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4-Bromobenzamidine Hydrochloride

    • Product Name 4-Bromobenzamidine Hydrochloride
    • Alias 4-Bromo-benzamidine hydrochloride
    • Einecs 629-865-4
    • 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

    898615

    Product Name 4-Bromobenzamidine Hydrochloride
    Cas Number 88674-45-9
    Molecular Formula C7H7BrN2·HCl
    Molecular Weight 235.51 g/mol
    Appearance White to off-white solid
    Melting Point 228-232 °C
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms p-Bromobenzamidine hydrochloride
    Chemical Class Amidines
    Smiles C1=CC(=CC=C1C(=N)N)Br.Cl

    As an accredited 4-Bromobenzamidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromobenzamidine Hydrochloride

    Applications of 4-Bromobenzamidine Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we specialize in the production and supply of high-purity 4-Bromobenzamidine Hydrochloride for targeted industrial sectors. Our chemical plays a critical functional role in several advanced downstream applications across life sciences and specialty synthesis. Here we detail its principal uses, formulated for regulatory alignment and process efficiency.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies utilize 4-Bromobenzamidine Hydrochloride as an intermediate for API construction, especially for molecules featuring benzamidine moieties or halogenated aromatic scaffolds. It typically enters amidine formation reactions or halogen-substituted amination steps, supporting small-molecule drug development. Its high purity and controlled chloride content keep impurity profiles within regulatory allowances. Chemists adjust the charge ratio depending on the reaction pathway, ensuring complete conversion with minimal by-products and streamlined purification suited for cGMP batch production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for related intermediates
    • US FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • Chinese Pharmacopoeia (ChP) for import/export registration

    Typical usage ratio

    • 0.9—1.2 molar equivalents relative to the target aromatic core
    • Dose adjusted by molecular complexity and impurity targets

    Downstream process integration

    • Fed to the reaction vessel during key amination or condensation steps
    • Present in conversion routes for amidine-containing API lead structures
    • Integrated in multi-step flow chemistry synthesis lines

    Final product types

    • Small-molecule therapeutic APIs
    • Investigational New Drug (IND) intermediates for oncology or antivirals
    • Reference standards and analytical substances for regulatory submission

    2. Agrochemical Intermediate Manufacturing

    Leading agrochemical formulators select 4-Bromobenzamidine Hydrochloride as a key building block for synthesizing pesticidal and fungicidal actives with specific brominated aromatic backbone. Its reactivity profile allows efficient coupling or cyclization reactions under stringent batch control. Our material enables direct integration into scalable, regulated agrochemical production lines, mainly for triazole or benzamidine-derived actives. Compliance with environmental and toxicological assessment standards remains a primary consideration during all formulation and scale-up stages.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • China MOA pesticide registration requirements

    Typical usage ratio

    • 0.8—1.1 molar equivalents to final active ingredient target
    • Adjusted based on impurity limits and environmental residue analysis

    Downstream process integration

    • Used in ring closure or functional group insertion during active synthesis
    • Added during batch or semi-batch step for triazole derivative formation
    • Undergoes purification before downstream formulation with carriers

    Final product types

    • Triazole fungicides with benzamidine structures
    • Brominated pesticide actives
    • Seed treatment agents

    3. Diagnostic and Biomedical Reagent Synthesis

    Producers of diagnostic kits and research reagents use 4-Bromobenzamidine Hydrochloride to synthesize enzyme inhibitors and antibody affinity purification ligands. Its unique amidine moiety serves as a functional core for covalent immobilization and selective binding. Controlled purity and residual salt levels ensure minimal assay interference and facilitate scale-up for GMP or ISO 13485-suited reagent grades. The adjustment of addition ratios depends on the desired ligand density and specific protein affinity specifications.

