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HS Code |
911676 |
| Product Name | p-Bromophenyl Hydrazine |
| Cas Number | 2272-44-2 |
| Molecular Formula | C6H7BrN2 |
| Molecular Weight | 187.04 |
| Appearance | Off-white to beige powder |
| Melting Point | 75-78°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥ 97% |
| Synonyms | 4-Bromophenylhydrazine |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited P-Bromophenyl Hydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g P-Bromophenyl Hydrazine comes in a sealed amber glass bottle, labeled with hazard warnings, product details, and batch number. |
| Shipping | P-Bromophenyl Hydrazine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be labeled as a hazardous material and handled with appropriate safety precautions. Transport must comply with local and international regulations, ensuring ventilation and avoiding sources of ignition, as the substance may be toxic or combustible. |
| Storage | **P-Bromophenyl Hydrazine** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, flame, and sources of ignition. Protect it from light and moisture. Store separately from oxidizing agents, acids, and strong bases. Proper labeling and secondary containment are recommended to prevent contamination and ensure safe handling. |
Applications of P-Bromophenyl Hydrazine in Industrial ManufacturingP-Bromophenyl Hydrazine serves as a critical specialty intermediate utilized by fine and specialty chemical manufacturers in demanding synthesis routes. Its unique chemical reactivity supports the construction of various high-value compounds across select downstream sectors, where strict compliance, precise formulation, and reliable process integration are compulsory throughout industrial-scale production. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical manufacturers incorporate P-Bromophenyl Hydrazine as a building block when designing hydrazone-based active pharmaceutical ingredients, particularly for molecules requiring halogen substitution patterns. The raw material’s precise reactivity ensures selectivity in condensation steps, which is vital for maintaining pharmaceutical-grade purity. Sourcing and batch traceability demands reinforce adherence to strict regulatory and audit requirements in these settings. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentAgrochemical firms use P-Bromophenyl Hydrazine in the synthesis of select herbicides and fungicides where phenylhydrazone structures convey target organism specificity. Its purity directly affects downstream activity and environmental profile, making raw material traceability and contamination control central to sustainable product qualification. Industry compliance standards
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3. Dye and Pigment IntermediatesProducers of high-performance dyes and pigments in the electronics, textile, or plastic sectors select P-Bromophenyl Hydrazine for its role in coupling reactions that introduce azo or hydrazone chromophores with tailored spectral properties. Its batch consistency ensures color reproducibility and compliance with migration and heavy metal limits mandated by end-use standards. Industry compliance standards
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4. Fine Chemical and Specialty Intermediate ManufacturingSynthesizers of fine chemicals exploit P-Bromophenyl Hydrazine to prepare specialty intermediates for subsequent use in complex molecule construction. Its ability to selectively introduce a bromophenyl hydrazine fragment allows for controlled molecular editing in advanced material science, fragrance chemical development, and reference standard production, where documentation and process transparency are imperative. Industry compliance standards
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5. Chemical Research and Academic ApplicationsIn university and industrial R&D laboratories, researchers include P-Bromophenyl Hydrazine as an enabling reagent for novel compound discovery, method development, and proof-of-concept scale synthesis. Detailed lot documentation, along with impurity certificates, underpin acceptance in grant-funded and compliance-governed projects. Industry compliance standards
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Every product has a history, and so does our experience with P-Bromophenyl Hydrazine. As a chemical manufacturer rooted in years of synthesis and scale-up, we have always approached this compound with a focus on reliability and reproducibility. Behind every bottle stands a team committed to thorough process design, starting from raw material checks and moving all the way through careful crystallization and drying protocols, because we understand that each batch must answer to both lab-scale demands and industrial users who rely on tight tolerances.
Our P-Bromophenyl Hydrazine comes under the model PBPH-98, where the number signals the minimum assay purity. Every gram starts its journey in reactors that have handled only dedicated halogenated intermediates—cross-contamination is not an option. We direct our attention to every stage, from bromination to final hydrazine coupling, ensuring clean conversion and minimal side-product formation. Carefully controlled temperatures and reaction rates allow for consistent color, melting range, and solubility profile, so users don’t face unpleasant surprises with solubility slopes or unwanted residues. Our output passes through charcoaling and tailored filtration, reducing trace metal impurities to levels rarely flagged in downstream analytical testing.
