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HS Code |
274658 |
| Chemical Name | 3-Fluorophenethylamine |
| Cas Number | 348-35-4 |
| Molecular Formula | C8H10FN |
| Molecular Weight | 139.17 g/mol |
| Iupac Name | 2-(3-fluorophenyl)ethan-1-amine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 202-204 °C |
| Density | 1.086 g/cm³ |
| Solubility In Water | Soluble |
| Smiles | C1=CC(=CC(=C1)F)CCN |
| Inchi | InChI=1S/C8H10FN/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6H,4-5,10H2 |
| Flash Point | 79.7 °C |
| Refractive Index | 1.540 |
As an accredited 3-Fluorophenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 3-Fluorophenethylamine (10 grams) features a sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | 3-Fluorophenethylamine is shipped in secure, leak-proof containers, compliant with chemical safety regulations. Packaging ensures protection from moisture and light. Proper labeling with hazard identification and handling instructions is included. Shipping is typically via certified carriers, following all local and international guidelines for transport of potentially hazardous materials. |
| Storage | 3-Fluorophenethylamine should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and store at ambient temperatures, and use appropriate personal protective equipment when handling to avoid exposure. |
Applications of 3-Fluorophenethylamine in Industrial Manufacturing3-Fluorophenethylamine supports specialized chemical synthesis across select downstream sectors. As the original producer, we supply this intermediate to facilities conducting regulated processes where purity, traceability, and process-specific performance are mission-critical. Below we detail dedicated industrial scenarios illustrating how manufacturers integrate this ingredient under established global compliance protocols. 1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Agents3-Fluorophenethylamine functions as a structural building block in the multi-step manufacturing of specific central nervous system (CNS) active pharmaceutical ingredients. The controlled introduction of the fluoroethylamine moiety enables precise modulation of pharmacological profiles in targeted compounds. API manufacturers incorporate this intermediate at defined stages of synthesis to achieve efficient ring functionalization, ensuring target molecule specificity and batch-to-batch consistency. Industry compliance standards
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2. Custom Synthesis for Agrochemical Discovery CompoundsR&D laboratories specializing in agrochemical development utilize 3-Fluorophenethylamine as an integral intermediate when constructing libraries of candidate molecules for crop protection activities. The fluoro substitution enhances selectivity by inhibiting metabolic degradation in target organisms, making the amine a preferred scaffold for the synthesis of trial herbicide and insecticide leads under exploratory screening programs. Industry compliance standards
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3. Key Intermediate for Specialty Dye SynthesisWithin the fine chemicals sector, producers of digital printing and high-performance textile dyes employ 3-Fluorophenethylamine to introduce fluorinated side-chains that influence dye shade, fastness, and affinity characteristics. Integrators tailor the amine’s addition to achieve specific chromophore profiles for use in demanding coloration systems such as disperse, vat, and reactive dyes. Industry compliance standards
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4. Intermediate for Advanced Materials and Monomer Synthesis (Electronics Applications)3-Fluorophenethylamine serves as a functional intermediate in the advanced materials segment, especially for monomer modification in organic electronic and photonic manufacturing. The incorporation of the fluoro-functional group supports fine-tuning of dielectric properties and charge-transport behavior in conjugated polymers and small-molecule semiconductors, essential for device miniaturization and long-term stability in OLED displays and organic solar cells. Industry compliance standards
Typical usage ratio
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The daily work in our production facility revolves around a simple idea: make each batch count, make each product reflect what we’ve learned from decades of chemistry. Our 3-Fluorophenethylamine (3-FPEA) comes from that ambition. This isn’t about chasing the latest trends in the specialty chemical market. It’s about lending genuine value through careful synthesis, precise handling, and real-world experience. When a customer thinks of a phenethylamine variant, the expectation goes beyond a chemical name and purity specification. It touches on trust. For us, trust is built in the reactors, with every charge, every analysis, and every conversation we have with the chemists who use our products.
3-Fluorophenethylamine stands as a clear, colorless liquid at room temperature, typically offered above 98% purity, distilled and analyzed to confirm low moisture and trace impurity levels. We don’t rely on assumptions. Each batch is held to established standards, with GC-MS and NMR data confirming identity and absence of residual byproducts. As direct manufacturers, we witness firsthand the difference a careful reductive amination or selective halogenation makes. Each stage is optimized for safety and yield, not only because it delivers a better product, but also because waste reduction matters both economically and environmentally.
