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HS Code |
386440 |
| Name | Indole-3-Ethanol |
| Chemical Formula | C10H11NO |
| Molecular Weight | 161.20 g/mol |
| Cas Number | 487-93-4 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 74-77°C |
| Boiling Point | 330.4°C at 760 mmHg |
| Density | 1.22 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | CC(C1=CC=CC2=C1NC=C2)O |
As an accredited Indole-3-Ethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Indole-3-Ethanol is packaged in a 25g amber glass bottle with a tamper-evident cap and chemical hazard labeling. |
| Shipping | Indole-3-Ethanol is shipped in tightly sealed containers, protected from light and moisture. It is classified as a non-hazardous substance but should be handled according to standard chemical safety protocols. Shipping complies with international and local regulations, and the product is packaged to prevent leaks or contamination during transit. |
| Storage | Indole-3-Ethanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Protect from light and moisture. Store at room temperature or as specified by the manufacturer to maintain chemical stability and prevent degradation. |
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Purity 98%: Indole-3-Ethanol with purity 98% is used in plant hormone research, where it enhances auxin signaling accuracy. Molecular weight 161.19 g/mol: Indole-3-Ethanol with molecular weight 161.19 g/mol is used in biosynthetic pathway elucidation, where it supports metabolic flux analysis. Melting point 51-54°C: Indole-3-Ethanol with melting point 51-54°C is used in seedling growth assays, where it ensures compound stability and homogeneity. Stability at pH 7: Indole-3-Ethanol with stability at pH 7 is used in hydroponic nutrient formulation, where it maintains bioactivity during plant exposure. Particle size <50 μm: Indole-3-Ethanol with particle size <50 μm is used in foliar spray preparations, where it improves dispersion and absorption efficiency. Solubility in ethanol 25 mg/mL: Indole-3-Ethanol with solubility in ethanol 25 mg/mL is used in agrochemical solution blends, where it allows for precise dosing and homogeneous mixtures. UV absorbance λmax 280 nm: Indole-3-Ethanol with UV absorbance λmax 280 nm is used in analytical quantification methods, where it facilitates sensitive detection and measurement. Thermal stability up to 95°C: Indole-3-Ethanol with thermal stability up to 95°C is used in heated bioreactor studies, where it prevents compound degradation during sustained processes. |
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Step into any modern lab or chemical research facility, and you’ll hear about the small group of compounds that quietly change the game for plant biology and pharmaceutical work. Indole-3-Ethanol—sometimes called tryptophol—stands at that intersection. It draws immediate attention from botanists, life science researchers, and formulation chemists because its structure, blending a stable indole ring with a two-carbon ethanol chain, opens doors for both study and practical use. Those familiar with plant growth regulators know just how important it is to pick compounds that can be trusted for their purity, consistency, and reliability during experimentation.
What keeps Indole-3-Ethanol in high demand stems from its unique role in tracing auxin biosynthesis and as a precursor for studying metabolic pathways. Unlike synthetic counterparts or mass-produced alternatives, it offers a rich background in published research and has proven itself for decades as more than just another reagent on the shelf. I remember running my own side-by-side tests with common derivatives: results from Indole-3-Ethanol brought clean, reproducible markers in chromatography and showed better compatibility with a variety of solvents. That’s the type of subtle edge you look for if you’ve spent years in wet labs, always chasing the next breakthrough.
This compound usually comes as a white to off-white crystalline powder, maintaining high stability under ordinary storage conditions. With a molecular weight of 161.19 g/mol and the formula C10H11NO, it remains manageable for both small benchtop assays and larger synthesis protocols. Researchers interested in signal transduction or who want to investigate tryptophan catabolism consistently gravitate toward Indole-3-Ethanol because they count on its clear metabolic fingerprint. Too many reagents float around with fuzzy origins or unpredictable impurities; here, you’re working with a cleaner baseline.
When used in plant biology, this molecule’s specificity shows during bioassays for trace auxin analogs and related growth experiments. Since auxins steer cell elongation, fruiting patterns, and plant tissue development, tracking compounds that interact with those pathways can save entire projects from false positives. For years, major journals have spotlighted Indole-3-Ethanol’s reliability versus isolated alternatives like indole-3-acetic acid or indole-3-butyric acid—those come with their own quirks, but more researchers find Indole-3-Ethanol works without unexpected side reactions or breakdown byproducts in plant cell cultures.
Anyone who’s compiled monthly purchase data or reviewed supply chain disruptions knows consistency can’t be taken for granted in the chemical trade. On the business and logistics side, single-source purity reduces batch-to-batch headaches. Not all suppliers handle quality control with care, but established producers of Indole-3-Ethanol often back every shipment with batch certificates, HPLC purity analysis, and detailed spectral data. Those aren’t just paper trails—they’re the bones of years of hard-earned trust. If a university or industrial lab has suffered through shoddy shipments before, they appreciate seeing those authentication documents, day in and day out.
