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7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One

    • Product Name 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One
    • Alias Bromazepam
    • Einecs 827-432-1
    • 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
    VTB
    Specifications

    HS Code

    163632

    Iupac Name 7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one
    Chemical Formula C15H10BrClN2O
    Molecular Weight 349.61 g/mol
    Appearance White to off-white crystalline powder
    Cas Number 107007-99-0
    Melting Point 220-225°C
    Solubility Slightly soluble in water, soluble in organic solvents like ethanol and DMSO
    Boiling Point Decomposes before boiling
    Density 1.56 g/cm³ (approximate)
    Pubchem Cid 10482662
    Smiles C1C(=O)NC2=CC=CC(Br)=C2N1C3=CC=CC=C3Cl
    Storage Conditions Store at 2-8°C, keep in a dry, well-ventilated place
    Synonyms Bromazepam intermediate, 7-bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

    As an accredited 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 5g amber glass vial, sealed with a tamper-evident cap, and labeled with safety and identification details.
    Shipping The chemical `7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One` is shipped in tightly sealed containers, protected from light and moisture. It is packed according to regulatory guidelines for hazardous substances, with proper labeling and documentation. Transport occurs via certified carriers, ensuring safety and compliance with local and international shipping regulations.
    Storage Store **7-Bromo-5-(2-Chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one** in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances. Ensure the storage area is secure and access is restricted to authorized personnel. Follow all local, state, and federal regulations for chemical storage and handling.
    Application of 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One

    Applications of 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One in Industrial Manufacturing

    7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One serves as a key intermediate in pharmaceutical manufacturing and fine chemical synthesis. As the original producer, we supply this raw material to multiple specialized downstream users operating within strictly regulated industrial segments. The following sections outline specific use cases across actual industrial application pathways.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Anxiolytic Drugs

    Pharmaceutical manufacturers utilize this compound primarily in the synthesis of benzodiazepine-based APIs targeted at central nervous system therapy. Production requires validated GMP process frameworks due to the stringent quality demands for human-use pharmaceutical intermediates. Formulators introduce the compound during the penultimate stage of API assembly, where controlled reaction parameters are set to ensure selectivity and minimize contamination risk. Final APIs produced from this route form the core ingredient for prescription anxiolytic medications distributed to global markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4 Part II
    • U.S. FDA 21 CFR Part 210/211 (cGMP for finished pharmaceuticals)
    • Ph. Eur., USP, JP monographs for benzodiazepine derivatives

    Typical usage ratio

    • 0.7–1.1 molar equivalents as dictated by stoichiometry in final API stage
    • Precise ratio adjusted for target batch size and critical impurity control

    Downstream process integration

    • Charged into the penultimate condensation or substitution reaction reactor
    • Follows isolation and purification prior to final API crystallization
    • Integrated within closed-system reactors to ensure containment

    Final product types

    • Benzodiazepine anxiolytics (e.g., formulations for diazepam or clonazepam analogues)
    • Psychotropic API ingredients for research and clinical use

    2. Custom Synthesis of Reference Standards for Analytical Laboratories

    Analytical reagent suppliers use this molecule in the development of benzodiazepine reference standards vital for quality control testing and forensic analysis. Chemical purity and traceability are mandatory, and batch documentation aligns with international testing guidelines. The raw material undergoes secondary synthesis and purification protocols to achieve purity above 99.5%, ensuring accurate calibration references for industry and government labs. End-use typically involves micro-scale aliquoting and certified packaging.

    Industry compliance standards

    • ISO 17034:2016 General requirements for the competence of reference material producers
    • ISO/IEC 17025:2017 Testing and calibration laboratories
    • Certificates of Analysis (CoA) for each lot

    Typical usage ratio

    • Starting material at 98–99.5% purity (input level: typically 10–50 g per batch)
    • Exact mass depends on the standard set production demand

    Downstream process integration

    • Processed in multi-step synthesis and finishing for analytical-grade reference substances
    • Recrystallized and then micro-dosed into certified vials under cleanroom conditions
    • Verification through LC-MS, GC-MS, and NMR ensures batch compliance

    Final product types

    • Certified benzodiazepine reference standards
    • Test kits for pharmaceutical QC laboratories
    • Traceable analytical controls for toxicology and forensic science labs