    Industry compliance standards

    • ISO 13485:2016 for Medical Devices — Quality Management Systems
    • US FDA 21 CFR Part 820 for in-vitro diagnostic devices
    • REACH Regulation (EC) No 1907/2006 chemical registration

    Typical usage ratio

    • 0.5—1.5 molar equivalents relative to resin or conjugation base
    • Optimized by ligand saturation and batch assay validation

    Downstream process integration

    • Incorporated during resin activation and ligand immobilization
    • Used during coupling of functionalized beads for affinity chromatography
    • Combined into formulation steps for buffered diagnostic reagents

    Final product types

    • Affinity chromatography resins
    • Diagnostic inhibitor cocktail components
    • Purification reagents for protein R&D

    4. Specialty Chemical Synthesis — Polymer Additives

    Chemical companies incorporate this raw material in the design and manufacture of custom polymers featuring halogenated benzamidine groups. It acts as a functional monomer or end-group, allowing for advanced polymers with engineered interaction properties for coatings, membranes, or electrochemical devices. Our manufacturing supports regular lot validation to meet specific customer polymerization protocols and downstream end-use compliance needs in advanced materials sectors.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty chemical manufacturing
    • EU REACH and polymer-specific registration guidelines
    • ASTM D883 terminology for plastics

    Typical usage ratio

    • 1—5% by mol in copolymer composition
    • Adjusted for polymer chain length and targeted functionalization degree

    Downstream process integration

    • Charged with other monomers in batch reactor polymerization
    • Fed to solution or emulsion polymerization steps for surface-active polymers
    • Added post-polymerization for chain-end functionalization

    Final product types

    • Antifouling membrane materials
    • Conductive coatings for sensors
    • Specialty resins for selective separation

    5. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Dye manufacturers use 4-Bromobenzamidine Hydrochloride as a core intermediate in the preparation of specialty azo and reactive dyes requiring electron-rich amidine substitutions. Its precise bromine positioning and high batch-to-batch consistency make it suitable for synthesizing dyes with strict shade, performance, and fastness requirements. The material typically undergoes diazotization or further substitution in controlled reactors, according to customer-specific dye molecule designs.

    Industry compliance standards

    • ISO 14001 for Environmental Management in dye production
    • EU REACH restrictions related to azo compounds
    • Chinese National Standard GB/T for textile chemicals

    Typical usage ratio

    • Typically 0.7—1.3 molar equivalents for coupling or substitution steps
    • Varies by target chromophore structure and waste minimization goals

    Downstream process integration

    • Applied as precursor for diazonium salt production
    • Used in final coupling step of specialty pigment synthesis
    • Incorporated into continuous synthesis and finishing lines

    Final product types

    • Specialty azo dyes for textiles
    • Waterborne reactive dyestuffs
    • High-performance organic pigments
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    More Introduction

    Meet 4-Bromobenzamidine Hydrochloride: A Key Reagent for Research Progress

    Understanding 4-Bromobenzamidine Hydrochloride

    Among specialty chemicals, 4-Bromobenzamidine Hydrochloride holds a unique spot. Recognized by its chemical structure as C7H7BrN2·HCl, this compound often finds its way onto researchers’ benches as a staple reagent. Sporting a white to off-white crystalline powder form, it dissolves well in water, which makes it practical for a range of experimental setups. Typical packaging comes in sealed jars or amber containers, guarding it from moisture and light, which can keep the compound stable over time.

    A Personal Story from the Lab Bench

    In years spent exploring biochemical mechanisms, especially protein-protein and protein-ligand interactions, timely access to compounds like 4-Bromobenzamidine Hydrochloride felt like finding a shortcut through a complicated process. When an experiment needed a selective trypsin inhibitor or a reliable anchor for molecular modeling, this compound emerged as a true workhorse. Its performance rarely gets flashy headlines, but those slow, steady improvements it brings to protocols matter.

    Specifications That Matter to the Researcher

    The product comes with a notable purity benchmark—typically above 98%. This level of purity means results stay consistent and researchers deal with fewer surprises in assay readouts. Modern labs pay close attention to contaminants like heavy metals or unwanted anions, so suppliers often provide detailed batch analysis by HPLC or NMR, not just a simple COA. Reliable documentation means fewer interruptions for quality checks and smoother documentation for those writing up publication data or filing patent applications. I’ve personally avoided unnecessary troubleshooting simply by switching to a batch of 4-Bromobenzamidine Hydrochloride with clearly reported quality metrics.

    Why This Compound?