Ask a dozen botanists how they leverage Indole-3-Ethanol, and you’ll gather answers connecting everything from root initiation assays to gene expression studies. What’s common across settings is its handy solubility in ethanol, DMSO, or water, which spares researchers the wasted time and frustration of slow dissolving reagents during time-sensitive runs. In my own experience, switching to this compound meant ditching longer prep sessions and cleaning out ambiguous residues from beakers. Less guesswork leads to clearer results.
Beyond plant research, pharmacologists turn to Indole-3-Ethanol for investigations around neurotransmitter biosynthesis or as a standard in evaluating tryptophan-derived metabolites. Its track record goes back to studies on microbial metabolism, ethanol tolerance, and immune modulation. These fields share a common need: a compound that holds up during storage and repeated freezing or thawing. Stability like this, both chemically and physically, can’t be glossed over after years watching lesser products weather or rot in their vials.
Students attack their research goals with more energy when they know what’s actually in their flask. Not all chemical models perform as expected when moved from controlled settings to real-world conditions, which makes Indole-3-Ethanol’s robust profile more appealing. Technicians and postdocs on tight deadlines bank on its moderate melting point to sidestep thermal degradation during short synthesis or evaporation cycles. Having run these processes myself, I can’t count the times well-chosen starting materials let me dodge late nights in the lab redoing spoiled steps.
Veteran research coordinators and quality assurance leads both notice the difference between pharmaceutical-grade Indole-3-Ethanol and generic technical grades floating around online. Take the time to compare documentation and you’ll see the critical distinctions: trace impurity thresholds, consistent particle sizes, detailed spectral fingerprints, and tightly monitored storage histories. Each of these compliance steps matters as soon as downstream regulations come into play—whether someone’s filing for a new study protocol or verifying certificates for a peer-reviewed publication.
Competition in the reagent and additive market gets fierce quickly, especially as suppliers chase both price and consistency. Some offer Indole-3-Ethanol in grades that seem too good to be true—often skipping on trustworthy supply chains or third-party lab testing. Those who have ordered from bargain suppliers usually end up with rogue batches, unexpected discoloration, or purity below what’s promised. Laboratories committed to robust results learn from those burned-out flasks and opt for certified sources, often only after an expensive lesson.
Standard versions of Indole-3-Ethanol outshine synthetic analogs and broad-spectrum auxin mimics by sidestepping the unpredictable breakdown paths that crop up under varied pH, light, or temperature conditions. Many common lab alternatives, like indole-3-acetonitrile or the more volatile ethyl analogs, lose potency or become unstable under the sorts of routine manipulations typical in day-to-day protocol work. Time after time, carefully archived stability trials show that properly stored Indole-3-Ethanol handles both short exposures to open air and longer stretches in cold storage with little loss of function or chemical drift.
If you compare protocols head-to-head, you’ll see that this compound integrates well within both traditional atomic absorption panels and modern mass spectrometry setups. That compatibility, shored up by thousands of use cases, gives it a wider appeal over competitors that show peculiarities—unexpected chromatogram spikes, extra background noise, mixed reaction yields, or even incomplete recovery from standard extraction procedures. Researchers know that even a small hiccup at this stage means costly reruns or lost grant cycles.
Looking over product notes from various producers, a few recurring themes show up where Indole-3-Ethanol leads: packaging with air-tight, light-shielded containers, pre-screened for moisture absorption, and always accompanied by transparent documentation. Unlike some alternatives that get rushed to buyers without bothering to include calibration records or spectral printouts, reputable brands offer all the details upfront. That kind of transparency lays the foundation for trust between supplier and scientist—and it’s not something achieved overnight.
In my own journey, working on long-term experiments in plant hormone research, having a reliable source for Indole-3-Ethanol meant switching from finger-crossing to systematic planning. Colleagues across disciplines—pharmacology, biochemistry, agronomy—echoed similar stories after switching away from mystery-batch chemicals. They saw their reproducibility scores climb, their false result rates fall, and their data get accepted at prestigious journals more often.
Thinking about it from an educator’s perspective, access to a product with built-in assurances means undergraduates and new researchers develop better habits—monitoring storage, checking batch numbers, ensuring solvent compatibility. These lessons stick longer than any lecture, and reinforce the value of careful materials selection. I’ve watched lab teams pivot toward suppliers who put effort behind their reporting protocols and batch analysis—a conversation that crops up not just during purchasing, but at every stage of analysis and data review.
Since many industries lean more heavily on risk reduction, buyers at pharmaceutical, food science, or biotechnology companies scrutinize every new chemical for recall histories and documented complaints. Much of the low-quality, high-risk product gets weeded out fast. Indole-3-Ethanol’s profile, supported by long-term safety data and trusted supplier histories, lands it in the preferred compound lists year after year. Laboratories that put in the effort to vet their sources see fewer headaches, less waste, and better regulatory compliance in markets where those details bring real-world legal or financial consequences.