    3. Intermediate in Contract Manufacturing of Specialty Benzodiazepine Derivatives

    Contract development and manufacturing organizations (CDMOs) access this chemical for custom projects involving specialty benzodiazepines, which serve niche therapeutic research and intellectual property extension programs. The ratio and route of use are tightly specified according to individual process development agreements, which may include scale-up from laboratory to pilot-plant quantities. Manufacturers maintain electronic batch records and process analytics to support regulatory submissions and patent filings.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • US FDA Drug Master File (DMF) requirements
    • cGMP operations under client-validated protocols

    Typical usage ratio

    • 0.5–1.3 equivalents depending on process design and targeted analogues
    • Ratio subject to project-specific yield, impurity profile, and downstream reactivity

    Downstream process integration

    • Employed during key functionalization or bridge formation steps
    • Synthesized under inert atmosphere, moisture control, and precise temperature cycling
    • Transferred by automated transfer lines into downstream continuous manufacturing reactors

    Final product types

    • Novel benzodiazepine chemical entities for early-phase clinical trials
    • Patent-expired drug intermediates customized for generic formulation

    4. Precursor for Fine Chemical Production in Research Chemical Supply

    Specialty fine chemical suppliers incorporate this molecule into the production of pure research-grade benzodiazepine compounds requested by academic laboratories and medicinal chemistry programs. Synthesis often occurs under small-batch or campaign-mode settings, with detailed batch traceability and solvent management to comply with chemical handling guidelines. Compounds synthesized from this precursor support preclinical research, biological pathway exploration, and structural activity studies.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for research and development
    • REACH Substance Registration (for the EU market)
    • UN Recommendations for the Transport of Dangerous Goods

    Typical usage ratio

    • 1.0–1.6 equivalents, based on the functional group conversion efficiency
    • Adjusted according to batch size (typical ranges 0.1–5 kg per campaign)

    Downstream process integration

    • Charged as main starting base in reflux or sealed tube reactions
    • Purified via preparative chromatography and solvent displacement
    • Packaged and labeled for direct research use by institutional laboratories

    Final product types

    • Research-only benzodiazepine analogues
    • Milled small-pack samples for medicinal chemistry studies
    • Tools for assay and bioactivity screening platforms
    Free Quote

    Competitive 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One: A Manufacturer’s Perspective

    Understanding 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One

    On the factory floor, chemistry isn't just a series of reactions in a vessel—it’s a deliberate process that demands attention to detail and practical insight. We produce 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One—a molecule engineered with precision and tracked all the way from raw material selection to finished batch. Colleagues in downstream industries refer to this compound by its chemical structure rather than catchy names, because what matters is what it does and how it performs under real-world conditions.

    Model, Batch and Quality Realities

    Every time we run a batch, we commit to a consistent model of synthesis designed for reliability at scale. We stick to precise stoichiometry, temperature control, and careful monitoring of intermediates. The result: a white to off-white solid, crystalline, with a purity that repeatedly tests above 99%. There isn't much patience here for unexplained yield drops or wandering impurity profiles. Our chemists track every variable—reaction times, solvent grades, filtration codes, and drying techniques—so the final product meets strict reproducibility standards batch after batch.

    Our facility’s equipment, from jacketed glass reactors to automated HPLC, isn’t there for show. These investment decisions stem from years of hard lessons about what can go wrong—a drift in water content, a heat spike, solvent contamination, or unforgiving variances in halogen reactivity. Hands-on experience counts at this stage. Technicians identify each lot by tightly controlled reference samples and not just by a series of lab numbers. That is the only way to maintain confidence with every outgoing shipment.

    Why Choose this Benzodiazepine Core?

    7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One fits into a narrow but critical space in the benzodiazepine family. Our process builds in the 2-chloro group on the phenyl ring and the 7-bromo substituent on the benzodiazepin core without requiring exotic reagents or unstable intermediates. This approach gives end users a stable base compound, with a heavy focus on limiting by-products that could interfere with later transformations—especially those involving amination, alkylation, or acylation steps.

    Comparing this material to broader-spectrum benzodiazepines, its unique substitution pattern changes both its reactivity and profile in downstream chemistry. Most labs using our product are not searching for general-purpose intermediates; they demand exactly this compound for well-justified reasons, usually linked to structural-activity studies, finished drug synthesis, or as marked reference standards. Our own workbench surveys have shown that the combination of bromo and chloro positioning relieves the synthetic chemist from multiple steps of protection and deprotection, translating directly into lower waste and reduced cycle times.

    By the Numbers: Specifications and Purity

    Routine purity checks rely on a battery of methods—high-performance liquid chromatography for percentage and organic volatility, melting point for physical identity, and NMR for fine structure confirmation. Solvent residuals matter to OEM partners, so we run GC and Karl Fischer titrations as part of release protocols. Each kilogram or smaller custom package passes through a rigorous inspection. On-site staff carry out hands-on verification, weighing, and final packing. This isn’t just a regulatory tickbox—missing a contaminant or skipping a simple water test can cascade to major project setbacks at the user’s end, especially if they're working at scale or in pharmaceutical environments.

