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2-Amino-4'-Bromoacetophenone Hydrochloride

    • Product Name 2-Amino-4'-Bromoacetophenone Hydrochloride
    • Einecs EINECS 629-725-7
    • 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
    VTB
    Specifications

    HS Code

    234173

    Product Name 2-Amino-4'-Bromoacetophenone Hydrochloride
    Molecular Formula C8H8BrNO·HCl
    Molecular Weight 250.52 g/mol
    Cas Number 5869-04-7
    Appearance Light yellow to beige solid
    Purity Typically ≥98%
    Melting Point 203-208°C
    Solubility Soluble in water and polar organic solvents
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms 2-Amino-1-(4-bromophenyl)ethanone hydrochloride
    Structural Formula C8H8BrNO·HCl
    Safety Hazards May cause irritation to skin, eyes, and respiratory tract

    As an accredited 2-Amino-4'-Bromoacetophenone Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 25 grams of 2-Amino-4'-Bromoacetophenone Hydrochloride, screw cap sealed, labeled with hazard and product details.
    Shipping 2-Amino-4'-Bromoacetophenone Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. The package complies with regulations for chemical transport, typically using robust, leak-proof packaging and appropriate hazard labeling. Temperature-stable environments are maintained, and all handling follows safety guidelines to prevent exposure or contamination during transit.
    Storage 2-Amino-4'-Bromoacetophenone Hydrochloride should be stored in a tightly sealed container, away from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizing agents. Always follow standard chemical storage protocols and ensure proper labeling for safe handling and identification.
    Application of 2-Amino-4'-Bromoacetophenone Hydrochloride

    Applications of 2-Amino-4'-Bromoacetophenone Hydrochloride in Industrial Manufacturing

    2-Amino-4'-Bromoacetophenone Hydrochloride is a key compound widely implemented in specific organic synthesis routes across the pharmaceutical, agrochemical, and specialty chemical industries. Our in-house production ensures consistent quality that aligns with the diverse requirements of downstream manufacturers. Below, we detail its principle application scenarios, including regulatory benchmarks, practical addition levels, integration into industrial workflows, and the resulting end-use products.

    1. Pharmaceutical Intermediate in Active Pharmaceutical Ingredient (API) Synthesis

    This compound serves as an advanced intermediate in the preparation of a range of pharmaceutical agents, particularly those involving bromo-substituted aromatic amines as core scaffolds. API manufacturers use it during core amide coupling or heterocycle construction steps, where controlled halogenation and amination are required, frequently for targeted oncology and antiviral drug molecules. Its batch-to-batch reproducibility supports multi-step GMP synthesis campaigns, which demand consistency in impurity profiles and specification controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs (if applicable in later stages)
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia (ChP) pre-API guidance

    Typical usage ratio

    • Reactant loading typically ranges from 0.5 to 1.2 molar equivalents relative to main substrate per reaction stage, adjusted according to target molecule and yield optimization; higher-end dosing is selected for steps with low conversion recovery.

    Downstream process integration

    • Material is charged after initial aromatic amino protection step, frequently as a key building block in the sequence preceding cyclization or functional group transformation; handled under inert nitrogen and dry conditions to prevent hydrochloride hydrolysis before use.

    Final product types

    • N-aryl substituted heterocycles (intermediates)
    • API candidates undergoing further derivatization
    • Pharmaceutical bulk actives post-processing

    2. Agrochemical Intermediate (Herbicide and Pesticide Synthesis)

    Agrochemical companies utilize this material as a precursor for synthesizing bromoacetophenone-based intermediates, which are subsequently transformed into selective herbicides or insecticidal compounds. Precision in substitution patterns achieved via its use enables more effective binding properties and better crop protection characteristics, and ensures downstream formulations remain within regulated impurity profiles for environmental application.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemical active ingredients
    • FAO/WHO Manual on the Development and Use of FAO and WHO Specifications for Chemical Pesticides
    • Regulation (EC) No 1107/2009 (EU)

    Typical usage ratio

    • Typically 0.8–1.5 molar equivalents per synthetic transformation, based on targeted yield and minimization of potential side reactions; higher ratios used in multi-substrate condensation reactions to maximize conversion rates.

    Downstream process integration

    • Integrated after halide exchange or nitration steps; introduced during condensation or coupling reactions for producing key intermediates prior to formulation blending and granulation.

    Final product types

    • Intermediate compounds for herbicidal products
    • Pre-formulation concentrates for pesticide actives
    • Active technical materials for post-processing

    3. Fine Chemical Manufacturing for Specialty Dye Intermediates

    Producers of specialty dyes deploy this building block in the synthesis of bromoaniline derivatives which impart unique lightfastness and color properties to textile and ink formulations. Consistent lot quality mitigates variability in chromophore formation and supports batch reproducibility critical for large-scale pigment manufacturing. Reaction control and impurity minimization are particularly important given downstream coloration and textile standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for dye intermediates (relevant for textiles)
    • REACH Regulation (EC) No 1907/2006 (EU) requirements for specialty chemicals
    • ISO 14001 Environmental Management

    Typical usage ratio

    • Applied at 0.6–1.0 equivalent per colorant precursor batch, fine-tuned based on chromophore structure and desired intensity; higher end for deeper shade dyes.

