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5-Bromo-2-Fluorobenzylamine Hydrochloride

    • Product Name 5-Bromo-2-Fluorobenzylamine Hydrochloride
    • Alias 5-Bromo-2-fluoro-benzylamine HCl
    • Einecs 801-039-7
    • 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

    327775

    Product Name 5-Bromo-2-Fluorobenzylamine Hydrochloride
    Cas Number 872365-15-6
    Molecular Formula C7H8BrFN·HCl
    Molecular Weight 240.51 g/mol
    Appearance White to off-white solid
    Melting Point 168-172°C
    Solubility Soluble in water, DMSO, methanol
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, tightly sealed
    Synonyms 5-Bromo-2-fluorobenzylamine hydrochloride
    Chemical Structure Benzylamine with bromine at position 5 and fluorine at position 2, HCl salt
    Smiles C1=CC(=C(C=C1Br)F)CN.Cl
    Inchikey AQESECBQAJWOBL-UHFFFAOYSA-N

    As an accredited 5-Bromo-2-Fluorobenzylamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Opaque, white HDPE bottle containing 25 grams, sealed with tamper-evident cap and labeled with product name, CAS, and safety information.
    Shipping 5-Bromo-2-Fluorobenzylamine Hydrochloride is shipped in tightly sealed, chemically resistant containers under ambient conditions. The package is clearly labeled, with appropriate hazard and handling identifiers, and conforms to international regulations for safe transport of chemical substances. Shipping documentation includes safety data and emergency contact information. Handle with gloves and avoid exposure.
    Storage **5-Bromo-2-Fluorobenzylamine Hydrochloride** should be stored in a tightly sealed container, protected from light and moisture. Keep at room temperature (20-25°C) in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and access only to trained personnel. Follow all standard safety and containment procedures for handling chemicals.
    Application of 5-Bromo-2-Fluorobenzylamine Hydrochloride

    Applications of 5-Bromo-2-Fluorobenzylamine Hydrochloride in Industrial Manufacturing

    As an established manufacturer of 5-Bromo-2-Fluorobenzylamine Hydrochloride, we serve numerous sectors in the advanced chemical industry by supplying this key aromatic amine intermediate. Below, we detail its implemented roles across essential downstream pathways, focusing on technical compliance, process integration, and application-specific formulation guidance.

    1. Pharmaceutical Intermediates for CNS Active Compounds

    This intermediate sees targeted use in the synthesis of central nervous system (CNS) candidate molecules, particularly during the assembly of substituted phenethylamines and related structures. It enters multistep synthetic routes, contributing a reactive benzylamine motif for coupling or condensation steps under GMP-controlled production environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USFDA 21 CFR Part 211 Current Good Manufacturing Practice
    • European Pharmacopoeia (Ph. Eur.) Section 5.10 for pharmaceutical intermediates
    • China GMP (2010 Revision) for chemical drug substances

    Typical usage ratio

    • 0.8–1.1 molar equivalent relative to the primary core intermediate; chemists refine addition based on desired stoichiometry and impurity profile management in lead optimization stages

    Downstream process integration

    • Introduced prior to amide or imine coupling in batch or continuous multi-reactor flows; frequently protected with Boc or Fmoc groups post-addition to minimize side reactions; purification follows using silica or crystallization protocols

    Final product types

    • Investigational new drugs (IND) with CNS activity
    • Reference standards for psychoactive pharmaceutical research
    • Late stage preclinical intermediates

    2. Agrochemical Building Block for Herbicide & Fungicide Synthesis

    In the agrochemical sector, this compound functions as an arylamine building block in the design of bromofluorinated active ingredients for modern herbicides and fungicides. The amine moiety enables straightforward insertion into target molecules intended for increased selectivity and crop safety.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • China GB/T 1600-2022 Quality Standards for Agrochemicals
    • REACH (EC 1907/2006) Chemical Safety Report for agricultural agents
    • OECD Principles of Good Laboratory Practice for registration batches