    Over several years, we’ve observed that minor specification drift often exposes deep-rooted issues—a problem with the crystal lattice, a micro-impurity that interferes with downstream halogen-metal exchanges, or an unreported batch of poorly purified starting material. Fixing these repeatedly has sharpened our readiness to adapt and improve SOPs in real time. There’s no shortcut here; every identified outlier means extra weeks in troubleshooting and validation.

    Usages Driven by Experience, Not Guesswork

    Demand for this compound comes from cutting-edge medicinal chemistry research, particularly teams engaged in new drug design. Some use this benzodiazepinone as a direct pharmacophore in their structure-activity research, exploring subtle differences in biological affinity driven by halogen placement. Others treat it as a protected scaffold as they build more complex molecules, leveraging its stability to explore variant analogues. Our product gets used in a variety of research, from CNS pipeline targets to experimental studies in receptor pharmacology.

    Getting technical support requests sheds light on real challenges faced downstream. A frequent topic: crystallization and compound handling. Even a slight shift in the dryness or particle size can impact later reactions or automated dispensing. Researchers reach out with questions about particle flow, reactivity under different solvent conditions, or persistence during chromatography. Having seen many of the same challenges in our own labs, we give feedback grounded in experience—not just theory. If a batch sticks, clumps, or dissolves unevenly, we refine granulation steps or adaptive drying protocols and retest under customer-specific conditions.

    What Sets this Compound Apart

    Real differentiation starts with understanding what goes wrong in the production and downstream use of similar benzodiazepine-like intermediates. Several competing products on the market take shortcuts at various points: skipping secondary drying, outsourcing early-stage formulation to less controlled facilities, or failing to monitor for ring-opened impurities. We get called to help troubleshoot these failures—sticky cakes, off-color fractions, or unexplained NMR signals—by labs that tried alternate suppliers.

    We build our value on upstream control. All starting materials pass in-house inspection. The intermediates, especially the halogenated precursors, undergo full profile characterization before scaling. Rejecting a suspect batch of 2-chlorophenyl starting material is standard, even if it means rerunning the whole synthesis. As for final handling, we pack under inert atmospheric conditions, seal packages immediately, and include chain-of-custody documentation—not for regulatory appearance, but to back up every gram shipped.

    Another important difference reflects the purification approach. Some suppliers rely on basic crystallization or minimal filtration. Our process incorporates multistep purification involving recrystallization with carefully chosen solvents and, if needed, column chromatography to ensure that not only visible impurities but also trace by-products are out of the way. We aim for the benchmark standards demanded by regulated markets, even if the final repository is a research lab.

    Facts About Handling, Stability, and Downstream Use

    Any compound’s reputation survives only as long as it proves robust beyond idealized lab settings. 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One faces multiple tests in scale-up environments: thermal cycling during transport, exposure to ambient humidity, or prolonged storage in drafty lab cabinets. Our own stability studies, born from necessity after seeing failed batches arrive at end-use sites, highlight a few critical truths.

    This compound prefers low humidity and cool, protected environments—ideally under nitrogen or argon for long-term storage. Neglected moisture barriers can introduce hydrolytic degradation, visible as color drift or, less obviously, as shifts in mass spec profiles. To counter this, we implemented double-barrier packaging: primary sealed bags within tight-sealing containers, both purged and tested for leaks after packing. Direct feedback from after-sales support shows significant improvement in product stability, cutting the incidence of user-reported failures by more than half.

    Shipping partners receive explicit instructions about transit temperatures and minimum handling times. Each courier ticket includes a log of conditions and time stamps, so we can trace back any shipping mishap. This hands-on approach stops compound degradation before it starts, protecting the integrity researchers rely on.

    Quality Control Without Shortcuts

    We don’t pretend that chemistry at a manufacturing scale is ever free of surprises. Production teams constantly train and retrain—taking pointers from observed errors, customer complaints, or unexpected shelf-life data. Every time an anomaly creeps into a batch, open review cycles involve analytical chemists, QC leads, and production staff together. Routinely, we update standard operating procedures to reflect new analytical insights or better filtration protocols.

