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HS Code |
476269 |
| Product Name | 3-Bromo-4-Fluorobenzylamine Hydrochloride |
| Cas Number | 868851-28-5 |
| Molecular Formula | C7H8BrFN·HCl |
| Molecular Weight | 244.51 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 160-166°C |
| Solubility | Soluble in water and DMSO |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | 3-Bromo-4-fluorobenzylamine hydrochloride |
| Smiles | C1=CC(=C(C=C1F)Br)CN.Cl |
| Inchikey | COYYIUWVHKDJEQ-UHFFFAOYSA-N |
As an accredited 3-Bromo-4-Fluorobenzylamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 3-Bromo-4-Fluorobenzylamine Hydrochloride is packaged in a sealed amber glass bottle with a white screw cap and label. |
| Shipping | 3-Bromo-4-Fluorobenzylamine Hydrochloride is shipped in secure, airtight containers compliant with chemical safety regulations. Packaging ensures protection from moisture, light, and physical damage. All shipping is handled by certified carriers, including appropriate hazard labeling and documentation, to ensure safe transport and delivery according to international and local regulatory requirements. |
| Storage | 3-Bromo-4-Fluorobenzylamine Hydrochloride should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature (15–25°C). Ensure proper labeling and keep away from food and drink to avoid accidental ingestion or contamination. |
Applications of 3-Bromo-4-Fluorobenzylamine Hydrochloride in Industrial ManufacturingAs an integrated manufacturer, we supply 3-Bromo-4-Fluorobenzylamine Hydrochloride for advanced synthesis in pharmaceutical, agrochemical, and specialty chemical sectors. Our experience with diverse downstream industries ensures industrial users benefit from consistent material quality and process-specific guidance for the product’s critical applications in high-value molecule construction. 1. Small-Molecule Pharmaceutical IntermediatesLeading API producers utilize 3-Bromo-4-Fluorobenzylamine Hydrochloride in constructing complex molecular scaffolds, particularly for the synthesis of CNS-active and oncology drug intermediates. Our material integrates at the stage of nucleophilic substitution and amide coupling when developing fluorinated benzylamine derivatives that improve metabolic stability and selectivity. Manufacturers rely on traceability and documentation to meet qualification for regulated pharmaceutical manufacturing and secure consistent batches for scale-up. Industry compliance standards
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2. Agrochemical Intermediate SynthesisDownstream agrochemical manufacturers select this compound for the targeted synthesis of advanced crop protection intermediates, especially those requiring fluorobenzyl motifs to increase selectivity and environmental persistence. It enters the pathway as a key amine building block in creating novel insecticidal and fungicidal actives and improves residue control in regulatory submissions by ensuring batch reproducibility. Industry compliance standards
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3. Dye and Pigment SynthesisManufacturers specializing in specialty dyes and pigments use the hydrochloride salt for producing colorants where electron-withdrawing bromine and fluorine substituents adjust chromophore properties for performance applications. It is especially valued in synthesizing intermediates for high-stability pigments suitable for inkjet printing, plastics coloring, and high-durability coatings, supporting enhanced hue and lightfastness expectations. Industry compliance standards
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4. Specialty Chemical Synthesis for Electronic MaterialsProducers in the electronics chemical sector employ this raw material in constructing intermediates for high-frequency and photonic device coatings. Its dual halogen functionality facilitates subsequent cross-coupling or further derivatization, enabling the manufacture of selective resins, resists, and molecular spacers for photolithography or printed circuit fabrication demanding defined electronic properties and structure-controlled interaction with substrates. Industry compliance standards
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5. Fine Chemical Building Block for Custom SynthesisContract and custom fine chemical synthesis services regularly specify this benzylamine hydrochloride derivative when developing new molecular entities for R&D. The product's dual halogen pattern enables selective subsequent functionalization, providing a controlled entry point for route scouting in both established and exploratory projects where new aromatic amine derivatives are required in low-volume, high-purity applications. Industry compliance standards
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Competitive 3-Bromo-4-Fluorobenzylamine Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.
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Our experience in producing 3-Bromo-4-Fluorobenzylamine Hydrochloride always starts with rigorous control at every step of synthesis. Chemists who work directly with benzylamine derivatives know that introducing both a bromine and a fluorine atom onto the aromatic ring can shift the reactivity in ways you can’t achieve with simpler amines or even other halogenated benzylamines. The practical value of this compound comes through in the way it shortens synthetic routes and helps fine-tune physical properties of pharmaceutical candidates or advanced materials.
You can tell a lot about a supplier’s understanding when they talk about halogen handling, purity thresholds, and how they avoid cross-contamination during isolation. In our shop, we commit to keeping moisture out and adapting the process to the desired hydrochloride salt form for stable storage and cleaner downstream applications. Those who have spent years on a reactor floor know that minimizing residual solvents and metal traces is not simply a checkbox on a spec sheet — it's about real-world reactivity, shelf-life, and regulatory trust.
