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HS Code |
682046 |
| Chemical Name | 4-Thiophen-2-Ylphenylamine |
| Molecular Formula | C10H9NS |
| Molecular Weight | 175.25 g/mol |
| Cas Number | 870831-98-8 |
| Appearance | Solid (usually off-white to light yellow powder) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | c1cc(ccc1N)c2sccc2 |
| Inchi | InChI=1S/C10H9NS/c11-9-4-2-8(3-5-9)10-6-1-7-12-10/h1-7H,11H2 |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Pubchem Cid | 15005215 |
As an accredited 4-Thiophen-2-Ylphenylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4-Thiophen-2-Ylphenylamine (10g) features an amber glass bottle with a tamper-evident seal and clear hazard labeling. |
| Shipping | 4-Thiophen-2-Ylphenylamine is shipped in sealed, chemical-resistant containers to ensure safety and stability during transit. Packaging complies with relevant regulations for hazardous materials. The chemical is typically shipped via ground or air freight, accompanied by proper documentation and labeling for identification and handling instructions. Temperature control may be applied if required. |
| Storage | 4-Thiophen-2-Ylphenylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep it away from direct sunlight, moisture, and sources of ignition. Use secondary containment to prevent spills, and ensure the storage area is clearly labeled and compliant with local chemical safety regulations. |
Applications of 4-Thiophen-2-Ylphenylamine in Industrial Manufacturing4-Thiophen-2-Ylphenylamine offers specific functionality as a building block in advanced materials and chemical synthesis. Our direct manufacturing expertise supports multiple precise uses, each with unique compliance, formulation, and integration requirements outlined here. 1. Organic Electronic Materials – OLED IntermediateThis compound serves as a core intermediate in synthesizing OLED emissive layers and hole transport materials. Its unique conjugated structure contributes to charge carrier mobility and color tuning in organic light-emitting diode applications. Formulators use it predominantly for blue and green light-emitting devices requiring stable molecular alignment in thin-film deposition. Industry compliance standards
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2. Dye and Pigment Manufacturing – Functional Azo CouplerThis material acts as a key coupling component in synthesizing high-performance organic dyes. Chemists utilize its aromatic amine group for introducing thiophene motifs into azo dye molecules, enhancing the chromatic stability and sulfur compatibility required in specialty inks and textile colorants. Industry compliance standards
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3. Pharmaceutical Research – Heterocyclic Active ScaffoldR&D groups incorporate this heteroaryl amine as a molecular fragment for lead compound discovery and medicinal chemistry programs. Its dual aromatic centers make it useful in constructing new molecular entities targeting kinase inhibition and central nervous system modulation. Precise handling, traceability, and quality assurance are essential at this early synthesis stage. Industry compliance standards
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4. Polymeric Material Synthesis – Functional Monomer/AdditiveFormulators use this amine-containing aromatic monomer for engineering specialty polymers including polythiophenes and advanced aromatic polyamides. Its presence in the backbone enhances electronic conductivity or imparts customized mechanical flexibility for niche markets such as anti-static materials and electronic encapsulants. Industry compliance standards
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5. Agrochemical R&D – Intermediate for Bioactive MoleculesSynthetic chemists employ this compound as a designed precursor in creating heterocyclic structures for herbicide and fungicide candidates. The thiophene motif supports bioactivity screens aiming at mode-of-action innovation. Rigorous trace impurity control and batch documentation are essential in pilot and scale-up synthesis for regulatory agencies. Industry compliance standards
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At our facility, the production of 4-Thiophen-2-Ylphenylamine isn’t just another batch in the reactor. We handle the entire process in-house, from the careful selection of raw materials to the final refinements and packaging. Once the raw intermediates reach our plant, we rely on years of synthesis experience and a tightly controlled environment to get the best out of each reaction. Watching the process unfold—at its peak, you know you’re getting a product with the consistency and purity that can make a difference.
The model out of our synthesis line is 4-Thiophen-2-Ylphenylamine with purity levels usually reaching above 98%. We offer this compound as a fine crystalline powder, typically light yellow, sometimes a bit deeper if trace thiophene byproducts stick around. Every minor variation in appearance tips us off to look closer at the batch history and adjust cleaning, drying, or filtration steps as necessary. The melting point sits right where it should—usually between 89 and 91 Celsius, which matches reference literature and our archived QC reports.
We ship in moisture-proof, airtight containers because even a few hours of humid air exposure can nudge the product off-spec. Each container has a batch code tied to full traceability and an internal analytical report, typically including HPLC spectrum, NMR, and elemental analysis. By keeping testing and packaging under one roof, we resolve deviations before orders ship out, rather than after the fact—the sooner an anomaly is caught, the less waste, the better the outcome for everyone.
