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HS Code |
110508 |
| Product Name | 7-Methylindole-3-Carboxaldehyde |
| Cas Number | 61823-45-6 |
| Molecular Formula | C10H9NO |
| Molecular Weight | 159.19 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 110-114 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO and methanol |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 7-Methyl-1H-indole-3-carboxaldehyde |
| Smiles | Cc1ccc2[nH]cc(C=O)c2c1 |
| Inchi | InChI=1S/C10H9NO/c1-7-2-3-8-9(6-12)5-11-10(8)4-7 |
As an accredited 7-Methylindole-3-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 7-Methylindole-3-Carboxaldehyde, tightly sealed with a screw cap and labeled with hazard warnings. |
| Shipping | 7-Methylindole-3-Carboxaldehyde is shipped in tightly sealed containers to prevent moisture and air exposure. The chemical is handled with care, following safety regulations, and is typically packaged in glass or plastic bottles with appropriate labeling. It is transported in compliance with local and international hazardous material shipping standards. |
| Storage | 7-Methylindole-3-carboxaldehyde should be stored in a cool, dry, well-ventilated area, protected from direct sunlight and moisture. Keep the container tightly sealed and stored away from incompatible substances such as strong oxidizing agents. Ensure storage in a chemically resistant, clearly labeled container. Handle with gloves and safety goggles to avoid skin and eye contact. Store at room temperature unless otherwise specified. |
Applications of 7-Methylindole-3-Carboxaldehyde in Industrial ManufacturingWe supply 7-Methylindole-3-Carboxaldehyde directly from our ISO-certified facilities to specialized industries where it plays a critical role as a building block and intermediate. Below, we detail its application across strictly selected, validated downstream manufacturing scenarios, emphasizing compliance, process integration, and typical usage parameters relevant for industrial formulators and process engineers. 1. Pharmaceutical API Intermediate SynthesisThis compound serves as a precursor in the synthesis of indole-based active pharmaceutical ingredients, particularly in the development of advanced oncology and neurology compounds within small-molecule pipelines. Manufacturing teams integrate it into targeted heterocyclic core constructions, where precise molecular modification is vital for downstream pharmacological profiling. Choice of batch or flow synthesis determines process scalability and impacts quality documentation compliance. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingChemical synthesis units use this material for formulating potent indole-based fungicides and herbicides where specificity in molecular substitution impacts biological target profiles. Technical-grade purity requirements remain high to avoid environmental legacy contaminants. Continuous or batch reactors facilitate integration into chlorination and cross-coupling sequences, and analytical teams closely monitor residual levels and trace by-products mandated by agricultural approval frameworks. Industry compliance standards
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3. Specialty Dye and Pigment SynthesisAdvanced dye houses and pigment manufacturers deploy this indole derivative for producing high-performance colorants, especially where lightfastness and molecular integrity are demanded by regulatory and customer specifications. The aldehyde enables specialty condensation reactions for producing heterocyclic pigments, with close monitoring of trace impurities and intermediates using chromatographic and spectrophotometric controls throughout the process chain. Industry compliance standards
Typical usage ratio
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4. Chemical R&D and Analytical Reference MaterialsContract research organizations and analytical laboratories source this compound as a defined reference standard for structure-activity relationship studies, metabolite profiling, and method development within regulated R&D pipelines. Sourcing focuses on traceable purity and stability, vital for method validation and calibration of precision analytical instruments, including HPLC and GC-MS, with full supporting documentation for audit trails. Industry compliance standards
Typical usage ratio
Downstream process integration
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Every compound has its role in the lab. Over years of manufacturing heterocyclic intermediates, we've seen how targeted changes in indole rings yield results that open up entire reaction pathways. 7-Methylindole-3-Carboxaldehyde (CAS 60723-98-2) has earned a spot in a variety of syntheses because its structure supports chemistries that demand selectivity at both the indole nitrogen and the aldehyde handle. In my daily work, noticing what separates one derivative from its cousin often spells the difference between a robust process and weeks of troubleshooting. It’s not just about purity or meeting a spectral standard — it’s about consistency under real process conditions.
