Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Bromoisoindoline Hydrochloride

    • Product Name 4-Bromoisoindoline Hydrochloride
    • Alias 4-Bromo-2,3-dihydro-1H-isoindole hydrochloride
    • Einecs 696-195-9
    • 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

    642100

    Product Name 4-Bromoisoindoline Hydrochloride
    Cas Number 1416129-89-8
    Molecular Formula C8H8BrN·HCl
    Molecular Weight 250.53 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water and DMSO
    Purity Typically ≥98%
    Storage Condition Store at 2-8°C, protected from light and moisture
    Synonyms 1,3-Dihydro-4-bromoisoindole hydrochloride
    Smiles C1CN(C2=CC=C(Br)C=C2)C1.Cl
    Application Used as a pharmaceutical intermediate
    Hs Code 29339990

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

    Packing & Storage
    Packing
    Shipping
    Storage
    Application of 4-Bromoisoindoline Hydrochloride

    Applications of 4-Bromoisoindoline Hydrochloride in Industrial Manufacturing

    As a direct producer, we supply 4-Bromoisoindoline Hydrochloride to established sectors with proven, scalable applications. Our technical experience ensures support from bench trials to commercial implementation. Below, we outline leading application domains, highlighting regulatory adherence, recommended formulation ranges, integration points, and the range of final products manufactured by our industrial partners.

    1. Pharmaceutical Intermediates—Atypical Antipsychotic Synthesis

    In the pharmaceutical sector, this material serves a critical role as a building block in the synthesis of several second-generation antipsychotic agents, especially within the isoindoline-based compound family. Reactions utilize its bromo functionality for regioselective coupling, supporting scalable multi-step processes. Strict regulatory controls and trace impurity monitoring apply throughout the process, from raw material introduction during heterocyclization to the purification of the final API intermediates used in neuropsychiatric drug manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient (API) manufacturing
    • Ph. Eur. and USP specifications for pharmaceutical intermediates
    • FDA and EMA inspection guidelines on starting material traceability
    • Data integrity standards per 21 CFR Part 11 for batch record management

    Typical usage ratio

    • 0.85–1.05 molar equivalents per synthetic batch, adjusted by process yield and impurity allowance

    Downstream process integration

    • Introduced in the initial or early-stage condensation or Suzuki coupling step to deliver halogenated isoindoline cores for further functionalization

    Final product types

    • Pharmaceutical APIs—Isoindoline-derived antipsychotics, anxiolytics, and adjunctive therapy drugs
    • Registered intermediate substances for contract manufacturing (CMO/CDMO)

    2. Agrochemical Intermediate Manufacturing—Herbicide Synthesis

    This compound provides a highly effective starting point for advanced herbicidal active ingredient synthesis, where its structural features enable selective ring construction reactions. Leading agrochemical producers rely on its predictable reactivity for efficient steps in constructing active molecules targeting grass and broadleaf weeds. Quality assurance focuses on residue minimization and controlled release profiles, with compliance to agchem-specific production and registration criteria throughout synthesis and downstream processing.

    Industry compliance standards

    • ISO 9001:2015 certified production protocols for agrochemical intermediates
    • FAO Manual on Development and Use of FAO Specifications for Plant Protection Products
    • China GB/T 1604-2008 for technical material purity in pesticide APIs
    • EU Regulation (EC) No 1107/2009 & US EPA FIFRA framework for product registrations

    Typical usage ratio

    • 0.9–1.2 moles per mole of target herbicide precursor, modified per conversion efficiency and downstream purification requirements

    Downstream process integration

    • Charged in the first or second condensation step to introduce halogen functionality prior to cyclization or amidation stages in active ingredient synthesis

    Final product types

    • Formulated herbicidal active ingredient technicals
    • Bulk intermediates for further synthetic modification (e.g., halogenated isoinolin derivatives for selective herbicidal agents)

