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1-(2,6-Dichlorophenyl)-2-Indolinone

    • Product Name 1-(2,6-Dichlorophenyl)-2-Indolinone
    • Alias Sunitinib
    • Einecs 259-592-4
    • 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

    657007

    Cas Number 2472-60-8
    Molecular Formula C14H9Cl2NO
    Molecular Weight 278.13
    Appearance Off-white to light yellow solid
    Purity Typically ≥98%
    Melting Point 166-170°C
    Solubility Slightly soluble in organic solvents, insoluble in water
    Chemical Structure Indolinone core with 2,6-dichlorophenyl substitution at N-1
    Storage Conditions Store at room temperature, dry and dark environment
    Synonyms 2,6-Dichloro-N-phenylindolin-2-one
    Iupac Name 1-(2,6-dichlorophenyl)-2,3-dihydro-1H-indol-2-one
    Ec Number 219-600-6

    As an accredited 1-(2,6-Dichlorophenyl)-2-Indolinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "1-(2,6-Dichlorophenyl)-2-Indolinone, ≥98%," featuring hazard warnings.
    Shipping 1-(2,6-Dichlorophenyl)-2-Indolinone is shipped in tightly sealed containers, protected from moisture and light. It is handled as a regulated chemical, following safety protocols, including labeling for hazardous materials. Shipping complies with local and international regulations to ensure safe transport, prevent leaks, and avoid exposure to heat, ignition sources, and incompatible substances.
    Storage 1-(2,6-Dichlorophenyl)-2-Indolinone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep it separate from incompatible substances such as strong oxidizing agents. Store at room temperature and label properly. Ensure access is restricted to trained personnel and follow all standard chemical storage guidelines.
    Application of 1-(2,6-Dichlorophenyl)-2-Indolinone

    Applications of 1-(2,6-Dichlorophenyl)-2-Indolinone in Industrial Manufacturing

    As a specialized manufacturer of 1-(2,6-Dichlorophenyl)-2-Indolinone, we support a range of industrial sectors that rely on our consistent quality and batch-to-batch reproducibility. This intermediate enters well-established production lines for advanced synthesis in the pharmaceutical, agrochemical, pigment, liquid crystal, and materials modification industries. Below we detail its real-world industrial application routes.

    1. Pharmaceutical Intermediate for Antineoplastic Drug Synthesis

    Major pharmaceutical manufacturers integrate 1-(2,6-Dichlorophenyl)-2-Indolinone as a crucial building block during the preparation of kinase inhibitor APIs. Its specific substitution pattern enables targeted functionalization, which supports the efficient construction of indolinone-based compounds prevalent in patented antitumor agents. Controlled synthesis ensures regulatory conformity, and our product supports direct scale-up in multi-kilogram cGMP campaigns through validated chemical steps.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/EP monographs (where applicable for final API)
    • FDA 21 CFR Part 211 (for drug substance synthesis)
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • 0.85 to 1.10 molar equivalents per target API intermediate, based on stoichiometry in the coupling stage.
    • Adjustable according to impurity profile requirements and reaction yield optimization during the process validation phase.

    Downstream process integration

    • Enters as a starting heterocyclic reactant in Suzuki-Miyaura or Buchwald-Hartwig couplings.
    • Functionalization, halogen-exchange, and further N-alkylation steps occur before API isolation.
    • Critical in the generation of pharmacologically active indolinone scaffolds.

    Final product types

    • Tyrosine kinase inhibitor drug substances (e.g., Sunitinib raw material stage)
    • Patented oncology therapeutics
    • Research-stage investigational drugs
    • Intermediates for medicinal chemistry screening libraries

    2. Agrochemical Precursor for Benzoxazinone Synthesis

    Agrochemical formulators use our indolinone as a core intermediate in the synthesis of chlorinated benzoxazinone derivatives, which serve as active ingredients or protective agents for crop protection. The compound’s specific dichlorophenyl configuration facilitates chlorination and ring expansion reactions while supporting rigorous batch documentation for traceability demanded by the agrochemical sector.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Good Laboratory Practice (GLP) OECD Guidelines for synthesis steps
    • REACH registration for chemical intermediates (EC No. mandatory in Europe)
    • China National Standard GB 38472 (Pesticide manufacturing)

    Typical usage ratio

    • 0.9–1.2 equivalents per batch depending on active ingredient requirements and conversion efficiency in subsequent steps.
    • Adjusted based on downstream derivatization and chlorination strategy within process optimization windows.

