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1-Acetyl-5-Bromoindoline

    • Product Name 1-Acetyl-5-Bromoindoline
    • Alias 1-Acetyl-5-bromo-2,3-dihydro-1H-indole
    • Einecs 700-849-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    755332

    Chemicalname 1-Acetyl-5-Bromoindoline
    Molecularformula C10H10BrNO
    Molecularweight 240.10 g/mol
    Casnumber 883531-58-2
    Appearance White to off-white solid
    Meltingpoint 95-98°C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, dichloromethane; slightly soluble in water
    Smiles CC(=O)N1CC2=C(C=C(C=C2)Br)C1
    Inchi InChI=1S/C10H10BrNO/c1-7(13)12-6-8-4-2-3-9(11)5-10(8)12/h2-5H,6H2,1H3
    Storagetemperature 2-8°C, keep container tightly closed
    Synonyms 5-Bromo-1-acetylindoline

    As an accredited 1-Acetyl-5-Bromoindoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 1-Acetyl-5-Bromoindoline, securely sealed, labeled with chemical name, purity, and safety information.
    Shipping 1-Acetyl-5-Bromoindoline is typically shipped in tightly sealed containers to prevent contamination and degradation. It is classified as a chemical substance and should be transported according to local and international regulations. Handle with care, store away from incompatible materials, and ensure proper labeling for safe and compliant delivery.
    Storage 1-Acetyl-5-Bromoindoline should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from sources of heat and ignition. Protect it from moisture and direct sunlight. Store it separately from oxidizing agents and strong acids to prevent possible hazardous reactions. Proper chemical labeling and secure storage are advised to ensure safety.
    Application of 1-Acetyl-5-Bromoindoline

    Applications of 1-Acetyl-5-Bromoindoline in Industrial Manufacturing

    As the original manufacturer of 1-Acetyl-5-Bromoindoline, we supply this specialty intermediate to selected industrial sectors with proven, reliable downstream deployments. Our focus remains on its precise integration into pharmaceutical synthesis, agrochemical development, advanced material research, pigment precursor chains, and specialty chemical production—where its chemical structure supports well-documented formulation and scale-up operations. Below, we outline the specific industrial applications, referencing industry compliance, recommended usage levels, process locations, and final goods established in these sectors.

    1. Pharmaceutical Active Ingredient Synthesis (API Intermediates)

    1-Acetyl-5-Bromoindoline serves as a specialized intermediate in multi-step syntheses for select active pharmaceutical ingredients featuring indoline core scaffolds. It remains vital in routes where halogenated or N-acyl-indoline fragments are introduced for antimicrobial, anxiolytic, or CNS-targeted drug development pipelines. The intermediate typically enters after initial coupling stages to enable further functionalization or cyclization, with process conditions strictly governed by pharmaceutical-grade GMP and impurity control protocols. Final APIs must satisfy region-specific regulatory frameworks before commercialization.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) requirements for starting materials and intermediates
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)
    • Chinese Pharmacopoeia intermediate quality standards

    Typical usage ratio

    • Employed at 0.4–1.2 molar equivalents relative to initial indoline or preceding scaffold intermediate in multi-kilogram synthesis campaigns; ratio adjusted based on desired yield and route specificity for target API structure

    Downstream process integration

    • Added after core indoline formation or cyclization step; reaction carried out in polar aprotic solvents (e.g., DMF, DMSO) under controlled temperature
    • Subsequent steps feature further functional group transformations (such as halogen-metal exchange, reductive amination, or acylation)
    • Intermediate holds for in-process QC before conversion to API

    Final product types

    • Small-molecule APIs for central nervous system disorders
    • Antibacterial/antifungal agents incorporating indoline structures
    • Intermediates for branded and generic pharmaceutical formulations