    Typical usage ratio

    • 5–15% (w/w) relative to total synthetic input for the aromatic segment; actual use refined in R&D to balance substitution levels and minimize downstream impurity generation

    Downstream process integration

    • Charged into intermediate coupling reactors following halogen exchange or substitution reactions; post-functionalization includes N-acylation and heterocycle formation under inert atmosphere conditions

    Final product types

    • Active pesticide technical concentrates
    • Assembled functionalized pre-mixes for further formulation
    • Agronomic field trial samples for regulatory submission

    3. Specialty Organic Synthesis for Fluorinated Fine Chemicals

    This material is deployed in the manufacture of specialty fluorinated compounds used in fine chemical applications, particularly for industries requiring high-purity aromatic intermediates. It delivers a controlled source of bromo and fluoro substituents tailored for custom molecule assembly in laboratory and pilot-plant settings.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for specialty chemical production
    • Responsible Care® Global Charter adherence for production safety
    • DIN EN ISO 14001 Environmental Management standards
    • ECHA (European Chemicals Agency) notification for custom synthesis

    Typical usage ratio

    • 15–30% (by molecular ratio) in custom syntheses; tailored input based on the complexity of the downstream target structure and substitution pattern required

    Downstream process integration

    • Introduced as a coupling or derivatizing agent during stepwise functional group installation in multi-gram to multi-kilogram batches; monitored via HPLC and NMR for batch-to-batch consistency

    Final product types

    • Fluorinated aromatic intermediates for electronics
    • Intermediate stocks for specialty reagent houses
    • Research compounds for structure–activity relationship studies

    4. Active Ingredient Precursor in Diagnostic Reagent Synthesis

    Contract manufacturers for IVD (in vitro diagnostic) reagents employ this hydrochloride salt as a customizable precursor for synthesizing tagged entities and diagnostic probes. Its high purity and distinct substitution pattern are essential for downstream conjugation to signaling moieties under traceable conditions.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management for IVD
    • USP General Chapter <1047> for Ancillary Materials
    • China YY/T 0287 Quality Management for Medical Devices
    • EU In Vitro Diagnostic Regulation (IVDR, 2017/746)

    Typical usage ratio

    • Adjusted 1–3% (w/w) in conjugation or derivatization formulations; final input based on the intended labeling density and probe specificity requirements

    Downstream process integration

    • Employed in solution or solid-phase synthesis during linker installation or fluorescent tagging; exhaustive washing and purification follows to ensure diagnostic-grade purity

    Final product types

    • Chemical conjugates for diagnostic assay kits
    • Labeled reagents for fluorescence and colorimetric detection
    • Analytical reference materials for laboratory QC

    5. Chemical Modification Agent in Material Science Research

    Advanced material developers utilize this compound as an amination and halogenation agent to tune properties of polymeric systems and engineered surfaces. Its role centers on introducing specific functional groups onto preformed matrices, enabling downstream modification of surface chemistry and interfacial behavior in R&D and pilot programs.

    Industry compliance standards

    • ISO/TS 80004-12:2016 Nanotechnologies—Engineering materials
    • ASTM E2879-13 Standard Guide for Laboratory Use in Material Synthesis
    • REACH Annex XVII for specialty substances in material innovation
    • In-house validated QC protocols for surface modification

    Typical usage ratio

    • 0.5–2.5% (w/w) relative to substrate matrix; optimized for uniform surface distribution and to control reaction completeness in custom experimental designs

    Downstream process integration

    • Applied during chemisorption or covalent tethering reactions; materials are typically incubated with functionalized solution under controlled pH and temperature to achieve reproducible modification

    Final product types

    • Modified polymeric films for electronic or sensing applications
    • Surface-activated substrates for nanotech prototyping
    • Research-scale material samples for prototype testing
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    Certification & Compliance
    More Introduction

    5-Bromo-2-Fluorobenzylamine Hydrochloride: An Experienced Manufacturer’s Perspective

    Direct Production, Honest Insights

    Every day on our site floor, our team works hands-on with a broad portfolio of specialty benzylamine derivatives. Among them, 5-Bromo-2-Fluorobenzylamine Hydrochloride stands out for its reliable performance, stable characteristics, and versatility in research and synthesis. Over the years, we have refined each detail of its manufacture. This brings confidence, not just for our clients in laboratories but also for our own team. Direct production gives us real visibility into what consistently works—no hearsay, only our collective experience.