Over the years, research and industry customers have taught us the value of consistency. 3-FPEA’s main role lies in synthesis—a building block that chemists reach for during the elaboration of active pharmaceutical ingredients, advanced intermediates, and functional materials. Small structural changes, such as the placement of a fluorine atom on the phenyl ring, open the door to activity modification that can be significant in drug discovery. Unlike unsubstituted phenethylamine, 3-FPEA introduces both electronic and metabolic differences. The meta-fluoro group brings a wrinkle to the electron distribution, often influencing receptor binding, metabolic stability, or process reactivity.
We don’t view these differences as abstract concepts. Process chemists want predictability. Medicinal chemists need subtlety. We have seen projects rise or fall on the back of purity spikes, inconsistent physical characteristics, or misidentified raw materials. The way 3-FPEA stirs, reacts, and stores places it apart from other halogenated or alkylated analogs. Customers have remarked on the clarity and freedom from colored tars in our product—a direct result of closely watched conditions and prompt isolation.
Some may wonder why we focus specifically on the 3-fluoro variant. Through direct collaboration with research labs and industrial innovators, we’ve learned that a small substituent jump—para to ortho to meta—can translate into meaningful results. In our own pilot studies, 3-FPEA enabled the preparation of urea, amide, and carbamate derivatives that resisted oxidative degradation far better compared to non-fluorinated controls. In certain peptide-based applications, the presence of the 3-fluoro group suppressed unwanted byproduct formation under standard coupling conditions.
Colleagues share stories of failed late-stage modifications attributed to overlooked differences in raw material quality. This perspective has shaped our own internal routines. Every release lot of 3-FPEA leaves the plant with a complete spectral envelope and impurity profile. Nothing is left to chance—not the storage drum linings, not the shipment temperature controls, not the transparency of the labeling.
Our team often discusses how real manufacturing shapes the chemical landscape. Bulk traders rarely see what happens after the product leaves the warehouse. We carry forward our experience with minor composition variations that can cause major headaches at kilolab or production scale. 3-Fluorophenethylamine handled without careful exclusion of water sometimes leads to yellowing and off-target reactivity in downstream transformations. The solvent choice during final purification impacts more than just yield. In one scale-up run, switching from toluene to ethyl acetate in the workup led to a lower water content and improved shelf life. These lessons form the backbone of our day-to-day guidance to partners.
On the practical side, 3-FPEA’s boiling point, density, and nitrogen content set it apart from similar arylethylamines. High-resolution QC sheets are available for all shipments. By working upstream, we minimize risks for our clients—wasted runs, contaminated reactors, or unexpected exotherms in reductive coupling reactions. Long years of direct communication with synthetic chemists make these habits non-negotiable for us.
We have seen the shifting regulatory terrain around phenethylamines. There are pitfalls—compliance questions, shipping delays due to ambiguous labeling or lack of up-to-date documentation. Our technical team tracks requirements closely, so shipments reach their destinations with all documentation in order. We maintain in-house experience with regional standards in Asia, Europe, and the Americas. Each destination has its own expectations and challenges, and we address them before they become shipping or customs problems.
From a safety perspective, our operators use contained systems, robust ventilation, and detailed incident logs. Real safety isn’t a slogan. It means making changes when a near-miss shows up in a campaign, revising batch procedures after feedback, and regular audits—no exceptions. For 3-FPEA, our protocols account for its amine nature, volatility, and activity at trace levels. The right PPE, storage, and emergency response training keep our people and facilities safe, and guarantee supply continuity for clients. Customers receive our own safety handling advice based on real operational experience, not generic documents.
As a chemical maker, disruptions and delays test both planning and relationships. 3-Fluorophenethylamine, like other specialty amines, depends on a stable stream of raw materials. Over the past decade, we responded to raw fluorinated intermediates becoming scarce during global shortages. We assessed alternative vendors, validated their supply chain reliability through site visits, and qualified more than one backup supplier for each upstream feedstock.
When the pressure mounts—a trade bottleneck, unexpected plant outage, new regulatory policy—we don’t pass the buck. Instead, our regular QC batch reports and ongoing customer updates keep users informed throughout every step. No one likes surprises in kilo or ton-scale reactions. We hold reserves and engage in regular forecasting meetings with our key clients, which helps us anticipate surges and dips in demand even six months out.
