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HS Code |
450592 |
| Chemical Name | 3-Acetoxy-5-Bromoindole |
| Cas Number | 376594-36-8 |
| Molecular Formula | C10H8BrNO2 |
| Molecular Weight | 254.08 g/mol |
| Appearance | Off-white to light yellow solid |
| Melting Point | 136-140°C |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Synonyms | 5-Bromo-1H-indol-3-yl acetate |
| Smiles | CC(=O)Oc1c[nH]c2ccc(Br)cc12 |
| Inchi | InChI=1S/C10H8BrNO2/c1-6(13)14-10-7-4-8(11)2-3-9(7)12-5-10/h2-5,12H,1H3 |
As an accredited 3-Acetoxy-5-Bromoindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 10g amber glass bottle, tightly sealed, with a clear label: 3-Acetoxy-5-Bromoindole, CAS number, and hazard warnings. |
| Shipping | 3-Acetoxy-5-Bromoindole is securely packaged in sealed containers to ensure stability and prevent contamination during transit. Shipping complies with chemical safety regulations, using padded, leak-proof materials and, where required, temperature control. All containers are clearly labeled with hazard information, and transport meets international standards for hazardous materials. |
| Storage | 3-Acetoxy-5-Bromoindole should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator). Avoid exposure to strong acids, bases, and oxidizing agents. Ensure proper chemical labeling and follow all relevant safety guidelines to prevent accidental exposure or degradation. |
Applications of 3-Acetoxy-5-Bromoindole in Industrial ManufacturingAs a specialized manufacturer of 3-Acetoxy-5-Bromoindole, we supply this advanced indole derivative to a select range of industrial sectors. This compound supports high-value synthesis pathways in pharmaceuticals, agrochemical research, advanced dye development, and functional material science. Each application requires precise compliance management, formulation control, and established integration within proprietary production processes. Below, we detail key industrial scenarios, explicitly mapping application parameters and related compliance frameworks. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisAPI producers utilize 3-Acetoxy-5-Bromoindole as a key intermediate when constructing complex indole frameworks, especially in stepwise synthesis of anti-cancer, anti-inflammatory, or CNS-active pharmaceuticals. This compound provides a functionalized scaffolding suitable for Suzuki-Miyaura and Buchwald-Hartwig coupling chemistry, which streamlines the introduction of bioactive substituents. In practice, strict change-control procedures ensure batch consistency and full traceability from intermediate to final dosage form for regulated pharmaceutical manufacturing pipelines. Industry compliance standards
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2. Advanced Agrochemical R&D (Herbicide and Plant Growth Regulator Precursors)Industrial agrochemical research teams use this compound when investigating novel indole-based bioactives. Its brominated acetoxy functionality enables rapid screening of new analogs by facilitating late-stage group modifications during plant growth regulator and herbicide synthesis. Typical applications include scale-up of lab-optimized lead structures for regulatory testing or field trials, with full documentation for environmental and operator safety compliance during processing. Industry compliance standards
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3. Organic Electronics and Functional Dye DevelopmentSpecialty chemical manufacturers use this indole derivative within R&D pipelines for organic semiconductors, OLED emitters, and high-performance functional dyes. Its brominated functional group is suitable for cross-coupling reactions, resulting in extended conjugated systems or tunable optoelectronic properties. Consistency in reagent purity and process traceability is essential for materials designed for optical films, sensor components, or display-related dyes under emerging international quality norms. Industry compliance standards
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4. Fine Chemicals for Advanced Laboratory ReagentsProducers of analytical and synthetic reagents employ this brominated indole as a specialty starting material for reference standard production and test kit development. Its unique substitution pattern provides a basis for bespoke small-molecule libraries or marker compounds used in research studies, stability testing, and method validation. Each manufacturing run follows reagent-grade quality control and documentation aligned with scientific reproducibility requirements. Industry compliance standards
Typical usage ratio
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We make 3-Acetoxy-5-Bromoindole for chemists who need genuine reliability in their building blocks. Over the years, feedback from customers running discovery labs, scaling up kilo quantities, or charting new pharmaceutical directions has shaped how we approach its manufacture. What some see as a niche reagent, we see as an essential step—one that makes or breaks long routes, drives SAR studies, and clears away roadblocks for innovators.
We don't just pack and ship; we start at the reactor wall, tuning conditions batch-by-batch to ensure both the 3-acetoxy group and the 5-bromo handle emerge with clean, distinct signals. Purity in this field can't tolerate margin for error, so we invest resources into both process and analytical controls, often rerunning thin-layer chromatography, HPLC, and NMR before a drum even leaves the facility. That precision keeps teams downstream from facing surprises at workup or scale-up.