On paper, 7-Methylindole-3-Carboxaldehyde looks simple enough: a methyl group at the 7-position, an aldehyde at the 3-position. That methyl substitution isn’t there for show. When we put this compound into reactions, that extra methyl group brings extra stability to the indole ring. This is more than theoretical; our teams have measured how the methyl group acts as an electron donor, which can affect both the reactivity and the physical handling of the compound. For chemists seeking to reduce side-product formation or who are optimizing routes feeding into active pharmaceutical ingredients, small tweaks like this methyl group become the linchpin in their process.
We’ve produced this compound for projects ranging from building complex natural products to supplying smaller groups evaluating novel kinase inhibitors. The precise placement of both substituents means it joins a fairly select group of indole chemistry building blocks, and its performance often reflects the subtle but meaningful differences from structurally similar options, like unsubstituted indole-3-carboxaldehyde or 5-methylindole-3-carboxaldehyde. Through direct feedback from chemists using our batches, we've found that these differences show up in yield, crystallinity, and compatibility with specific downstream steps, such as selective nucleophilic additions or condensation reactions.
Every batch we produce navigates the realities of scale; what works for ten grams looks different at ten kilograms. From our plant floor, the transition from bench to bulk comes with its own challenges. Impurity control, especially residual starting materials or positional isomers, demands attention at each stage. In the case of 7-Methylindole-3-Carboxaldehyde, we've developed crystallization procedures that favor consistent morphology, making this product easier to handle in automated dispensing systems. Our HPLC and GC methods pick up even trace impurities, and we've learned to tweak our solvent selections based on the slightest color or texture differences between lots. That’s just part of earning our customers’ trust—if you're running parallel syntheses or scaling up a lead compound, you can't afford surprises from your starting material.
The fine dust of certain indole derivatives used to plague both our operators and end-users; anyone who's handled tons of fine powder on a cold morning knows how static electricity can frustrate even the best process plan. We’ve worked out anti-caking methods and intelligent packaging to sidestep bottlenecks at the receiving dock. It’s small details like these, rooted in the real flow of chemicals from drums to reactors, that shape how well a product performs in your hands. People don’t always talk about packaging and flowability, but chemists with new projects appreciate not losing time fighting clogged instrumentation or lost powder.
We routinely supply 7-Methylindole-3-Carboxaldehyde for use in medicinal chemistry, from libraries screening for new antibacterial agents to projects advancing into preclinical trials. Researchers synthesizing new tryptamine derivatives or indolyl-based scaffolds find that methylation at the 7-position steers reactivity so they see fewer dead-end products. In one project, a partner described how this compound slotted cleanly into a Suzuki coupling, enabling higher yields and cleaner purifications compared to less substituted indole aldehydes.
One frequent use comes up in the synthesis of 7-methyltryptophan derivatives. The methyl group staves off problematic side reactions, letting chemists isolate their target amine in higher yields. Whether the end goal is an agrochemical or an investigational pharmaceutical, the reduced formation of difficult-to-remove byproducts has saved weeks in downstream processing. In peptide chemistry, specialists appreciate how the steric effect of the 7-methyl substitution leads to greater selectivity, reducing competitive acylations or alphatic exchanges during elongation strategies.
Some groups have reported that, compared to more electron-rich indole aldehydes, 7-Methylindole-3-Carboxaldehyde delivers a unique balance: enough reactivity to engage standard coupling partners, but not so much that it turns unwieldy in multi-step syntheses. This sweet spot lowers byproducts in both harsh and mild conditions, giving process chemists more leeway when balancing throughput against cost.
There’s no shortage of indole aldehydes, each with quirks that only show up after repeated use. Take indole-3-carboxaldehyde — without the methyl group, it’s more susceptible to oxidation and polymerization. 5-Methylindole-3-carboxaldehyde brings different electronic effects, shifting the way it handles acid or base catalysis or interacts in metal-mediated cross-couplings. These details matter during scale-up. We’ve observed that 7-Methylindole-3-Carboxaldehyde shows better shelf stability, especially in high humidity, and forms fewer unknowns after extended storage.