After many years supplying research groups, pilot plants, and downstream specialty manufacturers, we’ve watched 4-Thiophen-2-Ylphenylamine carve its niche. Researchers reach for it while developing new organic electronic materials. If you’re building conjugated polymers, OLEDs, or new sensor coatings, you’ll see its unique fused-heterocycle backbone show up in published structures and patent applications.
We get regular requests for 4-Thiophen-2-Ylphenylamine from teams working on advanced dyes and photoinitiator studies. The structure’s balance—having both an electron-rich thiophene and an amine-functionalized phenyl ring—unlocks stable, tunable materials that outperform simpler analogs. The amine group attaches efficiently to a range of other blocks or spacers, and the thiophene ring stabilizes charge transfer, which helps with conductivity and emission.
Over the years, customers have shown us real application examples: new polymer compositions, OLED shield layers, and high-performance coatings built off our outputs. Some demand larger orders of the same specification for pilot production. Each season brings new requests for tweaks—sometimes needing higher purity, sometimes matched melting point, sometimes a custom package size.
We run tight batch-to-batch QC. Our operators know that even small changes in solvent composition, temperature ramp, or agitation can push a batch in the wrong direction. Many specialty chemicals show some tolerance for these shifts, but with 4-Thiophen-2-Ylphenylamine, you spot result variations downstream fast. An inconsistent melting point will ripple into downstream polymerizations or functionalization.
We had one situation where a subtle impurity—a barely visible byproduct from suboptimal thiophene starting material—skewed a customer’s yield in a pilot OLED run. After troubleshooting together, we adjusted the feedstock screening and swapped out the reactor’s condensation control points. Since then, those issues haven’t resurfaced. Stories like this remind us why tight process control and firsthand data matter more than off-the-shelf comfort.
Generic amines might help with basic functionalization needs, and thiophene-only derivatives work if conjugation length isn’t crucial. Our product stands out because its structure fuses the phenyl and thiophene rings in a way that opens sharply different electronic possibilities. Substitutions on the phenyl or thiophene can alter the reactivity, but the 2-position linkage and the free amine together make this compound especially reactive in coupling, polymerization, and sensor applications.
Customers sometimes ask why we don’t stock several related thiophenylamines with different substitution patterns. Through years of feedback, the answer usually comes back to this: for organic electronic development, the 4-thiophen-2-yl structure with a direct amine—without further alkylation or halogenation—hits a sweet spot between solubility, conjugation, and functionalization potential.
Off-spec or impure 4-Thiophen-2-Ylphenylamine has tripped up more than a few projects we’ve seen. Some problems come down to trace unreacted phenylamine, which interferes with downstream polymerizations or causes color instability. Other times, isomeric byproducts—such as the 3-thiophene isomer—creep in from impure starting materials. Even at levels under 2%, these can throw off yield or introduce unpredictable side reactions.
Having our own in-house analytics pays off. The NMR spectrum should always show a clean aromatic window and a sharp signal around the amine protons—no unexpected broadening or missing peaks. HPLC should trace a clean single main peak. We’ve learned to recognize early warning flags and reject suspicious batches rather than risk reputational cost with long-time partners who rely on our chemists as much as our compounds.
We’ve stored batches for years in our climate-controlled rooms to watch for long-term drift. Kept dry and away from direct light, the compound holds up, but even a brief exposure to air or moisture can nudge the color darker and shift the melting point. Resellers sometimes ask us to decant into smaller vials or pack under argon for maximum shelf life—these requests match our own practices for internal QC samples.
Some users work in open labs, so we advise using the material within days of opening, storing in tightly capped, dry vials between uses. It doesn’t degrade with normal handling, but the painstaking efforts invested in high purity can all too easily go to waste if the container sits open on a humid bench over a weekend.
Handling aromatic amines and heterocycles requires careful attention to both worker safety and environmental stewardship. We run solvent capture systems and use carbon filtration on exhausts, not only to meet regulations but because we want a safe plant for our team and community. Our crystalline waste streams stay segregated and tracked so nothing slips into the wrong bin.
Adopting greener solvents and minimizing the use of heavy metal catalysts have become central in our process development the last several years. Reduced-waste synthesis methods aren’t only slogans—they show up as real cost savings in disposal and reduced environmental footprint. Downstream users increasingly ask about lifecycle data and environmental impact, so we share what we’ve learned in regular sustainability reports to our partners.