    Downstream process integration

    • Enters the diazotization or coupling stage following amino group functionalization, supporting direct pigment synthesis or as precursor for sulfonation and other derivatizations.

    Final product types

    • Azo dye intermediates
    • Bromoaniline-based pigments for specialty inks
    • High-performance textile colorants

    4. Research and Development (R&D) in Chemical Synthesis

    Chemical research institutes and innovation labs use this hydrochloride as a model substrate for the development of new organic synthesis methodologies, particularly for C–N and C–Br bond activation reactions. Structured sample lots support process optimization studies, impurity mapping, and mechanistic research for new synthetic routes targeting complex molecules. Strict traceability and high documentation standards are necessary to support publication- and patent-level research activities.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation
    • GLP (Good Laboratory Practice) for R&D synthesis
    • Material transfer and handling documentation as per institutional policy

    Typical usage ratio

    • Standard procedural test runs employ 0.1–1.0 mmol scale reactions in kinetic studies; scale-up studies adjust input material for each experimental design, often not exceeding 2 mmol per batch.

    Downstream process integration

    • Compound is introduced at the designated reaction step according to the specific experiment—usually in closed-vessel synthesis for safety and reaction pathway elucidation.

    Final product types

    • Reference intermediates for synthetic development
    • Analytical standards for mechanistic studies
    • Lead compounds for preclinical candidate screening
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    Certification & Compliance
    More Introduction

    2-Amino-4'-Bromoacetophenone Hydrochloride: Quality Matters in Specialty Chemistry

    The Realities of Working with 2-Amino-4'-Bromoacetophenone Hydrochloride

    We have spent years navigating the challenges and small victories that come with making 2-Amino-4'-Bromoacetophenone Hydrochloride for researchers and manufacturers. Little in this world sits still; that includes the chemistries demanded in the pharmaceutical and fine chemical sectors. This compound remains a regular request, not because it's the simplest to handle, but because it performs reliably in crucial synthesis steps, especially for advanced heterocyclic structures and key pharmaceutical intermediates.

    In our production line, we typically achieve purity levels above 99.5% as measured by HPLC, with batch-to-batch consistency verified through routine GC-MS and NMR analysis. Physical appearance ranges from off-white to pale yellow crystalline powder. Even slight differences in color can result from trace starting material variations, but what matters is the underlying consistency of the chemical backbone. Water content usually sits well below 0.5% thanks to careful drying and storage in sealed drums with desiccant pouches. We do not cut corners on those steps, since moisture leads to clumping, and clumping means headaches both for us and for downstream users.

    Why Users Rely on This Compound

    In our direct conversations with R&D chemists, most trace their need for 2-Amino-4'-Bromoacetophenone Hydrochloride to its role as a versatile building block rather than an end-use substance. Medicinal chemists favor its aminoketone motif for targeted syntheses, particularly in the production of substituted benzophenones, oxazoles, and benzimidazole derivatives. A few decades ago, access to functionalized acetophenones with both amine and halogen out-groups meant long routes with inefficient yields. Modern synthesis depends on short, robust steps—and this product fills one of those gaps.

    Our approach starts with the raw selection of acetophenone derivatives, tracking back two or three tiers deep in the supply chain. Some producers use low-grade precursors that introduce colored impurities and chemical instability. We favor fractionally distilled and chromatographically purified inputs, always. Customers tell us they notice: direct crystallization works better, HPLC chromatograms show cleaner peaks, and downstream protection or coupling reactions require less rework.

    Model, Packaging, and User Feedback

    Our standard offering weighs in at 250-gram or 500-gram net packs, though several bulk contracts have seen single-lot deliveries exceeding 10 kilograms. Vacuum-sealed, double-layer PE bags inside HDPE containers keep the compound stable during international transit, whether that's by sea or air. The label often includes real production batch data—yield percentage, spectroscopic fingerprints, and purity checks—because some buyers want more than just the word “high-purity.”

    Some end users ask about granule size or filtration properties; we note that most production falls within the 50–120 mesh size range. Granularity can matter for handling in automated feeders, but for those weighing by hand at the bench, it’s rarely a concern.

    We took feedback from university and industrial labs to adjust this—sometimes researchers want less dust, sometimes quick dissolvability. Real, hands-on input shapes batch parameters more than any spec sheet created for marketing.