    2. Crop Protection Compound Manufacturing (Agrochemical Intermediates)

    In crop protection R&D and large-scale agrochemical manufacturing, formulators use 1-Acetyl-5-Bromoindoline as a key intermediate when synthesizing certain insecticide and herbicide molecules that require bromo-substituted indoline rings. Its halogen functionality provides a handle for downstream cross-coupling or heterocycle formation, particularly in the assembly of selective mode-of-action agents. The integration of this raw material is subject to identity, purity, and trace impurity specifications as mandated by agrochemical quality systems and national pesticide regulations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • FAO/WHO guidelines for technical pesticide grade intermediates
    • GB 3796-2019 (China National Standard for pesticide production)
    • EU Regulation 1107/2009 (Plant Protection Product regulations)

    Typical usage ratio

    • Typically 0.8–1.5 equivalents per target synthetic scheme, adjusted depending on downstream pathway efficiency and final active ingredient substitution positions

    Downstream process integration

    • Introduced at the indoline core assembly stage prior to aromatic bromine displacement or Suzuki-Miyaura cross-coupling reactions
    • Reaction run in batch reactors under inert atmosphere; crude products isolated prior to further derivatization
    • Process monitored for residual indoline impurities and halide content

    Final product types

    • Intermediate and technical-grade insecticides
    • Precursor molecules for selective herbicides
    • Plant growth regulator synthesis intermediates

    3. Organic Pigment and Dye Precursor Production

    Within the specialty pigment and dye sector, downstream manufacturers utilize 1-Acetyl-5-Bromoindoline to enable structural diversification and color tuning of indoline-based chromophores. The brominated acetyl structure supports site-specific coupling reactions essential for synthesizing pigments with tailored electronic and optical properties, particularly for use in specialty inks, plastics coloration, and high-performance coatings. Stringent controls over trace impurities and color consistency are enforced under pigment regulatory standards.

    Industry compliance standards

    • ISO 18451-1 (Pigments and extenders—definitions and methods)
    • EU REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals)
    • FDA 21 CFR 74 Subpart B (Color Additives for Plastics and Inks)
    • Rohs/ELV for coloring components in electronics

    Typical usage ratio

    • Used at 1.0–2.5% molar basis in pigment precursor syntheses; the ratio is modulated based on chromophore ring extension requirements and light fastness targets

    Downstream process integration

    • Fed into condensation or cyclization stages where bromine enables directed cross-coupling
    • Subsequent purification relies on column chromatography or precipitation depending on desired pigment purity level
    • Final dye lots validated for hue, tinting strength, and trace residues

    Final product types

    • Organic pigments for plastics compounding
    • Disperse dyes for textile printing
    • Solvent-based coloration for coatings and inks

    4. Advanced Functional Material Development (Electronic and Optoelectronic Components)

    Material R&D teams employ 1-Acetyl-5-Bromoindoline as a chemical building block in the development of high-performance electronic and optoelectronic materials, particularly where indoline derivatives contribute to charge transport, molecular alignment, or dielectric properties. Applications include organic semiconductors, specialty resins for photolithography, and photoresponsive films. Manufacturing processes require consistent lot-to-lot composition, and final products face validation in accordance with semiconductor and electronics industry requirements.

    Industry compliance standards

    • IEC 60747-1 (Semiconductor devices—General requirements)
    • ISO 9001:2015 for supply chain traceability
    • JEDEC JESD46 (Procedures for part change notifications)
    • REACH and RoHS substance restrictions

    Typical usage ratio

    • Range from 0.5–1.3 molar equivalents in functional polymer or oligomer syntheses depending on target electronic properties and component architecture

    Downstream process integration

    • Inserted at monomer feed stage in polymerization or oligomer extension reactions, such as Stille or Heck couplings
    • Product isolation follows via solvent extraction and re-precipitation to remove unreacted intermediates
    • QC testing for conductivity, purity, and molecular weight distribution

    Final product types

    • Organic photovoltaic layer components
    • Light-sensitive resins for microfabrication
    • Organic thin film transistors (OTFTs)

    5. Specialty Fine Chemical Synthesis

    Manufacturers of niche fine chemicals turn to 1-Acetyl-5-Bromoindoline for fragment assembly in products such as analytical reference compounds, chemical probes, and molecular tools. Its structure provides a gateway to custom indoline analogs through controlled substitution or cross-coupling reactions, with high purity and defined isomer ratios mandatory for downstream applications. Formulation and isolation strategies are designed to prevent cross-contamination and support quality claims relevant to laboratory and industrial scale supply.