    3. Specialty Chemical Manufacturing—Functional Dye Precursors

    This compound is implemented in the specialty chemical sector as a core intermediate for the synthesis of advanced dye molecules, especially for coloring applications in electronics and high-performance fiber industries. Its bromo group activates nucleophilic substitution and cross-coupling reactions, vital for installing conjugated systems in specialty dyes. Process control extends through high purity blending and color stability validation, addressing both international chemical safety and specialty textile coloration standards.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for dye precursor registration
    • Oeko-Tex Standard 100 for restricted substance requirements in textiles
    • ISO 9001 for chemical manufacturing traceability
    • Compliance with ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) recommendations

    Typical usage ratio

    • 15–30% by mass in functional dye precursor formulations; exact ratio based on dye type and color depth requirements

    Downstream process integration

    • Dosed during initial coupling or cyclization stage, allowing further extension or variation in dye structure via Suzuki or Buchwald–Hartwig chemistries

    Final product types

    • Functional colorants for OLED and electronic displays
    • Specialty fiber dyes for high-performance technical textiles
    • Optical filter dyestuffs for industrial imaging applications

    4. Organic Electronics—Small Molecule Semiconductor Materials

    Electronic material producers integrate this intermediate for the construction of organic semiconductors and charge transport materials used in thin film transistors and photovoltaic layers. Its unique bromo-functionalized isoindoline core provides a nucleation site for electron transport extension, critical for molecular engineering in high-mobility, solution-processable organics. Production specifications focus on impurity profile control, with comprehensive batch release validation targeting stringent electronics industry requirements.

    Industry compliance standards

    • IEC 62899-202 Standard for printability in printed electronics
    • RoHS Directive 2011/65/EU for hazardous substances control
    • ISO 14001:2015 for environmentally responsible manufacturing
    • OEM-specific purity metrics and electronic grade raw material supply protocols

    Typical usage ratio

    • 5–25% by mole in organic semiconductor precursor syntheses, adjusted for device architecture and molecular weight targets

    Downstream process integration

    • Loaded during oligomer extension or ring closure, preceding substitution reactions in fabrication of conjugated electronic molecules

    Final product types

    • Organic light-emitting diode (OLED) charge transport layers
    • Small molecule semiconductors for TFT and flexible electronics
    • Solution-processable photovoltaic active materials

    5. Fine Chemical Production—Photoinitiator Precursors

    Within the fine chemical domain, formulators use the compound to prepare photoinitiator intermediates for UV-curable coatings, inks, and adhesives. Its reactivity supports selective halogen exchange and subsequent incorporation into aryl ether structures with precise absorption characteristics, demanded by UV-cure formulators. Each stage maintains rigorous documentation and QA according to chemical and industrial end-use legislation, with continuous in-line purity verification throughout synthesis and blending operations.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for quality and environmental management during fine chemical production
    • Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances
    • Substance registration per TSCA (US) or KKDIK (Turkey) for chemical imports
    • Product-specific EN 15051 for workplace exposure controls in powder handling

    Typical usage ratio

    • 10–18% by weight in photoinitiator synthesis, determined by target photo-crosslinking efficiency and absorption profile needed

    Downstream process integration

    • Fed into the key arylation or halogenation stage to set UV absorption wavelength parameters before final product isolation and formulation

    Final product types

    • Photoinitiator active compositions for UV-cured coatings
    • UV inkjet ink additive blends
    • Bonding adhesives with precision light-activation profiles
    Free Quote

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

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

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 4-Bromoisoindoline Hydrochloride: Setting a New Standard in Fine Chemical Applications

    Looking Beyond Standard Reagents

    For years, chemists and researchers have chased reliable reagents that can integrate seamlessly into the workflow and drive real, measurable progress. Having sorted through stacks of generic catalogues, I often felt the tedium—lists of substances, all promising purity but few delivering performance that stands out. 4-Bromoisoindoline Hydrochloride upends this monotony, stepping forward as a true asset for innovators in organic synthesis, drug discovery, and chemical development.

    Distinctive Features Shaping Choice

    4-Bromoisoindoline Hydrochloride, with its unique indoline backbone and a strategically placed bromine at the 4-position, brings a balance of reactivity and manageability. Its chemical fingerprint isn’t just a formality—chemists gravitate toward this compound specifically for transformations where selectivity matters. The hydrochloride salt ensures it stays solid and manageable at room temperature, which simplifies handling compared to some of the free base analogs out there that can be oils or unstable in air.

