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HS Code |
796696 |
| Product Name | 5-Bromoindole-2-Carboxylic Acid |
| Cas Number | 1631-73-8 |
| Molecular Formula | C9H6BrNO2 |
| Molecular Weight | 240.06 |
| Appearance | Light yellow to beige powder |
| Melting Point | 265-269°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in DMSO, moderately soluble in methanol |
| Storage Temperature | 2-8°C |
| Smiles | C1=CC2=C(C=C1Br)NC(=C2)C(=O)O |
| Inchi Key | KCRDCGYYNSXEEB-UHFFFAOYSA-N |
As an accredited 5-Bromoindole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A clear, sealed glass vial containing 10 grams of 5-Bromoindole-2-Carboxylic Acid, labeled with product details and safety information. |
| Shipping | 5-Bromoindole-2-Carboxylic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture ingress. Packaging complies with international regulations for hazardous materials. The shipment includes appropriate labeling and documentation, with temperature-sensitive handling if required. Transport follows safety protocols to ensure chemical integrity and regulatory compliance during transit. |
| Storage | **5-Bromoindole-2-carboxylic acid** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator). Avoid exposure to incompatible substances such as strong oxidizers. Ensure the storage area is clearly labeled and complies with standard laboratory chemical storage regulations. |
Applications of 5-Bromoindole-2-Carboxylic Acid in Industrial ManufacturingAs a direct manufacturer of 5-Bromoindole-2-Carboxylic Acid, we serve key sectors where this compound acts as a critical intermediate, primarily in the development and synthesis of advanced pharmaceuticals, fine chemicals, and specialty organic materials. The following sections detail the most widely documented industrial downstream applications, covering regulatory requirements, technical process integration, and finished product outcomes. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers use 5-Bromoindole-2-Carboxylic Acid as a core building block during multi-step synthesis of various small-molecule APIs, primarily those containing indole substructures for oncology and central nervous system indications. It enters critical halogenation and coupling reactions under GMP conditions, where its high purity minimizes side reactions, supporting efficient manufacturing of API precursors that demand strict control of trace impurities and residual solvents in the end product. Industry compliance standards
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2. Agrochemical Research Compound SynthesisDownstream agrochemical developers incorporate 5-Bromoindole-2-Carboxylic Acid in the synthesis of research-grade indole-based seed treatment agents and experimental herbicide candidates. Its role focuses on selective halogenation and ring functionalization, allowing property modulation for developing lead compounds before field-scale trials and regulatory submissions. Industry compliance standards
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3. Dye and Pigment Intermediate ManufacturingIndustrial specialty chemicals operations utilize this material as a functionalized indole source for the preparation of azo and heterocyclic dyes, where bromine substitution enhances chroma and lightfastness. The compound’s stability during high-temperature condensation reactions supports consistent batch yields of high-purity dye intermediates, demanded for further chemical modification and finished pigment synthesis. Industry compliance standards
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4. Advanced Organic Electronics R&DIn organic electronics research, 5-Bromoindole-2-Carboxylic Acid supports the synthesis of high-purity functional materials for organic semiconductors and OLED emitter development. Academic and industrial labs leverage its controlled halogen and carboxyl substitution pattern for precise coupling reactions, which facilitate the assembly of conjugated systems and active layers in prototype optoelectronic devices. Industry compliance standards
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Working each season with 5-Bromoindole-2-Carboxylic Acid on our shop floor and in our labs lets us pull back the curtain on what makes this compound genuinely useful in modern synthesis. Drawing on daily experience from the reactor to the drum and every step in between, we notice how this indole derivative holds a steady place in both research and production. 5-Bromoindole-2-Carboxylic Acid stands out not as a niche specialty but as a reliable mainstay for teams developing pharmaceuticals and complicated natural product analogs.