    The Chemistry Behind Reliability

    5-Bromo-2-Fluorobenzylamine Hydrochloride belongs to the benzylamine class of compounds, with the molecular formula C7H7BrFN·HCl. What sets this amine salt apart starts at the structural level. Handling bromine and fluorine substituted aromatic rings can be tricky, especially under large-scale operation conditions. We’ve spent years perfecting temperature controls, solvent combinations, and purification steps. Across each batch, our chemists check closely for color and particle consistency at every stage, aiming to keep the product free of colored impurities or inconsistent grain shapes. Our past missteps developed a set of standard operating procedures we rely on today; mistakes taught us more than any datasheet ever could.

    Our standard offering provides tight control of chemical purity, consistently exceeding 98%. Moisture content and residual solvents remain low; we screen rigorously for inorganic admixtures, as even traces risk reducing downstream reactivity or causing unwanted byproducts. We use HPLC and NMR for routine confirmation. Some clients, particularly those in pharmaceutical research, have unique requirements—perhaps a narrow particle size, or specific documentation supporting traceability. Having all manufacturing under our roof allows us to adjust workflows without delay. Specifications are not arbitrary: each value represents a potential variable we have tested against, suffered setbacks from, and finally mastered. Proper handling in our plant reduces degradation and keeps the hydrochloride form stable in long-term storage.

    Comparing with Other Benzylamine Derivatives

    Many research projects call for different aromatic substitutions or halogen patterns on the benzylamine backbone. Whether someone asks us for 4-bromo-2-fluorobenzylamine or an unhalogenated analog, there’s no one-size-fits-all answer. Bromine and fluorine both alter electron density around the ring and influence downstream chemistry. In our experience, the 5-bromo, 2-fluoro configuration reacts with milder nucleophiles without excessive activation or deactivation. This gives our customers more flexibility, particularly for lead compound development or advanced intermediate work. We engineered our process to minimize side-products arising from over-bromination or fluorination, two perennial issues in the field.

    Over time, it became clear that purity benchmarks from literature rarely account for stability through shipment or long-term storage. It is not enough to nail a target percentage on the day of production. Repeat sampling—three months, six months down the line—often reveals how unresolved impurities or even packaging choices shift the effective reactivity for our clients. By maintaining close records and making batch improvements based on this data, we not only deliver high initial purity, but also lower the risk of changes in compound behavior during its shelf life. Other suppliers sometimes simply relay what they have been told; as a direct manufacturer, our data comes straight from our own analytical runs. This transparency is core to how we see trust with our community.

    Applications That Shape Our Approach

    Over the years, we see most orders for 5-Bromo-2-Fluorobenzylamine Hydrochloride come from research groups tackling pharmaceuticals, materials, or specialty catalysts. The compound’s dual halogenation affects binding affinity and metabolism in drug discovery. We see demand from customers looking to prepare custom amides, ureas, or coupling intermediates. Synthetic organic chemists often remark on the utility of this product for fine-tuning electronic and steric effects during medicinal scaffold expansion. In catalyst development, its halogenated aromatic moiety acts as an essential handle for further functionalization.

    Our job includes listening to consistent feedback about solubility, melting point, and compatibility. For some, solubility in polar aprotic solvents means more to them than just a number on a data sheet. Early on, we ran into feedback from researchers getting glassy or overly sticky product, making it challenging to weigh or dissolve accurately. Those reports led us to new drying and storage protocols—now, each lot comes free-flowing and uniform, easy to handle on a benchtop. We maintain a focus beyond just the molecule’s identity, looking at its behavior in actual research settings. Once, a customer pursuing a novel peptide synthesis found issues with byproduct formation due to trace iron content; this inspired an overhaul of our purification route, now validated by routine ICP-MS checks for heavy metals.