    My own experience in bench-scale synthesis made me appreciate the difference between a standard building block and one that behaves predictably under rigorous lab conditions. Given a molecular formula of C8H8BrN·HCl, chemists typically receive a white to off-white crystalline powder. Its melting point—often checked as a matter of good lab practice—tends to fall within a reasonable, easily managed range, far apart from the unpredictable behavior of similar unrefined indoline derivatives.

    Precision in Modern Synthesis

    Pure, well-characterized intermediates open pathways that impure or overly reactive alternatives could block. The bromine at the 4-position isn’t just decoration; it unlocks access to Suzuki coupling reactions and various aromatic substitutions. Researchers can build upon this atom-efficient compound to reach new heterocycles, aromatic scaffolds, or introduce additional halogenation, all while sidestepping the persistent issues of by-product formation that so often plague multi-step sequences.

    In my work supporting process development teams, I’ve seen 4-Bromoisoindoline Hydrochloride outperform generic halogenated indolines in both consistency and yield. After all, nobody needs another product that saps morale because it appears pure on paper, then gives inconsistent conversion and leaves everyone guessing about what went wrong.

    Addressing Key User Needs

    Time in the lab is too precious for guesswork caused by uncertain specifications. Standard sources of 4-Bromoisoindoline Hydrochloride commit to traceable purity—commonly surpassing 98%. For teams concerned with trace metal or residual solvent contamination, high-purity lots come with certificates of analysis. Analytical data such as NMR, HPLC, and MS are not luxuries here—they become routine checks.

    A reliable compound helps streamline route scouting, lead optimization, or process scale-up. For contract research organizations, that means fewer surprises when delivering to pharmaceutical partners. I’ve relied on the dependability of this hydrochloride salt more than once when troubleshooting synthesis setbacks; its consistency saved both resources and reputation, especially when facing tight project deadlines.

    Comparing With Other Building Blocks

    Stack 4-Bromoisoindoline Hydrochloride side by side with its closest cousins—say, 4-chloro or unsubstituted isoindolines—and some clear differences emerge. The bromine’s properties offer a halfway point: more reactive than chlorine, yet less so than iodine, striking a manageable rate for Suzuki couplings or Buchwald–Hartwig aminations.

    I remember testing several halogenated indolines for a late-stage modification. The iodine compound worked fast but degraded under our conditions, kicking up side-products. The chloride was sluggish, making purification a nightmare. The bromo compound stood out—reacted thoroughly, minimal by-products, and clean workup. Paper comparisons can’t capture the hours—or weeks—saved with the right choice.

    Handling and Safety Observations

    Although 4-Bromoisoindoline Hydrochloride doesn’t rank among the most hazardous lab chemicals, every chemist is taught to approach any new reagent with healthy skepticism. Store in a dry, well-ventilated place away from direct sunlight and incompatible acids or bases. Not all handling advice is created equal: relying on properly sealed containers—moisture intrusion can affect performance or clumping, especially if environmental controls are lacking over weekends or holidays.

    My years organizing shared chemical spaces hammered home that little details, like robust bulk packaging or the right desiccant packs, matter far more than manufacturer guarantees. No researcher relishes returning on a Monday only to find reagents caked together and unusable—a scenario less likely with a stable hydrochloride salt.

    Impact on Research and Industrial Outcomes

    Research teams crave leverage in competitive environments. Academia prizes reproducibility just as much as pharma demands scalability. 4-Bromoisoindoline Hydrochloride slides comfortably into both settings. With its solid performance, it reliably serves as a springboard in medicinal chemistry campaigns, where logbooks track precious milligrams and synthetic steps stack up by the dozen.

    It’s about more than reaction schemes or cost per gram. Consider the high stakes during library generation or fragment-based drug design. With finite budgets and pressure to deliver hits, even minor inconsistencies in starting materials derail months of planning. My colleagues and I once mapped out a dozen indoline-based derivatives, only to have to rerun a third of the routes after discovering a batch of inferior starting material sabotaged early steps. Once we switched exclusively to verified 4-Bromoisoindoline Hydrochloride, those detours dwindled.