    Downstream process integration

    • Functions as lactam precursor in sequenced condensation and chlorination reactions.
    • Introduced during heterocycle formation before final active molecule isolation.
    • Accounted for within parent compound mass balance for regulatory submission.

    Final product types

    • Selective herbicide actives (benzoxazinone class)
    • Fungicidal intermediates for formulated crop protection agents
    • Early-stage building blocks for proprietary pesticide research
    • Seed treatment chemical precursors

    3. Intermediate for High-Performance Liquid Crystal Materials

    Manufacturers of liquid crystal materials leverage this indolinone derivative as a precision intermediate in the synthesis of mesogenic compounds. The rigid aromatic core structure is essential in tuning the phase transition temperatures and electro-optical characteristics of LC compounds. Consistency in supply and purity allows downstream users to meet the uniformity specifications required for display and optical device manufacturing.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic device safety
    • IEC 62321 testing for hazardous substances
    • Physical property conformity per customer proprietary specification sheets
    • ISO 9001:2015 certified quality management

    Typical usage ratio

    • 5–12 wt% within intermediate reaction mixtures as dictated by target mesogen structure.
    • Ratios adjusted depending on molecular alignment and dielectric property requirements.

    Downstream process integration

    • Introduced in the initial coupling or cyclization phase for heteroaromatic LC core formation.
    • Subjected to further functionalization (alkylation, halogenation) before final formulation.
    • Included in in-process control sampling per end-user standards.

    Final product types

    • TFT-LCD mixture components
    • Thermotropic liquid crystals for display panels
    • Optoelectronic device intermediates
    • Specialty LC mixtures for instrument and sensor displays

    4. Dye and Pigment Intermediate for Specialty Colorants

    Industrial pigment and dye producers utilize 1-(2,6-Dichlorophenyl)-2-Indolinone in the controlled synthesis of high-performance azo and heterocyclic colorants. The indolinone core provides chemical stability and enhances color fastness in coatings and plastics. Downstream users depend on rigorous impurity control and documentation that aligns with international chemical safety and dye applications standards.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • OEKO-TEX® Standard 100 (where applicable for textile dyes)
    • REACH Annex XVII (restrictions on hazardous substances)
    • GHS-compliant SDS documentation

    Typical usage ratio

    • 2–8 wt% as a coupling intermediate in pigment synthesis batches, based on required chroma and solubility.
    • Adjusted for pigment purity, tinting strength, and downstream formulation needs.

    Downstream process integration

    • Used in the synthesis of heterocyclic dye skeletons via condensation and substitution reactions.
    • Fed into pigment manufacturing lines before dispersion and finishing stages.
    • Monitored for residual levels in final pigment QC.

    Final product types

    • High-stability organic pigments for plastics
    • Special effect dyes for automotive coatings
    • Colorants for industrial inkjet printing
    • Specialty dyes for electronic and security printing
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    Certification & Compliance
    More Introduction

    1-(2,6-Dichlorophenyl)-2-Indolinone: Shaping Progress in Fine Chemical Innovation

    A Closer Look at 1-(2,6-Dichlorophenyl)-2-Indolinone

    Every day at our plant, the team works with compounds that define the practical side of chemistry. 1-(2,6-Dichlorophenyl)-2-Indolinone stands out as one of those specialty molecules that often flies under the radar, yet it drives a considerable portion of innovation in synthesis. With a careful arrangement of a dichlorophenyl ring fused to an indolinone core, this product brings together chemical stability and reactive potential. We produce this substance using established, reproducible methods that undergo continuous refinement. It's not a laboratory novelty—it's the result of industrial discipline paired with technical expertise.

