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3'-Iodoacetophenone

    • Product Name 3'-Iodoacetophenone
    • Einecs 219-015-8
    • 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

    835840

    Chemical Name 3'-Iodoacetophenone
    Cas Number 637-69-4
    Molecular Formula C8H7IO
    Molecular Weight 246.05 g/mol
    Appearance Pale yellow to light brown solid
    Melting Point 59-62°C
    Boiling Point 315°C
    Density 1.81 g/cm³
    Smiles CC(=O)C1=CC(=CC=C1)I
    Synonyms 3-Iodoacetophenone, m-Iodoacetophenone
    Refractive Index 1.6700
    Purity Typically >97%
    Storage Conditions Store in a cool, dry place away from light
    Solubility Slightly soluble in water; soluble in organic solvents
    Ec Number 211-299-8

    As an accredited 3'-Iodoacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3'-Iodoacetophenone is supplied in a 25g amber glass bottle, featuring a tightly sealed screw cap with hazard labeling and handling instructions.
    Shipping 3'-Iodoacetophenone is shipped in secure, chemical-resistant containers to prevent leaks and contamination. Packaging meets international safety regulations for hazardous chemicals. The product is transported under controlled conditions, avoiding extreme temperatures. Appropriate hazard labeling and documentation ensure safe handling during transit. Shipping is available to authorized locations only, complying with legal requirements.
    Storage 3'-Iodoacetophenone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. The container must be tightly closed and clearly labeled. Protect it from light and moisture. Store at room temperature or as recommended in the supplier’s safety data sheet (SDS). Use appropriate chemical storage cabinets if available.
    Application of 3'-Iodoacetophenone

    Applications of 3'-Iodoacetophenone in Industrial Manufacturing

    3'-Iodoacetophenone serves key intermediate roles for several specialized downstream sectors. As an experienced manufacturer, we focus on established applications where this compound directly enables the synthesis of advanced chemicals and pharmaceuticals. Below, we outline its role in select industrial segments based on current global practice.

    1. Pharmaceutical Intermediate for Antifungal and Antibacterial Agents

    Pharmaceutical manufacturers deploy 3'-Iodoacetophenone as an essential intermediate in the synthesis of specific antifungal and antibacterial APIs. This aromatic halide allows for precision iodination in the early steps of active ingredient construction, crucial for heterocycle assembly where halogen substitution patterns determine drug efficacy and metabolic behavior. Its reactivity supports efficient coupling and cyclization reactions—particularly for building substituted benzene frameworks used in many contemporary antimicrobials—while facilitating compliance with strict residual solvent and impurity profiles required by global regulatory bodies.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) and European Pharmacopeia (Ph. Eur.) monographs for relevant APIs
    • 21 CFR Part 211: US cGMP for finished pharmaceuticals
    • WHO Technical Report Series for API process validation

    Typical usage ratio

    • Batch formula typically utilizes 0.5–1.8 molar equivalents per target intermediate, adjusted based on intended substitution yield and purification protocol; parameters tuned during process scale-up and impurity optimization phases.

    Downstream process integration

    • Charged during stepwise halogenation or Suzuki coupling for aromatic ring assembly, followed by hydrogenation, hydrolysis, and crystallization within multi-step synthesis trains; handled and isolated in dedicated reactor trains to meet API regulatory audits.

    Final product types

    • Broad-spectrum antifungal finished drugs (e.g., triazole or imidazole derivatives)
    • Antibacterial APIs for topical and systemic administration
    • Custom pharmaceutical building blocks for CDMO supply chains

    2. Agrochemical Synthesis: Fungicide and Herbicide Intermediates

    Agrochemical formulators depend on the selective reactivity of 3'-Iodoacetophenone to produce halogenated intermediates essential for modern crop protection agents. Its controlled insertion at the meta position yields intermediates that undergo subsequent Grignard or Ullmann-type couplings, especially in the creation of specialty fungicides targeting persistent agricultural pathogens. Use in this sector emphasizes scalability, purity, and cost efficiency, supporting well-regulated manufacturing environments subject to international registration and export controls.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) technical specifications for active substances
    • ISO 9001:2015 for quality assurance in agricultural chemical manufacturing
    • REACH Annex II requirements for intermediates under EU regulations
    • China GB 2763 pesticide maximum residue limits for exported active ingredients

    Typical usage ratio

    • Employed at 0.7–1.5 mole equivalents per mole of target agrochemical core, with in-process adjustments for specific conversion rates and by-product suppression during scale-up.