Each batch that leaves our plant gets logged with not just the analytical data but also a summary of any process tweaks made. Through years of running production, we’ve found that real-world feedback drives meaningful changes—sometimes improving crystallization for faster filtering, sometimes enhancing drying to avoid caking, or even updating packaging to accommodate new automation on the customer side.
One large customer pointed out that even minor traces of dimethylamine, a byproduct from cleaning solvents, showed up by GC-MS on their side. After reviewing cleaning procedures, we changed the solvent lot, validated the new process, and saved days of troubleshooting in their lab. When we commit to quality, it isn’t just a claim on a certificate—it shows up each time someone reruns their NMR and finds exactly what they need, no more, and no less.
Unlike commodity-grade amines or thiophenes from catalogue vendors, our 4-Thiophen-2-Ylphenylamine arises from dedicated production lines preferred by advanced material researchers. As a manufacturer, we don’t blend down impurities, nor dilute output with stabilizers or carriers unless specifically requested. Each lot reflects adjustments made by skilled staff, with the flexibility to scale batches up for pilot purposes or divide into smaller research lots.
Many similar chemicals crowd the catalogues, but side-by-side testing shows that minor impurities or altered synthesis routes undermine the performance in sensitive applications. As one example, a batch sourced from a general-purpose importer showed faint extra peaks in HPLC—undetectable by older methods—a reminder that transparency in manufacturing and thorough in-house testing matter more than sourcing convenience or price. Our plant holds itself to the same standards demanded by the world’s leading polymer research labs and device manufacturers.
We treat traceability and transparency as inseparable from quality. Every batch number ties back to in-plant QC records, operator notes, and raw material lots. This system gives us more leverage to help when troubleshooting with a customer; real data backs up our response rather than guesswork or generic guidance. These habits developed over years of supporting both academic users and industrial teams, where time saved on re-qualification or issue diagnosis translates directly to value for both sides.
We do not pass responsibility down the chain; if an issue arises, our team investigates, reviews data, and shares actionable insights fast. We’ve seen how even the best process can hit surprises in scale-up or after storage, but keeping the conversation data-driven helps us adjust recipes, retrain staff, and share findings directly with those who rely on our output.
4-Thiophen-2-Ylphenylamine has supported wide-ranging research, from exploratory functional material studies to pre-commercial pilot runs in next-generation displays. As customers push the envelope designing new sensors or conductive materials, they need reliable, on-spec chemistry without unpredictable interruptions. Reliability comes from control—every tweak, every test, every feedback loop carried back to our reactor benches.
Some partners need minor customizations: different batch sizes, alternative grades, or packaging that matches their lab or line automation. We respond from a manufacturer’s perspective, adapting not to catalogues but to what actually works for end users. We operate on the principle that each order must match or exceed customer requirements, and we invest in the tools and expertise to make that possible.
R&D is accelerating in electronics, sensors, and advanced materials, and with it, expectations on specialty chemical suppliers. Speed matters, but so does precision and a willingness to listen. As more innovators look for atom-efficient, high-performance synthetic blocks, compounds like 4-Thiophen-2-Ylphenylamine prove their value through the downstream results they enable—repeatable yields, clear spectra, trusted scaling.
We rely on direct relationships with users—sometimes a research chemist, sometimes a process engineer—to find pain points early, diagnose new requirements, and bring forward solutions. Whether the challenge is tighter specs, improved sustainability data, or scaling production without sacrificing quality, the dialogue we have with partners shapes our plant far more than any industry standard. Our teams carry this feedback upstream so each improvement builds on lessons learned, making each batch better than the last.
Manufacturing specialty chemicals like 4-Thiophen-2-Ylphenylamine involves continuous learning. We study each finished batch, analyze every returned vial, and update protocols based on both success stories and setbacks. Our chemists revisit literature, adapt proven synthetic routes, and translate them to safe, scalable, and clean plant conditions. Failures force reflection, but most advances come through curiosity: what made this purification better, this filtration faster, or this test result clearer?
Stubborn contaminants or stubborn drying failures can halt a line or delay a shipment; spotting these early makes the difference between satisfied customers and missed opportunities. Pride in manufacturing means saying no to shortcuts and yes to every step that protects quality. Through all of this, it is the real-world results—publications, patents, new product launches—that speak to the value that a carefully manufactured specialty chemical brings.
Quality doesn’t just happen; it gets built, tested, and improved with each run. At every step, our focus sits firmly on how our 4-Thiophen-2-Ylphenylamine performs, not just in our reports but in the hands of those inventing tomorrow’s materials. We see ourselves a partner to innovators, offering reliability, traceability, and the know-how that only direct manufacturing experience brings. These habits keep our reactors running, our customers advancing, and our reputation growing batch by batch.