Our team targets an assay of no less than 98.0% for P-Bromophenyl Hydrazine by HPLC, with melting points in the 112-114°C range. The product appears as an off-white to faintly yellowish crystalline powder; sometimes, fresh batches trend paler, as expected with high-purity hydrazines. We run GC and LC-MS screens not only for assay, but to detect related phenyl hydrazines, halogenated tars, or acid halide byproducts. Many users ask about sulfur or nitrogen oxide residues. Over the years, we have refined our synthetic work-up steps to keep these far below 0.1%—a level confirmed on each lot. This figure matters for those using sensitive downstream syntheses, especially in medicinal or agrochemical applications.
Trace moisture is another concern we have addressed; consistent handling and final-stage vacuum drying mean our P-Bromophenyl Hydrazine averages below 0.5% water content by Karl Fischer. For users who need ultra-dry material, we offer pre-packed, desiccated bottles straight from our glove boxes, as atmospheric moisture pick-up puts the most sensitive reactions at risk. We store all final product in lined drums and seal bottles to prevent any bromine vapor migration—which has posed trouble in the past when packaging was neglected. Aging studies have led us to reinforce shelf-life expectations: the material holds its chemical integrity with less than 0.2% assay change over 24 months under cool, dry conditions.
Chemists choose P-Bromophenyl Hydrazine for its versatility in both research and production environments. The bromine on the para-position allows selective reactivity, serving as either a leaving group or a handle for further coupling. Researchers and process development teams continue to find value in this selectivity—especially when aiming to introduce new rings, extend conjugated systems, or test pharmacophores. Compared to unsubstituted phenyl hydrazine, the p-bromo derivative brings a different electronic profile to diazotization, cyclization, and azo coupling steps. Reagents with ortho or meta substitution tend to produce mixture problems; para selects cleanly in many systems.
Our conversations with clients in the pharmaceutical discovery sector show a consistent demand for P-Bromophenyl Hydrazine in scaffold construction, especially in intermediate steps for indoles, triazoles, and azo dyes. Biological screening groups appreciate the predictable reactivity, which supports parallel synthesis and structure-activity relationship trials. On the industrial scale, we’ve worked alongside teams needing several hundred kilograms per year, often for specialty pigment manufacture or as a building block for pesticide actives. The bromine’s electron-withdrawing properties modulate reactivity in a way that unsubstituted or ortho/para-methyl analogues cannot replicate, providing a valuable tool in synthetic strategy.
Producing hydrazines presents unique safety demands, with strict controls against hydrazine vapor, heat spikes, or unwanted side reactions. We train our operators to monitor not just temperature and pressure, but also to interpret visual and odor cues that precede decomposition events. It took several years of process tweaking—including solvent swaps and quench rate adjustments—to minimize exotherm risk during the bromination stage. Early batches sometimes showed variability in particle size and color, so we integrated in-line monitoring and real-time analytics, which allowed tighter grip over nucleation and growth in the final crystallization tank.
From time to time, supply chain changes or market-driven sourcing of precursors have forced us to re-validate starting material lots. Our lab responds by running small-scale pilot tests every time a supplier changes, preventing unknown contaminants or inconsistent performance from reaching our main plant. Hydrazine impurities can impact both chemical reactivity and safety, so we continue to invest in test method development—moving beyond standard titration and relying on more sensitive chromatographic techniques for batch release.
Younger chemists on our staff have brought forward digital tools for tracking and documenting process data, linking every batch number to its full production and test record. Customers tell us this traceability gives them confidence in material tracking, especially when audit time comes. We offer regulatory support for those in highly-regulated industries, drawing from our production documentation to answer questions about origin, lot history, and contaminant management.
In the world of aromatic hydrazines, not all products serve the same role. P-Bromophenyl Hydrazine distinguishes itself primarily through the reactivity profile provided by its para-bromo substitution. Unsubstituted phenyl hydrazine can sometimes lead to excessive byproduct formation due to its unbalanced reactivity, while ortho- and meta-bromo variants introduce steric bulk that hampers key reactions, such as cyclizations or nucleophilic substitutions.
Some customers have used meta- or ortho-chlorophenyl hydrazines, expecting similar results, only to encounter yield drops or chromatographic headaches when separating products. We have often been called to troubleshoot process workflows that need cleaner step outcomes. With p-bromo, the electron-withdrawing effect tightens selectivity, especially when handling transformations that are sensitive to electron density—like diazotization or condensation onto electron-rich partners. Our field experience, supported by direct feedback from customers, shows that para-halogens both stabilize the hydrazine and make it more predictable in complex, multistep syntheses.