    Industry compliance standards

    • ISO 17034 (Reference material producers—General requirements)
    • USP/NF for laboratory chemical reagent purity assessment
    • ISO/IEC 17025:2017 for testing and calibration laboratories
    • Safety Data Sheet (SDS) compliance under GHS for chemical handling

    Typical usage ratio

    • Typically 0.2–0.8 molar equivalents within targeted synthesis, with scaling examined case-by-case for specific molecular tool or probe generation

    Downstream process integration

    • Enters at substitution or cross-coupling phase; subsequent purification by HPLC or crystallization to achieve analytic purity
    • Batch tested for isomeric content, impurity spectrum, and batch traceability

    Final product types

    • Analytical standards for laboratory QC
    • Chemical probes for bioscience and pharmaceutical research
    • Specialty intermediates for fine chemical catalogs
    Free Quote

    Competitive 1-Acetyl-5-Bromoindoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Acetyl-5-Bromoindoline: A Practical Choice for Fine Chemical Synthesis

    Product Overview from Our Own Production Line

    From our years mixing reagents and troubleshooting reactors, 1-Acetyl-5-Bromoindoline stands out as a versatile building block in pharmaceutical and agrochemical synthesis. We pour a lot of expertise into every batch, keeping a close watch on purity and yield since downstream results depend on it. Our process has moved from pilot to full-scale production, and in that journey, we’ve ironed out every hitch connected to crystallization, purification, and handling stability. Getting reproducible, moisture-free material means fewer surprises for the chemists in the next stage, and that's something we take to heart.

    Physical Profile and Key Properties

    You’re looking for a compound that holds up well on the bench, delivers in solution, and doesn’t degrade under light lab conditions. 1-Acetyl-5-Bromoindoline presents as an off-white crystalline solid—no sticky residues, no cloudiness. Our product meets demanding specifications, with typical purities over 99% by HPLC, and we keep moisture levels below 0.5% to avoid side reactions. This allows for easy weighing and dependable solubility in common solvents such as dichloromethane, ethyl acetate, and even lower alcohols.

    Our proprietary process ensures the N-acetylation is clean. Every lot is free from unreacted indoline, so you won’t chase after byproducts or mixed signals in your spectra. This isn’t just theoretical lab talk. We confirm each delivery with real QC, not just COA figures, pulling random samples and verifying impurity profiles. That’s cut downtime for our regular clients, who are tired of chasing mystery peaks during their scale-ups.

    How We See Demand: Roots in Custom Chemistry

    Academic research groups and pilot drug development teams keep coming back for 1-Acetyl-5-Bromoindoline. It’s a favored intermediate when introducing an indoline motif—particularly with bromine offering a reactive handle for cross-coupling or further functionalization. If your route uses Suzuki, Buchwald-Hartwig, or Ullmann-type coupling, you’ll notice how the bromo position keeps options open for a wide range of linkages. That alone makes it more attractive than the plain indoline or acetylindoline variants that lack the halo functionality.

    We see the shift in modern medicinal chemistry toward modular synthetic networks. Having a pre-acetylated, brominated indoline out of the drum offers chemists more freedom to assemble analogs, without going through multistep raw material upgrading. The bottom line is time saved and higher creative turnover in the lab. Since we produce it ourselves, we notice demands shift as more groups look to expedite SAR campaigns or even optimize new pesticide leads.

    Why Chemists Prefer This Over Other Indoline Derivatives

    Off-the-shelf indolines often lack the specific mix of protection and reactivity. N-acetylation blocks unwanted side reactions and improves the selectivity in C–C and C–N bond formation. Chemists working with simple 5-bromoindoline run into trouble with multiple alkylations, polymerization, and tracking two N-based impurities that complicate things. By acetylating at the outset, we've cut out those headaches. The bromine at the 5-position isn’t just tacked on for show—it gives you the leverage for late-stage diversification, whether you're adding aryl, alkyl, or heteroaryl units through palladium, copper, or nickel catalysis.