I recall a collaboration with a team evaluating several indole derivatives for metathesis reactions. In head-to-head tests, using our 7-methyl derivative cut out the need for extra stabilization additives, which saved both cycle time and materials. The less reactive analogs either lagged in conversion or spawned extra byproducts that forced longer purifications.
Among screening teams looking for lead diversification, methylation often helps tune the hydrophobicity or partitioning behavior of candidate molecules. As synthesis demands pivot to meet evolving SAR data, these subtle changes make all the difference in library development, bioinformatics modeling, and later stages of purification. The methyl group on our product means users can predictably shift R-group scanning and SAR experiments — useful for those living at the border between medchem and process scale-up.
Every successful project depends on more than high-assay product. Trace solvent issues, low-level tars, even glassware residue can throw off scale-up and cost teams weeks. We make our 7-Methylindole-3-Carboxaldehyde in facilities fitted to control risk, and collect feedback not just from QC but from project leaders in pharma and fine chemical sectors. Feedback drove us to improve filtration and drying steps — not out of regulation-chasing, but because customers told us how subtle morphology differences could cause headaches in automated feeding.
We’ve supplied this compound in quantities ranging from grams to multi-kilogram runs, with batch records designed around traceability not as box-ticking, but as a tool for process troubleshooting. Several customers on accelerated delivery timelines rely on consistent batches to reduce analytical requalification. These long-term relationships, built from real-world performance data, tell us that even in an age of digital supply chains, the measure of a chemical is in its practical reliability.
Working with indole aldehydes, we’ve learned that color and odor provide clues to underlying purity, well before a chromatograph gives its verdict. We encourage our customers to share their observations openly; we routinely tweak our drying and crystallization times in response to reports of any out-of-spec changes. It’s a two-way street between manufacturer and lab, and years of doing this built a robust pipeline that adapts to new projects without sacrificing quality. We don’t take it for granted — we know how much of a difference good material makes at either end of the innovation lifecycle.
Not all advanced chemicals treat users kindly. Indole derivatives sometimes pose handling issues, from strong odors to tricky wettability. Our batches of 7-Methylindole-3-Carboxaldehyde ship with predictable physical profiles. This direct experience comes from cleaning up early batches wrecked by clumping or losses due to static, which we countered with appropriately sized, resealable containers and anti-static liners. From our site to your benchtop, the packaging holds up whether you're gleaning milligram samples or dumping a full drum for process campaigns.
Repeated cycles of batching and feedback convinced us never to overlook minor issues, like trace moisture. We’ve introduced robust moisture controls and often run Karl Fischer at release to catch water uptake from humid storage seasons. Chemists appreciate opening fresh product with the right texture and flow needed for direct weighing or loading into feed hoppers. By managing grain size and storage stability, we've reduced off-odors and elevated user experiences, even in demanding GMP environments.
Staff safety also matters. Our teams work closely with in-house health specialists to keep airborne exposure low and avoid excessive dust. During one scale-up campaign, we switched to semi-granular forms after operators flagged the usual fine powder as a respiratory nuisance. For the end user, that means fewer environmental or handling headaches, especially during frequent transfers between vessels during a busy shift.
Supply reliability and lead times count for as much as chemical reactivity. Anyone who’s had a project freeze up waiting for a critical building block knows the frustration. We maintain buffer inventory and track shipping conditions to cover for the realities of customs delays, seasonality, or logistics holdups. More than once, a project manager has called up in need of rapid turnaround for clinical manufacturing or a development pivot. We value those relationships, and our logistics teams treat every request as tied to a real-world outcome, not just a transactional shipment.
