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HS Code |
636948 |
| Iupac Name | 5-Methoxy-1H-indole-3-carboxylic acid |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.18 g/mol |
| Cas Number | 16727-59-0 |
| Appearance | Off-white to light yellow powder |
| Melting Point | 217-222°C |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=CC2=C(C=C1)NC=C2C(=O)O |
| Inchi | InChI=1S/C10H9NO3/c1-14-7-3-2-6-8(9(7)11-4-6)5-10(12)13/h2-5,11H,1H3,(H,12,13) |
| Pka | 2.7 (carboxylic acid group) |
| Storage Temperature | Store at 2-8°C |
| Pubchem Cid | 66097 |
| Logp | 1.56 |
| Synonyms | 5-Methoxyindole-3-carboxylic acid |
As an accredited 5-Methoxy-3-Indolecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle labeled “5-Methoxy-3-Indolecarboxylic Acid, 25 grams.” Features hazard warnings, CAS number, and lot number. |
| Shipping | 5-Methoxy-3-Indolecarboxylic Acid is shipped in sealed, chemically resistant containers to prevent contamination and degradation. Packages are clearly labeled according to regulatory standards. During transit, it is protected from moisture, extreme temperatures, and direct sunlight. Shipping complies with all applicable local, national, and international regulations for chemical transport. |
| Storage | 5-Methoxy-3-Indolecarboxylic 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 room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizing agents. Proper labeling and adherence to safety protocols are essential to ensure safe storage and handling. |
Applications of 5-Methoxy-3-Indolecarboxylic Acid in Industrial ManufacturingAs a specialized chemical producer, we supply 5-Methoxy-3-Indolecarboxylic Acid for integration into several core industrial sectors. Below, we outline its regulated use cases across four principal downstream markets, with details on compliance, dosing, process position, and finished outputs in each application channel. 1. Pharmaceutical Intermediate for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs)Pharmaceutical manufacturers use this compound primarily as an advanced intermediate during the synthesis of certain indole-based NSAIDs. Its indolecarboxylic structure enables stepwise chemical transformation. The product enters the ketone synthesis stage, where the 5-methoxy group improves reaction specificity and yield. Integration occurs under GMP-compliant cleanroom conditions, and material traceability is required for batch release. The end result is formation of key intermediates that are subsequently converted into finished pain relief medications after further processing and quality control. Industry compliance standards
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2. Agrochemical Intermediate for Plant Growth RegulatorsWithin crop protection manufacturing, 5-methoxy-3-indolecarboxylic acid functions in the synthesis of specialty auxin analogues—key ingredients in selective herbicides and plant growth regulators. Process engineers introduce the compound downstream of initial indole ring assembly, leveraging its methoxy group to direct regioselective modifications. Quality assurance procedures include spectral purity and residue profiling, as required for agricultural chemical registration and global export. Industry compliance standards
Typical usage ratio
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3. Fluorescent Dye Intermediate in Biochemical Reagent ManufacturingChemical and biotech firms rely on 5-methoxy-3-indolecarboxylic acid to build indole-based fluorophores used in diagnostic imaging and nucleic acid labeling. The compound enters the dye intermediate stage after carboxyl group activation. Strict analytical control ensures freedom from UV-active impurities and accurate substitution patterns. Final dye calibration requires trace-level verification by HPLC and LC-MS, to provide consistent photo-physical properties in downstream bioassays. Industry compliance standards
Typical usage ratio
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4. Specialty Fine Chemicals in OLED and Electronic Material SynthesisManufacturers in the electronic materials sector employ this indolecarboxylic acid as a core segment in heterocyclic conjugated polymer synthesis. Its unique substitution allows tuning of electron-donating properties required for new-generation OLED (organic light-emitting diode) materials and photonic applications. The incorporation occurs via palladium-catalyzed cross-coupling after carboxyl activation, where purity fluctuations directly affect the final film quality and device consistency. All process steps require electronic-grade starting material tracked under ISO quality systems for clean production. Industry compliance standards
Typical usage ratio
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In our daily production work, 5-Methoxy-3-Indolecarboxylic Acid stands out as a product that finds itself mentioned regularly among research chemists and industrial clients who care about reliable building blocks. Throughout years on the floor and in the process development lab, we’ve handled a range of indole derivatives, but only a few show the same dependability in synthesis as this compound.
Our routine work makes us keenly aware of its chemical formula, which reads C10H9NO3, and its molecular weight of around 191.19 g/mol. The white to off-white crystalline powder we ship out needs to meet high standards of purity, often tailored for precise applications in pharmaceutical research or specialty materials intermediates. We know well the way every small change in side chain or substituent on the indole backbone can affect downstream chemistry — especially its methoxy substitution at the fifth position, which helps to steer reactivity and compatibility in subsequent steps.
Reliable quality forms the heart of any manufacturing facility worth the name. In our plant, we've learned to respect the quirks of indole chemistry. The methoxy group at the 5-position challenges process engineers with its potential for demethylation and must be protected from unnecessary exposure to strong acids and bases during synthesis and isolation steps. Lab-scale work taught us a lot, but full-scale production brought its own lessons about filtration, solvent choice, and gentle drying.