    Compared to mono-functional or unprotected indolines, 1-Acetyl-5-Bromoindoline brings down byproduct formation and simplifies purification in both solution and solid-phase synthesis. This results in fewer purification cycles and better yields, especially noticeable when moving from gram to multi-kilogram scale. We developed our process to minimize nitrosamine and polybrominated impurities; these are critical from a regulatory and safety viewpoint, especially for any pharma client preparing for IND submissions.

    Handling and Storage: Lab-Proven Stability

    Our team has run stability studies under both controlled and open conditions. 1-Acetyl-5-Bromoindoline stores well at ambient temperatures, with no significant degradation noted over a year’s time, even under typical warehouse fluctuations. That's based on our own accelerated aging tests. You can open a drum and return for more, weeks later, without worrying about browning or odorous breakdown. For labs requiring milligram to kilogram quantities, that means less waste, fewer reorder rushes, and predictable inventory management.

    No one wants capricious solids that transform into oily masses or draw moisture. Early pilot lots taught us what tweaks were necessary—adjusting crystallization solvents, optimizing dryer times, and investing in nitrogen-purged packing lines. These updates weren't window dressing—they came from direct feedback from our own analytical staff and partners downstream. Now, our drums and bottles ship with protective liners that genuinely make a difference, not just a label claim.

    Uses in Research, Scale-Up, and Commercial Production

    Pharmaceutical R&D takes the lion’s share of volume, but advanced material researchers also rely on our 1-Acetyl-5-Bromoindoline for new dye and pigment concepts. Our product features in several patent filings linked to kinase inhibitor precursors, serotonin analogs, and CNS drug candidates. We also see crop science teams adapt this indoline for new herbicide scaffolds, where the acetyl and bromo groups open pathways for targeted ring closures.

    Because we manufacture and not merely resell, we get to collaborate directly with process chemists and troubleshoot with their engineers. We hear how the crystalline product simplifies dissolving, speeds up homogeneity, and tolerates a wider range of process conditions. More than once, a shift from a basic bromoindoline to our acetylated version meant one fewer distillation or a simpler workup.

    Often, a chemist is pressed for purity in late-stage intermediates, especially before building up more elaborate molecules. Crude brominations or acetylations performed in-house can cut corners, but they increase risk in regulated environments. Our customers have shown us their chromatograms—bands cleaner, fewer extraction steps, less time on the rotavap. That’s a difference measured not by slogans, but by achieved throughput.

    Operational Differences: Direct Production Means Better Consistency

    We’ve fielded plenty of questions about trace metals, residual solvents, and batch-to-batch consistency. Many of those problems stem from material funneled through two or three distributors, sometimes with little control over original process changes or plant hygiene. Our setup gives us the opportunity to adopt single-solvent operations, internal scavenging columns, and robust in-line analytical controls. There's no relabeling or repacking from unverified sources.

    Some competitors dilute the product into blends or introduce variable crystal forms. These shortcuts might meet short-term price targets but end up costing more downstream through increased solvent usage during purification. By running all stages—from bromination to acetylation to final drying—at our own facility, we've kept variability at bay and met tough audit requirements that many pharma clients insist on as standard.

    If a process manager or project chemist flags an issue, we log it internally, reevaluate the process map, and make rapid changes. Our technical support actually reaches the plant floor, not a call center. That’s made reviewers from both the QC side and customer audit teams much happier with the onboarding of our 1-Acetyl-5-Bromoindoline.

    Why Source Directly from a Manufacturer

    Shuffling through a long supply chain piles on both risk and cost, especially in today’s regulatory landscape. Fluctuations in raw materials, inconsistent temperature control during transit, and lack of origin traceability bring more than headaches—they bring genuine batch failures. We've experienced firsthand how a late or inferior intermediate upturns entire project timelines, prompting hasty rework or double-checking source documents for every lot.

    By making this compound ourselves, we keep a tighter rein on every variable. Traceability includes each reagent, timestamped batch records, and original QC signatures. If someone rings us up with a concern late at night, our own chemists and operations team are on hand to answer. That isn’t service spun for marketing; it’s a daily reality in fine chemical manufacturing.