Adoption of digital documentation platforms allows us to share batch histories, CoAs, and analytical results in secure, searchable ways. If questions arise about the color, odor, or purity drift in a single container, we track down the root cause immediately. Our team keeps meticulous records not because of GMP rules alone, but because we believe accountability matters. When something works, it’s the result of thousands of hours spent perfecting not just chemistry, but communication too.
Having synthesized and shipped several analogues, our team has ample reference points. While simple phenethylamine sees wide use thanks to its established synthetic routes, the 3-fluoro variant introduces a new level of reactivity control. We’ve compared reactivity in iron-catalyzed coupling reactions, Suzuki-type borylations, and Friedel-Crafts acylations. 3-FPEA shows sharper selectivity and improved stability under conditions that degrade more sensitive halogenated analogues.
Take, for example, the comparison with 4-fluorophenethylamine or the more heavily fluorinated variants. The meta-fluoro group on 3-FPEA changes both the electron density and the site accessibility for subsequent modifications. Our direct users have noticed that end products made from 3-FPEA show different pharmacokinetic properties, a detail that researchers can tie back to functional group placement. Safety data also shows distinct inhalation and dermal risk profiles between meta- and para- substituted products, underscoring why plant operators receive separate training for each.
Sometimes, the most satisfying moments come not from shipping tonnage or announcing a new catalogue item, but from collaborating on real technical problems. A pharma client once faced yield drops during scale-up of an N-carbamate derivative. Through side-by-side analytical trials and in-process monitoring, we noticed the key impurity derived from a trace over-halogenated byproduct in their purchased 3-FPEA. Our team traced the issue to a subtle change in crystallization temperature in our finishing step. We tuned the profile, implemented more stringent inspection, and saw defect rates drop. They passed the lessons along and improved their own process.
These improvements didn’t come from a spec sheet. They grew out of cycles of feedback, trial, error, and refinement—tools that every real manufacturer calls upon. Our engineers and QC analysts keep an open door to customers, ready to support method transfer, analytical troubleshooting, or process optimization at every stage.
We do not take shortcuts. Each bottle and drum of our 3-Fluorophenethylamine reflects a supply chain that reaches from bulk chemical plants to research universities. Our chemists, operators, and logistics staff are part of a larger story—one that balances batch reproducibility, regulatory requirements, and hands-on troubleshooting. The differentiators for us are the day-to-day controls: regular calibration checks, maintenance logs, and ongoing staff training. Chemical manufacturing means facing the unexpected—from power outages to unseasonal humidity swings to a shipping strike in a major port city. Through all this, keeping 3-FPEA’s quality and availability stable is a practical test of discipline.
Trust builds over time, in both small tasks and large. The chemist who receives our product invests their own reputation in the results. That’s never an abstract consideration for us. We address every complaint, answer every query, and integrate every justified feedback into future runs. Our long-term relationships with clients come from repeated proof that our attention to practical detail is not marketing talk—it’s how we work.
The specialty amine sector faces evolving challenges. Environmental standards tighten, customer specifications become more exacting, and market pressures demand both quality and agility. 3-Fluorophenethylamine stands as one example where adaptation has paid off. Continuous process review, investment in greener reagents, updated PPE and waste management protocols, and a careful selection of compatible solvents all contribute to success.
We participate in regular industry benchmarking activities, not only to compare output metrics but to spot fresh opportunities for process safety and environmental improvement. Routine engagement with the scientific community lets us hear first-hand about shifting research priorities—from new ligands to regulated active intermediates. We are quick to learn, and proud to teach what we have learned to both established customers and ambitious start-ups.
What sets us apart as a chemical producer isn’t product volume or catalog size, but persistent engagement and open communication. Clients benefit when we share both success stories and cautionary tales. These exchanges help us refine our methods, improve our documentation, and foster a cycle of improvement that touches everyone.
In the end, 3-Fluorophenethylamine, as produced in our facilities, features the sum of real operational lessons—purity that holds up to scale, documentation that stands up to audits, and service that reflects hands-on knowledge. We believe each customer, technician, and end user deserves not only a chemical with a name and a number, but a product backed by understood consequences, transparent traceability, and a partner who listens. In specialty amines, as in the rest of manufacturing, real value emerges from expertise in practice, not theory.