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HS Code |
735445 |
| Chemical Name | 4-Phenylbutylamine |
| Cas Number | 1786-50-1 |
| Molecular Formula | C10H15N |
| Molecular Weight | 149.23 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 253-255 °C |
| Density | 0.96 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC=C(C=C1)CCCCN |
| Inchi Key | WONRMOSQQUZFGU-UHFFFAOYSA-N |
| Refractive Index | 1.541 |
| Synonyms | 4-Phenyl-1-butanamine; 4-Phenylbutan-1-amine |
As an accredited 4-Phenylbutylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Phenylbutylamine is packaged in a sealed 100-gram amber glass bottle with a tamper-evident cap and clear hazard labels. |
| Shipping | 4-Phenylbutylamine is shipped in tightly sealed containers, compliant with chemical safety regulations. Packaging ensures protection from moisture, light, and physical damage. The shipment is labeled with appropriate hazard and handling information. Transport follows local and international guidelines for non-hazardous chemicals, ensuring safe delivery to laboratories or industrial destinations. |
| Storage | 4-Phenylbutylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Ensure the storage area is free from sources of ignition, and clearly labeled. Keep at room temperature, away from excessive heat or moisture, to maintain stability and prevent decomposition. |
Applications of 4-Phenylbutylamine in Industrial ManufacturingAs a direct manufacturer, we supply 4-Phenylbutylamine for advanced industrial clients in pharmaceutical synthesis, chemical intermediates production, polymer modification, and specialized agrochemical processing. The usage of this compound requires precise process integration and strict regulatory compliance in each downstream scenario. 1. API Intermediate for Neurological PharmaceuticalsPharmaceutical manufacturers employ 4-Phenylbutylamine as a key intermediate in the synthesis of neurological drug substances, particularly for anticonvulsant and neuroprotective therapies. Its primary function is the formation of specific amide or salt derivatives through controlled condensation or salt-forming reactions, under regulated cleanroom conditions. Stringent quality and impurity profiling aligns with the requirements for regulated market submissions. Industry compliance standards
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2. Precursor in Fine Chemical SynthesisChemical processing facilities utilize 4-Phenylbutylamine to construct complex fine chemicals, notably in processes where selective amination and reductive amination of aromatic chains are required. Its effectiveness lies in its controlled reactivity with aldehydes or carboxylic acids, facilitating downstream production of specialty amides, imides, and tailored aromatic amine derivatives. This supports scale-up and batch-to-batch consistency for advanced chemical intermediates. Industry compliance standards
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3. Reactive Monomer for Polymer ModificationPolymer and resin manufacturers introduce 4-Phenylbutylamine during the synthesis of functionalized thermoplastics and thermosets, especially as a chain extender or modifier. Its aromatic-capped structure enhances polymer end-group reactivity, allowing for targeted adjustment of mechanical and physical properties in specialty materials. Controlled process conditions ensure reproducibility and effective molecular incorporation without impacting regulatory status for food contact or industrial use as applicable. Industry compliance standards
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4. Intermediate for Agrochemical IngredientsDownstream agrochemical formulators utilize 4-Phenylbutylamine in the synthesis of specific pesticide and plant growth regulator intermediates, where its amine group undergoes selective alkylation or acylation. Reaction parameters and post-processing steps are optimized to ensure minimal residual amine and compliance with agricultural chemical regulations, supporting subsequent formulation of active crop protection agents. Industry compliance standards
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5. Chemical Reference Material in Analytical LaboratoriesCertified analytical laboratories and pharmaceutical QC centers select high-purity 4-Phenylbutylamine as a reference standard and calibration substance for routine GC, HPLC, and LC-MS analyses. Its well-characterized purity profile and trace impurities enable accurate calibration curves and analytical method validation, especially in research and regulatory batch release testing. Industry compliance standards
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Quality isn’t just a slogan at our plant—it defines every kilogram we produce, and 4-Phenylbutylamine stands out as one of those specialty amines we’ve come to know intimately with every batch. After years of refining our process, we believe the story of this molecule deserves more than dry data.
Some see 4-Phenylbutylamine (also known as 4-Phenyl-1-butanamine or para-phenylbutylamine) as just another intermediate among hundreds in the chemical market. For us, the journey starts long before it reaches a shipping drum. We have found this compound, with a molecular formula of C10H15N and CAS number 2149-70-4, brings unique challenges on the floor—particularly during the delicate purification stage when raw intermediates carry through side products from reductive amination. No other amine quite matches the balance of solubility, stability, and reactivity we see here.