    Not all amidines handle bromine like 4-Bromobenzamidine Hydrochloride does. The para-positioned bromine atom shifts the compound’s reactivity profile, compared to its unhalogenated cousins. Chemists note improved binding affinity in some target classes, especially where electron-withdrawing groups tune ligand properties. That means researchers looking to make subtle structural tweaks in drug design often reach for 4-Bromobenzamidine Hydrochloride.

    The hydrochloride salt form also helps. It increases solubility in polar media—often necessary for biological assays or for clean-up steps such as chromatography. By contrast, the freebase form can sometimes behave sluggishly in solution or cause precipitation, putting long experimental runs at risk. Anyone who’s lost days because of cloudy buffers knows the headache that brings, especially before a big conference submission.

    Applications Across Scientific Fields

    Synthetic organic chemistry often revolves around precision and efficiency. 4-Bromobenzamidine Hydrochloride acts as a cornerstone for building more complex heterocycles (like benzimidazoles or triazines). Because the bromine site tolerates robust cross-coupling reactions—Suzuki, Heck, and others—it can be fitted with varied aryl or vinyl groups, expanding the reach of accessible molecules. I recall one collaborative effort in medicinal chemistry that streamlined a year’s work by tapping into just this property.

    Enzymology and protein chemistry also benefit. Researchers use it to inhibit serine proteases by mimicking substrate geometry, which makes it easier to study enzyme kinetics without runaway reactions. Reliable inhibition means more accurate measurement of enzyme concentrations and less variability in reported activity. To someone who’s tried to reproduce half a dozen enzyme assay protocols, these details carve the line between publishable results and another round of troubleshooting.

    Structural biology applications come up less in casual conversation but deserve mention. Some crystallographers use bromine-containing ligands like this one to aid protein structure determination. The anomalous signal from bromine atoms is valuable in phasing methods—a technical detail, perhaps, but one that often unlocks new levels of insight about protein folds or binding sites.

    What Sets 4-Bromobenzamidine Hydrochloride Apart?

    Several factors distinguish this compound in the lineup of benzamidine derivatives. The key difference is selectivity: while plain benzamidine blocks a range of proteases, the bromo-substitution at the para position modifies activity profiles. In drug lead discovery, being able to fine-tune molecular interactions—either dampening off-target effects or boosting affinity—matters for both efficacy and safety. Medicinal chemists sometimes remark that bromine handles like a little steering wheel, nudging molecules into better shape for docking or metabolism.

    The hydrochloride salt doesn’t just boost solubility; it keeps handling simple. Some competitive products force researchers to dissolve compounds in organic solvents, which can mess with downstream assays or require more waste management. With 4-Bromobenzamidine Hydrochloride, many protocols stick with water or buffer—a bonus for clean, straightforward work in both academic and pharma labs.

    Another point is stability. Not every amidine holds up well to open air or variable humidity. The hydrochloride form resists breakdown far longer under ambient conditions, reducing the need for repeated stock solution prep or fretful freezer storage. Anyone deep into kinetic assays or high-throughput screening appreciates not having to double-check compound freshness every week.

    Quality, Safety, and the Question of Trust

    Trust grows from predictable performance. Any chemical, especially one reserved for biological experiments, can’t just look white and powdery. 4-Bromobenzamidine Hydrochloride sourced from reputable suppliers will include trace metal analysis, moisture content reporting, and microimpurity data. Analytical labs use tools like HPLC, FTIR, and high-resolution MS to back up claims—so researchers can focus on the science, not policing impurities.

    On the safety front, 4-Bromobenzamidine Hydrochloride doesn’t carry hazards that immediately stand out in boldface compared to other lab reagents. Usual laboratory practices matter most: wearing gloves, using proper ventilation, and keeping logs. It pays to consult the SDS before the first use and follow institutional protocols. I’ve found that briefing the team once before a project kicks off saves everyone from stumbles halfway through.

