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HS Code |
482418 |
| Name | 6-Methoxy-1H-Indole-3-Carboxylic Acid |
| Synonyms | 6-Methoxyindole-3-carboxylic acid |
| Cas Number | 2525-90-4 |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.18 g/mol |
| Appearance | Off-white to light yellow solid |
| Melting Point | 252-256 °C |
| Solubility | Slightly soluble in water, soluble in DMSO and methanol |
| Purity | Typically ≥98% |
| Smiles | COc1ccc2[nH]cc(C(=O)O)c2c1 |
| Inchi | InChI=1S/C10H9NO3/c1-14-8-3-2-6-5-7(10(12)13)4-11-9(6)8/h2-5,11H,1H3,(H,12,13) |
| Storage Temperature | 2-8 °C |
| Pka | Estimated 4.1 (carboxylic acid group) |
| Logp | Estimated 1.6 |
| Usage | Intermediate for pharmaceutical research |
As an accredited 6-Methoxy-1H-Indole-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 6-Methoxy-1H-Indole-3-Carboxylic Acid, securely sealed with a tamper-evident cap. |
| Shipping | 6-Methoxy-1H-Indole-3-Carboxylic Acid is shipped in sealed, airtight containers to prevent moisture and contamination. The packaging complies with chemical safety standards, and is protected from light and extreme temperatures. All shipments include appropriate labeling and documentation, ensuring secure transport and handling according to regulatory requirements. Delivery times vary by destination and carrier. |
| Storage | 6-Methoxy-1H-indole-3-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Store in accordance with local chemical safety regulations and ensure proper labeling to prevent accidental misuse. |
Applications of 6-Methoxy-1H-Indole-3-Carboxylic Acid in Industrial Manufacturing6-Methoxy-1H-Indole-3-Carboxylic Acid serves as a critical chemical intermediate in several high-value downstream sectors, where its indole structure enables precise molecular modifications. Our manufacturing process guarantees compliance with industry standards to meet the specific quality demands of each application. The following sections detail key application scenarios based on actual industry practice. 1. Pharmaceutical API and Intermediate SynthesisThis compound is widely utilized by pharmaceutical manufacturers during multistep synthetic processes for preparing indole-based active pharmaceutical ingredients, particularly in oncology and central nervous system (CNS) drug discovery programs. The presence of the 6-methoxy group allows medicinal chemists to introduce further substitutions, supporting analog development for optimized receptor binding profiles. Accurate quality controls and traceability are required throughout the supply chain to satisfy regulatory filing and registration of APIs. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentIn the agrochemical industry, 6-Methoxy-1H-Indole-3-Carboxylic Acid functions as a precursor in the synthesis of novel indole-type herbicides and plant growth regulators. Downstream formulation specialists value the compound for its ability to form stable, targeted molecules displaying improved selectivity and biodegradability profiles in crop protection products. Tight process controls are necessary to prevent residual monomer contamination in commercial-scale synthesis. Industry compliance standards
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3. Dye and Pigment Intermediate ManufacturingChemical producers in the dye sector exploit the aromatic stability and functional group reactivity of this indole compound to manufacture specialty high-purity pigments. Oxidative coupling and ring modification allow for tunable color properties, enabling textile and ink makers to design colorfast, light-stable dye molecules. Precise dosing and impurity profiling are closely monitored under dye industry batch processing controls. Industry compliance standards
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4. Electronic and Photonic Material SynthesisAdvanced electronics and photonics material manufacturers integrate this indole acid as an initial component in the assembly of organic semiconductors, OLED modifications, and sensor dye compounds. The molecule’s methoxy-substituted aromatic ring provides valuable photophysical properties and chemical stability, supporting the fabrication of efficient charge-transport or light-emitting materials. Production lines require rigorous control of trace metal and residual solvent levels to meet electronics industry reliability benchmarks. Industry compliance standards
Typical usage ratio
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Our journey began with a focus on indole derivatives, tackling the complexities that lie behind every synthesis. Among these, 6-Methoxy-1H-Indole-3-Carboxylic Acid stands out. This compound, often abbreviated as 6-MICA, represents the culmination of years of refining techniques and understanding the subtleties of indole chemistry. Direct experience on the production floor has shown that this molecule holds a well-regarded place in both research and industrial application.
6-Methoxy-1H-Indole-3-Carboxylic Acid features a methoxy group at the 6-position and a carboxylic acid at position 3 of the indole ring. Chemists working at the bench notice distinct differences in reactivity and solubility compared to its unsubstituted relatives. This substitution pattern offers unique electronic and steric properties, making the compound especially attractive for those who need to modify biological activity or tailor synthetic routes during pharmaceutical or materials research.