Years in the industry have shown me that even the best chemical can’t solve problems if used carelessly or stashed in a corner to gather dust. Smart labs know integrating Indole-3-Ethanol means accounting for every input: temperature tracking, light exposure, precise weighing, solvent selection, and even scheduling of shipments to avoid excessive warehouse stays. Sourcing from producers who match specs and stand behind their work with batch transparency makes the entire pipeline—from order to assay—run smoother.
Innovation doesn’t just happen at the benchtop. Many teams run pilot studies to compare Indole-3-Ethanol versus so-called low-cost, off-brand alternatives, documenting everything: how long dissolution takes, how many pipetting errors crop up, and which contaminants slip through into final products. Over time, their logs fill up with evidence for why one source becomes the go-to while the bargains never get reordered. This real-world feedback loop, especially when pooled between academic partners and industrial customers, drives both incremental improvements in bulk product quality and stronger supplier-user communication.
Breaking away from bulk commodity thinking, some producers now offer innovations like pre-portioned vials for smaller research labs or vacuum-sealed multi-use packs with tracking codes for inventory-sensitive facilities. While these changes rarely make it into glossy product brochures, anyone on the ground floor of supply chain management knows that packaging and handling details like these cut waste and loss over time. For new or under-resourced research teams, picking high-quality Indole-3-Ethanol in manageable packaging brings more data reliability without driving up costs from spoilage or over-ordering.
Not every story about Indole-3-Ethanol shines, though. Issues still come up around counterfeit imports, questionable shelf-lives, and spotty documentation from anonymous internet sellers. Seasoned lab techs learn to recognize warning signs: off-smelling vials, missing characterization sheets, or unexplained price drops. These experiences underscore why industry-wide cooperation—across suppliers, distributors, and end-users—remains critical for product confidence. The days of taking claims at face value are long gone; everyone in the pipeline has a role, from auditing batch records to flagging suspected non-conformances early.
Transparency doesn’t just build goodwill. It drives smarter research, faster troubleshooting, and gives scientific teams—whether in academia or commercial R&D—the peace of mind to try new ideas without fear of mysterious sample variables. As a result, the labs sticking with clearly documented, peer-reviewed grades of Indole-3-Ethanol not only deliver more credible papers and product candidates; they set the bar for safer, more reproducible science.
Some push for digital batch tracking, blockchain verification, and stricter third-party independent audits throughout the chemical supply chain. These practices bring new levels of trust to the high-stakes worlds of pharmaceutical development and large-scale agricultural innovation, where recalls or missed targets can wipe out years of effort. While upfront investment can seem daunting for smaller outfits, labs that embrace these practices find themselves fielding fewer surprises, both in terms of funding and regulatory inquiries.
Looking to the future, everyone from growers to clinicians stands to benefit as reliable producers of Indole-3-Ethanol champion greener manufacturing practices and prioritize safe, traceable transport. The industry’s shift toward batch-to-batch transparency, renewable packaging, and less resource-intensive synthesis steps echoes long-term demands for sustainable chemical supply. Environmental stewardship isn’t just a buzzword for funding applications—it’s fast becoming a baseline for staying competitive as research evolves and public scrutiny deepens.
Teams who show up to international conferences or publish in respected journals often share back stories about how a single compound—sourced from a trustworthy vendor—unlocked months of progress or let them scale pilot projects into full-scale field trials. Indole-3-Ethanol consistently pops up in those narratives because its technical and practical foundations go deep. The demand for clear sourcing goes hand-in-hand with new technologies for data logging, sample integrity checks, and international compliance.
I’ve watched as industry collectives, including both legacy chemical houses and young startups, put effort into voluntary certifications and third-party verification networks. These moves keep everyone on even ground and open the doors for more open dialog between buyers and producers. Some of the best products—and the tightest collaborations—are forged in this kind of transparent ecosystem, where everyone shares responsibility for outcomes that ripple from the petri dish to the global market.
Experienced researchers and newcomers alike benefit from critical conversations about sourcing: not just what Indole-3-Ethanol can do, but how each batch supports or undermines the broader pursuit of reliable science. Trust can’t be bought off a shelf or conjured with low prices. It takes years of openness, real documentation, and honest responses from both sides—producer and user. As standards rise in labs around the world, Indole-3-Ethanol’s strong legacy stands as a case study in the power of transparency, verification, and quality-first thinking.
Every advance—whether in understanding plant development, mapping metabolic networks, or synthesizing new molecules—rests on the promise that raw materials live up to their billing. The journey from research question to breakthrough pivots on thousands of these smaller decisions. Picking a reliable, transparent source of Indole-3-Ethanol remains one of those choices that pays off time and again for science, the market, and most importantly, for the people aiming to move each field forward.