We lean on robust HPLC, NMR, and IR analysis to check for common traces: residual solvents, potential methylation byproducts, and incomplete hydrolysis that can show up when production steps run less than optimally. The analytical team and production staff work in tight communication, and regular audits of batches help identify even small deviations. Mistakes happen, but spotting them early means losing less time and fewer resources later.
Our end-users drive the demand for 5-Methoxy-3-Indolecarboxylic Acid. Regular customers in medicinal chemistry order it for early-stage candidates where the indole core must support various pharmacologically active groups. The methoxy group serves more than decoration — it’s known to impact both compound solubility and metabolic stability of the resulting drug molecules.
Specialty pigment and dye researchers value how the methoxy group at the 5-position can adjust shade and behavior without inviting color instability. We supply small, research-scale lots for screening efforts, as well as multi-kilogram batches to those who have advanced to pilot or production scale, always keeping customer feedback in mind. The feedback loop with formulators, bench chemists, and technical managers has pushed us to adjust packing forms, moisture protection, and batch sizing so that adoption stays easy and losses minimal.
It’s not just the name that sets this compound apart within the indolecarboxylic acid family. The methoxy group at the 5-position matters in both the lab and the production plant. We’ve worked with unsubstituted indole-3-carboxylic acid, and the differences become clear during reactions. The methoxy group brings added electron-donating properties, which affects nucleophilic attack in common coupling and condensation processes.
Some customers ask for the 5-hydroxy or 7-methoxy derivatives, and we make and supply those, too. Yet, the 5-methoxy variant balances reactivity and stability for downstream transformations, especially for those making tryptamine analogs or other bioactive molecules. The methoxy group’s steric influence sometimes blocks unwanted side reactions, sparing users from extra purification headaches down the road.
From a handling perspective, the crystalline form tends to offer improved flow properties compared to some stickier, more hygroscopic indoles. That makes a difference in automated powder dispensing or when feeding larger reactors. Lab techs appreciate less caking, and downstream cleaning goes quicker — an often-overlooked efficiency in busy operations.
Product requirements from research labs differ sharply from those in process scale-up or manufacturing. We’ve learned to keep communication open with technical teams at customer sites, taking feedback on what works and what doesn’t. We adjust batch purification parameters for those who need purities above 98 percent, especially for clinical research or materials where trace byproducts cause significant issues. For others heading into exploratory chemistry, we can tune specs a bit, delivering a more cost-effective product that keeps their project on budget.
Storage and packaging needs grow as customers work through pilot batches and scale their own processes. The 5-methoxy substitution offers some benefit: these materials handle air exposure better than their hydroxy analogs, reducing degradation during storage or shipping. Yet, no indolecarboxylic acid appreciates extended exposure to moisture or open air, so packaging methods rely on the right gas flushing, low-permeability bags, and secondary containment. We change pack size per customer project, from small sealed bottles for R&D teams to multi-kilo drums lined with moisture barriers where regular partial use occurs.
Process chemistry for 5-Methoxy-3-Indolecarboxylic Acid taught us that each upstream intermediate must meet tight specs, because trace over-alkylation or incomplete substitution quickly shows up as impurity. Early batches were plagued by slight fennel-like odors from side products — nothing a spec sheet would tell you, but something that could taint the next coupling reaction for a customer working on a delicate chiral synthesis.
Continuous improvement remains a backbone of any proper shop. Operators send real-time notes to QC and R&D about crystal size, solution color, or flow rates, and those tiny tweaks save the headaches of batch failures. Standard protocols help, but every production campaign brings new surprises, usually linked to raw material quality changes or ambient humidity swings.
Energy consumption and sustainability targets matter, too. Switching to greener solvents and lowering process temperatures where possible makes a difference in plant energy use and waste output. We revisit each synthesis route yearly, balancing yield, safety, and cost against environmental impact. Recycling solvents and treating wastewater properly carry costs, but keeping local and global regulations in mind prevents trouble in the long run.
Indole derivatives form a large group, but some look quite similar at first glance. Take 3-indolecarboxylic acid and 5-hydroxy-3-indolecarboxylic acid: both show up in similar research spaces. The 5-methoxy substitution sets this variant apart by its influence on hydrogen bonding and reactivity, which changes solubility profiles and rates in common coupling reactions. Budgets and timelines favor products that deliver repeatable results, and customers stick with us because our process keeps trace impurities predictable and at bay. Those who work with methoxy rather than hydroxy patterns also enjoy a longer shelf life, so less ends up wasted or spoiled.
We don’t neglect feedback from researchers who ask about novel indole scaffolds, including multi-methoxy or fused-ring variants. Each difference in substitution pattern demands a hard look at both cost of goods and downstream safety considerations. Sometimes, minor changes in raw materials make a big difference in environmental reviews and permit renewals — another real-world factor influencing what leaves our doors. Documented process transparency sets a professional operation apart, earning ongoing customer trust in regulated and application-critical markets.
