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HS Code |
584019 |
| Product Name | 6-Fluoroindole-3-Acetic Acid |
| Cas Number | 34221-55-9 |
| Molecular Formula | C10H8FNO2 |
| Molecular Weight | 193.18 |
| Appearance | Solid, usually crystalline powder |
| Purity | Typically ≥98% (varies by supplier) |
| Melting Point | 195-197°C |
| Solubility | Slightly soluble in water; soluble in organic solvents such as DMSO, methanol |
| Synonyms | 6-Fluoro-1H-indole-3-acetic acid |
| Storage Temperature | 2-8°C (Refrigerated) |
| Chemical Class | Indole derivative |
| Smiles | c1cc2c(cc1F)nc(c2)CC(=O)O |
| Application | Plant growth regulator; research chemical |
As an accredited 6-Fluoroindole-3-Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 5 g amber glass vial with a secure screw cap, labeled clearly with chemical name and purity. |
| Shipping | 6-Fluoroindole-3-Acetic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. Packaging complies with regulatory standards for hazardous materials, labeled for safe handling. During transit, it is protected from moisture, direct sunlight, and extreme temperatures. Appropriate documentation accompanies each shipment for safe and legal transport. |
| Storage | 6-Fluoroindole-3-acetic acid should be stored in a tightly sealed container at 2–8 °C, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Handle in a well-ventilated area and avoid unnecessary exposure. Keep the chemical in a cool, dry place, clearly labeled, and ensure access is limited to trained personnel. |
Applications of 6-Fluoroindole-3-Acetic Acid in Industrial ManufacturingAs a direct manufacturer, we supply 6-Fluoroindole-3-Acetic Acid to downstream industries where advanced plant growth regulator technology and high specificity for molecular modification are critical. This material supports industrial applications limited to scientifically established uses in agricultural biotechnology, plant tissue culture, agrochemical research, and advanced plant breeding. Here we provide detailed application insights, including compliance standards, dosage guidance, process positioning, and details on end product development, compliant with practical industrial requirements. 1. Plant Growth Regulator Formulation for Commercial AgricultureMajor agricultural product manufacturers utilize this molecule as a next-generation auxin analog to drive targeted plant growth modulation in high-value crops, including fruits, vegetables, and field crops. By substituting a fluorine atom at the indole ring, formulators achieve enhanced physiological activity and metabolic stability, which supports precision farming and growth synchronization in controlled environments. Industry compliance standards
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2. Industrial Plant Tissue Culture Media ProductionSpecialty plant tissue culture laboratories and media producers incorporate this compound to trigger cell division, promote rooting, and coordinate shoot formation in micropropagation lines for elite horticultural and forestry species. The fluorinated analog improves callus formation rates and controls physiological responses where traditional auxins show limitations. Industry compliance standards
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3. Active Ingredient in Advanced Agrochemical R&D ProgramsResearchers and industrial-scale chemical discovery programs employ 6-Fluoroindole-3-Acetic Acid as a molecular scaffold for generating new classes of plant hormone analogs and bioactive derivatives through fluorinated moiety insertion. This application supports the development of proprietary auxin derivatives for patentable agrochemical portfolios and high-throughput screening. Industry compliance standards
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4. Breeding Program Reagent for Trait Improvement InitiativesSeed producers and commercial breeding stations working on yield, stress resistance, or phenotypic uniformity in field crops or ornamentals select this compound as a direct treatment in mutation induction, doubled haploid production, and breeding station phenotypic screening. The specific fluorine substitution brings improved control over morphogenetic events, facilitating trait stabilization. Industry compliance standards
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Experience in the manufacture of auxin derivatives has taught us the value of precision, both in synthesis and characterization. 6-Fluoroindole-3-Acetic Acid, for those of us working on the production line and in the development lab, isn’t just another variant of IAA derivatives; it represents a carefully controlled approach toward bringing subtlety and specificity to plant hormone biotechnology. Our approach starts right from raw material sourcing, travels through each purification stage, and ends with batch-to-batch consistency that botanists and agronomists can actually rely on in research and field applications.
We designate our batches as F-IAA6, with purity consistently above 98%. Our technicians keep an eye on spectral verification to prevent isomeric contamination; this isn’t a point of pride but a necessity. Unlike bulk commodity synthesis, handling 6-Fluoroindole-3-Acetic Acid calls for a sharply honed process. Introducing fluorine into the indole scaffold alters both biological functionality and chemical behavior—solubility shifts, affinities change, and shelf life varies from what you’d expect from basic IAA. We’ve witnessed reduced degradation in sample storage, an effect that many agronomists recognize as key for stock solutions lingering between greenhouse trials.
This molecule turns heads in plant physiology research. Researchers have shown how substitution at the 6th position of the indole ring can transform plant auxin response—driving cell elongation, influencing gravitropic response, and modulating root or shoot development with a specificity that classic IAA cannot deliver. Our clients frequently report clearer dose-response curves and improved reproducibility. The addition of a fluorine atom at the 6-position isn’t random; it creates a more persistent auxin analog that resists metabolic breakdown both in solution and in living tissues. This means scientists spend less time repeating inconsistent experiments and more time exploring genuine plant hormone signaling pathways. We’ve seen this translate, in practice, to more reproducible research publications and fewer concerns about batch variability.