Meticulous process controls define the purity levels that we maintain batch after batch. Our technical teams commit to high standards, with final specifications supported by precise HPLC and NMR analysis. In practical terms, 6-MICA comes as an off-white to light tan powder, and our chemists vouch for its stability when handled properly. Moisture content and trace impurities present hurdles that we address by maximizing control over drying steps, using reliable storage conditions, and verifying every lot before release.
The model of 6-Methoxy-1H-Indole-3-Carboxylic Acid we supply reflects our experience working with demanding synthesis procedures. We regularly see researchers request a minimum purity of 98%, but internal feedback reminds us that even minor contaminants may interfere in biological screens or downstream coupling reactions. By witnessing failed reactions due to slight off-specification material, we set in-house acceptance tighter than the industry norm, not just meeting but often surpassing published reports.
Many research groups value 6-MICA in the development of tryptophan-derived analogues, enzyme inhibitors, and fluorescent labels. Scientists synthesize peptides, explore small molecule libraries, and test novel scaffolds using this building block. Over the years, open conversations with clients have allowed us to gather insights into new applications. Some incorporate 6-MICA into solid-phase peptide synthesis, banking on its robust carboxyl function that resists side-reactions under standard coupling conditions.
Direct feedback from medicinal chemists emphasizes its value in lead optimization projects. The methoxy group blocks metabolic hydroxylation sites, and the carboxylic acid offers a handle for further structural manipulation. For those transitioning from small-scale exploratory projects to larger batch requirements, reliable sourcing makes a dramatic difference in both speed and success rates. Several end users have described successful scale-ups to pilot plant batches, relying on our consistent quality to meet rigorous documentation and traceability demands.
Our teams take pride in more than just matching a chemical structure. Real differences between various indole-3-carboxylic acid derivatives can make or break a project. For example, 5-methoxy and 7-methoxy analogues share similar names, but anyone who has tried substituting will know that the electronic environment shifts dramatically. Different methoxy positions lead to pronounced changes not only in reactivity but also in solubility profiles and overall stability. Internal studies have confirmed that reagents tailored for one analogue may fail under the same conditions for another—altered pKa, steric accessibility, and conjugation must all be considered.
Many buyers assume that any indole-3-carboxylic acid will meet their needs. Having run repeated optimization cycles, we point out that each substitution shifts the entire behavior of a synthetic protocol. 6-MICA delivers greater oxidative stability than its unsubstituted relative; this feature matters during storage and transport, especially in humid or variable temperature environments. In contrast, other analogues may present higher risks of degradation or hydrolysis, and we address these through both packaging and procedural advice.
Chemists on our production teams have learned that laboratory syntheses rarely scale linearly. Early attempts produced yields lower than expected; side-products proved stubbornly hard to remove. Over time, continuous collaboration with both academic groups and industrial partners refined our operating conditions. By running multiple crystallization and filtration steps, and scrutinizing each intermediate, we reached a protocol that confers both high purity and repeatability.
Long experience highlights that introducing a methoxy group to the indole core increases complexity. Electrophilic substitution requires exacting conditions, especially for a clean introduction at the 6-position. We select reagents with low residual metal content and monitor each step for over-reaction or degradation. Drying conditions, especially after the introduction of the carboxylic acid, can affect the final material dramatically. As a result, our quality assurance focuses not only on the end product but on each stage of the process.
Our years of manufacturing have demonstrated how a single batch out of specification costs time, resources, and trust. For scale-up projects in particular, our teams always discuss the critical stages with the end user, adapting particle size, reagents, or solvent systems suited to their specific downstream application—rather than providing a one-size-fits-all option that may disappoint later.
Quality arises from transparent conversation. Our clients have shared stories of other suppliers where the compound arrives with unexpected moisture or discoloration, creating confusion and halting valuable work. These cases underscore why every container that leaves our site is tracked and signed off by chemists who understand not just the paperwork, but the chemistry behind the product.
Our own troubleshooting stages for any reported inconsistency begin by retracing every part of the journey, from incoming raw material to the packed bottle. If a problem arises, production teams collaborate directly with research scientists, seldom outsourcing or passing along responsibility. Lessons learned from each deviation get logged into our living production manual, raising the bar on future releases. With each client report and project update, we refine both documentation and technical protocols to reduce the time between inquiry and solution, preventing small errors from snowballing into project-ending delays.
Our reputation in indole chemistry developed slowly, through repeated, verifiable delivery of consistent batches. By participating in peer-reviewed collaborations, our technical staff observed how nuanced requirements change across research fields. Material qualified for synthetic chemistry may need further assurance for life science or analytical applications. Some customers provide their own methods for verification; we welcome this level of scrutiny, providing sample quantities for independent analysis. Feedback collected over time shaped our technical bulletins and instructional guidelines, all with the aim of helping users extract the maximum value from each acquisition of 6-MICA.