    Product Model and Form

    We manufacture our 1-(2,6-Dichlorophenyl)-2-Indolinone under strict conditions that focus on purity and batch consistency. The appearance is usually that of a pale solid—sometimes an off-white, sometimes leaning slightly yellow, based on starting material lot and reaction time. Each batch receives careful attention from our analytical staff: thin-layer chromatography checks for trace byproducts, and HPLC tracks peak integration for every gram produced. Melting point is checked, along with spectral confirmation, to stay aligned with requirements set by technical users. We avoid unnecessary over-polishing that would drive up costs without offering added value.

    For our customers, the available particle range avoids excessive fines that complicate handling and discourage accurate weighing for research and pilot work. Dust control measures in our main packaging area ensure workplace hygiene and minimize the risk of contamination to the compound itself. The packaging lines use lined fiber drums or HDPE containers, depending on shipment size and end-user feedback. Each package label bears only the necessary regulatory identifications and lot coding for total traceability back to raw materials and process times.

    Delivering Consistent Chemistry

    Our process chemistry team has written and refined every step in-house. The goal isn’t just to tick boxes for regulatory submissions—each improvement leads back to real-world uses. Over several years, we have seen consistent requests for batch uniformity and a need to limit unwanted isomers during the formation of the indolinone core. Our reactor controls now maintain a tight thermal profile, avoided side reactions from water ingress, and efficient recovery on dichloro intermediates, which drives higher output and less reprocessing waste.

    We have worked directly with several process scale-up groups. Unlike traders or brokers who saber off samples from various sources, our hands-on involvement in the reaction and purification steps means we spot quality shifts before they leave the gate. Instrument calibration, reagent sourcing, and even routine maintenance logbooks all play a part in guaranteeing that the indolinone you receive tomorrow matches the one you ordered last quarter. Regular meetings with downstream processors have confirmed that our lots reduce downtime in their own operations, especially when complex reactions involve this compound as a core intermediate.

    The Role of 1-(2,6-Dichlorophenyl)-2-Indolinone in Advanced Synthesis

    Chemists who’ve handled indolinones will tell you these compounds bridge gaps between research and application. Our product carries a dichlorophenyl substitution at the 2,6-positions, which grants a blend of electron-withdrawing effect and steric edge. These traits allow developers to reach into heterocyclic frameworks, constructing novel pharmaceutical candidates, crop protection agents, and materials science prototypes. A respected research team once noted to us that the chlorine pattern not only enhances selectivity in Suzuki couplings but also allows for further substitution, creating entire families of structurally related compounds. That control has a direct impact on developing commercial drugs with unique activity profiles and patentable novelty, especially when they seek to avoid overlapping prior art in the literature.

    On the industrial side, our clients use this indolinone to extend into several downstream analogs. Once, a partner involved in photoactive material design outlined how the compound's specific substitution prevented photodegradation during outdoor field use. Another syntheses project pointed to the molecule's freedom from long-lived tars—an issue plaguing other phenylindolinones. Each real-world case reinforces that a careful upstream synthesis, rather than a focus on mere cost per kilo, defines a manufacturing route that fits advanced demands.

    The Factor of Purity: Going Beyond High Numbers

    A compound’s stated purity has always been a topic of debate, often leading to inflated claims or over-emphasis on test results. For 1-(2,6-Dichlorophenyl)-2-Indolinone, the reality is straightforward—practical, consistent purity outweighs marginal increases. Spectra reveal that trace byproducts, if left unchecked, can disrupt both small molecule transformations and biocatalytic steps further along the chain. Our years of data show that most challenges arise from neglected detail, such as minor solvent carryover or incomplete crystallization. By holding batch review meetings after every run, our operation managers flag trends and send samples for confirmatory analysis, which then feeds into equipment cleanout routines and process tightening.

