|
HS Code |
156224 |
| Chemical Name | 5-Chlorooxindole |
| Cas Number | 35461-26-8 |
| Molecular Formula | C8H6ClNO |
| Molecular Weight | 167.59 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 202-205°C |
| Solubility | Slightly soluble in water; soluble in organic solvents such as DMSO and ethanol |
| Purity | Typically ≥ 98% |
| Inchi | InChI=1S/C8H6ClNO/c9-6-2-1-5-4-10-8(11)7(5)3-6/h1-3,10-11H,4H2 |
| Smiles | C1C2=C(C=C(C=C2)Cl)C(=O)N1 |
As an accredited 5-Chlorooxindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-Chlorooxindole is supplied in a 25-gram amber glass bottle with a tightly sealed cap and clear hazard labeling. |
| Shipping | 5-Chlorooxindole is shipped in tightly sealed, chemical-resistant containers to prevent moisture or air exposure. It is transported following standard regulations for laboratory chemicals, with clear labeling and safety documentation included. Packages are cushioned to minimize breakage, and temperature control is provided if required to maintain compound stability during transit. |
| Storage | 5-Chlorooxindole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. It should be kept away from sources of ignition, incompatible chemicals, and moisture. Store at room temperature, and ensure the storage area follows all relevant chemical safety protocols. Clearly label the container and restrict access to trained personnel. |
Applications of 5-Chlorooxindole in Industrial Manufacturing5-Chlorooxindole serves as a key intermediate in several advanced industrial sectors, supporting downstream producers with reliable integration into high-value product syntheses. As a direct manufacturer with established quality systems, we serve partners that require consistent application knowledge and regulatory compliance for complex, scale-driven formulations. Below, we detail primary industrial domains where this specialty intermediate delivers critical function, mapped to precise sector requirements and manufacturing workflows. 1. Active Pharmaceutical Ingredient (API) Synthesis for Anticancer AgentsPharmaceutical manufacturers employ 5-chlorooxindole as a building block in the synthesis of targeted small-molecule oncology therapies, notably for indole-based kinase inhibitor APIs. The material’s chloro-substitution pattern enables downstream functional group modifications and ring closures central to drug scaffold construction, meeting the high-purity thresholds necessary for regulated high-potency API facilities. Operators usually integrate this intermediate in medicinal chemistry and later scale-up for pilot and commercial manufacturing, where every additive meets stringent traceability and analytical control to comply with worldwide GMP mandates. Industry compliance standards
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2. Agrochemical Intermediate Production for Fungicide SynthesisMajor agrochemical companies utilize the compound as a core intermediate in the synthesis of modern, highly selective fungicidal actives. Its electrophilic chloro group and indole core support downstream ring transformations unique to strobilurin and azole analog development. These applications require high batch-to-batch reproducibility, as the quality of the intermediate impacts field efficacy, product registration, and maximum residue levels in end-use crops. Our production adheres to plant protection active substance standards enforced in regulated international markets. Industry compliance standards
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3. Dye and Pigment Intermediate for Specialty ColorantsDownstream dyestuff and organic pigment manufacturers incorporate 5-chlorooxindole to generate vivid, high-stability color bases for inks, plastics, and specialty coatings. The halogenated indole structure supports unique coupling and diazotization routes, essential for lightfast azo and indole dyes used in high-spec print and packaging applications. End-users require assured purity and trace impurity control to meet color consistency and environmental safety requirements for industrial and consumer markets. Industry compliance standards
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4. Organic Electronics Material SynthesisProducers of organic semiconductor and photovoltaic materials use 5-chlorooxindole as a synthetic platform for constructing advanced indole-derivatized conjugated backbones. Its chloro functionality provides accessible entry points for palladium-catalyzed cross-coupling, supporting precise monomer tailoring in organic field-effect transistor and OLED fabrication. Firms focusing on high purity and defect-free polymerization depend on consistent impurity profiles, as optical and electrical characteristics of finished devices are directly tied to the quality of the originating building block. Industry compliance standards
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At our manufacturing site, 5-Chlorooxindole represents more than just a chemical product code or a CAS number on an SDS. It marks a story of consistent effort, continuous process tuning, and measured decision-making, from raw stock selection through crystallization and drying. Models like the MM10385 draw on years of refining our batch reaction and purification systems, turning a tricky indole halogenation into something reliable and scaleable. Customers in the pharmaceutical and agrochemical fields demand purity, yield, and surety against byproduct contamination—especially with specialty indoles, which refuse to behave like bulk intermediates. Our focus on 5-Chlorooxindole’s material and stepwise process control means we don’t just chase theoretical yields; we prioritize what goes in the drum, what you see after opening the bag, and the traceability behind every kilogram.