    Downstream process integration

    • Incorporated during first- or second-stage aromatic derivatization, preceding etherification or amination for lead fungicide or herbicide actives; integrated within continuous or semi-batch synthesis units for large-scale plant operations.

    Final product types

    • Fungicide active ingredients for seed and foliar treatment
    • Herbicide precursor compounds
    • Intermediate isolates for proprietary agrochemical blends

    3. Dye and Pigment Intermediate Manufacturing

    Within dye and pigment production chains, 3'-Iodoacetophenone functions as a crucial nucleophilic aromatic precursor for synthesizing complex, high-performance colorants. The iodo functional group enables controlled substitution reactions such as Buchwald-Hartwig aminations or Sonogashira couplings, forming extended conjugated systems indispensable for constructing specialty colorants used in inks, plastics, and high-durability industrial coatings. Manufacturers rely on this building block when purity and substitution specificity are critical for product color stability and regulatory compliance.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substance levels in textile dyes
    • EN 71-3:2019 safety requirements for pigments in toys
    • ISO 9001:2015 Quality Management Systems for colorant manufacturing
    • FDA CFR Title 21, Part 74: Color additives for food contact plastics (if applicable)

    Typical usage ratio

    • Formulators select 0.6–1.2 molar equivalents per pigment core, depending on desired halogen density and batch-throughput parameters. Ratios tuned for hue intensity, fastness, and batch uniformity during process QC cycles.

    Downstream process integration

    • Introduced during early aromatic halogenation steps or as a functionalized intermediate feedstock for palladium-catalyzed coupling stages; enters synthesis line prior to azo, anthraquinone, or phthalocyanine functionalization in pigment reactor trains.

    Final product types

    • Synthetic and specialty dyes for textile, inkjet, and coated paper applications
    • Pigment dispersions for automotive, industrial, and plastic coloration
    • Precursor intermediates for advanced effect pigments

    4. Active Ingredient Precursor for Fine Chemical Synthesis

    Producers of fine chemicals leverage 3'-Iodoacetophenone’s precision halogenation to construct specialized aromatic compounds used across advanced sectors—from electronic-grade intermediates to UV absorbers for polymers. Its unique reactivity provides a route to meta-substituted aromatic scaffolds, which serve as key nodes in further functionalization of high-value chemicals where trace impurity levels must remain exceptionally low. Controlled handling, coupled with tailored purification procedures, ensure integration meets process validation and custom specification requirements for sophisticated end-use applications.

    Industry compliance standards

    • ISO 9001:2015 certification for fine chemical production processes
    • ROHS Directive 2011/65/EU for electronic additives
    • FDA 21 CFR for polymer additives intended for food contact applications (if relevant)
    • REACH pre-registration and notification requirements for specialty chemicals

    Typical usage ratio

    • Adopted at 0.8–1.4 mole equivalents, fine-tuned for the specific aromatic transformations required. Volumes and ratios set according to downstream functional group compatibility and impurity management strategies per customer SOPs.

    Downstream process integration

    • Charged as a starting halide for direct arylation, metal-catalyzed cross-coupling, or as an advanced intermediate prior to sulfonation, alkylation, or condensation steps; handled within closed or inerted synthesis modules designed for high-purity operations.

