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1-Methylindole-2-Carboxylic Acid

    • Product Name 1-Methylindole-2-Carboxylic Acid
    • Alias 1-Methyl-2-indolecarboxylic acid
    • Einecs 625-359-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    611584

    Productname 1-Methylindole-2-Carboxylic Acid
    Casnumber 6949-41-7
    Molecularformula C10H9NO2
    Molecularweight 175.19 g/mol
    Appearance Off-white to light brown powder
    Meltingpoint 195-198°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Chemicalclass Indole derivative
    Smiles Cn1cc2ccccc2c1C(=O)O
    Inchi InChI=1S/C10H9NO2/c1-11-6-8-4-2-3-5-7(8)9(11)10(12)13/h2-6H,1H3,(H,12,13)
    Storageconditions Store at room temperature, keep container tightly closed

    As an accredited 1-Methylindole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Methylindole-2-Carboxylic Acid, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping 1-Methylindole-2-Carboxylic Acid is shipped in secure, airtight containers to prevent contamination and moisture exposure. Packaging complies with regulations for chemical transport, ensuring safe handling. Shipping documents include safety data sheets (SDS), and transit may require temperature control. Handle with appropriate personal protective equipment (PPE) upon receipt.
    Storage **Storage for 1-Methylindole-2-Carboxylic Acid:** Store in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizers. Keep at room temperature in a cool, dry, well-ventilated area. Avoid excessive heat. Label the container clearly, and handle under appropriate safety conditions, including the use of gloves and eye protection to prevent skin or eye contact.
    Application of 1-Methylindole-2-Carboxylic Acid

    Applications of 1-Methylindole-2-Carboxylic Acid in Industrial Manufacturing

    As a direct manufacturer, we support advanced industrial production with reliably supplied 1-Methylindole-2-Carboxylic Acid, a specialized intermediate valued for its chemical structure and reactivity. Its performance under demanding process conditions makes it integral to select high-value chemical manufacturing chains. Below, we present detailed application scenarios, grounded in real downstream sectors utilizing the compound for precise functional roles.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound in the synthesis of several indole-derived APIs, where its unique carboxy group placement is crucial during ring-closing and selective functionalization steps. Production facilities incorporate it for development of molecules including tryptophan derivatives and targeted kinase inhibitors, requiring careful process controls to ensure purity at each stage for regulatory approval. Optimizing dosing depends on the stepwise demands of the particular heterocycle being generated and subsequent purification efficiencies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 2 for Chemical API Intermediates
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia Monographs (where applicable for final APIs)

    Typical usage ratio

    • Formulation input varies from 0.8 molar equivalents (as limiting reagent) up to equimolar or 1.2 equivalents, adjusted based on coupling efficiency and yield in the synthetic sequence.

    Downstream process integration

    • Charged into multi-step batch reactors as a key intermediate after initial raw material purification, entering during amidation, esterification, or cyclization stages depending on the API molecular scaffold.

    Final product types

    • Small-molecule kinase inhibitors
    • Psychoactive indole pharmaceutical APIs
    • Custom pharmaceutical contract synthesis outputs for regulated markets

    2. Agrochemical Active Ingredient Precursor

    In the agrochemical industry, 1-Methylindole-2-Carboxylic Acid serves as a fundamental building block for selective herbicide and fungicide formulations. Process engineers require consistent input quality for downstream coupling and sulfonation reactions that yield complex active agents with improved environmental profiles. Each crop protection agent's technical specification dictates how the feedstock is proportioned and when it is introduced to maximize transformation rates and minimize side product formation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 Laboratory Accreditation (batch testing)
    • Chinese National Standard GB 2763 (Maximum Residue Levels for Pesticides)
    • REACH Registration (for Europe-bound formulations)

    Typical usage ratio

    • Dosage typically ranges from 5–12% w/w of total intermediate mix, depending on downstream coupling route and desired active agrochemical yield.

    Downstream process integration

    • Introduced post-nitration but before chlorination in the synthesis line, or as the substrate for indole core modifications in continuous flow or batch processing environments.

    Final product types

    • Pre-cursor intermediates for selective herbicides
    • Fungicidal agent scaffolds for crop protection
    • Registered active ingredient mixtures for European and Asian markets

    3. Fine Chemical Dye Intermediate Manufacturing

    Producers of advanced specialty dyes rely on well-characterized indole derivatives to create stable chromophores for high-performance textile and ink sectors. 1-Methylindole-2-Carboxylic Acid's molecular structure supports regioselective transformations, introducing carboxyl or methyl functionalities necessary for the synthesis of colorants that meet durability and color fastness standards. Adjustment of its concentration occurs according to target color profile and compatibility with applied batch or continuous processing protocols.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • ZDHC MRSL (chemical safety in dye manufacture)
    • EU REACH SVHC List (for dye intermediates)
    • ISO 9001 Quality Management for Chemical Manufacturing

    Typical usage ratio

    • Applied as 7–15% of core input mass in dye precursor synthesis; variation determined by target molecular weight and batch-to-batch yield optimization.