Decades of manufacturing experience have carved out key distinctions between fluorinated indole acetic acids and their non-fluorinated counterparts. During recrystallization, for instance, our technicians monitor not just yield but polymorph formation, knowing that even subtle differences can shift plant response profiles. Our plant uses robust vacuum drying, ensuring low residual water and no alcohol carryover—a crucial point for researchers working with water-sensitive plant tissues. There’s a reason so many developmental biology labs come straight to factories like ours rather than resellers; direct contact gives them confidence in what landed on their bench yesterday.
Our workbench sampling over thousands of kilograms has told us one truth: not all indole-3-acetic acids behave the same. The fluorine substitution at C6 makes this molecule more stable under UV and oxidative conditions compared to parent IAA, so long-term assays or outdoor field experiments don’t suffer from unexpected breakdown. Plant biochemists we’ve supplied tell us they see consistently heightened auxin activity in bioassays such as the classic Lepidium sativum root elongation test. Compared to 5-fluoro or unsubstituted IAA, the 6-position fluorine often displays unique dose-response kinetics and stronger resistance to conjugation in plant cells. This partly explains why researchers ask for this specific regioisomer above all others for mechanistic plant growth studies.
On the manufacturing floor, it is impossible to ignore feedback from the field. We’ve heard from irrigation chemists who tested 6-Fluoroindole-3-Acetic Acid in nurseries and row crops, noting more predictable rooting patterns, especially under temperature swings that degrade standard IAA. Some trialists have reported that limited use in micropropagation cut down on hyperhydricity, a common issue found with less stable auxins. Biology departments working on model species, from Arabidopsis to tomato root cultures, have remarked on sharper lateral root formation with less browning of sensitive explants. The feedback loop from growers and scientists directs our ongoing process refinements, influencing small tweaks in washing, drying, and final filtration. In our experience, direct end-user input always trumps theoretical speculation in shaping production priorities.
We can speak to the reality of lab storage, with daily batch samples taking up shelves in our own quality assurance department. Our records, backed by weekly HPLC and NMR checks, confirm that 6-Fluoroindole-3-Acetic Acid retains integrity under refrigerated or room temperature conditions far better than many non-halogenated auxins. This is not just idle laboratory chatter; university researchers and agricultural product formulators request stability data from us for regulatory filings and grant proposals. With lower rates of oxidative decomposition, this molecule doesn’t require elaborate inert-gas storage for typical short-to-medium term use. This kind of practical durability helps plan experiments in research facilities where high-frequency use or staff rotation can introduce lapses in chemical care.
Purity in plant growth regulators influences biological activity in more ways than just potency. Traces of isomeric, halogenated byproducts can block site-specific auxin receptors or activate off-target cellular responses. From hands-on troubleshooting, our chemists know that poor purification or improper crystallization brings stubborn fouling in tissue culture pipelines. Aggregation, precipitation, or unexplainable variance in explant growth can almost always be traced back to off-grade reagent. We address these practical problems at the source, adapting raw material qualification and tweaking solvent gradients based on our in-process analytics. Our in-house staff never hesitate to run additional melting point or chromatographic checks for clients about to undertake long-term field studies, since an extra 24 hours of confirmation saves weeks of troubleshooting down the road.
Many of our first-time buyers arrive with a list of packaging questions. Toxicology researchers and seed companies handle chemicals very differently. We package 6-Fluoroindole-3-Acetic Acid in sealed amber glass or HDPE, always under low humidity. Those working in tropical environments often ask about possible condensation, so our approach has evolved toward more robust desiccant and vacuum sealing, even for small milligram vials. Our field notes show that minimizing atmospheric moisture during filling prevents caking or unplanned hydrolysis by the time the package lands in the researcher’s hands. Rapid access and direct exchanges between the plant and university or commercial labs have led us to adjust even minor labeling protocols based on what actually helps technicians in practice.
Synthesizing halogenated indole compounds requires careful attention to environmental impact. Our factory replaced chlorinated solvents in most process steps, not solely for regulatory compliance but because it prevents hazardous waste. We direct much of the captured waste toward recovery streams, reducing solvent use and allowing for the recycling of non-reactive materials back into upstream processes. Monitoring by-products and secondary waste ensures that the footstep of our manufacturing remains lighter, responding both to local waste handlers and the broader demands of global regulatory bodies. Experience teaches that the discipline needed for this kind of chemical stewardship often pays off in reduced costs and fewer regulatory downtime events, ultimately letting us deliver a more reliable product to researchers with clear documentation from batch to batch.