With our in-house approach, every batch starts with a direct focus on purity and integrity. The structure—C9H6BrNO2, CAS 885-77-8—describes only a fraction of the story. Each run, we measure grain characteristics, particle texture, and solubility to ensure a consistent and reproducible output. From handling to packaging, our teams understand how small variations impact downstream chemistry and formulation.
One insight that comes with years in chemical manufacturing is the difference process control makes. The route chosen to synthesize an indole carboxylic acid can shift yield or impurity profile. For 5-Bromoindole-2-Carboxylic Acid, controlling the bromination and subsequent carboxylation steps keeps both the 5-bromo position clean and the acid group free from overreaction or decarboxylation. Minor slip-ups here introduce byproducts that waste time for formulators or create environmental headaches.
Because we manage reaction temperatures and reagent addition—never rushing or skimping on intermediate purifications—we keep heavy metals, halogenated side products, and colored residuals far below accepted thresholds. Precision here directly translates to trust in every subsequent coupling or derivatization using this building block. Every kilogram leaving our plant has been checked and rechecked for these issues.
No one sees the quirks and practical problems of 5-Bromoindole-2-Carboxylic Acid’s journey quite like the people loading it from jacketed flasks into dryers, sievers, and sealed containers. The solid form can pick up moisture if stored for too long in humid air. We solve this by double-vacuum drying and nitrogen-purging the product directly into lined drums—real measures only a manufacturer can appreciate.
A lot of material in circulation comes from repackagers or traders with no connection to the actual chemical processes behind the powder. If you ask about sources of off-white flakes or faint odors, how color might affect your LC/MS results, or why carboxylic acids sometimes fail to dissolve—these aren’t idle questions to us. Our staff can pull batch records, note reagent lots, and explain outcomes. If a patch of product shows a drift in melting point or unexpected fluorescence, we know whether the issue appeared at bromination, quenching, or drying, and not just by deduction but by tracking the full run from raw material inspection to the last seal on the drum.
Industry analysts might once have accepted a purity of 97%. Our teams raised that bar years ago. We routinely hit at least 99% by HPLC, because every extra decimal makes a difference in syntheses that tolerate little leeway. Residual solvents—especially chlorinated and aromatic ones—are kept well below 300 ppm. Water content stays under 0.5%. We established these benchmarks by listening to research chemists frustrated by hard-to-dry acids, or scale-up groups chasing fewer code-red batch failures.
Monitoring particle size distribution has made downstream handling radically smoother for our clients. We mill and sieve to a fine powder, but not so aggressively as to encourage static or dust loss. Chunky crude may save us processing time, but it clogs hoppers and feeder lines. Over-milling, on the other hand, makes static cling or dusting a constant risk. Our granulation sits at a point where blending, measuring, and suspending creates minimal loss and uniform dosing.
On the instrumental side, we respond to feedback by adding tighter controls: GC-MS for traces of precursor amines, updated IR for functional group integrity, and laser scattering for particle size checks before each shipment. Our quality specialists keep these metrics transparent, both for us and for clients scaling to pilot production or regulatory review. Every process improvement results from concrete troubleshooting on the shop floor, not distant speculation.
The primary users of 5-Bromoindole-2-Carboxylic Acid come from pharmaceutical discovery and custom synthesis. Many ask for this intermediate because it allows rapid access to indole-based drugs, kinase inhibitors, or experimental agrochemical candidates. The bromo substitution opens up cross-coupling methods—Suzuki, Stille, Buchwald—providing an easy anchor for aryl, vinyl, or heterocyclic appendages. The carboxylic acid group means researchers can cyclize, amidate, or append solubilizing or bioactive fragments without lengthy protecting group strategies.
Handling and storage advice we give stems from common pitfalls we see. Allowing the product to sit exposed to humid lab air can affect not only weighing but also reproducibility in multistep syntheses. For long-term stability, we developed vacuum-sealed, foil-lined packaging that stays robust when shipped by land or air. Feedback from users who faced dissolution problems after storing open jars prompted us to adapt the lining process.