The business of manufacturing halo-indoles doesn’t offer shortcuts or generic specs if you want to avoid headaches in scaling or regulatory review. With 5-Chlorooxindole, isomer formation and parent oxindole contamination have tested our patience in the past. Some batches from our earliest years showed variable yields, and more than a few gram-scale crystallizations stuck together and delayed washing. Experience taught us that full conversion is only part of the story. So we bracket temperature ramps and quench points within narrow bands. We keep an eye on trace aniline and dimer formation, using targeted solvent choices and slow addition rates. Specification sheets for our main model guarantee at least 99% HPLC purity, but tighter control on color, moisture, and particle morphology gives customers fewer surprises on downstream workups.
Routine testing catches nitrosamine hazards and choro-aniline formation. We prefer to over-report trace impurities so the supply chain managers we partner with never get unexpected shelf-life drop-offs or inconsistent performance in subsequent transformations. That’s feedback from past years: one customer traced an unexpected TLC shadow back to a half-percent impurity in some off-market product. Since then, every lot receives comprehensive screening beyond what minimum regulatory asks for. Working closely with solvents and crystallizers fine-tunes our purification and consistently delivers that off-white-to-pale product, right down to the last drum.
We remain a manufacturer, not a blending house. That matters in small-molecule chemistry. There’s a gap between repacking intermediates and troubleshooting precise process bottlenecks. Dyes and API start materials can be picky—often intolerant of extra chlorides or oxidizing residues. If a customer calls with a question about a certain batch, our in-house chemists can talk through process notes on that exact run. No blank stares, no deflection to “standard specs.” Over time, this willingness to trace the details and explain methods builds trust, especially in process transfer or validation projects. Last year an api plant flagged a change in melting point and color—our production log showed a change in drying pressure one day. Good documentation let us address the issue in hours, not weeks.
By sticking with rigorous documentation and refusing to blend away problems, our reputation rides on authenticity and accountability. No third-party warehousing, no surprise relabeling. Each batch of 5-Chlorooxindole gets its own notebook entry and storage code. Downstream, if the material doesn’t fit your spec for reactivity or color, we’ll investigate openly—right down to raw material COA review and retention sample checks. This kind of direct connection beats any “off-the-shelf” trade stockpiling or lowest-bidder supply chain every time, especially for regulated end users.
Not all oxindoles behave the same in the reactor, and chemists who’ve handled halogenations or tried to fix failed couplings know why. Our experience with 5-Chlorooxindole builds on earlier work with 6-chloro analogs and 7-bromo-oxindoles. Each one comes with separate hazard profiles, varying by the site of halogenation and its downstream applications. Compared to the 6-chloro version, 5-Chlorooxindole tends to favor cleaner ring closure and consistently shows higher tolerance in coupling steps for pharmaceutical intermediate prep, especially Suzuki or Buchwald reactions.
While our facilities also supply unsubstituted oxindole, the presence of a chlorine atom at position 5 makes a real difference in electronic behavior. Certain agrochemical syntheses select 5-chloro substitution for selective biological targeting or better stepwise functionalization. During scale-up trials for custom intermediates, we noticed the 5-chloro analog resisted over-chlorination and minimized double-chloride formation when compared to similar products from traders. Each subtle difference between these halogenated indoles shapes future steps, from cross-coupling to direct reduction.
The hydrogen-bonding and planarity of 5-Chlorooxindole also impact its physical handing—important during formulation, granulation, or direct tableting for research quantities. Customers who have used alternative chloro- or bromo-oxindoles often report issues with caking, slow dissolution, or unanticipated side reactions. Careful process control during our manufacture addresses these challenges with predictable lot-to-lot behavior. You won’t find the same quality swing or uncertainty that sometimes shows up in bulk market intermediates not tracked back to the original manufacturing process.
Most of our output finds its way into specialty pharma syntheses, including kinase inhibitor development and small-molecule modification. Medicinal chemists provide steady feedback, sharing insights from reaction screens: some value the precise reactivity profile, others focus on ease of purification. Researchers working in crop science have leveraged its halogenated core for targeted pesticide active synthesis, taking advantage of the more predictable byproduct profile and clean mass spectrum it provides during pilot-scale optimization. These are not theoretical benefits. More than one plant manager has admitted to us that a poorly made batch can tie up a kilo-scale run for weeks, forcing chromatography where none should be needed. Our own customers get to avoid these pain points, as many have confirmed in post-campaign audits.
Some industrial clients have moved up to multi-kilo requirements as their pipeline matures from R&D to phase I/II scale-up. They arrive at this step with process bottlenecks already ironed out, thanks to the deliberate absence of the kinds of trace foreign matter that can plague scale-up. By tracking individual impurity trends from the gram scale to the drum lot, we help our partners avoid guessing games or downstream rework. This matters—a single percent drop in purity, or an unforeseen insoluble fraction, can wipe out the savings from “cheaper” supply.
