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3-Indolepropionic Acid

    • Product Name 3-Indolepropionic Acid
    • Alias IPA
    • Einecs 212-281-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    270593

    Chemicalname 3-Indolepropionic Acid
    Casnumber 830-96-6
    Molecularformula C11H11NO2
    Molecularweight 189.21 g/mol
    Appearance White to off-white powder
    Meltingpoint 137-139 °C
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Boilingpoint 412.5 °C at 760 mmHg
    Storagetemperature 2-8 °C
    Ph 4.0-4.5 (10 mM in water)
    Synonyms Indole-3-propionic acid, IPA

    As an accredited 3-Indolepropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Indolepropionic Acid is packaged in a 25g amber glass bottle, sealed, with a clear label indicating hazard and storage instructions.
    Shipping 3-Indolepropionic Acid is shipped in secure, tightly sealed containers to prevent contamination and degradation. The containers are clearly labeled and stored under cool, dry conditions away from incompatible substances. Standard shipping typically follows all applicable regulations and safety guidelines for handling and transporting chemical compounds to ensure safe delivery.
    Storage 3-Indolepropionic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at a cool temperature, preferably in a refrigerator (2–8°C), and away from incompatible substances such as strong oxidizing agents. Ensure the storage area is well-ventilated and that proper labeling is present to avoid accidental misuse or contamination. Handle with appropriate protective equipment.
    Application of 3-Indolepropionic Acid

    Applications of 3-Indolepropionic Acid in Industrial Manufacturing

    3-Indolepropionic Acid (IPA) serves as an advanced specialty intermediate in several technical industries, where manufacturers integrate it for its potent antioxidant and metabolic modulation properties. We supply high-purity IPA designed for consistent performance and traceability throughout stringent downstream processes. The following application scenarios detail exclusive sectors and protocols currently employing this material in volume production.

    1. Pharmaceutical API Intermediate Synthesis

    Leading pharmaceutical companies utilize IPA as a building block and protective antioxidant during the synthesis of select neuroprotective and metabolic drug candidates, such as precursors for new-generation small-molecule medications. Manufacturer R&D teams formulate API intermediates in tightly regulated environments, requiring alignment with global pharmacopoeia and continuous in-process QC analytics to assure purity and safety.

    Industry compliance standards

    • US Pharmacopeia (USP)
    • European Pharmacopeia (Ph. Eur.)
    • ICH Q7A GMP guidelines
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • 0.03–0.2 molar equivalents per target API, adjusted based on desired molecular complexity and batch synthesis conditions

    Downstream process integration

    • Introduced during mid-stage coupling or protection steps as an intermediate, followed by controlled purification and conversion to advanced molecules

    Final product types

    • Pharmaceutical grade intermediates
    • Active pharmaceutical ingredients (APIs) for CNS and metabolic therapies
    • Custom research molecules

    2. Antioxidant Formulations for Functional Foods

    Food manufacturers adopt IPA as a potent antioxidative additive in the fortification of health snacks, functional beverages, and nutritional supplements. Its integration into food matrices enhances oxidative stability and supports shelf-life extension, while R&D and QC teams must ensure ingredient compliance with local food safety and additive frameworks.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius
    • GB 2760 National Food Safety Standard for Food Additives (China)
    • FDA 21 CFR Part 170–199 (US Food Additive Regulations)
    • FSSC 22000 certified production (where applicable)

    Typical usage ratio

    • 10–80 mg per kg of final food product, with fine-tuning linked to target product shelf-life and local maximum residue allowances

    Downstream process integration

    • Dosed at the blending stage for beverages and directly into dry mixes for bars and powders, followed by uniform dispersion using industrial mixers under controlled temperature

    Final product types

    • Prebiotic beverages
    • Functional nutrition bars
    • Dietary supplement powders
    • Food fortification premixes