We typically provide 3-Bromo-4-Fluorobenzylamine Hydrochloride in batches with a minimum assay of 98%, but consistently hitting 99%+ levels is not luck; it requires batch records, in-process controls, analytic calibration, and sometimes a willingness to throw out yield in favor of purity. The model our lab follows is based on feedback we’ve received from synthetic chemists. This feedback reflects real challenges: trace impurities from starting materials, unwanted dehalogenation, or byproducts from incomplete reactions. By controlling temperature ramp rates, carefully timing addition of hydrochloric acid, and monitoring the color and appearance of the product through each wash, we keep consistency high and batch rejection rare.
Solid samples arrive as off-white to light tan crystalline powder, a tone that often signals the absence of over-oxidized or decomposed material. Moisture content, often kept well below 1%, makes a difference not only during storage but also in coupling steps where wet material can produce stubborn side products. Some clients on fast-paced timelines ask about flow chemistry production or kilogram-scale orders. We routinely scale from gram to tens-of-kilos, keeping the same attention to both impurity profiles and polymorphs—nobody wants material that dissolves unpredictably or changes form on storage.
We’ve supplied this compound primarily to pharmaceutical R&D and advanced material labs. In pharmaceuticals, it often serves as a core building block or intermediate for synthesizing active ingredient precursors. The presence of both bromine and fluorine on the benzylamine core opens the door to site-selective cross-coupling, whether you favor Suzuki, Buchwald-Hartwig, or nucleophilic aromatic substitution. We have found that the hydrochloride salt form grants extra handling ease, from weighing to solubility in both water and polar organics. We receive consistent reports from customers who run multi-step syntheses that the hydrochloride version reduces issues with loss of volatile free base, keeps handling safer, and improves consistency in yields downstream.
Some researchers in materials science come back to our product for its utility in fabricating customized polymers or electronic components. Substituted benzylamines like this one insert precisely into backbone chains and tune electronic effects in ways that simple anilines or unsubstituted amines cannot. The bromine function can serve for further derivatization, including direct arylation or incorporation into more elaborate structures. For specialists in ligand design or catalysis, the simultaneous presence of both halogens makes a difference in tweaking electron density and reactivity.
Any chemist who has run parallel experiments with compounds like 4-Fluorobenzylamine, 3-Bromobenzylamine, or classic unsubstituted benzylamine will immediately notice three things with this compound: reactivity, selectivity, and stability shift noticeably. In cross-coupling, the bromo group offers smooth reactivity with palladium or nickel catalysts, allowing tighter control over substitution patterns compared to non-halogenated analogs. The added fluorine atom pulls electron density and changes both solubility and hydrogen bonding in final products. In our manufacturing batches, we verify these changes not just through HPLC but also through real-world downstream coupling trials, often collaborating with customers to verify that our interpretations in the lab stand up in field applications.
Some manufacturers struggle to keep cross-contaminants low when switching between various halogenated benzylamines. Our facility dedicates separate lines for this class, eliminating issues traced to shared reactors, filter cloths, or even solvent lines. The practical difference comes down to cleaning protocols, air handling, and dedicated analytical equipment. Experience shows that customers who switch between the 3-bromo-4-fluoro version and single-halogenated variants comment on lower formation of isomeric byproducts and easier purification—valuable advantages when running time-sensitive synthetic campaigns.
On the plant floor, controlling the introduction of fluorine and bromine on the aromatic ring always calls for precise stoichiometry and order of addition. Over the years, we have learned that the choice of solvent and acid work-up greatly changes both the yield and the crystallinity of the final hydrochloride. Crews with experience know that skipping thorough drying between synthetic steps ends up costing both in downstream purity and ease of isolation. Our staff has dealt firsthand with the challenges of halogenated contamination, especially during summer humidity: the slightest misstep and you end up with clumps, slower crystallization, or, worst of all, a persistent off-color in the product.
We have adopted batch control protocols that flag issues at the blending stage and prioritize in-process FT-IR checks. Those who’ve worked in kilo labs realize that not every impurity gets caught by a final assay—watchful eyes during filtration and solvent exchange matter as much as what goes into the HPLC run. It’s not uncommon to lose yield to a cautious cut, tossing away the “tails” of a batch to guarantee that only the purest fraction gets packed. Attention to anhydrous processing not only achieves better analytical results but also means that downstream users—medicinal chemists or polymer scientists—spend less time troubleshooting weird assay deviations.
Our team has trained extensively in handling benzylamines and halogenated intermediates. Classic concerns—skin exposure, inhalation, environmental release—become much more pressing at scale. We don’t just follow procedures on paper. Actual incidents (near-misses with bromine off-gassing or skin contact during neutralizations) have shaped our emphasis on PPE, air extraction, containment systems, and staff training. People on the production floor don’t forget lessons learned during setup or at 3AM shift turnovers.