    Where It Fits In Modern Synthesis Strategies

    The road to innovative compounds often winds through nitty-gritty bench work—aromatic substitutions, cyclization, derivatization. 4-Bromoisoindoline Hydrochloride doesn’t dominate headlines, but it underpins reliable transformations in both small-scale methods and bulk production. Its modest profile conceals its ability to influence both prototype development and commercial synthesis.

    Process chemists appreciate that certain crude intermediates can linger in “maybe it’ll work” territory for months before someone delivers a tightly specified, easy-to-reorder variant—something this product offers. Pathways that looked difficult become routine as robust reagents like this one lower the probability of failed runs and convoluted purifications.

    Broadening Applications—Moving From Lab to Scale-Up

    Academic groups might use grams as they chase new chemical space. Industry teams can quickly scale to kilograms without revalidating old routes. I’ve watched startups pivot overnight from medicinal chemistry to pilot production—with only minor tweaks needed in protocols thanks to the qualities of this compound. This feels increasingly important as timelines shrink and the push to demonstrate proof-of-concept speeds up across the sector.

    In contract manufacturing, flexibility is king. The hydrochloride salt form facilitates easier weighing, less static charging, and fewer headaches compared to more volatile, oilier alternatives. It cuts out one more small—but essential—variable that could otherwise gum up automated dispensing or batch vessel transfers.

    Environmental and Regulatory Considerations

    Stringent attitudes now surround the chemicals that enter pharmaceutical and agricultural supply chains. Concerns about trace impurities, heavy metals, or solvent residues trace back to the reliability of the starting materials. High-purity 4-Bromoisoindoline Hydrochloride fits tighter regulatory benchmarks set for fine chemicals used directly or indirectly in new molecular entities. Its wide distribution through reputable channels adds layers of confidence, both for regulatory audits and for securing downstream Quality Assurance.

    Over the last decade, I’ve observed more regulatory agencies scrutinizing supplier documentation, lot traceability, and even minor synthetic by-products. Being able to offer clean, certificate-backed batches of 4-Bromoisoindoline Hydrochloride gives project managers an edge, whether they’re dealing with an internal review or an external audit.

    Rough Edges—Facing Challenges

    It’s easy to overstate the case for any reagent in a catalog. Like all halogenated aromatics, 4-Bromoisoindoline Hydrochloride must still fit the right project. Some reactions demand higher reactivity; others need substitution patterns the 4-position can’t accommodate. For highly functionalized targets or rare transformations, the indoline backbone might not line up with the strictest needs. There’s no universal solution, but stacking your toolkit with a versatile, consistent performer removes more roadblocks than it creates.

    Some users have flagged issues sourcing ultra-high-purity lots at very large scale, especially if they expect tight tolerances on polymorphism or particle size. I haven’t personally faced this snag, but I’ve sat in project meetings where late-stage process tweaks spiraled because a kilo-lot varied ever so slightly from a research-grade sample. More dialogue with suppliers—about particle morphology, re-crystallization solvents, or trace impurity analysis—almost always solved these challenges before they mutated into production delays.

    Solutions for Real-World Demands

    The finest results emerge from a blend of tight analytical controls and close partnerships between buyers and technical support. Don’t wait until a hiccup disrupts the workflow—build feedback into procurement, track lot history, and request supporting analytical data from trusted vendors. In practice, I’ve seen research directors rejig project charts simply because one reliable building block arrived ahead of schedule, plus an up-to-date Quality Assurance report landed in their inbox without having to chase a supplier a dozen times.

    For companies scaling from preclinical work into regulatory submission, this proactive approach dovetails with QbD—Quality by Design—principles now often expected by regulators. The hydrochloride form also spares one step in salt formation, side-stepping an added variable during final purification in the lab or plant module.