    3. Research Reagents for Analytical and Life Science Labs

    Specialty chemical producers formulate IPA into high-purity analytical reagents for life science R&D institutions, focused on oxidative stress assays, detection of indole derivatives, and brain-gut axis investigations. Consistent reagent grade quality and batch reproducibility are key, along with supporting documentation for regulatory laboratory consumers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • REACH Registration for laboratory chemicals
    • OECD Good Laboratory Practice (GLP)
    • Analytical standards (HPLC/GC verified)

    Typical usage ratio

    • Prepared as 10-500 μM solutions in buffer systems for in vitro bioassays; solid-form usage based on experimental protocol requirements

    Downstream process integration

    • Dissolved or suspended at the bench or within automated reagent pack assembly lines, filtered, and QC-tested prior to distribution to research users

    Final product types

    • Calibrated HPLC standards
    • Cell culture antioxidants for oxidative stress models
    • Custom reagent solutions for metabolite quantification
    • Life science assay kits

    4. Advanced Cosmeceuticals and Personal Care Actives

    IPA’s ability to stabilize sensitive bioactives and inhibit radical formation makes it valuable in the personal care sector, particularly in skincare serums and anti-aging formulations. Cosmetic manufacturers must meet global cosmetic safety guidelines and stability standards when incorporating this ingredient at substantiated functional levels.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • Cosmetic Ingredient Review (CIR) database
    • ISO 22716 Good Manufacturing Practices for Cosmetics
    • Health Canada Cosmetic Ingredient Hotlist

    Typical usage ratio

    • 0.01–0.1% w/w, with variation based on skin tolerance testing and intended antioxidant activity claims

    Downstream process integration

    • Introduced into emulsions post-cooling phase to minimize thermal degradation, then homogenized before filling and stability testing

    Final product types

    • High-end facial serums
    • Day/night antioxidant creams
    • Specialty skin repair lotions
    • Topical recovery gels
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    Competitive 3-Indolepropionic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Inside Our 3-Indolepropionic Acid: A Manufacturer’s Take

    Looking Closely at 3-Indolepropionic Acid

    From the moment we started producing 3-Indolepropionic Acid (IPA, CAS 830-96-6), we noticed how different it performed compared to many aromatic carboxylic acids. IPA stands out, not because of its strange name or niche reputation, but because its structure opens doors in multiple applications from pharmaceutical research to advanced material synthesis. Over years of direct manufacturing, we’ve learned production tricks that impact its purity, stability, and readiness for demanding R&D.

    What Makes Our IPA Different

    Many chemical manufacturers pump out similar-sounding indole derivatives, but none echo the oxidation stability or long shelf life we have cultivated for IPA. Each batch comes with a guarantee on purity, with HPLC specs pushing past 99% in most lots. We did not reach these numbers by luck. Precise control during synthesis — from initial cyclization through purification steps — cuts down on typical side-products such as indole-acetate and indole-butyrate, which easily creep in when shortcuts tempt untrained hands or when older equipment runs the show.

    Indole derivatives often challenge even experienced teams. Tryptophan, indole-3-butyric acid, and indole-3-acetic acid each bring their quirks, oxidizing or degrading unless stored in ideal conditions. IPA, once protected during production, gives a strong edge in thermal and photostability. Users working late nights or running long experiments see fewer surprises in their results. Years ago, some customers told us they jumped between suppliers, finding half-full flasks sedimented or yellowed within months. This kind of avoidable waste does not happen where raw material selection and airtight process management set the tone from day one.

    Our Model and Approach

    We label our main product line as IPA-9905, marking out its minimum 99.0% assay by HPLC and its suitability for both lab-scale and pilot-plant work. Particle sizing is not an afterthought—standard ranges run 60–120 mesh, fine enough for most syntheses but still easy to handle. We keep an eye on the shelf life with regular stability checks. It’s not unusual for advanced users to ask about bulk quantities in industrial containers, so our drum packaging uses high-grade liners to keep the acid dry and protected from light.