A shared sense of responsibility emerges among chemists who see firsthand the impact of interrupted experiments and lost time. These experiences guide our day-to-day commitment, nudging us to treat every batch as if it were required for an in-house research project, not just an anonymous invoice. We update our storage and transport guidelines as supply chain risks evolve, always factoring in the realities faced by scientists working in varied climates or timelines. Sensitive to the needs of both major laboratories and small startups, we scale quantities and documentation support accordingly, never sacrificing precision for expedience.
In one notable project, a pharmaceutical team requested a large, single-lot batch to support a time-sensitive screen for kinase inhibitors. The material—prepared under custom specs for particle size—arrived on time, but an unexpected analytical anomaly arose at the client’s site. Working in parallel, our QC lab and theirs exchanged raw data within hours, cross-verifying method calibration and reference spectra. Both sides traced the minor variance to a freshly calibrated HPLC column, avoiding unnecessary delays or doubts about material integrity.
Elsewhere, a natural products group ran into a common roadblock: rapid degradation of purchased indole derivatives during long-term storage. They turned to us for better packaging, and our team responded by reviewing barrier film properties and humidity controls at each step of distribution. Months later, their results confirmed stable performance, with no loss of material quality.
We also routinely adjust lot sizes to help academic labs meet budget constraints, allowing for secure, smaller batches without increased risk of cross-contamination. Knowing that different workflows demand different quantities and packaging systems, we treat each inquiry with technical attention instead of relying on off-the-shelf solutions.
First-hand experience with repeated returns and complaints about “off” material drilled in the need for careful attention to storage. Even small traces of moisture can change the behavior of 6-Methoxy-1H-Indole-3-Carboxylic Acid in a reaction setup. Over the years, our teams refined vacuum-sealing techniques and selected desiccant types based on direct failure analysis. We take into consideration end-user storage conditions, offering practical advice alongside the product, from avoiding prolonged air exposure to the use of tightly sealed glass containers.
We have replaced traditional bulk packaging with smaller, sealed units for labs requiring frequent, small-scale syntheses. Each change stems from investigating customer environments: some work in dry deserts, others in humid climates. Recognizing these variables reduces unnecessary spoilage and keeps each batch useful far longer. Handling guidance extends beyond dry instructions and often includes anecdotal insights gleaned from hard-won experience.
As a manufacturer, we do not just observe supply chain gaps—we deal with them daily. Fragile materials like 6-MICA are susceptible to shocks during transit and storage. Several years ago, repeated returns highlighted the inadequacy of certain common freight carriers. In response, we overhauled our logistics partnerships, tested alternative shipping containers, and expanded temperature monitoring. Now, even transcontinental shipments arrive without visible or analytical degradation.
We also identify the limits of our material. For example, researchers once attempted to substitute 6-MICA for other tryptophan analogues in photophysical studies, only to find unexpected shifts in absorption spectra. Our technical feedback pointed out the electronic consequences of that methoxy group, guiding the scientists toward more suitable derivatives instead of leaving them to puzzle through misplaced expectations.
With each batch that crosses our line, insights grow. Technical advances in purification and solid-phase extraction technology continue to inform changes to our own workflow, often sparked by requests from innovative end-users. We reshape purification methods and sampling protocols in response to these developments. Cross-functional discussions—involving those who make, test, and use the compound—shape what we do next, from refining chromatographic conditions to adjusting labeling for greater clarity and regulatory compliance.
Many lessons come from failed attempts. During our initial manufacturing campaigns, certain reaction byproducts stubbornly resisted removal, costing us valuable time. Instead of dismissing these difficulties, we documented process variables that made a difference, such as small temperature changes or alternative buffer systems. The result: consistent, scalable results that now underpin every lot of 6-MICA that leaves our factory.
Being a true manufacturer demands more than hitting specifications. We keep communication open at all stages, from providing live updates during scale-up runs to consulting with end users about solvent systems and purification strategies. Our chemists do the work themselves, building a shared vocabulary with research partners over time. Each insight, whether generated from customer queries or internal quality reviews, becomes a checklist item—documented for both regulatory diligence and end user support.
We publish detailed COA reports, but we also welcome additional verification and custom testing. Technicians remain ready to talk through issues, not just refer clients to paperwork. Over the long term, these collaborative exchanges reduce misunderstandings and keep project momentum going, even when demands shift unexpectedly.
Manufacturing 6-Methoxy-1H-Indole-3-Carboxylic Acid means more than meeting a target formula: it calls for hands-on knowledge, deep process control, and ongoing communication with users. Every improvement stems from lessons learned on the line, feedback from those at the bench, and a commitment to scientific collaboration. Our belief is simple: quality comes from experience, and every gram should support progress, not hold it back.