    Adapting Specifications to Actual Needs

    No product leaves our plant labeled “generic.” Each specification we offer reflects the sort of requests and feedback we’ve accumulated as a bulk manufacturer. Typical properties—solid hydrochloride salt, a pale off-white to white appearance, free of visible particles or discoloration—stand the test of time against real-world requirements. Water content, often overlooked, can have a major impact on certain sensitive coupling reactions. To control this, we use vacuum drying and package under dry nitrogen. Granule sizing is not just for looks; it affects weighing accuracy and dissolution. Based on laboratory and pilot-scale feedback, we adjusted our processing to keep clumping or dust to a minimum. We document each step, producing paperwork that stands up to scrutiny—both from clients and from regulatory auditors.

    We do not stick to rigid batch sizes. Student groups often need as little as a few grams for new reaction screening, while larger projects may require kilos. Our operation scales accordingly. This flexibility does more than keep us nimble; it brings us face-to-face with the practical mistakes and pain points that only emerge during actual usage. After all, unexpected behaviors in a gram-scale pilot can magnify into major headaches at the kilo scale, especially when converting into higher value compounds.

    Tracing Challenges and Discovering Solutions

    Years in the business reinforce that chemistry refuses to be rushed, even as clients push for rapid turnarounds. Early attempts to scale our process brought a series of learning moments. For instance, the hydrochloride form seemed stable under bench conditions but started to degrade under humid summer air. This threatened both purity and handling, leading us to revise our entire packaging setup. Now, each unit ships in moisture-resistant containers, sometimes under inert atmosphere, depending on the client’s storage profile. We saw a sharp drop in complaints around product caking or color shift.

    Supply chain challenges have driven us to value local sourcing and reliable raw material partnerships. The global pandemic revealed the risks of long, opaque supply lines. Any minor contamination—from incorrect bromination agents or off-ratio solvents—shows up quickly during purification. We perform incoming goods inspection for every critical reagent, clearing only those with validated purity and consistency. We invest in analytical tools that give instant feedback. While this raises our own baseline costs, it protects the whole value chain—delays and rework down the road cost both us and our collaborators far more than any marginal savings at the front end.

    Why Direct Manufacturing Makes the Difference

    Control remains central—over method, materials, data, and outcomes. Making 5-Bromo-2-Fluorobenzylamine Hydrochloride ourselves, we know the backward links of every lot, down to the barrel of solvent or batch of bromine. If a problem comes up—say, slight yellowing or micro-scale residuals after filtration—we track it to the source, adjust, and follow up. Third-party trading or long distribution chains can’t offer this level of truth. We field calls from research partners working late or facing a critical experimental bottleneck; nobody needs to wait for overseas approval or scramble for answers. Understanding the routine failures and unpredictabilities of synthetic organic chemistry brings empathy for those at the bench, and pushes us to keep improving, cycle after cycle.

    We do not rely on theoretical knowledge alone. Walking the lab floor, we see how humidity, minor equipment drift, or inconsistencies in chilling during workup affect the end product. The value in tightening these up becomes clear every time a client’s work proceeds uninterrupted, reactions lean toward expected yields, and no time is wasted troubleshooting raw material quirks.

    Environmental and Safety Realities

    Bromine and fluorine chemistry demands a level of respect for safety and waste management. Processes for 5-Bromo-2-Fluorobenzylamine Hydrochloride generate halogenated byproducts that need proper treatment. Our plant uses a combination of in-line scrubbers and closed systems. Not every operator appreciates these hazards until export or disposal headaches arise. Direct management of every step lets us minimize environmental footprint while keeping our team and clients protected from exposure. Regular third-party audits keep our procedures transparent and well documented.