    We do not claim unattainable purity just for marketing brochures. Several academic and industry partners have shown us how real purity affects downstream yield and reproducibility—especially in medicinal chemistry, where only a few percentage points difference can tilt a reaction towards side-products or wasted resolving steps. By opting for reliable crystallization and proper filtration, our process creates a product ideal for scale-up work, as well as delicate benchtop manipulations. Missteps at this stage can cost weeks or months for R&D partners, and we see ourselves as an enabler of reliable productivity, not just a supplier of raw chemical mass.

    Comparison: 1-(2,6-Dichlorophenyl)-2-Indolinone Against Similar Compounds

    Through more than a decade of work on indolinones, patterns start to appear between variously substituted molecules. Mono-chloro versions, for example, cannot block metabolic oxidation as efficiently, giving unpredictable results in in vivo screens. Unsubstituted indolinones tend to undergo polymerization or give reactive sites for unwanted nitration or halogenation steps, especially when used in material science research. Tri-chloro indolinones drift beyond acceptable toxicity thresholds for many pharmaceutical projects—and purification becomes needlessly arduous.

    Comparing the 2,6-dichloro arrangement directly to meta or para chloros only, we observe that electron density shuttling around the ring shifts NMR signals and affects how Pd-catalyzed cross-couplings behave under moderate pressure. Researchers have sent us spectra involving meta-dichloro indolinones, but they soon report sluggish conversion when scaling up, leading to abandoned projects. Our version with 2,6-chlorines strikes the right compromise between chemical stability and removable protection, according to friendly laboratory notes we’ve reviewed. These qualities translate to a better outcomes in process chemistry applications, where control leads to fewer purification cycles and cost savings.

    Production Scale and Commitment

    Many specialty chemicals hover in the gap between “lab scale” and “commercial scale”—leaving buyers stranded trying to bridge the difference. Our investment in reactor size and downstream finishing equipment follows from genuine orders, not speculation. We have grown from pilot vials to full drums, led by direct consultation with end-users who describe pain points and request specific batch sizes. Our core 1-(2,6-Dichlorophenyl)-2-Indolinone design supports kilo to multi-ton runs. We have listened to technical transfer teams and responded by building redundancy into reactor scheduling, adjusting filtration rates, and improving solvent recovery. The result has been timely delivery for partners scaling research programs while managing their own changing timelines and compliance hurdles.

    Shipping and handling never take a back seat. We have developed stepwise scheduling with our freight partners, ensuring safe, compliant movement across routes that avoid temperature swings and excessive handling. Regular risk review meetings involve shipping logistics staff, plant chemists, and analytical leads, so no shipment leaves our site without review. Several customer audits have praised the transparency of our batch records and lot tracking protocols—a direct result of seeing too many horror stories involving suspicious origins or missing paperwork from generic traders. Every year, we invest in quality-of-life improvements for our warehouse and logistics teams because their hands literally touch every step our chemistry takes beyond the reaction vessel.

    Environmental and Regulatory Attention

    Every manufacturer handling chlorinated aromatics faces scrutiny over environmental impact. Disposing of chlorinated waste requires strict oversight—there's no room for shortcuts. We've improved our solvent recycling rates and direct thermal oxidizer connections to cut VOC releases from the process area. The company runs regular waste audits alongside government-licensed handlers. Waste labelling and storage conditions receive constant review from our EHS committee, and process routes undergo regular assessment so future improvements remain in sight. Auditors often quiz us about historical data patterns, and we're able to share detailed logs thanks to a company ethos that doesn’t cut corners just to meet quota. Real world experience has taught us that cost savings from good environmental controls always beat damage control over accidental releases or non-compliance fines.

    We have worked with partners in multiple jurisdictions, and every market brings a new set of compliance challenges—ranging from Safety Data Sheet accuracy to permit renewals and customs details. Close contact with downstream technical teams helps us predict which changes may affect allowable limits, packaging, or reporting formats. Each year, new standards emerge, and our staff spend time with regulatory watchdogs and industry associations to stay current. Sometimes, product specifications shift mid-batch—requiring us to pivot or repackage shipments to satisfy client requirements. This close feedback loop promotes factual, open communication rather than vague promises about regulatory readiness.

