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3-Bromo-4-Fluorobenzylamine Hydrochloride

    • Product Name 3-Bromo-4-Fluorobenzylamine Hydrochloride
    • Alias 3-Bromo-4-fluorobenzylamine HCl
    • Einecs 841-639-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    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 & Storage
    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.
    Application of 3-Bromo-4-Fluorobenzylamine Hydrochloride

    Applications of 3-Bromo-4-Fluorobenzylamine Hydrochloride in Industrial Manufacturing

    As 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 Intermediates

    Leading 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapters (pertaining to impurities, residual solvents)
    • European Pharmacopoeia General Notices
    • FDA Drug Master File (when filed by API manufacturers)

    Typical usage ratio

    • Used at 1.1–1.5 molar equivalents relative to core substrate; precise loading refined via route optimization to minimize excess amid high-value intermediates. Range adjusted to control impurity profile and achieve high target yield.

    Downstream process integration

    • Dosed during intermediate formation via direct amination, acylation, or reductive amination in multi-step synthesis. Entry point: After halogenation or prior to final deprotection/purification of pharma intermediates.

    Final product types

    • CNS-active pharmaceutical intermediates
    • Antitumor agent intermediates
    • Complex fluorinated benzylamines for generic and proprietary APIs
    • Reference standards and analytical intermediates for pharma QC labs

    2. Agrochemical Intermediate Synthesis

    Downstream 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

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 Quality Management Systems
    • European Union Regulation (EC) No 1107/2009 on Plant Protection Products
    • OECD Good Laboratory Practice (GLP) for regulatory studies

    Typical usage ratio

    • Inputs vary from 0.8 to 1.3 molar equivalents based on downstream coupling route and active ingredient complexity. Modulation based on cost and conversion efficiency in continuous and semi-batch operations.

    Downstream process integration

    • Incorporated during the synthesis of heterocyclic rings or as a nucleophilic component in the Mannich reaction. Used post-halide introduction, enabling streamlined modification of active-site functionality.

    Final product types

    • Active ingredient intermediates for cereal and vegetable crop protection
    • Fungicide scaffolds incorporating fluorinated benzylamine subunits
    • Custom synthesis blocks for proprietary agrochemical development
    • Analytical standards for pesticide residue monitoring

    3. Dye and Pigment Synthesis

    Manufacturers 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

    • REACH Regulation (EC) No 1907/2006 for Chemicals Registration
    • ISO 9001:2015 (for dye and pigment quality control)
    • ETAD Code of Practice for Responsible Manufacturing
    • Control of Substances Hazardous to Health (COSHH - UK) for worker safety

    Typical usage ratio

    • Incorporated at 0.2–0.6 mol ratios, calculated from the primary condensation substrate, with adjustments for process color yield and desired solubility characteristics in solvent-based dispersions.

    Downstream process integration

    • Added prior to ring-closure or azo coupling reactions, enabling introduction of functionalized amine moieties into aromatic pigment backbones for shade and durability tuning.

    Final product types

    • High-performance organic pigments for plastics
    • Inkjet printer dyes and toners
    • Automotive and industrial coatings pigments
    • Specialty colorants for electronics and packaging

    4. Specialty Chemical Synthesis for Electronic Materials

    Producers 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

    • RoHS Directive (2011/65/EU) for hazardous substances
    • IPC-4101 Laminate and Prepreg Materials Standards
    • ISO 14001:2015 Environmental Management System
    • Chemical Substances Control Law (Japan, if exported to Japanese circuit manufacturers)

    Typical usage ratio

    • Incorporated at 0.1–0.4 mol fractions, depending on resin matrix and electronic requirements for dielectric constant, solubility, or mechanical performance. Ratio optimized for reactivity in Suzuki or Buchwald–Hartwig reactions.

    Downstream process integration

    • Added during advanced resin or monomer synthesis prior to polymerization, directly enabling formation of functional intermediates with halogenated aromatic structures. Entry point: after initial ring synthesis or before final functional group modification.

    Final product types

    • Photoresist intermediates for semiconductor processing
    • Specialty resins for printed circuit boards
    • Dielectric and encapsulation materials for microelectronics
    • Functional coatings for optoelectronic applications

    5. Fine Chemical Building Block for Custom Synthesis

    Contract 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

    • ISO 9001:2015 Quality Management System
    • GMP-like documentation for custom synthesis (when end-use is pharma/agro research)
    • IUPAC Nomenclature and Analytical Standards
    • GHS SDS Preparation and REACH Pre-registration (as required by project scope)

    Typical usage ratio

    • Ranges from 0.05 to 3 equivalents as per synthetic design. Early-phase R&D favors stoichiometric excess for reaction scouting; production optimization reduces loading for cost efficiency and minimize side products.

    Downstream process integration

    • Introduced at defined steps such as amidation, reductive amination, or C–N cross-coupling, based on project requirements. Used either as a terminal modification or in multi-stage functionalization during process development.

    Final product types

    • Specialty aromatic amine building blocks for academia and industry projects
    • Targeted reference intermediates for analytical method validation
    • Reactive scaffolds for pharmaceutical, agrochemical, or materials research
    • Intermediates submitted to patent filings and structure–activity R&D studies
    Free Quote

    Competitive 3-Bromo-4-Fluorobenzylamine Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    3-Bromo-4-Fluorobenzylamine Hydrochloride: Building Blocks for Precision Chemistry

    Understanding 3-Bromo-4-Fluorobenzylamine Hydrochloride in Everyday Manufacturing

    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.

    Specification and Model Choices Backed by Hands-On Experience

    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.

    How Usage Trends Shape Quality Commitments

    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.

    Comparing 3-Bromo-4-Fluorobenzylamine Hydrochloride to Related Products

    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.

    Managing Production and Quality: Hands-On Lessons

    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.

    Safety and Environmental Practices Honed Over Time

    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.

    Ensuring Consistency and Traceability for Sensitive Applications

    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.

    Supporting New Directions in Research and Scale-Up

    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.

    Troubleshooting and Continuous Improvement from the Source

    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.

    Product Differentiation That Matters in the Lab

    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.

    Customer Relationships Shape Our Approach

    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.

    Trust Built Through Transparency and Reliability

    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.