Academic and industrial projects also use this compound in high-throughput library synthesis. Demand for tight specification tolerance goes up in these settings, since automated pipetting and parallel processing flag any deviation in powder flow, solubility, or trace impurity. Our floor teams and QC analysts consistently test the material for both solubility (in DMF, DMSO, NMP, and basic water) and dusting issues.
We’ve seen research teams abandon other 5-substituted indole acids on account of unreliable supply chains or solvent instability. Reports sometimes reach us of sticky, clumped powders or yellow-to-brown discoloration—typical of byproduct bromination or oxidation during storage. Consistent structure and handling differentiate our product from those whose provenance or treatment are unclear.
Troubleshooting new runs with a team means spotting problems fast. We’ve caught instances where a minor shift in starting material purity altered the final product’s performance in coupling reactions. Traces of dibrominated indole carry over only when raw material handling gets rushed. We track each raw material through rigorous incoming quality checks—analyses for purity, byproduct content, and residual moisture—knowing how they affect final yields and purity.
Some users notice subtle differences in the crystalline form depending on storage conditions. The structural polymorph a batch settles into can shift reactivity in solution, usually surfacing only in large-scale coupling steps. To head this off, we tailor cooling and crystallization steps, working from pilot batches before locking procedures for production. Customer feedback prompted us to investigate and solve polymorphic drift, not just once, but thousands of times through both anecdotal and documented returns or follow-ups.
Color is another telltale sign for anyone making or buying 5-Bromoindole-2-Carboxylic Acid. Faint pink or yellow color hints at oxidation or incomplete washing. We adjust wash protocols and sometimes double the purification pass if we see even a minor color shift. The effort more than pays off in clear, reproducible signals on clients’ detectors or analytical systems. Handling color as a real-world metric brings more value to customers than just ticking a specification box.
People often ask what sets this acid apart from its close chemical neighbors—like 5-Bromoindole or 5-Bromoindole-3-Carboxylic Acid. Small as the structural difference may seem, the 2-carboxylic acid opens a window into distinct reactivity and downstream possibilities. The 3-carboxylic acid, often compared side-by-side, reacts differently in amidation and cyclization, leading researchers down other synthesis routes.
We manufacture both the 2- and 3-carboxylic variants, so we’ve tracked the performance of each in hundreds of projects. The 2-carboxylic compound aligns better with Suzuki-Miyaura and other palladium-catalyzed couplings at the 5-position, especially for late-stage diversification of natural product analogs and kinase inhibitor scaffolds. Our technical staff also notes that the electronic and steric properties of the acid at the 2-position suppress undesired polymerization or dimerization during scale-up, problems more common with the 3-acid.
Non-brominated indole-2-carboxylic acid lacks the same vector for functionalization via modern cross-coupling chemistry. Without the bromo handle, expanding the family of derivatives moves much slower or demands lengthy pre-functionalization—delays unacceptable to high-throughput discovery or process development. For those aiming at patentable compounds or one-pot transformations, brominated scaffolds provide unmatched flexibility.
Some producers routinely supply broader ranges of indole derivatives, but not all maintain the strict environmental or safety safeguards we do. Bromo chemistry can risk forming volatile organics or generating hazardous halogenated waste. We balance process efficiency against worker safety and environmental responsibility, using in-line scrubbers, solvent recapture, and waste minimization built into our synthesis setups.
The greatest changes in our process did not start from abstract design but from sincere customer requests and collaborative troubleshooting. Labs running combinatorial chemistry demanded not just chemical purity but a narrow, predictable particle size. Drug developers asked for details on trace halogen or residual catalyst levels, to match the climate of tightening regulations and audit controls. Every improvement, from drum design to solvent removal, grew out of these concrete problems and iterative feedback.
Shipping product overseas threw up the challenge of keeping material intact and desiccated across temperature swings and humid transits. Our packaging engineers worked with logistics staff to devise foil linings and vacuum seals resilient to days or weeks in cargo holds. Those complications—opacity, weight limits, puncture resistance—emerged only through direct hands-on experience, not theoretical discussion.