    Downstream process integration

    • Reacted during early-stage aromatic amination or diazotization steps for indole-based chromophore formation, prior to sulfonation or metallization in dyehouses.

    Final product types

    • Indole-based specialty textile dyes
    • High-value ink pigments for security printing
    • Colorants for industrial coating and plastics sectors

    4. Specialty Polymer Modifier Synthesis

    Polymer manufacturers incorporate 1-Methylindole-2-Carboxylic Acid as a reactive monomer or chain modifier in bespoke polymer blends for electronics and high-temperature insulation applications. Its ability to confer rigidity or introduce specific functional groups supports tailored polymer design. The ratio of addition reflects the necessary degree of functionalization, typically finalized after initial lab-scale extrusion or polymerization trials for scalability.

    Industry compliance standards

    • IEC 60695-11-10: Fire hazard testing for polymer electrical components
    • UL 94 (Flammability rating for plastics)
    • ISO 14001 Environmental Management (for production waste handling)
    • RoHS Directive 2011/65/EU (electronics material compliance)

    Typical usage ratio

    • Added at 1.5–5% w/w in copolymer or specialty polymer masterbatch, with further optimization depending on produced resin’s property targets.

    Downstream process integration

    • Introduced into reaction kettles or extruders during chain propagation or grafting phase, preceding the addition of base polymer backbones.

    Final product types

    • Flame-retardant electronic encapsulation materials
    • Anti-static and high-performance insulation resins
    • Customized engineering plastics for automotive electronics
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    Certification & Compliance
    More Introduction

    1-Methylindole-2-Carboxylic Acid: A Perspective from the Manufacturer’s Bench

    Introduction to 1-Methylindole-2-Carboxylic Acid

    Working in chemical manufacturing, we gain insight into both the substance itself and the needs of chemists and technologists who keep asking for quality and reliability. 1-Methylindole-2-Carboxylic Acid continues to attract attention from researchers, pharmaceutical innovators, and process chemists. The formula—C10H9NO2—may look straightforward on the page, but once this compound emerges from the reactor under the right conditions, its promise and its challenges become clear. We make it in our facility because it opens pathways for novel heterocyclic synthesis: it offers specificity that simpler indoles or carboxylic acids often lack.

    Model and Specifications Sourced from the Laboratory and Plant Floor

    Through years in the plant, we’ve grown familiar with the fine floury crystal of 1-Methylindole-2-Carboxylic Acid. The model in our workshop refers to material tested in lots ranging from gram up to multiple-kilogram scale. Melting points sit consistently in the 187 to 190 degree Celsius range, a figure we confirm from every batch using capillary tubes and digital devices equally, because precision is a habit that saves headaches before they start. We insist on purity levels crossing 98% because every application tolerates its own range of contaminants, but when it comes to 1-methylindole derivatives, a cleaner product gives much better yield and reproducibility downstream.

    Our analytical runs depend on HPLC and NMR. Each batch leaves the plant with full spectra archived. Experienced chemists recognize the unmistakable singlet around 3.7 ppm in proton NMR—methyl on the nitrogen. The carboxyl's presence is confirmed by carbonyl signals unmistakable by their downfield position. We watch the flow of solvents, carefully adjust the acidity at every stage, and avoid strong oxidizers that can yellow the product or lead to unwanted side-products. Every shift, there is discussion between the operators and the quality lab about small improvements: filtration times, the best antisolvent for crystallization, and how to minimize agglomeration so the powder handles well in the customer’s hands.

    How 1-Methylindole-2-Carboxylic Acid is Used in the Real World

    From our vantage point as producers, we see several customers and collaborations shaping the real demand for this molecule. Most interest centers on its role as a building block in active pharmaceutical ingredients (APIs), research compounds, and complex dyes. In the pharmaceutical sector, 1-Methylindole-2-Carboxylic Acid takes on significance because it acts as a reliable intermediate in the synthesis of tryptamine analogs and related heterocyclic structures. Medicinal chemists push us for ever-greater purity and consistency to feed discovery campaigns and pilot scaleups, because downstream steps demand a consistent starting material for reliable SAR profiling. Medicinal chemistry teams, especially those working on serotonin receptor ligands, have told us they depend on its methyl N-substitution to block unwanted side reactions that simpler indole acids encourage.