Our 3-Acetoxy-5-Bromoindole comes in a free-flowing, high-purity crystalline form, optimized for weighing accuracy and stable storage. Consistency batch-to-batch matters far more than pretty packaging, especially when buyers depend on tight timelines or have ongoing projects reliant on single-source supply. We've heard stories from research teams forced into late-stage troubleshooting due to unexpected impurities in their intermediates—something a manufacturer can avoid only by investing in rigorous production systems and honest self-inspection. That's why we blend experience, analytical tools, and a real commitment to transparency in every lot we release.
On the synthetic chemistry floor, we've seen end users care most about minimizing waste and maximizing clean conversions. Our product keeps sidelining issues like uncontrolled hydrolysis or variable melting points, both of which can complicate design and scale-up. We avoid seeding our batches with excess inhibitors or anti-caking agents that could interfere with end-stage steps. Having run reactions ourselves, we understand that above all, a reagent should behave predictably from flask to flask.
It takes hard-earned patience to get the acetoxy group installed at the 3-position without dragging in over-acetylation or unwanted quinone-type byproducts. Our lab teams worked months fine-tuning solvents, monitoring temperatures, and keeping bromination from wandering into the wrong position. The result? Fewer headaches for downstream chemists who rely on this indole to stay monofunctional until they want it to react. Years ago, competing materials sourced through secondary trading houses kept mixing structural isomers or showing faint colored streaks on HPLC. Now, our product's unambiguous signatures let users run transformations with peace of mind.
3-Acetoxy-5-Bromoindole finds itself in modern suites of heterocycle diversification, fitting neatly into cross-coupling, palladium-catalyzed operations, or direct arylation strategies. Teams advancing kinase inhibitors or CNS-acting drug leads have integrated it at late and early stages, leveraging the bromine for Suzuki or Buchwald-Hartwig couplings, and the acetoxy for subsequent deprotection. We heard from a customer running a dozen synthesis iterations per week—the uniformity of our intermediate shaved hours off their workups by avoiding repeated impurity purging.
This indole derivative also supports agrochemical programs in seed companies and pigment developers working at the material science frontier. The combination of a protected 3-position and an electron-withdrawing bromine opens synthetic flexibility that goes beyond the pharmacy. Researchers value not having to shield and deprotect with extra steps, especially if those steps introduce toxic byproducts or require hard-to-source reagents.
We worked with a mid-sized biotech facing sudden scale pressure on a promising analog series. Our 3-Acetoxy-5-Bromoindole gave them a cleaner conversion at the gram and multi-kilo mark, saving hundreds of labor hours on undesired hydrolysis products. Every cycle they lost running extra washes cost days; each clean run restored both budget and morale.
Having made indole derivatives from scratch, we know how subtle changes shift reaction outcomes. Take the difference between 3-Acetoxy-5-Bromoindole and its closest cousins. Using unprotected 5-bromoindole often brings uncontrolled side-products, especially under oxidative or strongly basic conditions. The acetoxy group stabilizes the molecule in standard stockroom humidity, makes handling safer, and prevents undesired N-alkylation or ring-opening unless specifically triggered.
Some groups have tried using unbrominated or multi-brominated indoles to bypass certain steps. We see those choices play out in more waste, lower selectivity, and extra purification cycles. Nothing replaces the direct access to C5 functionalization that our product offers—especially once users discover that skipping the protection step can mean incorporating unpredictable contaminants or masking minor instabilities until the scale magnifies them into real batch failures.
By producing the 3-acetoxy, 5-bromo variant, we offer an indole ready for programmable diversification. This approach lets med chemists or materials teams focus directly on the desired substitutions at the right stage—especially important for SAR loops or patent-space investigations that punish wasted cycles and lengthy chromatography.
A good product doesn't only pass in-house QA; it survives real customers' toughest conditions. Our quality team runs each lot through repeat analytical checks—NMR, LC-MS, water content, and residual solvents—all tied to actual retention samples, not just a slip of paper. We keep every batch logged with deep traceability, so researchers or regulatory teams can trace their key intermediate from delivered vial back to the day it came off the reactor.
Some labs write in with requests for process chemistry guidance or want to adapt to a continuous reactor. Our records help decode any anomalies in reactivity. When one client faced a subtle exotherm in coupling runs, we pulled our in-process control data to help develop safer loading and addition rates, reducing their risk of runaway reaction and enabling them to continue hitting their targets.
Shipments always come from our facility using only transport services that follow real, enforceable standards. We skip third-party broker storage, keeping material integrity controlled from synthesis to customer.