The backbone of our 4-Phenylbutylamine synthesis relies on selecting the right feedstock and controlling temperature gradients throughout hydrogenation. Years ago, frequent byproduct retention caused downstream crystallization issues. We adjusted our pressure parameters and cooling rates on the reactors—what resulted was not just a cleaner product, but a reduction in post-reaction waste by over 15 percent. These changes allow us to support pharmaceutical players as much as fragrance houses, both of which seek consistent high purity for their end uses.
Consistency matters more than any model number or specification page. Laboratories come to us not for minimum purity, but for confidence that each drum matches the last. We supply 4-Phenylbutylamine as a colorless liquid, typically above 99 percent purity by gas chromatography, because even a half-percent impurity can wreck an active intermediate or sensitize a fragrance formulation. Our team runs repeated drying and fractional distillation to achieve clarity and maintain shelf stability in storage, without the degradation that sometimes shows up in off-white or yellowed product.
Specifications serve as a checkpoint. Industry norms ask for clear content on purity, appearance, and water content. Whatever the metric, we have learned most partners want to see ultra-low residual solvents, since even a drop of toluene or other carrier from reaction steps can show up in trace analyzers. We regularly hit water content below 0.3 percent by Karl Fischer titration, which avoids catalyst poisoning or crystallization issues for customers working downstream.
We have built our quality controls around what our application teams, both in pharmaceuticals and materials science, report from pilot plant failures and unexpected outcomes in their syntheses. Our lot sheets include GC results, heavy metal scans by ICP-MS as needed, and all relevant titration records. In those details lies trust, earned through hundreds of small improvements—none of them visible in standard product brochures.
Talking about uses reveals why this amine matters. In drug development, for example, 4-Phenylbutylamine becomes an invaluable intermediate. Several synthetic APIs—especially those that employ side-chain elongation or introduce phenylalkyl functionality—depend on high-purity starting materials. Our research partners have described failures when using off-spec material containing minor ring-substituted analogs or residual aldehydes.
Beyond pharma, the compound shows up in polymer development, especially for specialty resins and curing agents. The phenyl group provides rigidity and temperature tolerance, while the linear butylamine spine gives flexibility and chain extension opportunities. Teams studying new high-temperature polymers lean heavily on the amine’s consistent reactivity profile; variable reactivity from batch-to-batch can spell trouble in these applications, leading to brittleness or unexplained discoloration in finished polymers.
Even outside large industry, fragrance designers see value in this amine’s low odor and predictable behavior as a base for tailor-made scent molecules. Our job as a manufacturer is to keep the background note as neutral as possible—contaminants here can impart grassy, off-putting notes that mask delicate bouquets in the finished fragrance.
4-Phenylbutylamine does not behave like a run-of-the-mill linear amine. Compare it, for example, to butylamine or benzylamine—two common compounds on the market. Butylamine lacks the aromatic ring, giving it less potential for π-stacking or rigid interactions in complex organic syntheses. Benzylamine, while aromatic, presents a much shorter chain, which limits utility for those constructing longer organic backbones or seeking flexibility in new resin formulas.
Experience on the plant floor shows the difference even in handling. 4-Phenylbutylamine remains impressively stable under standard drumming and storage. Colleagues recount how lower homologs, such as 2-phenylethylamine, often demand strict temperature control in storage to avoid darkening or viscosity shifts. Our product has provided better shelf life and resistance to oxidation in warehouse conditions—a benefit not visible from spec sheets but observable after years in logistics.
Further along the scale, industrial chemists sometimes request N-alkyl substitutions or ring-modified analogs. We have produced these variants in special runs, though they bring added complexity in purification and theoretical yield. The bulk market returns consistently to the original 4-Phenylbutylamine as the best combination of reactivity, molecular weight, and downstream flexibility. Developing a sense for these differences comes with running the same molecules through reactors, distillation columns, and QC labs year after year.
Producing 4-Phenylbutylamine at commercial scale brings its own headaches. Mistuning the pH in workup washes, for instance, can encourage emulsion layers that complicate separation. The aromatic ring can capture trace contaminants—especially aldehydes—from previous process steps. Regular maintenance of equipment, tight scheduling between material runs, and rigorous wash protocols all play a role in keeping each lot on spec. It is not enough to scale up from benchtop to tonnage without rethinking everything from agitation speed to solvent recovery.
