|
HS Code |
483536 |
| Productname | 3-Phthalimidopropionic Acid |
| Casnumber | 5241-95-8 |
| Molecularformula | C11H9NO4 |
| Molecularweight | 219.19 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 156-160°C |
| Solubility | Slightly soluble in water, soluble in DMSO and ethanol |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8°C |
| Smiles | O=C1C2=CC=CC=C2C(=O)N1CCC(=O)O |
| Inchikey | OHEXPZUCZCILCX-UHFFFAOYSA-N |
As an accredited 3-Phthalimidopropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a screw cap, labeled "3-Phthalimidopropionic Acid, C11H9NO4," featuring hazard and handling instructions. |
| Shipping | 3-Phthalimidopropionic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is transported under ambient conditions unless otherwise specified, following regulations for non-hazardous chemicals. Packaging ensures stability and protection from physical damage during transit. Always check the accompanying safety data sheet for specific handling and storage instructions. |
| Storage | 3-Phthalimidopropionic Acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. It should be protected from direct sunlight and sources of ignition. Proper labeling and secure location are essential to prevent accidental exposure or contamination. Store at room temperature unless otherwise specified by the manufacturer. |
Applications of 3-Phthalimidopropionic Acid in Industrial Manufacturing3-Phthalimidopropionic Acid serves specialized roles in multiple industrial chemical sectors, especially in synthesis of pharmaceuticals, specialty polymers, and advanced chemical intermediates. As an experienced manufacturer, we directly supply this raw material to downstream producers who require consistency, compliance, and technical adaptability for scale-up production. 1. Pharmaceutical Intermediates: Peptide Drug Synthesis3-Phthalimidopropionic Acid enables the protection of amino groups in peptide synthesis, providing a stable phthalimido group crucial for multi-step chain assembly. It enters the process during the early-stage coupling reactions to block reactive sites, ensuring selective bond formation for downstream deprotection and elongation phases. Such use forms part of the route to key peptide-based active pharmaceutical ingredients (APIs), especially those involving lysine and proline derivatives. Manufacturers rely on this raw material to achieve clean, scalable reactions with minimal byproduct formation and consistent purity. Industry compliance standards
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2. Fine Chemical Synthesis: Succinate DerivativesChemical manufacturers use 3-Phthalimidopropionic Acid as a key intermediate for building succinic acid derivatives via controlled deprotection and decarboxylation routes. These derivatives play a central role in organic synthesis strategies for agrochemicals, liquid crystals, and monomer production. The acid function and phthalimido group contribute to high-selectivity reactions in batch and continuous flow systems, supporting downstream applications that demand traceability and reproducibility for final compound registration. Industry compliance standards
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3. Advanced Polymer Additives ProductionDownstream polymer manufacturers utilize 3-Phthalimidopropionic Acid when developing functional additives for engineering plastics. The compound’s structure enables effective incorporation into polymer matrices, modifying thermal and mechanical properties. Its introduction occurs at the pre-polymerization stage or during the compounding process. The acid group forms copolymers or acts as a chain transfer agent, controlling molecular weight distribution in high-performance resin systems designated for electronics, automotive, and aerospace applications. Industry compliance standards
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4. Specialty Agrochemical Intermediate Manufacturing3-Phthalimidopropionic Acid finds targeted use in the preparation of plant growth regulators and protected nitrogen-release compounds. Agrochemical formulators rely on the acid for selective functionalization, introducing amide or imide groups into precursor molecules. Its application improves the stability of slow-release fertilizers and enhances uptake characteristics in soil and foliar treatments. Integration occurs as part of multi-step synthetic schemes under stringent process controls for active ingredient formation. Industry compliance standards
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Working at the intersection of organic synthesis and advanced material building blocks, we see the quiet importance of molecules like 3-phthalimidopropionic acid every day. Textile additives, pharmaceutical intermediates, and specialty chemical research labs request it with regularity. Over the years, we've observed how this modest compound grows into varied roles across both established and cutting-edge industries.
As we operate in batches each cycle, 3-phthalimidopropionic acid comes straight from our reactors as a white solid with dependable purity. Its formula, C11H9NO4, sits long on the minds of our chemists as they calibrate both the weight and molar output at each stage. High structural reliability comes from stringent control of heating and crystallization, so our lots rarely stray from the 99% range by HPLC analysis.