    Supporting Reproducibility in Modern Science

    The reproducibility crisis in science isn’t just about statistics or experimental design—it’s about the building blocks themselves. When someone details their use of 4-Bromobenzamidine Hydrochloride and reports the supplier, model number, and batch analysis, that creates a firmer foundation for others to repeat and expand the research. Good documentation and consistently high-quality materials don’t just help the original researcher: they keep whole fields moving forward at a steadier pace. I’ve witnessed how switching from generic or uncharacterized amidines to rigorously evaluated 4-Bromobenzamidine Hydrochloride improved repeatability across multiple student projects in an academic setting.

    Barriers and Solutions in Sourcing

    Easy access to chemical reagents can’t always be taken for granted. Some parts of the world face import restrictions, high costs, or inconsistent supplier reliability. This tends to hit smaller labs and startups the hardest. One approach that makes a difference is building coop-style pooling agreements—so institutions in the same region purchase and share high-quality batches, lowering per-user cost and improving traceability.

    Online resources have also changed the game. Open-access forums now host peer reviews of chemical suppliers. Users share lot numbers and NMR scans, so the research community can collectively spot quality dips or supplier changes before they disrupt experiments. I’ve relied more than once on posted verification data to decide which supplier to trust for a critical order.

    Why Many Stick with This Compound

    Switching up key components in the middle of a research campaign eats up time and resources. 4-Bromobenzamidine Hydrochloride gets recommended through word-of-mouth or laboratory protocols because it performs predictably, batch after batch. In multi-year research trajectories, having constants matters—saving both troubleshooting cycles and, frankly, a lot of headaches.

    Competitive products exist, including other halogenated benzamidines or different amidine salts, but they don’t hit quite the same balance between solubility, stability, and selectivity. Some alternatives might suit very specialized needs—like alternative salt forms for organic synthesis under non-aqueous conditions—but for the majority, this hydrochloride’s broad compatibility wins out.

    Tips for Maximizing Success with 4-Bromobenzamidine Hydrochloride

    A few field-tested habits help keep experiments on track:

    The Bigger Picture: From Building Blocks to Big Discoveries

    4-Bromobenzamidine Hydrochloride might seem like a small piece in vast scientific machinery, but its real-world impact travels further than it looks on a stockroom shelf. Every discovery in enzymology, medicinal chemistry, or structural biology draws momentum from the reliability of the reagents at hand. When research groups find a product that offers clear documentation, batch-to-batch reliability, and a good shelf life, future findings become more robust—and the whole process gets a little faster, a little more trustworthy.

    This isn’t just about ticking boxes on a chemical order form. Behind each batch are teams focused on synthesis, purification, packaging, and shipping, making careful choices at every step to keep quality high. Users play a vital role in closing the loop—reporting back outcomes, sharing publication data, and flagging any quality issues early. The relationship between supplier and scientist builds resilience into the research ecosystem.

    Looking Forward: Needs and Innovations on the Horizon

    Innovation doesn’t stand still. There’s a rising demand for “greener” chemistry and reduced-waste manufacturing—even for specialty reagents. Some suppliers now focus on minimizing hazardous byproducts during amidine synthesis, or switching to energy-saving purification steps. Labs looking toward sustainable certification or LEED credits pay attention to these sources, knowing that every small improvement adds up.

    Digital infrastructure also gets better every year. Automated calibration, blockchain batch tracing, and QR-coded bottles now appear even for specialty chemicals. Keeping full transparency means not just knowing what’s in the jar, but also tracing its path from synthesis to bench. In future, widespread adoption of these digital tools can mean quicker recalls if trouble arises, faster troubleshooting, and new efficiencies for inventory management.

    Summary: Why Experience Makes the Difference

    Reliability doesn’t shout, but it shapes every experiment. Using 4-Bromobenzamidine Hydrochloride, countless researchers have gained sharper reproducibility, easier handling, and smoother workflows. These advantages echo through every round of troubleshooting skipped, every result confidently published, and every late-night eureka moment that stands up to a second look.

    Sometimes it’s the unsung ingredients that unlock new breakthroughs. 4-Bromobenzamidine Hydrochloride, with its distinct position among benzamidine derivatives, underpins a wide range of discoveries. Whether lending precision to syntheses, supporting sharp enzyme inhibition, or assisting with clear protein crystal phasing, this compound proves its value time and again. For those serious about building on a firm foundation, attention to quality and detail here pays long-term dividends across entire research careers.