    Comparisons with Similar Compounds

    It’s easy to overlook how minor changes in substituents change the behavior of an acetophenone derivative. We have fielded many calls—often from high-throughput pharma groups—seeking either the free base, the bromide, or the hydroxy analog. The hydrochloride salt generally offers superior stability in ambient environments, with better resistance to hydrolysis and atmospheric moisture than either the free base or acetic acid salt. That means longer shelf life and less degradation-related waste.

    Some users who switch from 2-Amino-4'-Chloroacetophenone Hydrochloride find reactivity slower in key coupling steps, largely because of the differing halogen effects on the aromatic ring. The bromo compound delivers a better balance between reactivity and selectivity in palladium-catalyzed aminations and heterocycle closures, and experienced process chemists notice yield increases as well as easier purification in those downstream steps.

    A frequent question comes up from custom synthesis labs: “Can I just swap in 2-Amino-4'-Bromoacetophenone free base?” Not easily. The hydrochloride salt form gives better solubility in polar solvents and forms cleaner solutions for controlled reactions. Free base stocks are prone to slow oxidation and occasional off-odors, indicating minor impurities. Only in highly moisture-controlled environments do those risks disappear.

    Handling, Storage, and Real-World Constraints

    Even with robust packaging, we’ve seen labs skip proper storage—leaving a freshly opened drum on a humid shelf, for instance. Clumping, caking, and stickiness show up quickly, so we always recommend sealed storage in low-humidity cabinets. Temperature plays its part. Labs in tropical regions sometimes report product softening or minor discoloration, particularly if exposed to sunlight. We learned to ship product in insulated containers for certain destinations. These are lessons you only pick up after dozens of hard-earned delivery reports.

    On the production side, this compound requires scrupulous exclusion of trace iron and copper. Undesirable transition metal contamination can catalyze unwanted side reactions and compromise product integrity. Years ago, we diagnosed a recurring off-color in one customer’s finished pharmaceutical ingredient. We traced it back to metal contamination in a single lot of this intermediate. The cause? A filter housing swap that introduced a new grade of steel with poorer surface finish. We retooled the filtration setup with PTFE, and the returns to normal purity were immediate.

    In every batch, the final step involves drying under controlled vacuum at low temperature, followed by triple-checking water content. There is no shortcut here—the least amount of retained moisture impacts both solubility and physical appearance. Afterward, we conduct spot checks for residual solvents. Meeting pharmacopeial limits protects both the downstream user and, ultimately, the integrity of client research.

    Transparency, Traceability, and Supply Security

    Several years ago, a batch of imported 2-Amino-4'-Bromoacetophenone Hydrochloride hit our market at unusually low price. Upon investigation, it failed NMR testing and delivered irreproducible results in Suzuki reactions. Transparency matters—producers should document batch lineage, testing protocols, and raw material sources. We issue signed certificates of analysis, and when asked, we provide 2D NMR and chromatogram datasets, not just surface-level PDFs.

    Traceability practices changed in recent years, especially after some high-profile contaminant scares in the pharmaceutical industry. Buyers want to know how often a lot gets tested, or which subcontractor handled the packaging. Our records log every stage from initial synthesis to drum filling, noting who signed off at each checkpoint. If an issue arises, we trace back in hours, not weeks. Real peace of mind grows from this operational discipline.

    Supply reliability is another hard-won lesson. A few years back, a raw material shortage in one upstream specialty chemical left our output bottlenecked for nearly a month. We diversified sources and keep safety stocks adequate for three months of forecasted orders. That way, buyers don’t wait for their R&D timelines or process launches. Consistent supply isn’t always flashy, but in real-world chemical manufacturing, reliability trumps a few cents of savings every time.

    Sustainability and Process Refinement

    Attention has shifted toward greener syntheses and more environmentally conscious practices. Manufacturing 2-Amino-4'-Bromoacetophenone Hydrochloride traditionally generates halogenated waste and uses significant solvent volumes. Several years ago, we retrofitted our reactors with solvent recovery units, bringing solvent recycling rates up to 95%. That slashed annual disposal costs while reducing environmental footprint—the local water treatment facility confirmed a drop in trace halogen load in their intake by half.

    R&D teams work on milder halogenation conditions. In the early days, process steps called for extended high-temperature reflux and strong oxidants. Today, improvements let us run reactions at lower temperatures with less corrosive agents, boosting both yield and safety. We stopped using carbon tetrachloride long ago and phased out hazardous chlorinated solvents entirely in favor of greener alternatives. Lessons learned on the shop floor—such as unblocking condensers or rebalancing reflux rates after a process tweak—feed straight back into each next optimization cycle.

    Waste minimization extends to packaging too. Poly drums are returnable after one-time internal liner replacement, and we encourage buyers to reuse if their protocols allow. Smaller quantities ship in recyclable, antistatic pouches, a change that came directly from lab manager feedback about powder loss and static charges building up inside cheap LDPE bags. These practical adjustments save money and downtime just as much as they save landfill space.