Some research partners in emerging markets flagged instability in off-brand or gray market materials. Strange melting points, unexpected odors, and decomposition after a short shelf life all point to poor handling, residual solvents, or cross-contamination. Our investment in supply chain traceability means anyone using our product can track its journey from initial bromination reaction to final drum seal, not just at the batch level but by every significant handling or rework event.
Clients working in drug discovery or scale-up have little use for arms-length assurances or “compliant” language. They want to know how a compound will behave under stress, in challenging coupling reactions, or after months of storage. Our years in the industry mean every innovation we make traces back to a straightforward test: will this batch keep downstream chemistry running smoothly, reproducibly, and at scale?
Failure in one batch can throw off weeks of work in a contract research lab. That’s why a manufacturer’s enduring focus lands on removing residual solvents, eliminating visible color and dust, and maintaining reliable particle characteristics. Hearing about time lost to a sticky, half-dried acid or a powder that won’t pour on a balance motivates us to do better. We walk through those same challenges every day, so solving them goes beyond mere compliance—it’s personal.
We host technical Q&A every quarter with our production crew, shipping partners, and QC analysts to track repeat issues, gather fresh ideas, and fine-tune steps based on what the benchmarks require. Nothing surfaces improvement opportunities like first-hand feedback from scientists at the bench and plant operators on the loading dock.
Supply chain problems—lost material, unidentified byproducts, inconsistent sourcing—surface more often when intermediaries obscure the real story of a compound’s production. Working directly with manufacturers means less guesswork, faster troubleshooting, and full access to the details that shape research outcomes. Buying from a firsthand producer means every question about appearance, stability, trace content, or flow comes answered by someone with actual facility access and practical know-how, not a generic spec sheet.
We welcome site audits, online consultations, and ongoing technical support for every batch we ship. Requests for alternate solvent screens, reprocessing, or tighter melting range targets never get shunted to a trading desk. The people addressing those requests walk the same shop floor and run the same reactors that produced each lot in question.
Direct feedback from end users grows into better practice for us. Thinking back to days spent troubleshooting backlogged orders or late-night rework runs, experience shows results come quickest when producer and client work side by side. Our production team sees each batch of 5-Bromoindole-2-Carboxylic Acid not just as pounds of powder, but as the foundation for the next round of discoveries, drugs, or advanced materials emerging from our customers’ labs.
No chemical intermediate stands still. With each passing year, regulations tighten, downstream expectations grow, and the push for efficiency rises. Our teams revisit every protocol—reagent selection, solvent removal, drum filling, and documentation—seeking to eliminate outdated steps and boost both safety and performance.
Sustainability requires finding greener alternatives for waste removal, reducing hazardous reagents, and boosting solvent recapture. We make these shifts not because they are mandated, but because they make the business and the broader environment healthier. Mastering the manufacture of a bromoindole carboxylic acid is as much about respect for our crew and our customers as about hitting hard data points.
Looking ahead, we keep investing in both equipment and training, learning from every batch issue and customer result. If a certain approach can lower residuals or reduce batch-to-batch color drift, we push for adoption across all lines. Open lines of communication, skilled operators, and a willingness to fix mistakes mark the difference between adequate production and real leadership in specialty chemicals like this.
Every kilogram of 5-Bromoindole-2-Carboxylic Acid carries not just value in its structure but the cumulative learning from thousands of production runs, quality audits, and direct user feedback. Where others may see just another commoditized intermediate, we see a daily test of process, precision, and response to those who rely on dependable, well-made material.
Standing behind our product stems from knowing each detail—from reagents to final packaging—has been tuned over years of effort. Every shift, our team tracks not just numbers but real-world outcomes, securing confidence in each transfer of this critical building block. We welcome technical discussion and practical inquiry from those in the trenches, sharing what we’ve learned about making and delivering chemical intermediates that form the backbone of pioneering science everywhere.