Years of supplying both leading academic laboratories and commercial agricultural biotech companies have given us a front-row seat to the evolving demands of auxin research. High-throughput screening platforms, CRISPR/Cas-driven plant transformation pipelines, and detailed kinetic analyses all require starting materials that don’t compromise experimental reproducibility. Our batches of 6-Fluoroindole-3-Acetic Acid regularly feed into translational projects funded by international grants. We often get requests for custom batch documentation, including chromatograms and residual solvent data tailored to a specific research protocol. Our relationships with field researchers keep us grounded in the practical demands of day-to-day experimental work; serving these needs means openness about our own process data, acknowledging both process strengths and limitations.
No chemical is a silver bullet in biological experimentation. We field plenty of questions from researchers about interaction with soil microbiota, uptake efficiency in different plant systems, and compatibility with mixture partners in plant cocktails. We keep direct records of actual user outcomes, rather than just relying on published literature, and we see consistent patterns. For instance, applications in hydroponic systems can lead to accumulation issues, so dilution protocols and application intervals require adjustment from traditional field use. Where users report interference in symbiotic nodulation or microbial growth inhibition, we can point to fluorine’s subtle yet impactful effect—often beneficial for hormone signaling, occasionally disruptive in rhizosphere balance. By collecting feedback from trials, we help partners adapt dosing and timing strategies, rather than simply handing over chemical vials with printed instructions.
We see ourselves less as distant manufacturers and more as collaborative partners for every batch shipped. Beyond the standard certificate of analysis, our staff engage directly with research teams to interpret analytical data, digging into questions of secondary peaks or unusual spectral signatures when irregularities arise. Feedback from users sometimes leads us to revisit synthesis routes or tweak purification columns. While this means extra work on our end, the resulting trust and camaraderie benefit everyone in the chain. In a field where minor impurities or untracked degradation can derail months of research, our team’s approach to transparency and ongoing support stands as the single best insurance against disappointment or costly delays. We never consider our job finished once a shipment leaves the plant; instead, each bottle is part of a feedback cycle that sharpens both our product and the science built on it.
Most of those who buy from us aim to improve crop yields, unlock robust plant development, or probe the deep molecular roots of hormone signaling in plants. Users working on tissue culture protocols for recalcitrant species often tell us that 6-Fluoroindole-3-Acetic Acid offers greater cloning efficiency and healthier callus development. Horticultural technology providers describe their own in-house trials showing improved transplant root establishment, notably under stressful sunlight or suboptimal irrigation conditions that would degrade lesser-stable compounds. Research into herbicide resistance sometimes uses 6-Fluoroindole-3-Acetic Acid to dissect auxin transport pathways, a field long plagued by the instability and unpredictable turnover of less stable analogs.
These applied results didn’t just happen overnight. They represent years of dialogue between manufacturing, application, and research partners—each one feeding back hard-earned lessons on what works in specific species, climates, and systems. This iterative loop, covering everything from chemical synthesis procedures to application tips, provides much of the practical knowledge that keeps this compound valuable to real-world plant science.
Feedback from commercial nurseries and university trial stations push us to constant improvement. Repeated input about ease of dissolution has led us to fine-tune particle size without sacrificing purity. Requests for lower dusting and improved wetting ability from greenhouse mixing rooms influence our post-synthesis milling and sieving protocols. Issues like static buildup in dry handling—hard to appreciate unless you're staring at the residue on a weighing balance day after day—lead to adaptations in packaging antistatic agents or subtler container design changes. We take user frustrations seriously, and each solution builds into the next manufacturing cycle, helping us avoid the pitfalls of treating specialty chemicals as if they were just another commodity.
Few things matter more to us than building trust with those who actually use our products. Direct partnerships have shown us that co-development outpaces rigid supplier relationships. Researchers sometimes request custom batches with defined particle sizes, moisture content, or even specific counter-ion forms for downstream work. Our plant responds better to those customization requests since our engineers walk the floors daily and can make adjustments on the spot instead of wading through layers of distribution markup or opaque supply chains. This open-door policy has two effects: it brings new technical challenges straight to our in-house chemists, and it means new ideas for product development come straight from those who rely on our chemicals to turn research questions into real-world solutions.
Our involvement in the development and manufacture of 6-Fluoroindole-3-Acetic Acid over the years has meant more than just routine batch production. Engagement with cutting-edge research, keeping current with scientific advancements in the understanding of plant hormone analogs, has shaped how we approach catalyst selection, purification protocol, and final QC. We invest in upgrading our spectral analysis and impurity profiling each year, not just to satisfy regulatory agencies, but to match the rising bar set by world-leading plant science programs. The lessons we’ve learned, and mistakes we’ve corrected, are embedded in every part of our routine. Returning customers and published acknowledgments in high-impact journals highlight just how pivotal manufacturing partnership can be in the quest for breakthroughs in plant biology and agriculture.
Manufacturing is never just a technical exercise; it is a contract with each scientist and grower who places trust in our bottles. The chemical itself—6-Fluoroindole-3-Acetic Acid—only delivers extraordinary results when handled with an extraordinary commitment to detail, safety, and continual improvement, all of which draw on the experiences shared by both our staff and our partners in the field. With each cycle of production, feedback, and adaptation, we strengthen this trust, and in so doing, we uphold the highest standards demanded by cutting-edge plant science today and tomorrow.