Other sectors—such as specialty pigment and polymer research—tap into the unique electronic structure of 5-Chlorooxindole for exploratory syntheses or analog launches. Our experience tells us the clearer and more stable the starting compound, the less troubleshooting needed after mixing, compounding, or curing. Over years of supporting these teams, we’ve prioritized building an analytical package with full spectra, materials compatibility data, and predictive shelf-life tracking that stands up to third-party verification.
Customers come to us when their projects demand a higher level of process familiarity—beyond a quick stock buy. It’s not unusual for our technical team to set up pilot lots with altered solvent selection or modified filtration to match a customer’s specific downstream requirements. An example from the last quarter: a partner required a slightly coarser crystal cut for direct tableting, intended to eliminate dusting in final equipment. Experience working close to the process let us adjust drying and crystal seeding in-house rather than tacking on a crude screening step. No unnecessary blending, no unpredictable fines in the final product.
When a batch fails internal inspection, we don’t hide it or send it out for “market discount.” That failed lot becomes a learning tool. We break down the misstep—sometimes a hot spot in the reactor jacket, at other times an impurity spike traced back to a new charge of base. Internal SOPs document not just the successful runs but the near-misses, helping the next batch avoid the same fate. We can point to specific improvements implemented, from updated jacket PID tuning to revised solvent polishing routines, and share these openly with customers. Transparency at this level doesn’t just build trust; it delivers practical results for supply partners.
We work harder for small-batch or one-time requirements than a simple “make to stock” trader could. That means investing real time in documentation, process validation, and customer feedback channels. Custom analytical runs, repeat sampling, and in-depth root cause investigations for any off-specification lot form part of our daily operations. If new regulations or handling requirements appear in a customer’s industry, we adapt production protocol and quality reporting rather than pretending universal compliance exists. These experiences set a real manufacturer apart.
Static process lines rarely stand up to evolving customer needs or tightening industry scrutiny. To keep processes efficient but robust, our team regularly re-examines step sequences, purification loops, and packaging protocols, all while keeping existing customer supply timelines undisturbed. These ongoing tweaks go into test lots before full-scale adoption, ensuring the end user receives consistent product, not an unannounced process variant.
Regular investment in new stirring gear, filtration media, and automation systems reflects both a response to industry pressures and a commitment to our craft. Operator experience counts—when a process technician catches a departure from expected LOD or observes a finer change in product granularity, we treat that as actionable information, not background noise. Many refinements come not from top-down mandates but from daily production debriefs, in which floor technicians and chemists compare outcomes to previous logs and voice any detection of deviation. This iterative approach, rather than sudden swings, pushes our product line to a higher reliability level.
We manufacture using best-in-practice solvent recovery systems, in-plant filtration, and targeted waste management. By separating chlorination and neutralization zones, we minimize risk to both workers and the environment. We monitor VOC and chlorinated byproduct levels using in-house GC and regular third-party checks. Our efforts come from a responsibility to our crew and the wider community. Down the chain, this mindset translates to product traceability, stable supply, and a clear audit trail for each delivery.
Industry standards shift, and so do regulatory frameworks around halo-aromatic manufacture, storage, and transport. Rather than reacting to the letter of regulation after notice, we track updates with practical contingency planning. A policy of over-disclosure on impurities and trace byproducts protects both customer and end user, while also future-proofing against regulatory tightening. This proactive attitude comes from lived experience—past gaps in industry self-policing have led to tighter scrutiny, but those who already maintained robust records had nothing to hide.
Supplying 5-Chlorooxindole brings lessons, both as a chemical process and an evolving business practice. Winning over supply-chain decision makers and lab chemists alike doesn’t depend on jargon or bare minimum specs. We build on what we learn, treat every lot as a chapter in a much longer story, and answer questions directly and in detail, drawing on our logs, know-how, and pride in our work.
For large enterprises scaling up to new chemical platforms or startup ventures trialing fresh analogs, 5-Chlorooxindole supplies cannot be approached as a faceless transaction. Traceability, transparent methods, and honest communication are not optional add-ons—they’re built into every bag, drum, and delivery document leaving our facility. Years of close work with process chemists, production managers, and R&D teams have shown us that a little more attention paid up front prevents a dozen headaches down the line.
By focusing on accountable, hands-on manufacturing with traceable origins, we secure long-term partnerships—not just single sale orders. The result: a consistently reliable 5-Chlorooxindole supply that supports innovation, keeps auditors satisfied, and gives the users downstream fewer surprises and more options, campaign after campaign.