    Choice Shaped by Experience and Fact

    Product literature and catalog “descriptions” might jumble together a string of claims, but frontline users—chemists, engineers, pharmaceuticals scientists—look for more. Over a decade of practical lab work, I’ve grown to prioritize reliable sources, responsive support, and full access to batch-level analytical data. Every gram of 4-Bromoisoindoline Hydrochloride has to meet real-world expectations, not just check boxes on a specification sheet.

    As a seasoned hand in organic synthesis and scale-up, I’m not swayed by glossy brochures. Instead, I’ve come back to this compound specifically for projects that reward consistent yields, manageable storage, and reproducible outcomes. It’s the difference between passing an internal milestone and watching a promising lead vanish beneath a pile of troubleshooting tickets. From collaborating with academic teams to steering contract development projects, that trust becomes decisive.

    The Path Forward—Continuous Improvement

    Markets, techniques, and target molecules shift year by year. Laboratories push boundaries, and manufacturing teams seek more streamlined, greener, higher-outcome processes. High-purity, analytical-verified 4-Bromoisoindoline Hydrochloride occupies a spot in most advanced chemistry toolkits. Suppliers who listen to researchers’ needs for tighter control over impurities, solvents, and salt forms remain ahead in the race.

    While nobody in the chemical sciences expects miracles from a single reagent, more researchers share feedback and data with manufacturers—sometimes pointing out gaps in documentation, sometimes urging development of finer grades for specialty applications. In my career, I’ve joined roundtables that direct vendor leaders to extend their support—batch histories, expert troubleshooting, even training for new grad students finding their feet in advanced synthesis.

    Practical Use Cases and Impact Stories

    As more researchers document their work in publications, case studies, and patent filings, the role of 4-Bromoisoindoline Hydrochloride keeps expanding. In the literature, it anchors fragment coupling, heterocycle creation, and targeted amine construction efforts. Each project captures a different facet of its utility—academic groups proving mechanisms, pharma teams generating patentable derivatives, and CROs aiming to streamline offerings.

    Tales abound of stalled campaigns resurrected by a switch to purer, verifiable lots—sometimes through a single direct phone call to a dedicated account manager who digs up the right analytical certificate or gets a fresh batch issued overnight. One cannot overestimate the importance of substances that fit into these workflows, with qualities known, documented, and trusted.

    Whether it’s academic research or industrial late-stage functionalization, knowing you have access to a compound with this degree of reliability changes the pace of discovery. The impact skips beyond the lab bench. It rolls through decision meetings, Intellectual Property filings, regulatory dossiers, and investment pitches built on auditable, reproducible claims.

    Supply Chain and Future Prospects

    Direct conversations with technical sales and R&D support teams have strengthened my confidence in top-tier supply chains supporting 4-Bromoisoindoline Hydrochloride. Transparency in logistics, priority for climate-controlled transit, and backup inventory stand out as invaluable supports, especially during the supply disruptions that have hit the chemical market in recent years.

    As supply chains entangle further with regulatory requirements, suppliers who document batch origin, keep thorough transit logs, and offer live QC tracking win trust. No researcher can afford to roll the dice on uncertain sourcing. Secure packaging, tracked shipments, and responsive shipments make life easier for both lab managers and procurement leads.

    Looking ahead, demands on specialty building blocks will likely grow. Contract manufacturing organizations, biotech startups, and scale-up facilities want more certainty, not less. It’s safe to say that as these standards rise, 4-Bromoisoindoline Hydrochloride will keep deserving a place in project plans for both straightforward derivatizations and ambitious, multi-step campaigns.

    Final Thoughts

    Every chemical product tells a different story once it leaves the catalogue page and reaches the reality of the laboratory. For those of us committed to results—data-backed, reproducible, and reliable—the choice of starting materials matters sharply. Years of hands-on synthesis, scale-up consulting, and working through regulatory ladders have distilled my criteria for what defines a “go-to” compound. 4-Bromoisoindoline Hydrochloride has earned that status, not through grand claims, but from steady, on-the-ground performance, responsive support, and clear analytical data that eases the day-to-day grind of modern chemistry.

    With each successful run, every resolved bottleneck, and all the incremental advances in molecular design, a dependable reagent proves itself over and over—quietly supporting the search for tomorrow’s breakthroughs.