    In the context of material science and dyes, the methyl and the carboxy positioning allows for a fine-tuned entry into larger aromatic frameworks. Research groups in organic electronics or sensor development point out that the substitution pattern makes it easier to design donor-acceptor systems or fluorescent motifs. Some users exploit the acid group directly, forming esters or amides as coupling partners for their more specialized molecules. Even the seemingly straightforward action of forming an amide with an amine reveals the product’s value: the methyl on nitrogen blocks certain routes, leaving others open, helping the chemist direct reactivity with confidence.

    What Sets Our 1-Methylindole-2-Carboxylic Acid Apart from Related Compounds

    We’ve made, tested, and compared the unmodified indole-2-carboxylic acid, the 1-methylindole itself, and their regioisomers through multiple years on the line. The methylation at N1 confers better solubility in common organic solvents than unsubstituted analogs, and this aids in both processing and reactivity when it’s handed off to downstream laboratories or plants. Chemists who start with unprotected indole typically have to manage unpredictable N-H reactivity, but here they find none of the base lability or the polymerization issues characteristic of unsubstituted indole acids during certain acylations or metalations.

    From a manufacturer’s perspective, working with the 1-methyl derivative results in fewer nuisances during isolation and purification after N-protection or deprotection reactions. The benefit for the end user—our partners in R&D and production—is that the methyl group allows for more straightforward, predictable synthetic design. The acid’s ready availability in purified, high-quality form cuts steps from synthetic workflows. For anyone who has wrestled with column chromatography of less well-behaved indoles, the improved handling during crystallization and workup saves hours if not days in the lab and plant.

    Some customers request the 5- or 7-substituted analogs, which we also target on a custom basis, but the 2-carboxylic acid variant with 1-methyl substitution translates to consistent reactivity, especially in carbon–carbon coupling or amidation steps. Literature comparisons bear this out: 1-methylation eliminates competitive N-alkylation that can complicate later stapling or ring-locking transformations. In scale-up runs, especially those aiming for multi-hundred gram or kilogram output, this yields tighter reaction profiles and better isolated yields than the more reactive parent indoles.

    From Manufacturing Line to Research Bench: Meeting Demands for Reproducibility and Safety

    Consistency drives most of what we do, guided by the demanding standards of our clients and regulatory expectations. Every batch of 1-Methylindole-2-Carboxylic Acid receives scrutiny for moisture, color, and trace impurities. Workers know the signature scent—a faint, phenolic nose with a hint of sweet, not unlike other methylated indoles. We train for safe handling, given its moderate hazard profile. Personal protective equipment stands ready; air handling and dust control get regular checks. The powder form dispenses well, without excessive static or clumping, an outcome of repeated rounds of optimization in drying and packaging. Long-term stability studies continue; we store reference samples in desiccators and check them at intervals for changes in appearance or composition. Researchers want assurance that a shipment will be as reliable weeks or months later as the day it leaves us.

    The scaling of this molecule didn’t arrive overnight. We spent months refining the synthesis route, balancing cost, efficiency, and environmental compliance. Early pilot lots often highlighted the risk of side-product formation at higher temperatures. We learned that a slow acidification and prompt separation during workup make all the difference in purity—and in customer satisfaction. As an upstream manufacturer, we take feedback directly from repeat clients. One customer mentioned receiving material from another source that clumped or discolored, issues that led to batch failures. Through careful attention to drying and packaging, we mitigate such failures—simple bagging only exacerbates static and caking, so we moved to anti-static double-layered packaging for large lots.

    Compliance, Traceability, and Environmental Responsibility

    Around the plant, sustainability is more than a buzzword. Processes are built around minimizing toxic by-products and maximizing the use of recyclable solvents. We operate under ISO management guidelines. Tracking the flow of starting materials—indole, sodium methylate, CO2, and the rest—enables us to control not just chemical yield, but also waste and emissions. We recover and reuse a high percentage of our organic solvents, filtering and purifying them for the next production cycle.

    As both producer and partner, we respond quickly to requests for documentation. Every lot is accompanied by a certificate of analysis, not as an afterthought but as a necessity for those who must track every reagent in a stringent lab notebook or regulatory filing. Sophisticated clients request batch histories to trace every input to its origin, a practice we encourage. We archive reactions in electronic systems, and our QA teams maintain scrupulous logs. Regular inspections ensure nothing escapes our notice, whether it’s a drifting melting point or the faintest hint of peroxide formation on an old sample.