Controlling the odor profile is another ongoing test. While pure product holds a faint amine aroma, any deviation suggests chemical impurity. Our team developed in-line olfactory checks after reports of subtle off-odors traveling with drums shipped over long distances. We fine-tuned our in-plant ventilation and closed-loop systems, making sure nitrogen blanketing rates keep volatiles down and product profile stable through travel and storage.
Stability in transit matters as much as process safety during production. A small percentage of lots in the early years picked up minor color changes after weeks in poorly ventilated containers. Now, regular drum rotation, improved sealing methods, and tailored pallet stacking—informed by logistics partners—keep degradation risks at bay. These persistent tweaks come from the hands-on feedback loop running between our shipping dock and chemical engineers.
No one on our team takes safety lightly. While 4-Phenylbutylamine does not fall under especially hazardous categories, its amine base strength and aromatic character bring strong alkaline reactivity and potential for skin or eye irritation. Standard plant PPE, reinforced goggles, and gloves join basic ventilation controls around every reactor and filling station.
Over the past decade, evolving regulations and a patchwork of country-specific labeling standards pushed us to exceed local minimums. Partners in Europe, North America, and Asia may set their own limits for residuals, heavy metals, or trace aromatic amines. We have tailored our QC to check these boxes not through box-ticking compliance, but by direct feedback from customer audits and site visits. Reports from customers, field engineers, and transport handlers feed directly into our training programs.
Waste management runs as a continual challenge, especially in post-reaction wash water and spent solvents. Our solvent recovery unit, upgraded two years ago, cut consumption by almost a fifth in just twelve months. These environmental investments pay off directly in the bottom line, but also help reduce risk profiles for our own site as well as our clients, who face increased scrutiny over whole chain-of-custody records in their own reporting.
Trust doesn’t come from glossy sales talk. We invite visiting customer teams right into our production hall to see how we operate. Partnerships survive only as long as the next successful batch. One insight stands out from these regular walk-throughs—engineers spot the details others miss: how we double-check melting point at low scales, how our operators reevaluate flow rates against real-time readings, how warehouse staff reject drums at the faintest sign of seal compromise.
Requests for custom specs, such as reduced impurity thresholds or alternate solvent carriers, come through regularly. We do not always accept short-turnaround custom projects, but when someone presents a solid technical case, we assign a joint team to map the synthesis route and optimization targets. Several times, this led to new insights in purification or scale-up, which have improved our overall process and often benefited other products on the same line.
Interest in 4-Phenylbutylamine continues to grow, driven by new needs in biologically active scaffolds and tougher high-performance polymers. Market signals from Asia and North America point toward increasing application diversity, especially as collaborative research models blend pharma with advanced materials.
Feedback now cycles faster between customer labs and our technical teams. Glass reactors running new condensation cyclizations tell us in weeks what used to take months to filter through by sales reports. The growing importance of open, transparent data sharing compels us to keep analytical methods up to date; anyone can provide a spec sheet, but proof comes from sample-by-sample reporting for every lot, shared securely through customer portals.
Sustainability also plays a larger role than it did just a few years ago. We reengineer supply chains to favor renewable solvents and locally sourced feedstocks whenever supply allows. As environmental audits go deeper across the industry, our team brings in new mass balance calculations and clean-up methods, learning in real time what changes hold for large-volume production.
Working with 4-Phenylbutylamine taught us every molecule has its own story. A process improvement that yields advantage for this product may not translate to others, and customer feedback reveals that success rests as much in daily familiarity as in innovation. Production teams learn to recognize subtle shifts by sight, scent, and even drum weight. There is no substitute for years on the floor, walking the reaction lines, fine-tuning parameters, and comparing notes with chemists and engineers working at the receiving end.
We believe 4-Phenylbutylamine’s real-world value comes out not in data sheets, but in the hands-on experience of those whose jobs depend on its performance, purity, and dependability. Staying close to the synthesis, open to improvement, and alert to user feedback keeps us moving forward each day. As fellow manufacturers or end users know, trust in raw materials builds on what can be measured, seen, and repeatedly delivered—and it is this standard we hold for every batch rolling out of our doors.