing 2-Hydroxy-5-Nitrobenzyl Bromide for over a decade has taught us a lot about what people need, and how subtle changes in a molecule can change everything downstream. This compound, which many know by its CAS number 20441-47-8, stands out in the landscape of benzyl halides thanks to its distinctive functional groups. The hydroxy and nitro substituents, positioned ortho and para to the methyl bromide, give this molecule properties that chemists rely on for selective reactivity. Over the years, feedback from labs and production lines tells us that details matter when comparing it to its close cousins, so what we bring to the table strikes the balance between purity, control, and integration.
Our main offering sticks to a model optimized for research and process consistency. People working with 2-Hydroxy-5-Nitrobenzyl Bromide notice quickly when impurities or poor handling intervene, especially in high-sensitivity work like building blocks for complex organic molecules, pharmaceuticals, or agrochemical intermediates. Because bromides like this tend toward hydrolysis and decomposition without proper controls, we package and ship every batch only after strict residual solvent and impurity checks. Our routine brings the purity above 98.5%, routinely hitting the expected melting range around 85–88°C, and keeping color, moisture, and volatility in check. Stability remains reliable for months, given storage in an inert, dry environment—users regularly tell us the difference shows up in sharper yields and easier purification stages down the road.
In the world of benzyl bromides, adding both hydroxy and nitro groups changes reactivity and selectivity. The bromomethyl position carries good leaving-group potential, making this compound ideal for benzylation reactions, especially with molecules that need both an activating group (the nitro’s electron withdrawal) and a handle for further transformations or conjugations. Customers have shown us their data: choosing this reagent over less functionalized bromides leads to better site-selectivity or more straightforward workups. The hydroxy group at position 2 also allows direct access to ether and ester derivatives, and the nitro group offers potential for reduction, giving chemists more flexibility to tune a synthetic pathway. This is not just a rearrangement of atoms on paper—graduate students, QC teams, and project leads send us their praise for how these features translate into real research milestones.
Working directly with this compound every week, our chemists have learned how to handle its quirks. The greatest challenge affects scale-ups. Bromination must go cleanly, but the nitro group’s presence makes uncontrolled reactions more likely, sometimes leading to side-products or harsh conditions that damage the product. Water and bases must be scrupulously avoided after the final bromination stage, so our reactors stay inert and get purged repeatedly before and after every run. Years ago, scale-up attempts without disciplined process design led to inconsistent colors and melting points—a sign of variable purity or polymer formation. Today, we use high-performance HPLC and GC methods to monitor progress, reject off-spec intermediates, and time our washes and solvent changes more precisely.
In our experience, paying close attention to handling—especially drying and quick packing—keeps the degradation in check. Once, a transport delay coupled with insufficient water-protection caused an entire lot of several kilograms to darken, increasing impurities and ruining a client’s trial. The learning was expensive, but it made us overhaul our end-to-end handling protocols. This experience means today’s batches consistently meet user needs and ship with only minimal losses to instability.
Many researchers consider whether to use 2-Hydroxy-5-Nitrobenzyl Bromide or substitute with something else. Regular benzyl bromide comes up a lot, but without the hydroxy and nitro groups, the scope for post-bromination chemistry narrows. In contrast, 5-nitro-o-cresol can work where a methyl group would suffice, but missing the bromide limits uses to nucleophilic substitution scenarios. We’ve had frequent conversations with clients who try generic benzyl bromide and see sluggish reactivity or unwanted side-reactions, only to switch to our compound and find both rate and selectivity improve, especially in etherification and esterification, where the electron-withdrawing groups drive the reaction forward.
Feedback from scale-up process engineers also points to an easier isolation when using our benzyl bromide—especially during crystallizations and monitoring organic filtrates—thanks to changes in solubility and polarity from its substituents. These “little” differences cut dozens of person-hours over a year for production lines pushing out intermediates for APIs or agrochemicals.
People sometimes overlook the nuances of a specification sheet and regret it later during troubleshooting. In the case of 2-Hydroxy-5-Nitrobenzyl Bromide, we see the same flags every quarter: color drifting outside the pale yellow range, water content rising above the threshold, and melting point dropping. To rule out process mistakes, our QC group audits every drum against a comprehensive set of criteria—purity (HPLC), trace water (Karl Fischer), residual solvents, and occasionally, NMR for challenge cases. This hand-on protocol developed because relying purely on default specs left significant risks for end-users. Some of our partners tried switching suppliers on single-use lots, but then found their downstream products underperformed.
We decided early on to actively invite feedback from both bench chemists and pilot plant teams so that our production keeps up with the pace of the research world. Biotech and pharma clients now often bring us specific solubility, impurity, or stability requirements for their own optimizations—we respond with tailored campaigns and cross-calibration between analytical labs to eliminate quality surprises. Over time, this tight feedback loop means fewer late surprises during purification, and less downtime on client reactors.
In our hands, 2-Hydroxy-5-Nitrobenzyl Bromide performs best in carefully controlled environments. We recommend using dry, inert handling stations—gloveboxes or Schlenk lines—when weighing and transferring, as atmospheric moisture can initiate slow decomposition over a matter of hours. Storage in airtight containers, tightly sealed and away from heat and light, buys months of stability. If you’re scaling beyond laboratory scale, always purge transfer lines and vessels with nitrogen, because even brief ambient exposure can generate colored byproduct that gums up later purifications.