On the environmental front, our process incorporates solvent recapture for both the initial halogenation and amine purification steps. We strive for waste minimization and recovery, not just because of regulatory requirements, but out of respect for both our staff and our neighbors. Our experience has taught us that regular audits and process reviews keep the operation lean and ensure compliance, and proactive waste reduction eases pressure on effluent treatment further down the line.
Our clients in pharmaceutical R&D or specialty materials demand traceable lots, detailed batch histories, and transparent documentation. We can track every lot of 3-Bromo-4-Fluorobenzylamine Hydrochloride back to its raw halogen inputs and document every handling and purging cycle. Having robust records allowed us in the past to rapidly identify, recall, and replace a single batch with a QC deviation, protecting customers’ programs from costly setbacks. Direct experience shows that supply chain trust depends far more on willingness to stand behind each drum than any certificate or inspection result.
We regularly invite customer audits and have tailored parts of our operation to meet requirements from both US and European pharmaceutical partners. Practical know-how with impromptu “spot audits” and regular third-party inspections has improved our process hygiene and in-process monitoring. This open-door approach doesn’t add cost — if anything, it keeps our crew sharp and the product flow reliable for customers facing regulatory scrutiny or tight project deadlines.
We see demands shifting as customers move from milligram-scale exploratory syntheses to pilot plants and early-phase clinical manufacturing. We have supported partners transitioning from glassware to kilo-scale reactors, providing insight into solvent swaps, salt selection, and packaging solutions geared for time-sensitive programs. As projects scale, subtle differences in mixing, residence time, and crystallization can change the physical appearance and performance of 3-Bromo-4-Fluorobenzylamine Hydrochloride. Our technical team backs up each order with practical advice, whether it’s for re-dissolution, further derivatizations, or handling protocols to avoid caking and degradation.
Researchers often ask about the role of specific batch variants on yields in challenging transformations, such as amide coupling or heterocycle formation. We offer samples and technical support because it leads to a tighter feedback loop — learning how applied research in the lab reflects back into process optimization on our end. In some cases, we have adjusted our isolation protocol to meet specific dissolution rates or particle size requirements, always taking customer results as the ultimate test of process success.
No process runs perfectly forever, and even decades-old protocols demand troubleshooting when raw materials or equipment change. Our operators spot issues in real time—gassing rates in addition vessels, unexpected color shifts, slow filtration, or odd odors signal the need for immediate attention or batch hold. Over years, we have adjusted raw material suppliers, replaced filtration media that leached contaminants, and revised drying parameters on feedback from both QC results and operators' gut sense.
Customers in medicinal or polymer chemistry sometimes hit snags due to minor differences in reactivity or solubility between lots. We offer open, unfiltered communication about process changes and batch records, helping researchers correct for these differences on their end in real time. Instead of hiding deviations, we respond with transparency, pulling in both process chemists and analytics staff. This attitude has stopped more costly problems at the source than any high-gloss advertisement ever could.
Talk about "differentiation" can get abstract, but scientists on the bench recognize distinctions the moment they handle the product. Single-halogenated benzylamines often lack fine control over reactivity, and the subtle tweak of both bromine and fluorine on the ring allows for more tailored downstream design in both pharma and material science. Users report reduced need for purification in their own departments, and the higher batch-to-batch reproducibility means less wasted effort chasing inconsistencies.
The difference also comes in storage and prep time. Our hydrochloride salt resists humidity-driven clumping and oxidative discoloration. Over the seasons, as ambient conditions in warehouses and labs fluctuate, our customers have reported reduced cases of caking, easier resuspension, and fewer headaches related to unreliable weighing.
Over time, sincere relationships with researchers and scale-up teams have shaped our decision-making. Instead of dictating specs from behind a desk, we keep lines open for candid feedback and field-specific requests. Some customers require finer particle size, others demand bulletproof documentation for regulatory filings, and a few need specialized inert atmosphere packaging. By treating feedback as an asset rather than a burden, our team stays flexible and invests resources where they count toward real bottlenecks, not cosmetic improvements.
Having long-term customers who share final application details with us helps close the gap between process chemistry and end-use performance. Whether it’s for early clinical candidate synthesis or niche optoelectronic components, our ultimate goal is to make sure the product arriving in the lab delivers not only on paper, but in every measurable way during experimentation and scale-up.
Many in this industry have faced letdowns — unreliable shipments, withheld batch data, last-minute changes in supply chains, or inconsistent material quality. We openly acknowledge that trust is earned primarily through consistency and accountability. We focus our manufacturing approach on process discipline, hands-on monitoring, and direct support for every customer, so that one shipment leads to the next not because of marketing claims, but due to years of performance and open engagement.
Feedback, both positive and critical, informs every aspect of our process adjustments. If a customer experiences an issue or needs documentation updates for regulatory submission, we address those needs directly, backed by the full traceability and production records from our facility. At the end of the day, manufacturing 3-Bromo-4-Fluorobenzylamine Hydrochloride is not simply a technical routine, but a continual process of earning and maintaining the kind of trust that carries a research program from the bench to the plant and, eventually, to market.