    Long-Term Perspective from the Lab Bench and the Factory Floor

    Walking the factory floor at shift change, we hear stories directly from line chemists—about how minor tweaks to pH adjustment or stirrer blade angle bettered crystal formation and cut down filtration times. These seemingly minor improvements often matter more to final product usability than adjustments spelled out in any paper. In the lab, our process chemists keep tabs on how incremental batch data accumulates. This continuous performance monitoring drives future process tweaks, shaping a product that’s less a generic commodity and more a tool that end users can count on, year after year.

    This approach—grounded in feedback, hard data, and respect for small but crucial process details—lets us deliver 2-Amino-4'-Bromoacetophenone Hydrochloride that professionals trust. We field regular questions from field scientists about batch suitability for specific peptide coupling sequences, or whether our salt form supports regioselective addition in their in-house synthetic targets. Our reply never dodges the nuances. Instead, we draw from our test records, our accumulated experience, and the direct feedback from those same scientists. The product on the shelf today reflects years of these exchanges.

    Practical Applications and Synthesis Pathways

    In pharmaceutical R&D, the main users pull this intermediate off the shelf for multi-step syntheses, especially where aromatic halogenation is required as a precursor to C–N or C–C bond formation. The positioning of the amino and bromo groups means chemoselective transformations take place smoothly, minimizing the unpredictability of side reactions. It slots naturally into synthetic sequences for several classes of kinase inhibitors and custom heterocyclic compounds. Performing Suzuki, Buchwald–Hartwig, and Ullmann couplings calls for substrates that don’t fall apart in the presence of palladium or copper complexes. Over the years, chemists have told us this particular hydrochloride form gives higher yields than its free base analog.

    One small pharmaceutical firm ran a direct comparison—side-by-side runs with in-house synthesized versus our commercial grade. Their result: cleaner crude after condensation, faster crystallization, and solvent use reduced by 15 percent. We continue to gather these third-party case studies, using them to inform future adjustments to the process, packaging, and quality checks.

    Beyond pharma, dye manufacturers sometimes request custom batch sizes. In dye intermediates, amine protection and subsequent halogen exchange go more smoothly owing to the product’s robust salt form. In agricultural research, molecules closely related to this structure serve as bioactive agents or monitoring tags, and the hydrochloride provides reliable shelf stability during long shipping times to international testing fields. This reflects our experience that, while the pharmaceutical sector is the largest user base, specialty chemicals that don’t degrade under light are gaining traction in broader industries too.

    Day-to-Day Challenges in Manufacturing

    Making 2-Amino-4'-Bromoacetophenone Hydrochloride involves its fair share of day-to-day challenges. The bromo-selective synthesis needs control at each temperature ramp to avoid dimer and trimer formation. Waste heat can easily destroy product or generate off-odors, so process supervision means active management, not passive observation. Workers track shifts in color and particle formation visually at each filter cake separation—records show small but important differences between operator groups and even time of day for optimal syrup removal. Only long-term experience reveals which minute changes make for cleaner end product.

    Safety never takes a backseat. We supply operators with appropriate PPE and continually revise work instructions to reflect practical hazards encountered, such as dust accumulation in enclosed auger systems or static discharge near the bagging line. These stories hardly make glossy reports at industry conferences, but they define the real-world manufacturing landscape. For us, talking openly about these issues with downstream buyers builds trust that goes beyond simply selling a commodity.

    Openness: Key to Progress

    We do not claim perfection in every batch. Minor issues crop up—a slightly lower melting point or faintly stronger odor on occasion—usually tracing to upstream raw material changes or rare fluctuation in process water quality. Bringing these quirks to our users’ attention rather than sweeping them aside builds credibility and, over the years, forges strong partnerships. It also means many of our customers come to us first when they need derivative variants or new salt forms for exploratory chemistry.

    This openness means we readily share full analytical records, and send sample packs for user QC ahead of full delivery. We listen when buyers report unexpected chromatogram results—often those findings point to edge cases not documented in the literature. Our philosophy: real progress in specialty chemistry grows from continuous communication, operational discipline, and sharing lessons learned.

    The Path Forward

    Looking forward, 2-Amino-4'-Bromoacetophenone Hydrochloride will continue to hold a valuable place in modern chemistry. As synthetic strategies evolve, requirements for regulatory compliance, safety, and environmental stewardship will tighten. For us, these drivers aren’t barriers, but opportunities to iterate and refine, to build stronger working relationships, and to participate actively in a community where reliable, thoroughly characterized products fuel discovery and innovation. Every improvement—be it in purity, handling convenience, packaging, or process safety—comes from lived experience and ongoing dialogue with our customers. That is a future worth building, one batch at a time.