    How IPA Is Actually Used

    IPA has built a dedicated following in both research circles and specialty production lines. In the pharma sector, it often pops up in antioxidant research, thanks to its ability to reliably quench free radicals in radical scavenging assays. Other labs come to us looking to study IPA’s neuroprotective behavior, as early literature points toward reduced cellular damage in oxidative stress models. These interests are not abstract. Real value comes from years of replicability — the predictability of IPA’s chemical backbone translates to reliable assay outputs, tighter dosage development in pilot trials, and fewer failed batches downstream.

    Materials scientists have a different target. They use IPA as a precursor when constructing new polymer architectures, particularly in the search for novel bonds where a stable carboxylic acid supports delicate indole ring chemistry. In our conversations with such teams, they tell us that many other indole acids break down or react unpredictably; IPA stays viable even during multi-hour high-temperature steps. Those who have spent months on failed reactions appreciate this kind of peace of mind.

    Comparing IPA With Similar Compounds

    The world does not lack for indole chemicals. Anyone who has compared indole-3-acetic acid (IAA) or indole-3-butyric acid (IBA) with our IPA already sees the differences in solubility curves, reactivity, and degradation rates. IAA finds extensive use as a plant growth regulator, but ask anyone who needs strict antioxidant properties, and IPA wins by a long shot. Many labs fall into the trap of swapping compounds, only to learn that the electron distribution in IPA’s propionic side chain offers a uniquely persistent antioxidant action that IAA and IBA struggle to match.

    Our technical teams field many questions about mixing or co-applying different indoles. Early on, we did plenty of side-by-side stability trials: IPA routinely resisted both hydrolysis and air oxidation in buffered solutions where IAA faded. These measurable differences explain why advanced R&D groups insist on IPA for their screening libraries or when developing new lead compounds for neuroprotection. Likewise, materials engineers running high-load reactions care about IPA’s clean decomposition profile; fewer byproducts appear on GC-MS or LC reports, helping avoid costly downstream purification work.

    Lessons Learned About Consistency

    As a chemical maker, it’s easy to promise high purity, but time exposes any weaknesses. We learned quickly that many common glassware and tubing choices leach trace metal ions that catalyze indole ring breakdown. Years ago, we overhauled our line to include low-leach reactor systems: stainless steel, high-purity PTFE, quartz. Our analytics team runs dozens of stability samples each quarter, with extra controls to pre-emptively catch trends before any off-spec batch could hit a customer’s bench.

    Sometimes a researcher calls, frustrated about inconsistent melting points or discoloration in IPA purchased from unknown sources. The culprit is usually trace synthesis byproducts or mishandled drying. Our own drying protocol involves a staged, low-temperature vacuum process monitored by inline moisture analyzers. Outbound QA checks solvent residues, water, elemental impurities, and checks for even faint levels of heavy metals. With experience, you build up an internal database to spot warning signs, long before a final bottle is sealed.

    Why We Insist on Transparency

    Outside labs tell us that visibility into batch-level data helps them run tighter experiments. We publish real spectra, chromatograms, and impurity profiles for each batch shipped. A big-name customer once explained how a previous supplier’s lack of transparency cost them months in repeat synthesis—missed data leading to wasted time and budget. From our side, this transparency comes from experience; by being open, we create a feedback loop where customers and our own operators constantly raise the bar.

    We encourage partners to request full documentation: COAs with every technical detail, origin data for precursor chemicals, even test scripts upon request. This is not empty reassurance; it closes the trust gap and lets advanced research teams talk process improvements directly with our chemists.

    Handling, Storage, and Real-World Usability

    IPA holds up well under normal lab conditions, though sunlight and high heat accelerate its breakdown. Some manufacturers cut corners, leaving product in semi-translucent drums or packing with insufficient desiccants. Our operations crew stores all IPA in light-proof, nitrogen-flushed containers straight from dryer to shipment. This care prevents the oxidative yellowing that competitors’ IPA commonly shows just a few weeks after delivery.