Many researchers push for faster syntheses and skip precautions, only to find the reaction solution picks up color or yields trail off. Years of troubleshooting batches have shown us that fresh bottles open to room air for hours lead to evident performance decline; keeping containers out only as long as needed preserves sensitive features and cleanliness. Usual PPE and local exhaust work well, as the compound volatilizes only slightly, but avoiding direct skin and eye contact is always good practice due to the reactivity and potential irritant character of aromatic bromides.
Reflecting on hundreds of batches, it’s clear that no two lots of a specialty intermediate like 2-Hydroxy-5-Nitrobenzyl Bromide behave exactly the same in different industries and applications. Medicinal chemists rely on it to deliver benzyl-protected phenols via alkylation, then selectively cleave the hydroxy group for key steps. Polymer industries and specialty dye makers exploit unique color properties and electronic configurations, as both the hydroxy and nitro groups influence UV and visible spectra—information our technical support team shares to help labs push the boundaries of product formulation.
Quality-differentiated production, not just commodity synthesis, remains our core value. Mass-produced benzyl bromide from large suppliers rarely includes the custom controls on purity, physical presentation, and robust traceability per lot that our most demanding clients need. Whether the need focuses on high-throughput resin development or process chemistry for API candidates, the added substitutions on this benzyl bromide backbone deliver increased selectivity and reliability, supporting chemists who face tight deadlines and regulatory constraints.
Running a chemical manufacturing line means never losing sight of environmental compliance and responsible stewardship. The aromatic nitro and bromide groups present specific wastewater treatment challenges, so all our work-up and washing fluids pass through DCS-monitored, multi-stage treatments: neutralization, activated carbon, and separation for halide recovery. What we learned from earlier accidents (years ago, a bromide waste tank failure led to weeks of costly cleanup) continues to shape our mentality: pay the upfront cost of good engineering and staff education, recoup the investment in safe operations, and earn customers’ trust when they audit our plant.
Proactive solvent recycling and close attention to fugitive emissions keep our impact well below allowable limits. None of this is an afterthought—more than a quarter of our annual maintenance budget supports inspection rounds, operator certifications, and improvements in real-time monitoring. Responsible manufacturing of specialty intermediates like 2-Hydroxy-5-Nitrobenzyl Bromide can’t happen at arm’s length; it takes vigilance, record-keeping, and staff with the authority to stop lines if they spot problems.
We have seen enough process upsets and quirks to appreciate that the science of production intersects constantly with old-fashioned trial and error. Early attempts to increase throughput led to crystallization fouling and color drifts in two consecutive campaigns. Several batches failed analytical release because our dryers cycled too quickly, causing superficial dryness but hidden residual moisture. Instead of hiding these setbacks, our team involves both the lab and plant operators in routine post-mortems. The resulting actions—slowing filter rates, extending vacuum drying periods, and cross-checking sampling points—drove up our reliability scores based on actual client feedback.
Chemistry at scale brings surprises that a few grams in a university lab never reveal. We invest in operator cross-training between small-batch and multi-hundred-kilo runs to make sure lessons translate across every size of order. Clients have told us they value this reliability above any other factor, as failed intermediates can cost months of work or ruin expensive downstream syntheses. For every outlier batch, the root cause becomes a lesson for the entire team, not just the line that produced it.
One of the clearest advantages we bring comes from the staff who make and test every batch. Our chemists and operators don’t just follow procedures set in stone—they participate in monthly roundtables, bring their improvement ideas, and sometimes even spot changes in routine noise or appearance that signal early batch issues. This vigilance means our 2-Hydroxy-5-Nitrobenzyl Bromide regularly exceeds customer standards. Relationships with end-users—from startups prototyping new smart polymers to international pharma giants—grow from mutual respect and consistency.
Our team recognizes that specialty chemicals support people and businesses building next-generation products, not only today’s finished goods. Visible improvements in reaction efficiency, yield, and product stability start in the small details: how we inspect raw materials, confirm structures with NMR and LCMS, and respond to urgent rerun requests after a customer’s trial. A supplier’s job, in our view, is to listen first, then respond with what really matters.
Raw material variability sometimes throws a wrench in plans. Our procurement group sources from vetted partners with track records in both quality and ethical compliance, rotating suppliers as prices and performance shift over time. Trade interruptions, transport delays, and sudden regulatory changes have forced us to double up on inventory, qualifying second-source alternatives with side-by-side testing. Some years, this plan costs more, but we’ve found it protects both us and our customers from unpredictable disruptions.
Supply-demand cycles hit specialty intermediates unpredictably, as a handful of end-users can sharply change market volumes. Instead of waiting for bottlenecks to surface, we invest in logistics planning and buffer stock, absorbing price swings and volume surges so that customers—researchers and production managers alike—find 2-Hydroxy-5-Nitrobenzyl Bromide on hand for their needs.
Nobody wins in specialty manufacturing by standing still. Listening to clients who use our compounds in challenging synthetic routes has kept us adapting, adjusting, and refining both chemistry and delivery. Over the years, we have improved packaging to reduce static or clumping, introduced easy-tear liners that freshen one-batch at a time, and revisited documentation so that even regulatory-savvy partners receive the data they need without delay.
Products like 2-Hydroxy-5-Nitrobenzyl Bromide are more than lines on a price sheet for us—they reflect persistent effort, investment in quality processes, and dedication to the people who rely on what comes out of our reactors. From hands-on attention in purification through to safe and predictable transport, we measure ourselves by how well our chemicals deliver for science and manufacturing progress.