Even with fluctuating global demand, our output plans anticipate upswing in sourcing due to regulatory shifts or customer portfolio changes. It all feeds back into monthly procurement and predictive manufacturing cycles, ensuring fewer bottlenecks or rationed supplies. Nothing stings more than having to tell a trustworthy lab that their timelines slip because a drum stalled at a port. We’ve built backup supplier strategies and communicate transparently about realistic ETAs, based on genuine inventory status, not wishful thinking.
For multinational customers facing regulatory inspection schedules, our documentation support draws on decades of actual audits. Full traceability includes both certificate data and batch-level performance notes taken during scaling, giving confidence without requalification cycles. Our QA team maintains a running log of customer feedback and regulatory interactions, so every document serves both compliance and practical process improvement purposes.
Chemicals with therapeutic potential often attract scrutiny from both safety and regulatory viewpoints. Because 7-Methylindole-3-Carboxaldehyde falls into a class of intermediates used in advanced pharmaceutical and agrochemical syntheses, we maintain compliance updates for REACH, as well as region-specific requirements for North America, Europe, and Asia when relevant. We collect and report hazard data for standard workplace safety, and closely monitor changes in exposure guidelines.
Most indole derivatives pose low to moderate hazard profiles, with the greatest risks arising during high-volume handling or in settings with poor ventilation. As a manufacturer, we keep up to date with evolving occupational safety standards and share best practices with our partners. By tracking analytical lot performance under varied storage and handling regimes, we maintain current safety data and offer real-life advice for best practices in the lab, not just what’s printed on paper.
We’ve enacted annual reviews of all safety documentation, led by both chemists and production supervisors rather than administrative staff. That means hazards are evaluated in line with actual exposure routes, waste disposal, and downstream reactivity, guarding against surprises in either scale-up or final use environments. Our staff undergo regular training in contained handling and emergency procedures, lessons we pass on to downstream partners on request.
The chemical industry loves to declare itself future-ready, but in our experience, that only works for those who stay close to feedback from daily users. Our ongoing refinements to 7-Methylindole-3-Carboxaldehyde production trace right back to conversations with both first-time buyers and seasoned process teams. It’s never just the certificate of analysis that drives satisfaction, but responsiveness to changing project needs, scheduling pressures, and regulatory updates.
Recently, we revised our lot documentation format to reflect customer input about the need for faster digital access during regulatory audits. Our core IT and compliance colleagues developed an online portal tailored for batch-specific download and search, saving hours during urgent submissions. Feedback about minor aspects, such as label readability or packaging changes, has also driven real improvement in daily workflows for both our teams and end users.
As manufacturing partners, we measure our performance not only by repeat purchase rates, but by the number of customer suggestions adopted over the last year. That stream of feedback — whether about batch consistency, physical format, or ease of ordering — helps us zero in on what really matters in an industry where reliability counts as much as innovation.
Each year, the landscape for heterocyclic building blocks evolves in tune with scientific innovation. Researchers pivot strategies based on new mechanistic insights, while regulatory climates shift and new therapeutic demands rise. Working directly as a manufacturer, our challenge and privilege is keeping our production nimble enough to support fast-moving discovery teams while maintaining stability for those scaling to commercial output.
Collaborating with both large and small research outfits gives us a window into next-generation uses for 7-Methylindole-3-Carboxaldehyde, from new bioconjugation strategies to metabolic labeling for diagnostics. We recognize that what works for one application may call for subtle changes in physical specifications or analytical standards for another. Our plant and quality labs adapt quickly, responding not just to standard product requests but to new analytical needs, diverse reaction conditions, and sustainability targets.
In the years ahead, we’ll continue sharing knowledge rooted in plant-level experience, project outcomes, and genuine innovation partnerships. The essentials won’t change: give users the product they need, in the form that lets them work efficiently and safely, and keep lines of communication open. Our continued focus on real-world results, not just technical compliance, shapes every batch of 7-Methylindole-3-Carboxaldehyde we release. We invite feedback from every customer, every project team, as we keep refining both our process and our partnerships, supporting innovation in labs and plants worldwide.