    We monitor all effluent streams for residual organic matter. The filtration and recovery units run continuously during each operation run. Solid waste, much of it spent filtercake, is shipped to licensed handlers who process materials for safe destruction or, if feasible, for raw material recovery. Nothing leaves the site until it meets strict compliance standards, and our teams regularly conduct drills and safety audits. It’s not enough to meet today’s regulations; we plan ahead for anticipated changes, knowing that transparency is the foundation of long-term survival in the chemical industry.

    Supporting Innovation and Responsive Scale-Up

    We see ourselves not simply as vendors but as partners to innovation. Synthetic chemistry is a field shaped by trial, error, and incremental improvement, and our plant often serves as the extension of the research laboratory for our customers. Some request custom particle size or lot size; others want modified packaging or expedited testing. Our team’s years of hands-on knowledge mean we respond with practical solutions: grinding finer for those with special dissolution needs, or offering a more granular lot history for process development chemists who need to verify every input.

    End users often ask about the scalability of reactions using our 1-Methylindole-2-Carboxylic Acid. Every synthetic chemist learns that what works on milligram scale becomes treacherous when scaled to kilograms. By producing regular technical bulletins based on our own scale-up runs, we help partners bridge the gap from discovery chemistry to pilot plant. Customers share their own reaction outcomes, and we build those lessons back into process controls and formulation tweaks.

    Lessons Learned: Quality, Trust, and Continuous Improvement

    Real value in chemical manufacturing is proven not by a single batch but by performance over time. We have seen product inquiries surge when a newly published academic route uses our material in a key step, but repeat business comes from customers who report “no surprises” in the behavior of the product across multiple purchases. Trust builds slowly. Our operators understand the cost of a failed batch to the downstream customer—a setback not just in dollars but in time, morale, and momentum for the project.

    Feedback loops from process chemists, R&D groups, and regulatory reviewers shape how we approach production. The focus remains always on robust quality: verifying each intervention along the process, documenting it, and sharing both strengths and limitations with clients. We talk openly about critical points—like the need for strictly dry conditions during certain operations, or the trouble a bit of haze in the crystallization filtrate can cause. When issues arise, our approach is open communication paired with corrective action. This has led to improved formulations, better packaging, and continuous investment in employee training.

    Looking Ahead: Customer Needs and Industry Trends

    The evolving landscape of drug discovery, specialty materials, and multi-step organic synthesis keeps us focused on improving every link in the manufacturing chain. We note rising demand for not only high-purity batches but also predictive documentation on stability and performance in difficult reaction environments. Some customers pursue green chemistry goals, asking for solvent-free approaches or reduced residual heavy metals. We adapt where feasible, running development trials to balance performance and environmental footprint.

    Sourcing of key raw materials—especially high-grade indole—remains critical. Over recent years, price swings and availability shifts for key upstream chemicals pushed us to qualify secondary and even tertiary suppliers. We audit those partners stringently. Events overseas sometimes pinch supply chains, testing our ability to deliver on time and on spec. In response, we’ve adopted a more proactive communication stance. Customers now receive early warning if there’s even a hint of delay risk, and our supply teams keep redundant safety stocks for key intermediates.

    Collaborative Chemistry: Building Future Opportunities

    Manufacturing 1-Methylindole-2-Carboxylic Acid does not happen in a vacuum. The process, the knowledge, and the responsiveness come from decades of collective work. Our chemists work closely with academic groups and private R&D teams. We routinely discuss routes for further derivatization, potential synthetic shortcuts, and alternative methods that reduce waste or improve yields. In-house, we host regular sessions where plant chemists and quality analysts meet to review lab results, compare batch-to-batch performance, and set goals for the next set of improvements.

    Some of our most important process innovations have come from problems our partners encountered at their own scale-up stage. One pharma collaborator had trouble forming a key amide bond because trace moisture introduced from packaging spoiled a sensitive coupling reagent. After visiting their lab, we adjusted our drying and packaging cycling. The result: improved success rates for their API synthesis, and fewer failed reactions.

    As research groups push into ever more complex targets, we see demand shifting toward even tighter impurity profiles and traceability. Our analytical chemists already run LC-MS scans down to ppm levels for customers who require it. We have invested in new analytical equipment and automated data logging, so we can track each lot from starting material to final product, responding rapidly to changing regulatory environments.

    In Conclusion: A Manufacturer's Perspective

    Producing 1-Methylindole-2-Carboxylic Acid involves a blend of old-fashioned craftsmanship and rigorous scientific discipline. Through every run, every improvement, and every challenge, our focus remains on delivering a product that meets or surpasses the flexing demands of modern pharmaceutical and specialty chemical production. For us, the molecule is not just a line item or a specification—it is the outcome of planning, hard work, and continuous interaction with those who depend on it. As trends continue to shift, we stand ready to adapt our processes and take on new challenges, grounded by our commitment to both quality and partnership.