    Final product types

    • Electronic intermediates for OLED or semiconductor applications
    • UV-stabilizing additives for industrial polymers
    • Custom reagent intermediates for contract manufacturing
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    Certification & Compliance
    More Introduction

    3'-Iodoacetophenone: A Closer Look from a Chemical Manufacturer’s Perspective

    What Sets 3'-Iodoacetophenone Apart

    In our daily rounds on the manufacturing floor, we keep a close eye on both the raw materials flowing in and the specialties that exit our reactors. 3'-Iodoacetophenone stands out among the host of iodoaromatics that cross the line for one simple reason: reliability in downstream chemistry. Across several years, chemists have come to trust this compound when exact substitution matters. With the iodine at the 3’ position on the acetophenone scaffold, it provides a distinctive starting point for selective cross-coupling reactions—most notably, Suzuki and Sonogashira couplings. These reactions have driven much of the organic synthesis work in medicinal chemistry and fine chemical production over the last decade, and they require building blocks that don’t play games with purity or reactivity.

    A Look at the Substance Itself

    We keep 3'-Iodoacetophenone in production as both a technical and high-purity grade, serving requests from R&D teams as well as kilo-lab users scaling to pilot plant quantities. Its chemical formula, C8H7IO, captures the core: a benzene ring bearing an acetyl group and a single iodine atom at the meta position. As is typical with iodinated aromatics, it offers firm reactivity with palladium and copper catalysts, something most seasoned synthetic chemists expect. The molecular weight—a tick over 246 g/mol—places it in a sweet spot where handling remains flexible for analytical work and bulk synthesis alike. We provide certificates of analysis with every batch, focusing on the metrics that working chemists care about: GC purity, iodine content, residual solvents, and visible traces of byproducts.

    Importance from a Manufacturer’s Viewpoint

    As a producer with hands-on experience, what matters most is not just the molecule in isolation, but how it fits into real-world production. 3'-Iodoacetophenone often plays its part in the first leg of a synthetic route toward more complex pharmaceuticals, agrochemicals, and specialty ligands. The acetophenone serves as a useful “anchor,” letting chemists add new groups at the meta position without interfering at other sites. This predictability reduces wasted steps, saves on purification efforts, and helps projects maintain a tighter control on costs.

    In a lot of recent projects—especially in the field of kinase inhibitor research and advanced polymer additives—we’ve seen customers choose 3'-Iodoacetophenone over its ortho- or para-isomers. The reason is less about theory and more about practice: the reactivity at the 3’ location gives a unique avenue of substitution, avoiding the sort of unwanted side reactions that crop up with 2’- or 4’-iodoacetophenones. Working directly with medicinal chemists, we receive regular feedback on these outcomes, reinforcing our decision to keep this compound in regular supply.

    Handling and Storage: Lessons Learned Over Time

    Through batches large and small, one thing becomes clear—iodinated intermediates reward careful handling. Our staff deals with 3'-Iodoacetophenone daily, and we’ve put procedures in place to keep degradation to a minimum. Unlike some more volatile building blocks, this aromatic ketone displays enough stability under standard warehouse storage, provided containers stay sealed and exposure to strong light stays limited. Humidity doesn’t pose much risk, but routine visual checks remain a staple of our QA. Containers with solid flakes or crystals still yield material that complies with more than 98% GC purity, which represents the threshold our long-term partners demand.

    Transport to customer labs doesn’t throw up any special challenges compared with chlorinated or brominated analogs. Where we’ve seen issues in the past, they usually come down to packaging errors outside the factory. By packing in tight-sealing fluoropolymer bottles and including desiccants for longer transits, we sidestep most concerns. Our technical staff remains reachable throughout the supply chain—a practice that saves weeks of delays if a question crops up mid-delivery.

    Comparing 3'-Iodoacetophenone to Related Intermediates

    Many researchers eventually face the question: Why settle on 3'-Iodoacetophenone versus the 2'- or 4'- versions, or even the bromo and chloro analogs? Drawing on several years of production and custom synthesis, we can say that the answer ties back to the type of bonds chemists want at the next step. The iodine atom at the 3’ position activates the molecule for oxidative insertion reactions, and it does so exceptionally cleanly compared to the bromo or chloro equivalents. For Suzuki couplings or direct arylations, this means shorter reaction times, higher yields, and fewer purification headaches. From a purely practical standpoint, the Iodine at the 3’ site represents a sweet spot for both selectivity and reactivity.