    Users comment on clean-handling feel, the ease with which the powder dispenses or dissolves. No clumping, minimal dust, no off-odors. This may sound minor, but in batch preparation or scale-up, time lost due to handling headaches adds up. We receive fewer complaints about caking or flow issues than in our early days, something we attribute directly to tweaks in crystallization rate and drying environment.

    Scaling Up: Meeting Bulk and Custom Needs

    IPA users span from benchtop researchers to full-scale pilot plants. Along the way, we’ve handled odd volume requests (from tens of grams to hundreds of kilograms) and built relationships with glassware makers, drum manufacturers, and shipping experts so that each shipment matches customer requirements. Customization means more than just repackaging. Several users needed particle size modification, or wanted premeasured aliquots for one-time applications. We worked directly with their teams, adjusting crystal growth conditions, sieve schedules, or blend ratios to meet those needs.

    Large-scale users need documentation for regulatory reviews, especially when IPA goes into preclinical or toxicity studies. We developed a full suite of traceability statements, and thanks to automated batch controls, can pull full production records for any shipment. Our regulatory group tracks emerging guidelines from major bodies, reviewing regularly to stay compliant and anticipate customer questions before they turn into pain points.

    Value for Interdisciplinary Teams

    IPA does not live in a pharmaceutical silo. In environmental and crop sciences, its robust antioxidant activity makes it useful as a control standard for soil testing and root exudate analyses. Industrial chemists continue to describe creative applications as a starting material for new hybrid molecules. Every month, we field requests for technical input: can IPA serve double duty as both an antioxidant reference and a synthetic intermediate? Will its reactivity withstand alkali rinse in a continuous reaction? We run short test batches and share all results so prospective clients can make informed decisions before scaling.

    A few developers in the biotech startup scene told us that IPA was the ‘missing link’ for optimizing oxidative stress detection kits. By engaging early and sharing application notes—chromatography data, solubility checks, simple but meaningful stress tests—we’ve seen more startups launch with robust protocols that avoid costly supply chain stumbles.

    State of the Art, Future Directions

    Continuous investment in analytics and process improvements pays off in small but critical ways. Last year, we introduced a new in-line NMR check, adding yet another layer to our QC workflow. It’s easy to overload a product page with generic claims, but real value comes from consistent, testable results over time.

    Researchers repeatedly report that their IPA from mainstream catalog brands shows wider lot-to-lot variation than samples from our plants. We attribute that to our refusal to pool intermediates from different sources or to cut corners on solvent recovery. Production scale-ups often bring variability, so our engineers live on the line, adjusting distillation and crystallization with every reactor turn. It is methodical work, but getting the details right means customers face fewer troubleshooting calls or failed screens.

    Direct Feedback—Closing the Loop

    IPAs story in our plant is shaped by our customers—the ones who call up late with spectral questions or tell us face-to-face what went wrong or right. Regular follow-up and joint application trials keep the process honest. When someone uncovers a tricky impurity, we build it into future controls. Trusted partnerships, in R&D as in supply, mean fewer surprises, faster development, and shared victories—important in a field where lost weeks can mean lost opportunities.

    For every new use case, we document the results, update production notes, and share findings in technical bulletins. No two users run the same experiments, so we learn something with every order. Our collective experience, shaped by hundreds of real-world projects, feeds back into the purity, stability, and reliability any client can expect from each bottle or drum of our 3-Indolepropionic Acid.

    A Manufacturer’s Perspective on Real Value

    We have made 3-Indolepropionic Acid for long enough to see the difference between commodity chemistry and carefully controlled synthesis. Clean product means less downstream waste, clearer spectra, tighter data, and above all, trust from the teams whose success depends on reliable supply. From storeroom controls to analytical lab work, every step in our chain draws on years in the business and real feedback from our partners.

    Every gram represents an accumulation of practice, refinement, and ongoing dialogue with the people who actually use this molecule, day in and day out. This is where the true value, and the unique strengths, of our IPA emerge — not as another line on a catalog, but as a product built by those who know it from the inside out.