Our standard preparation aligns with the tetrahedral phthalimide core linked to a three-carbon propionic fragment—a motif well known for its stability during storage and resistance to hydrolysis. Each drum, lined and double-sealed, leaves only after final confirmation of melting point, free acid content, and residue on ignition.
Colleagues in pharmaceuticals appreciate a material that resists degradation by moisture and light. Synthesis steps remain predictable with 3-phthalimidopropionic acid, letting the amide bond formation stand out in multi-step API projects. The compound’s molecular framework sits close enough to common amino acids to serve as a protected glutamic acid analog, which gives medicinal chemists more room for late-stage diversion. As a backbone for peptide coupling or as a precursor for N-alkylated amines, it often enters pilot-scale campaigns before hitting full-scale GMP batch production.
Polymer developers reach for this acid when they need a hard-wearing intermediate that links well with acrylates or forms part of the backbone in imide-rich resins. The bulk shipments heading for their lines show little caking or clumping, even in high-humidity areas. Consistent melting range keeps process lines running without tuning, whether the acid dissolves in DMF for a condensation or in acetonitrile for a controlled oligomer addition.
Outside pure synthesis, research labs prize this molecule for bioconjugate experiments and linker studies. Attaching fluorescent or bioactive moieties proceeds cleanly at the terminal carboxyl group, letting postdoctoral teams skip unnecessary purification cycles. Some teams favor it for small molecule library work, banking on its minimal byproduct profile during cyclization reactions.
Our plant sees hundreds of kilograms of 3-phthalimidopropionic acid each month. Operators check every reaction for color and crystal clarity, since even a faint tinge can signal an upstream impurity that could derail downstream reactions. Skilled technicians manage drying, watching for telltale shifts in sample texture. Too rapid a vacuum phase and the crystals cake; too slow and the bulk density drops, making downstream handling an ordeal.
We confront small challenges—some lots turn sticky under humid conditions, so buffered desiccators become part of our routine. The acid travels best in ambient shipping, but only if triple-layered containers match atmospheric pressure to avoid condensation. Over time, the plant team learns to keep lint, paper dust, and even stray polypropylene weights away during weigh-outs, since static attracts everything in a cleanroom.
Compared to shorter-chain phthalimido acids or those based on succinimide skeletons, 3-phthalimidopropionic acid remains robust in the face of nucleophilic attack. It holds up longer in solution and resists unwanted side reactions when subjected to strong coupling reagents. We’ve received feedback from process development groups who’ve switched from phthalimidoacetic acid due to breakdown issues; their yield numbers confirm the long-chain acid carries less risk of amide cleavage or hydration.
We make both 3-phthalimido and 4-phthalimidopropionic acid on occasion. Field results consistently show that the meta isomer retains solubility in polar solvents while minimizing reactivity at the wrong position. For most, this means downstream conversion proceeds with fewer isomeric impurities, streamlining purification. Chemical suppliers often source their material from traders unsure which isomer came off the line; since we manufacture at-source, traceability and correct assignment never become guesswork.
As for cost, our larger-scale process sheds both solvent and energy use, which keeps overall pricing fair. Single-step batchers sometimes struggle to match the same price-to-purity ratio, especially as raw material volatility grows. As demand fluctuates, direct oversight on our warehouse floor keeps stock levels steady, without resorting to speculative storage.
Modern chemistry leans hard on process safety and environmental control. Solvent capture systems continually operate during our production of 3-phthalimidopropionic acid so emissions never build to hazardous levels. Operators regularly rotate solvent drums and replace spent molecular sieves to drive down waste. The phthalic anhydride pathway we use yields high percent conversion, so our mother liquors generate less organic residue than routes using phthalic acid direct.
We lower our energy burden by recycling hot wash streams through the cooling tower, which helps offset both cost and emissions. Watching energy meters over a shift can teach any plant manager where the waste lies—in our experience, tracking by batch rather than monthly aggregate brings results. Our routine meetings show savings even from what might look like insignificant tweaks: changing water purge times, recalibrating jacket temperatures, and tightening cleaning cycles.