    Supporting Complex Synthesis: Practical Insights from Production

    Lab synthesis offers a playground for creativity, but bringing a molecule like 1-(2,6-Dichlorophenyl)-2-Indolinone into real-world production means addressing bottlenecks and technical snags that never emerge in test tubes. Reactor loading times, agitation speeds, solvent quality, and crystallization rates all become significant. Our staff lab has compiled years of reaction notes—showing where the process tolerates substitutions and where it fails. For example, batch notes reveal that excess heat during base addition leads to skipped steps and yield losses. On the purification end, our team learned through experience the correct charcoal treatment avoids off-white streaks and solid-state impurities.

    Our support for partners doesn’t end after delivery. Several R&D teams call us into technical troubleshooting meetings to discuss unexpected yields or batch inconsistencies in successive syntheses using our product. We value this feedback, as it brings an opportunity to diagnose and tune parameters, benefitting both sides. Our manufacturing focus means we gain practical knowledge about subtle interactions—sometimes related to stirrer design or minor solvent residues that slow downstream steps. This kind of seasoned perspective sets apart real makers from middlemen simply shuffling goods per order.

    Addressing Industry Changes and Looking Forward

    As regulations tighten and requirements for traceability become stricter, the specialty chemical market shifts. Batch records must go beyond bare minimums, and sustainability audits have teeth. We rely on hundred percent in-house managed process control—from monitoring raw material sourcing to reviewing plant emissions and product stewardship practices. More than routine paperwork, daily plant meetings encourage ideas about process improvements and material conservation, building a real sense of ownership in our manufacturing staff. Chemists involved at each step pass along recommendations that reduce waste or uncover routes that save energy, yielding both financial and environmental rewards.

    Interest in 1-(2,6-Dichlorophenyl)-2-Indolinone continues to rise, particularly among organizations that want full transparency about their supply chain. They don't want vagueness about origin or process—they want a phone call straight to the production line if issues arise. When pilot projects fizzle, it is usually linked back to supply instability. By anchoring the product line with thorough, plant-checked records, we aim to become a partner who lessens risk. Over time, these relationships often evolve into technical collaborations, where our feedback sharpens future product requirements or reveals new applications for derivatives that only emerge through practical plant-scale experience.

    Why We Continue to Invest in 1-(2,6-Dichlorophenyl)-2-Indolinone

    Profit margins on specialty chemicals rarely draw headlines, but the assuredness of supplying a crucial material that keeps development moving forward does. Our investment in this product answers a clear pull from clients who’ve tested enough samples to know the difference between real manufacturing and simple repackaging. Day by day, our plant adapts to evolving needs—modifying particle size distributions, leveraging washed versus unwashed filtration routes, or shifting packaging selections based on incoming feedback.

    Lessons picked up from early pilots have spread across our teams, nurturing a foundation that respects chemical realities over paper promises. As users request new derivatives or share insights about performance limits in multi-step synthesis, the company remains responsive. Many breakthroughs resulted not from generic blue-sky research, but from careful observations shared by production-floor chemists and scale-up partners. For our staff, there’s pride in seeing a finished drum head out to support an international drug discovery campaign or a next-generation crop protection project, knowing every package tells the story of determined chemical manufacturing done right.

    Concluding Perspective: Crafting Reliability with Each Batch

    1-(2,6-Dichlorophenyl)-2-Indolinone represents more than a line item in a catalog. It embodies dependable chemistry that keeps moving the modern world forward. Our promise to the customers, the researchers, and the engineers is simple—nothing leaves our gates that doesn’t pass our own practical standards. Our factory floor balances experience, regulatory discipline, and modern analytics, tying together the many threads needed to support a chemically complex, opportunity-rich product like this. There will always be easy ways to source chemicals on the internet, but repeatable, trusted supply remains the province of real production teams who carry hard-won skill and a commitment to improvement. Here, we bet on the value of honest, expert-driven manufacturing—one batch at a time.