    From experience, we see para or ortho isomers finding use in certain polymer synthesis protocols, but the meta position holds value in fine-tuning electronic effects during pharmaceutical discovery. The interplay between the acetophenone’s carbonyl group and the iodine modulates the ring’s reactivity just enough to make targeted transformations more predictable. In our pilot plant, we’ve watched as slight adjustments in temperature or solvent bring out the differences between isomers—results that only become clear with repeated batch runs and careful record-keeping.

    Other iodoaromatics may compete on price per kilo or availability, yet they often fall behind on ease of purification or downstream product quality. Our chemists spent several years optimizing the crystallization process for 3'-Iodoacetophenone, shaving off impurities that once plagued multi-step syntheses. This kind of process improvement narrows batch variability—a key concern in pharma projects where regulatory submissions tolerate little deviation.

    Common Challenges and Solutions

    Like most halogenated intermediates, 3'-Iodoacetophenone raises two big flags in our process: supply of iodine raw materials and consistency in halogenation. The global market for elemental iodine fluctuates. We’ve faced pricing swings and periodic shortages that test any long-term supply chain. By contracting with reliable iodine suppliers and holding extra reserves, our plant hasn’t missed a customer order in over five years. There’s no shortcut; years of relationship-building form the backbone of a stable supply process.

    Achieving uniform halogenation across batches remains a technical challenge. Too much unreacted acetophenone, or an excess of polyiodinated byproducts, can ruin a lot. Our analytical team pulls real-time HPLC and GC data on every tank, dialing in reactant ratios and process temperature. Continuous feedback from R&D chemists who sample each new batch keeps the operation honest. In the rare event that a lot drifts out of spec, it gets flagged for in-house rework, not shipment. Customers remember the batches that run smoothly—this becomes our reputation, not the one-off problem.

    We’ve reduced waste stream toxicity with scrubbing setups, recapturing valuable iodine for reuse in the next run. Early on, some disposal routes ate into our margins and taxed our utilities. By recycling raw iodine and adjusting reaction conditions to favor near-quantitative conversion, we’ve trimmed both environmental footprint and overhead. This approach shows tangible results over years, cutting both costs and compliance headaches.

    Real-World Usage in Synthesis

    Over hundreds of conversations with client labs, one pattern never strays far: 3'-Iodoacetophenone gets deployed as a linchpin in multi-step synthesis. For biopharmaceutical projects, the meta-iodo group opens up substitution patterns that methyl or phenyl analogs can’t match. The compound readily undergoes cross-coupling to introduce new arenes or heterocycles, serving as a bridge to statins, kinase inhibitors, or less common APIs. As the research community pivots toward ever more complex molecular architectures, we’ve had to keep up. Users report back that our material’s low level of metal contaminants—especially palladium and copper—lets them run coupling reactions without fear of trace metals jeopardizing downstream purifications.

    Polymer chemists represent the second group seeking meta-iodo intermediates for highly controlled monomer insertion. These users need batch-to-batch consistency, and they usually demand multi-kilogram quantities—sometimes on short notice. Our flexibility in scaling up delivers this, but it’s the stable crystallinity of our product that draws repeat business. Good handling properties mean the compound dissolves swiftly and reproducibly, whether the next step calls for a Büchner funnel or automated feed system.

    We’ve collaborated with several industrial users who specialize in dye manufacture or electronic materials. In those sectors, subtle differences in meta-substitution shift colorfastness or electron transfer properties, so deviations in material source become all too obvious on the final line. Years of close work with these partners refine our workflow, and we fold those lessons into every operational tweak and QA review. From our side of the fence, building in such feedback never represents wasted time.