    One of the most revealing lessons arrived when a series of external labs flagged a low-level impurity missed by the supplier’s checks at that time. It took a combined effort of method redevelopment, external reference calibration, and blind spike testing to ferret out the trace contaminant. The end result was not just a remedied product, but a permanently revised QC method, an instruction set now benchmarked for all similar arylated benzodiazepine derivatives.

    Quality, by our measure, means being willing to halt a run if analytical doubts arise, even with scheduling pressure. We put accuracy over output, as every faulty shipment harms long-term relationships—partners remember errors far longer than on-time but under-characterized product delivery.

    Supply Chain and Feedback Loop

    Every production cycle begins with careful sourcing. We refuse to compromise on upstream suppliers. Reagents, especially halogenated aromatics, require thorough identity and purity checks before unloading. Our sourcing managers work with a limited set of long-term suppliers whose reliability passes year-by-year scrutiny. Anything uncertain triggers source substitution or even celebration postponement, because shipping out substandard material isn't worth the downstream disruption.

    Our customer feedback loop crosses continents, as research labs and drug development teams send back observations and suggestions. Every formal complaint triggers a root cause review. In one instance, a persistent but low-level odor from a specific lot led to a complete overhaul of solvent choice and recovery systems. Users should feel confident that their shipments meet expectation not due to chance, but through deliberate, repetitive validation at every stage.

    Supporting Responsible and Safe Use

    Safety concerns run deep for us, as handling halogenated benzodiazepinones brings real risks—both to our team and to those working farther down the line. We invest in continuous training, not as a compliance gesture, but because on-the-ground experience shapes safety culture more effectively than reciting checklists. Reports of off-gas reactions or accidental spills don’t get swept away. Instead, teams dissect these incidents to extract lessons, building an in-house knowledge base that supplements standard literature.

    We stress clear labeling, full documentation, and transparency about known risks or limitation. Even with high-purity material, benzodiazepinones like this require attentive handling under fume hoods and vigilant waste management. Following proper risk assessments and robust PPE policies go beyond a regulatory checkbox—they prevent real injuries in actual workspaces. Documentation packages include all available safety data, exposure limits, and suggestions for safe scaling up.

    Ongoing Improvement—Feedback Fuels Innovation

    This product’s journey from the reactor to the end-user’s bench never truly ends. Each batch shipped out represents both an achievement and a new opportunity. Customers return time and again with difficult questions on reactivity, compatibility with new reagents, or underappreciated process improvements. Our R&D team takes these as direct challenges. In some cases, user feedback on purification steps sparks new innovations in solvent recovery, energy use, or even greener process routes. The most creative ideas don’t come from the top down, but from daily troubleshooting and true collaboration with partners.

    For instance, difficulties dissolving the compound under specific buffers led us to develop granulation and micronization options on request. Other customers requested more tailored solvent packaging, so we upgraded our storage and mini-batch delivery system, allowing for flexibility in shipping and reduced waste at the user's end.

    Industry Trust Built on Experience and Results

    The market rarely gives second chances for quality lapses, and word of mouth in this field travels fast. Over time, our track record earned the trust of top-tier organizations—from independent medicinal chemistry labs focused on exploratory synthesis to mature pharma outfits running controlled process scale-up. Most partners stick with us after small trial orders, often referencing consistency, reliability, and the absence of unpleasant surprises.

    In the rare event problems occur, ownership and rapid response set the standard. We keep open lines with end-users, reviewing specifications, proposing workaround solutions, or even replacing shipments at our expense where justified. Every lesson enters our internal knowledge bank, helping refine both processes and outcomes for future production runs.

    Looking Forward: Challenges and Solutions

    As research and industry expectations grow more sophisticated, maintaining a bench-to-factory supply chain for 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One presents both headaches and opportunities. Scaling up without losing control of key parameters calls for constant attention to equipment maintenance, staff education, and data-driven process tweaks. The molecule’s reactivity means that even slight protocol deviations can ripple through project timelines.

    We see opportunities in sustainability as well—optimizing solvents, recycling waste streams, and minimizing halogenated byproducts. Feedback from green chemistry advocates has shaped recent internal projects, like closed-loop purification and solvent swap systems. These changes not only cut costs but also address regulatory and environmental scrutiny, a reality every chemical manufacturer must face.

    Day-to-day, our team approaches every production cycle of 7-Bromo-5-(2-Chlorophenyl)-1,3-Dihydro-2H-1,4-Benzodiazepin-2-One with the same mindset: careful, tested, and open to iteration. Each kilogram leaving our site carries not only the compound, but the accumulated experience of a manufacturer who knows that chemistry remains unforgiving of careless shortcuts, yet rewards patient, disciplined effort.