Making complex intermediates means facing regulations that evolve as science advances and regulators learn from the field. We commit to both the letter and the intent of these rules—ensuring downstream users don't face compliance trouble or unanswerable audits. Our certifications reflect direct audits and yearly process reviews. The documentation for our 3-Acetoxy-5-Bromoindole aligns with requirements for process transparency, hazardous material handling, and batch-specific quality systems.
We saw increased scrutiny of indole derivatives after a surge in synthetic research aimed at psychoactive compounds. Because of this, our data systems track every shipment and keep an accurate materials ledger available for verification. Customers working under Good Manufacturing Practices (GMP) receive full documentation, but even early R&D teams can access comprehensive batch histories and know exactly what went into each sample. That peace of mind matters when grant auditors or regulatory representatives look for proof of diligence.
Long-term relationships with chemical regulators help us navigate changes in international shipping, labeling, and environmental guidelines. We don't gamble on loopholes or unknown transport channels—if import restrictions or new HazMat frameworks emerge, we update both our internal procedures and customer advisories as soon as we validate the new system internally.
Everyone in our field is learning that "routine processes" aren’t enough. Solvent waste, mutagenic impurities, and energy intensity factor into every kilogram made. Our plant engineers replaced halogenated solvent streams with greener options where process safety allows. This came out of our own hazard reviews and industry push for cleaner synthesis.
Waste minimization drives our method development. Each step in the 3-Acetoxy-5-Bromoindole route is tracked on in-house mass balances. We work toward step reductions that lower both solvent and energy consumption, not just for cost, but because our community expects us to hand down a cleaner industry than we inherited. We constantly field ideas from both our staff and end users, weighing partner suggestions on purification or recycling streams. This has already yielded a drop in hazardous waste outputs, which benefits both our local footprint and our customers’ downstream disposal obligations.
We also consider packaging. Our shipments use only recyclable drums and minimize secondary plastics where stability allows. For kilo and sub-kilo orders, we default to glass or HDPE containers with robust sealing. These choices come from direct research and repeated customer outreach—not just internal audits.
Reliability in rare intermediates means real security for research groups facing deadlines on grant milestones or running phase-gated R&D cycles. Over the last year, global transport snarls and raw material bottlenecks taught every chemical manufacturer how to adapt or lose relevance. We stock core inputs for 3-Acetoxy-5-Bromoindole on a rolling basis, double-check supplier documentation, and keep a safety margin in both process capacity and finished goods inventory.
We make our logistics decisions based on actual production rhythms, with delivery schedules designed to match demand spikes and avoid false promises to both small-batch customers and long-term contracts. Large buyers can pre-book capacity; smaller groups see their samples shipped direct from production, not languishing in a warehouse. We do not commit to clients unless we can honor delivery windows—a philosophy earned through tough quarters and customer crises that tested our entire supply chain.
We take pride in our direct relationships with buyers. Technical support requests come straight to our synthesis experts, not an outsourced help desk. If someone encounters a problem with a reaction involving our 3-Acetoxy-5-Bromoindole, we work alongside their chemists to resolve it—whether that's troubleshooting batch variability, offering swap samples, or adjusting delivery timing to real-world project pivots.
Pharmaceutical firms turning out new kinase inhibitors rely on rapid iteration. One client reported that delayed shipments from other sources cost months of effort on a high-stakes program. We stepped in with validated, on-hand material, supplying lots that kept their lead compounds moving down the timeline. Our experienced synthesis chemists talked them through every facet of handling, purification, and scale-up, sidestepping the kinds of delays that burn precious budget and staff energy.
Elsewhere, research into organic semiconductors found our indole intermediate allowed for a direct and selective route to a key material for next-gen displays. The researchers needed consistent reactivity at the bromine center, but some alternatives introduced unpredictable substitutions or contaminated the core. Our attention to regioselectivity throughout years of manufacturing paid off: the product they received avoided the pitfalls seen with competitor batches, keeping R&D on pace and within restriction limits for impurities.
As synthetic chemistry uncovers tougher targets, the demand for reliable, functionally rich indole intermediates grows. We listen closely to fellow chemists and corporate partners—where processes can be improved, we channel those suggestions right back into our method development. Every failed attempt, every successful scale-up, and every support ticket finds its way into our approach, making sure even small tweaks mean fewer disruptions for the next customer.
Our 3-Acetoxy-5-Bromoindole reflects a philosophy grounded in experience: produce clean, predictable, and precisely analyzed building blocks, keep customer communication open and practical, and evolve quickly as both science and regulation change. We stand by the chemical, the people who use it, and the innovations it makes possible.