In pigment and dye chemistry, this substitution pattern brings out unique absorbance characteristics due to the resonance effects conferred by para-bromo groups. Literature surveys and internal testing over the years confirm that even small changes, like moving the bromine to a different ring position, have measurable impacts on colorfastness, tonality, or light stability of the resulting compounds.
The physical form of our product sets it apart from some lower-quality offerings we have encountered in the market. Instead of a dusty or amorphous solid, our crystalline output allows for easier handling, precise weighing, and consistent reactivity—attributes downstream users frequently mention. Finer particles tend to pick up moisture and degrade faster, so our batch-wise control of particle size is not just a matter of appearance but of shelf-life and functional value.
Every synthesis team finds that reliable intermediates cut down on troubleshooting time. Our own labs have used P-Bromophenyl Hydrazine for model reaction studies, exploring both its traditional role in cyclizations and its growing use in cross-coupling or catalytic transformations. Our users in agrochemical development often report successful runs in both known and exploratory reaction schemes—such as constructing heterocycles with improved environmental stability or processability.
Early-stage discovery scientists using small quantities favor our 10 g and 100 g packs, which come pre-verified for batch purity and impurity level. Process engineers and production chemists ordering kilo lots see value in our scale-up support, where technology transfer conversations include not only the chemical itself, but transport, storage guidance, and insights into material compatibility in their reactors. With hydrazines, safe and informed product integration can mean the difference between a routine scale-up and problematic reactivity.
Azo and formazan dye houses continue to standardize on our P-Bromophenyl Hydrazine because they observe cleaner color transitions and better reproducibility compared to less pure or inhomogeneous batches from commodity sources. While many dyes derived from this hydrazine are not new, continuous improvements in purity and performance play a role where downstream regulatory and environmental pressures increase. We often help customers understand how small gains in precursor quality lead directly to improved product results, including better shelf life and performance in light- or abrasion-resistance testing.
Manufacturing and supplying P-Bromophenyl Hydrazine comes with ethical and legal responsibilities. We follow a strict code to evaluate environmental and worker safety impacts, which means ongoing review and improvement of exhaust treatment systems and spill control measures throughout the plant. Hydrazine intermediates call for protected handling at every stage. No process, no matter how automated, replaces alert personnel who know the warning signs of degradation or system upset.
Waste minimization and resource efficiency feature in every production review. Our engineering team reviews not just reaction yields, but solvent reclamation, recycle opportunities, and byproduct treatment. Over the last five years, these efforts have dropped our process waste factor by nearly 30% for P-Bromophenyl Hydrazine, reducing both environmental footprint and operational costs for our partners. We share these results transparently with our customers, as many must document and defend their supply chain sustainability.
As industry regulators globally introduce sharper reporting and control mechanisms for hazardous precursors, we have woven compliance into every order. Routine support for product registration, shipping documentation, and supply chain traceability has become part of our everyday workflow—not an afterthought. Each customer faces their own regulatory landscape; we are committed to sharing our knowledge about best practices, changes in global regulations, and lessons learned from decades at the manufacturing line.
Experience has shaped our process for P-Bromophenyl Hydrazine, but progress never stalls. Research into cleaner and more energy-efficient syntheses continues, with active investments in new catalyst systems and solvent development. Open communication channels allow our production team to hear directly from chemists in the field, whose feedback often leads to process adjustments. We have revised purification steps and packaging specifications based on real-world insights—sometimes replacing older protocols entirely in response to emerging industry needs.
Our material goes through not just in-house QA, but often parallel runs in customer labs and external validation. This shared approach strengthens both confidence in the product and long-term relationships with customers. We keep a close eye on any challenge faced in handling, storage, or downstream processing and work closely to identify and resolve root causes. Regular site visits and technical consultations bring the manufacturer’s insight directly to the hands of those using the product.
Though P-Bromophenyl Hydrazine may appear a routine building block, every batch reflects diligent cooperation between synthesis, analytical, safety, and customer support teams. Manufacturing is not simply about producing a chemical—it’s about delivering reproducibility and safety, ensuring every downstream innovation stands on stable ground.
Ongoing customer feedback and engagement with evolving synthetic trends will continue to shape both how we produce P-Bromophenyl Hydrazine and how we serve those who put it to use. Our aim is not to supply a commodity, but to provide a dependable tool, and to walk alongside every chemist and production engineer who chooses our product for their work.