    We found early that waste stream management should be proactive—not reactive. Approaching this product’s synthesis, our engineering teams trialed different catalyst and neutralization strategies, reducing hazardous outputs by over 25% in the last two years. Safety training goes hand-in-hand; our workforce receives regular updates, and we maintain clear documentation for regulatory compliance. This pays off during audits and, more importantly, keeps incidents rare.

    Product Evolution and Client Partnership

    5-Bromo-2-Fluorobenzylamine Hydrochloride has changed in more ways than just production technique. Feedback from end users—frustration about product stickiness, or surprise at improved purity—shapes our ongoing work. Almost every new lot can include small tweaks: a higher degree of dryness, changes in particle size, tighter packaging seals, or adjusted documentation for specific regulatory requests. We see the research and development cycle as a two-way street: our data and process improvements feed back into our client partnerships, raising the standard not just for us, but for the field as a whole.

    Many clients once struggled with downstream protocols, such as Boc protection or urea derivatization, when residual acids or salts complicated purification. Our support teams worked directly with their labs, jointly identifying small impurities as culprits, and then circling back to adjust our protocols. This level of collaboration makes for stronger, longer-term relationships. It also keeps us honest, rooting our improvements in tasks and setbacks shared at the research front line. Each success story—a peptide with clean coupling, or a fragment library built without supply snags—marks a tangible improvement over what we could claim years ago.

    The Ongoing Puzzle of Quality and Consistency

    Direct manufacturing feels at times like solving a never-ending puzzle. Products like 5-Bromo-2-Fluorobenzylamine Hydrochloride develop an identity around their details: composition, storage, packaging, and the absence—or presence—of almost invisible impurities. We chase away complacency. Every week delivers small surprises; what worked for one lot sometimes falters in the next, driven by upstream shifts or a change in one critical process parameter. Our teams invest in deliberate redundancy—cross-checking analytical data, re-running routine purity screens, and archiving samples for later review.

    Quality assurance means more than just getting an assay number above a certain mark. For clients in medicinal chemistry, a trace impurity can derail months of SAR work. One of our long-term pharmaceutical partners once traced a failed coupling to a sulfonate impurity we had not previously monitored. Learning from that, we extended our panel of tests, even when not explicitly requested. Research and manufacturing are dynamic and interconnected; our job is to anticipate needs before problems surface at the bench.

    Packaging That Matches Real-World Use

    Shipping and storing 5-Bromo-2-Fluorobenzylamine Hydrochloride isn’t just an afterthought. Early batches left our facility in basic glassware or simple liners, but recurring complaints about clumping and moisture absorption led us to rethink the process completely. Today, shipment happens only in double barrier pouches with a desiccant packet, sealed inside heavy-duty drums or laboratory-scale bottles, always under dry and inert gas. Each package includes batch-specific documentation—a detail frequently overlooked in broader supply chains. This approach avoids shipment loss and keeps the product ready for use, as feedback from hundreds of individual researchers has shown.

    Many of these improvements came from repeated failure and investigation. Minor particle migration or static build-up during transport used to cause unanticipated handling headaches; anti-static liners and powder funnel inserts now prevent these headaches. Experience here teaches humility—a product that looks perfect in our facility can change in unpredictable ways over the journey to your lab. Addressing this “last mile” detail directly means our clients work without avoidable delays or surprises.

    Transparency and Continuous Improvement

    With each batch of 5-Bromo-2-Fluorobenzylamine Hydrochloride, we document key parameters: source reagents, dates, operators, batch sizes, in-process yields, purity checks, and stability status. No number stands alone: before an order ships, every parameter is double-checked and signed by a dedicated supervisor. Questions about a past lot—whether three months or two years ago—drive us to pull up stored samples and data, always ready to trace back any issue.

    We support open communication about complications or unexpected test results from client laboratories. Each time a researcher brings up an anomaly, we work together to verify, reproduce, and resolve. Successful manufacturing is not a stand-alone achievement, but the result of learning from shared experience up and down the value chain. We look forward to a future built on this trust—rooted in quality, transparency, and shared experience in chemical science.