    The Market Shift: Building Trust Through Quality and Accountability

    Market demand for 1-Acetyl-5-Bromoindoline keeps rising as R&D groups pivot to flexible, parallel synthesis approaches. We’ve spoken with procurement officers feeling burned by inconsistent supply and mysterious impurity spikes. Now, more chemical users ask to source directly from plants like ours, not just for reliability but for transparency in documentation and responsiveness on technical queries.

    Customers looking to develop their own in-house projects bring us early-stage questions on process compatibility, solvent interactions, and scale-up extrapolation. We make it part of our offering to share our real-world insights, including how different solvents and bases affect bromine lability, and how acetyl group retention fares under various workup and purification conditions. Fostering trust means honestly sharing what works and where challenges lurk—whether that's a tendency toward light-induced deacetylation under certain wavelengths, or lessons from isolating products at higher loads in continuous flow settings.

    Supply, Scalability, and Customization: Keeping Ahead of Demand

    Our plant’s capacity is designed to accommodate both steady long-term contracts and faster turnarounds for urgent projects. We’ve done kilo to multi-ton batches, and we can tweak specs for moisture, particle size, or packaging in lockstep with your process requirements. This flexibility arose from years of working with both big pharma sites and tech-driven startups. By staying agile in our workflow, we're able to deliver more quickly and with fewer last-minute hiccups.

    Requests for co-crystal-friendly grades, ultra-low residual solvents, and custom shipping container solutions come through regularly. We’re geared up to handle those, often rolling out new quality modules based on not just regulatory demands, but fieldside feedback from synthesis chemists actually running the campaigns. Adjusting specs on-the-fly is never trivial, but in-house oversight makes it possible.

    Practical Considerations in Synthesis and Downstream Applications

    Synthetic routes using 1-Acetyl-5-Bromoindoline actually clear up a lot of headaches compared to starting with raw indoline or unprotected bromoindolines. N-acetyl protection simplifies NMR spectra and reduces hodgepodge peak clusters. The bromo group’s presence widens the palette for late-stage diversification, making synthesis more modular and less error-prone. By contrast, N–H bromoindolines create more unidentified byproduct concerns, particularly during scale-up. Our customers have shown us how our acetylated version directly influences increased throughput—fewer column chromatographies, fewer batch failures, and easier isolation tracking.

    Process engineers worrying about environmental loading appreciate less waste from minimized purification cycles. Handling a material that dissolves sharply and filters efficiently makes all the difference in a busy kilo lab or pilot plant, and it’s something our ops team obsesses over. Even the smallest changes in physical form—from crystalline modifications to particle sizing—are based on hours of bench-top trials to hit just the right performance window.

    Environmental Impact and Safety Practices

    Chemical plants shoulder a responsibility to communities and customers, not just regulators. Handling brominated intermediates comes with environmental and safety challenges. We employ closed-transfer handling, full secondary containment, and water scrubbing systems for off-gassing. Our acetylation step uses lower-toxicity reagents and continuous emissions tracking to keep our footprint minimal. By tightening these controls, we’ve not only met, but often exceeded, the requirements set by environmental authorities and client audit teams.

    For those using 1-Acetyl-5-Bromoindoline further downstream, responsible management extends to waste minimization and safe byproduct handling. We share safety and disposal know-how based on both regulatory standards and what we’ve seen work best in practice. Our safety data isn’t generic—it draws from our own incidents and lessons learned, not just paperwork compliance.

    Concluding View: Quality Built on Real-World Challenges

    In sum, our approach to 1-Acetyl-5-Bromoindoline stretches far past blending and packing. Every improvement in purity or handling has roots in real project bottlenecks and the gradual refinement of every stage—sourcing, reaction, isolation, inspection, and shipment. Our relationship with users goes beyond customer service—it reaches into problem solving, technical exchange, and long-term partnerships. That’s what makes our product not just another batch of chemical, but a working solution for research and production chemists who measure results by what moves the next step forward.