As markets stretch from life sciences to materials science, incoming requests for 3-phthalimidopropionic acid land with varied technical demands. Some require tighter particle sizing, some demand lower metal content, others want a two-year shelf life at room temperature. Here, on-site testing pays dividends. Whether an order comes in for 1 kg or 1000, every drum carries its own full assay sheet with spectral data, since many QC departments insist on cross-validation before greenlighting a new vendor. We gladly supply reference samples and reserve tank lots for returning partners, supporting both pilot-scale and commercial-grade runs side by side.
We see no sense in gating technical documents behind paywalls or NDAs. Trusted partners receive full COA detail and updated impurity maps with every batch revision. This reflects feedback—we save time and trouble on all sides by eliminating second-guessing. Instead of passing questions down a chain of resellers, direct communication gets problems aired and solved, whether it’s a solubility hiccup or a scale-up blockage.
Our technical group regularly talks through applications in protein modification or linker chemistry, sharing process hints hard-won through years of hands-on trials. Sometimes our customers face a formulation challenge or a bottleneck that isn’t obvious in theory; we work side by side until the workflow runs cleanly. This collaborative exchange is less about sales tactics and more about chemist-to-chemist respect, which we believe underpins all lasting B2B relationships in specialty chemistry.
3-phthalimidopropionic acid ships well under ambient conditions, yet care during transfer and weighing limits dust and contact. Personal protective equipment—nitrile gloves, goggles, lab coats—remains standard in both our shop floor and at external labs. Dry, cool conditions suit long-term storage, and most clients keep their acid sealed in original drums for up to two years, with shelf checks twice a year especially in regions with high seasonal swings.
Disposal after use stays straightforward for most, since our acid lacks halogens and decomposes predictably under incineration. Local waste regulations guide us far more than global edicts. We routinely audit disposal streams in our own operation, flagging any step that could slip outside compliance. Spills mean manual cleanup, no robots or aspirators; the powder clings, so a second pass always follows after initial sweep-up. Long hours of experience have shown our teams that missed trace contamination seeds future headaches, especially in the high-purity applications that dominate our business.
Few things set a producer apart like listening closely. Over the last decade, feedback from university research leads, regional formulation houses, and multinational pharma has driven how we refine our product and processes. Customers have helped us identify unwanted traces—remaining phthalic anhydride or color bodies—that only become clear in later stages of finished goods. We take these lessons directly to our strategy sessions.
On occasion, new process requests land on our desk: a greener solvent swap, a request for higher temperature crystallization, or an appeal to knock down peroxide traces below low ppb. We don’t treat these as burdens but as mile markers, guiding us to push internal controls a little further every quarter. Dedicated chemists manage pilot batches tailored to such requests, working long hand-in-glove with partners parsing every signal from their own QC teams. We constantly improve our documentation based on these dialogue loops, so our batch records tell the whole story—not just the checkmarks.
Plenty of our proudest moments come from seeing 3-phthalimidopropionic acid play its role in successful synthesis projects, new materials, or published research. Universities have turned to it as a stable handle for complex building blocks in peptide engineering projects. Companies in the coatings and resins sector slot it into new formulations where previous options failed due to brittleness or side reactions. Clinical-stage pharma counts on reliable supply of this acid to unblock challenging scale-ups, especially as synthetic protocols move from benchtop prototypes to manufacturing plant output.
As our catalog expands, we pay special attention to customer stories showing how 3-phthalimidopropionic acid bridges chemistry between research and reality. A handful of process changes year over year can make a world of difference, blunting the edge of day-to-day uncertainty while keeping the innovation pipeline open. Customers come back not for dramatic claims, but for steady, reliable material that fits seamlessly into difficult workflows.
We invite fellow chemists, developers, and researchers to share their requirements or observations. A product’s full advantage emerges only in continuous dialogue and honest adjustment. 3-phthalimidopropionic acid, as manufactured here from phthalic anhydride via controlled addition and crystallization, remains one of those quietly vital building blocks: steady, well-understood, and always open to refinement. We don’t claim glamour, just ongoing, hands-on attention to quality and practical value in every drum that leaves our floor.
From our perspective, 3-phthalimidopropionic acid doesn’t headline chemical news, but its importance runs deep through the threads of practical chemistry. Every new batch grows out of old lessons and fresh conversations—between our line operators, research partners, and the chemists who handle the powder on their own benches. We trust this compound because we know its origins, its quirks, and its value to the technicians, innovators, and manufacturers who count on it for consistency, reliability, and peace of mind across applications. If you work with it, your experience helps shape the next generation of production—one lot at a time.