Experienced operators develop habits that keep operations smooth and safe. Indolecarboxylic acids do not pose the same hazards as some of the more aggressive intermediates we manufacture, but respect for proper PPE and ventilation still holds. The methoxy group provides some shielding from rapid oxidation, yet trace impurities can still autooxidize and bring unpleasant discoloration or off-odors if left in stock too long.
Splitting up major supply batches for staggered delivery or extended shelf life solves real storage headaches for customers with sporadic but critical needs. Internal tracking of lot numbers and full batch history also helps quickly address any concerns. This isn’t just a matter of records; it gives confidence to customers extending into clinical research or regulated process environments where accountability matters.
R&D teams face pressure to deliver new molecules within shrinking timelines. We hear from medicinal chemists under crunch, process teams who must transfer reactions from milligrams to kilograms, and contract manufacturers seeking reliable supply continuity as their own clients draw closer to commercialization. We don’t treat scale-up work like an afterthought. Each switch from lab- to pilot-scale brings process variables into sharp relief: agitation rate, filtration speed, slurry behavior, solvent miscibility.
We’ve even supported direct collaboration on DOEs and process mapping, offering technical data from our own scale-up files so customers avoid known bottlenecks. Sharing what works — and what’s been a dead end — often saves weeks of repeated mistakes for the next group in line. We regard these projects as real partnerships; every successful launch strengthens long-term ties and improves internal manufacturing discipline for all involved.
Managing byproducts and waste streams takes real attention. Methoxy-bearing indolecarboxylic acids have fewer corrosive or acutely toxic intermediates than some aromatic amines, but our approach ensures all spent solvent gets tracked, neutralized, and disposed of safely. Wastewater treatment in the plant adheres to local and international regulation, with periodic review and outside audits keeping compliance strong.
Where feasible, solvent recovery reduces overall waste. Methanol and related alcohols figure prominently in the synthesis, so engineering teams prioritize their collection and reuse. This not only cuts costs but also lessens our overall environmental impact. Our efforts in these areas mirror growing expectations across the industry for cleaner, more responsible operations. Customers care about the impact of their raw material supply chain, and questions about environmental compliance come more often than years past.
Every so often, changes in regulatory status for related compounds or shifts in end-market requirements drive demand in new directions. For example, pigment applications focus more on color fastness and long-term stability, while pharmaceutical users scrutinize even minor impurities for toxicological reasons. We welcome this prospect, since it keeps internal teams attentive to fine process details and pushes us to refine our batch records.
When new regulatory challenges emerge — such as revised ICH guidelines on elemental impurities or more stringent transport labeling for fine chemicals — we keep lines open with shippers, customers, and our compliance team to head off supply interruptions. Revising documentation, batch labelling, and shipping protocols sometimes presses our administrative staff as much as production, but meeting these demands keeps customer confidence high.
Customers today want more than just a physical product. Regular requests for data on origin, traceability, and ESG (environmental, social, governance) metrics put manufacturers under more scrutiny. Rather than a burden, we treat this as an opportunity — as transparency helps cement long-term business relationships. We maintain open documentation on raw material sourcing, production metrics, and supply-chain risks. Market demand sometimes spikes when a research field points toward new synthetic applications for this indole structure, and agile production lets us respond rapidly.
Broader shifts in the chemical industry — including supply disruptions from geopolitical instability, pandemics, or raw material shortages — affect pricing and availability. We keep inventory levels mapped to both steady customers and fluctuating research demand, aiming to avoid either prolonged lead times or wasteful overstocks. Global partners appreciate prompt communication about changes, and sharing production outlook helps customers plan their projects with fewer surprises.
Looking back over years of production, cumulative improvements in crystallization, drying, and packaging have made the supply of 5-Methoxy-3-Indolecarboxylic Acid ever more reliable and convenient for downstream chemistry. The next steps focus on more sustainable synthesis routes, using greener raw materials and tighter process control with automated instrumentation.
We support development of new derivatives and analogs rooted in customer interest, running pilot campaigns in partnership with university labs or company research teams. These collaborations hone our process for handling new indolecarboxylic acid scaffolds and keep us closely tied to trends in drug discovery and specialty chemicals. Improved batch control, trace impurity management, and packaged product documentation evolve from these shared experiences.
5-Methoxy-3-Indolecarboxylic Acid remains a key intermediate for researchers and manufacturers with projects in pharmaceuticals, agrochemicals, advanced materials, and specialty pigments. Our approach, drawn from years of direct production and problem-solving along the way, ensures consistent supply and support for all stages of customer routes — from bench to plant floor.
This product’s reliability comes from practical investment in process development, a focus on safe handling and regulatory compliance, and a continuous learning culture across both manufacturing and support teams. Keeping pace with evolving customer needs, we commit to regular, honest feedback and agile responses that keep each supply chain running without surprises. Those who work regularly with indole chemistry know the value of a dependable partner who treats batch-to-batch consistency, traceability, and process transparency as everyday facts, not marketing lines. That’s how a manufacturer builds trust — serving both the technical and the practical priorities of today’s advanced chemical users.