    Quality Control: The Stories Behind the Numbers

    Our labs run more than just the minimum analytics required to tick off a certificate of analysis. Each batch undergoes GC and HPLC purity checks, trace halogen content, and physical testing for melting point and crystallinity. Where a customer requests added data, such as residual solvent or specific heavy metal analysis, we pull in third-party validation. Even so, the most revealing data often emerge through direct conversations with chemists who see our product perform—or falter—on their benches.

    Several years ago, a pharmaceutical customer flagged a slight shift in reaction profile traced to minor batch contamination from a common solvent. Addressing this issue required not just equipment cleaning but also an update of staff training and source controls. While that event set us back at the time, it led to a tighter, more robust workflow—one that serves every shipment since. We view these feedback loops as organic parts of a manufacturer’s evolution, not as isolated mistakes.

    The Marketplace and Regulatory Picture

    3'-Iodoacetophenone doesn’t fall under major controlled substance regulations, but downstream applications sometimes touch on tightly governed sectors. Our experience with documentation and traceability helps customers satisfy ever more rigorous audit demands from both internal QA and outside inspectors. Full tracking from raw material purchase to final packaging stands as standard—not an afterthought. We maintain records for several years per regulatory best practices, tied to batch numbers and shipment histories.

    Customers in Europe or North America sometimes request extra materials safety or REACH-related paperwork. Our staff responds to these requirements as needed, while staying mindful that over-regulation adds needless delay. By focusing routine QA on the specific compliance regimes request per customer, we prevent supply chain bottlenecks. The investment in thorough analytics and documented traceability grows more important as clients move from lab to clinical or commercial scale.

    Trends and Technology Shifts

    During the span of our production of 3'-Iodoacetophenone, reaction technologies keep shifting. Traditional batch reactors now share the floor with flow systems and automated synthesisers. These advances hold promise, but also push manufacturers like us to adjust particle size, solubility, and stability for new protocols. Smaller-scale modular reactors in custom synthesis drive us to test product fit across various platforms. The days of one-size-fits-all materials fade as clients demand formats that suit robots alongside technicians in a hood.

    Meanwhile, green chemistry gains real ground. Where feasible, we favor solvent choices and process tweaks that cut emissions and byproduct formation. The supply of “green” solvents sometimes challenges older continuous processes, but customer feedback and developmental partnerships help adapt reactors and post-processing to meet updated standards. The push for higher purity and lower environmental impact runs in parallel—there is real business as well as philosophical incentive for manufacturers to get ahead of shifting expectations.

    Customer Relationships and Long-Term Value

    Decades of production have taught us that the real value of a specialty intermediate like 3'-Iodoacetophenone doesn’t end with quality assurance or prompt shipment. Customer feedback makes clear that suppliers who take an active interest in end-use see more repeat business, and less friction if a challenge arises. Our technical staff frequently discusses reaction setup, isolation, and troubleshooting with chemists working on tight timelines. Sharing observations about what worked—or failed—in our own scale-up efforts gives clients a practical compass, not just a line on a safety data sheet.

    Repeat customers cite our willingness to adapt container sizes, update documentation for specific projects, and anticipate special logistic needs. These lessons turn up in operational meetings every month, shaping batch scales and scheduling for the following quarter. Chemical manufacturing ties its fate closely to its customer base, and only by listening, adjusting, and supporting does a company remain relevant over the long term.

    Final Notes: Learning in Practice

    Any lengthy experience as a chemical manufacturer leads to the same truth: Even a reliable product like 3'-Iodoacetophenone finds its limits and surprises in daily operations. Occasional hiccups in supply or process prompt real improvements that benefit more than one product line. Trust grows in layers—through honest problem-solving, open technical discussion, and a willingness to put science ahead of shortcuts. Every improvement in purity, every tweak to yield, and every hour spent troubleshooting translates into tangible value down the line. Chemists keep coming back not out of blind habit, but because their experience matches the claims we make. We learn just as much from their bench-scale results as we do from the numbers on a certificate. In our view, that ongoing partnership is the best foundation for both growth and real-world innovation.