|
HS Code |
764825 |
| Cas Number | 1193-02-8 |
| Molecular Formula | C6H7NS |
| Molecular Weight | 125.19 g/mol |
| Appearance | Light yellow to brown powder |
| Melting Point | 37-41 °C |
| Boiling Point | 284 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.18 g/cm³ |
| Flash Point | 154 °C |
| Refractive Index | 1.700 |
| Pubchem Id | 66297 |
As an accredited 4-Aminothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Aminothiophenol, 25g, comes in a sealed amber glass bottle with a secure screw cap and a detailed hazard label. |
| Shipping | 4-Aminothiophenol is shipped in securely sealed containers to prevent leaks and protect against moisture and light. The chemical is classified as hazardous and should be transported following applicable regulations for harmful substances. Proper labeling and documentation are required, and it must be handled and stored in a cool, well-ventilated area during transit. |
| Storage | 4-Aminothiophenol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. It should be kept away from strong oxidizing agents, acids, and sources of ignition. Proper labeling is essential, and it should be stored in compliance with local chemical storage regulations. Personal protective equipment should be used when handling. |
Competitive 4-Aminothiophenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Years of hands-on production in specialty chemicals teaches a manufacturer not just to see a molecule as a chemical name. You observe its behavior, purity, smell, the unpredictable quirks it shows during synthesis. 4-Aminothiophenol, often recognized by its chemical formula C6H7NS, belongs to the family of aromatic thiols. The structure gives it a dual nature: an amino group and a thiol group present on the benzene ring. This unique pairing brings certain reactivity not seen in simpler mono-functional aromatics.
Every batch of 4-Aminothiophenol walks a tightrope between color, moisture sensitivity, and the demand for high purity. During recrystallization, even a slight shift in temperature shows up immediately in product performance—crucial for end uses in electronics and advanced material science. As a manufacturer, you don’t just weigh grams and check columns on a certificate—real production insists on checking every flask, every raw material’s odor, and the subtle fizz when the raw intermediate hits the acid. These details, more than a specification sheet, determine reliability.
Most customers ask for a white to pale yellow crystalline powder with a purity of at least 99%. Chromatographic scans tell more: single-digit ppm levels for common impurities like aniline or phenol derivatives, and absolute dryness is a must if surface-modification work is at stake. Anyone who’s run the vacuum dryer at midnight to save an order knows how fickle trace moisture proves—it can ruin a whole run of sensor device coatings downstream. Standard packaging in tight-sealed poly-lined drums keeps out oxygen, which otherwise starts to yellow the product, especially in humid climates.
Particle size doesn’t usually get much attention in procurement meetings, but in the actual reactor, flowability changes the story. For some clients, sub-millimeter granules speed up blending with metal powders. For others, a fine powder helps in suspensions for ink formulations—neither one gets satisfied by stock “off-the-shelf” powders. This is a reason manufacturers offer sieved lots on recurring orders; small tweaks in the process keep the next kilo from clogging a feed or clumping up in a dispensing funnel.
The so-called ‘end use’ for 4-Aminothiophenol often gets described in generalities—labels like “intermediate” or “chemical building block” cloud the real work being done. Manufacturers follow these applications into the R&D labs that develop sensors, into workshops turning out biomedical assay kits, and even to the team at a printed electronics startup who measure an extra ten seconds of etching time because their surface modification layer picked up 0.2% more aminothiophenol.
In surface chemistry, the thiol group bonds rapidly with gold substrates, which opens the door for self-assembled monolayer technology. The amino group faces outward, anchoring further functionalization. Anyone working in this field quickly learns the headaches of oxidized impurities—one bad lot can leave researchers redoing entire surface prep runs. This is where batch traceability, consistent quality, and clear communication from us as the producer matter more than any certificate.
Beyond sensors, 4-Aminothiophenol finds use in dye and pigment synthesis. The diamine functionality lets it serve as a bridge for covalent bonding in organic synthesis. Certain pharmaceutical intermediates, especially in early-stage research, test the boundaries of this molecule’s reactivity; the same is true for some custom aromatic ligands in coordination chemistry. In practice, these uses demand small custom runs, quick turnarounds, and absolute clarity on shipment history. Flexible production scheduling becomes less about efficiency and more about fostering reliable partnerships.
There are plenty of aromatic thiols and aromatic amines on the market, each carving out their own category. 4-Aminothiophenol stands at a crossroads between standard thiophenol and aniline derivatives. For instance, compared to simple thiophenol, the presence of the para-amino group increases water solubility and adds an extra dimension in electrophilic reactions. This pays dividends in surface assembly for electronics, because post-modification steps need reactivity tailored by the amino function.
Contrast this with 2-aminothiophenol—the ortho isomer. The difference in position seems subtle on paper, but anyone synthesizing these compounds will confirm that ortho analogs run pungent, oxidize more quickly, and show different melting points. In gold surface applications, para-substituted aminothiophenol layers form better-aligned films. There’s no substitute for this experience; it’s not just an issue of structure, but a measurable difference in lab results.
Compared to para-phenylenediamine, 4-Aminothiophenol introduces a sulfur component, significantly changing downstream reactivity and electronic effects on the ring. In dye and pigment formulations, this can affect shade stability and compatibility with certain resins. The stability of the sulfur group in aminothiophenol, compared to the oxygen in analogues like 4-aminophenol, comes through in high-temperature or oxidative conditions, allowing it to stand in where oxygenated phenols might fail.
We have often received requests for product “equivalents” but it takes process-level experience to advise where a simple swap would ruin a batch. Close communication with researchers clarifies that some processes depend on the sharp nucleophilicity of the thiol group, while others choose aminothiophenol for its unique ability to bridge metal surfaces and organic matrices.
Every manufacturer faces moments that fall outside normal quality control. Through scaling up the process for 4-Aminothiophenol, subtle changes in the starting material’s aromatic purity, transition metal catalyst residues, and batch-to-batch aging show up in the finished product. Even a trace of sulfur dioxide from incomplete drying creates perceptible off-odors—something an experienced handler detects immediately, and which is critical to remove since many uses, particularly in electronic device prep, are sensitive to sulfur contaminants.
Raw materials need careful sourcing. Aniline must meet not just analytical specifications, but also remain fresh enough to avoid excessive by-product formation during synthesis. Storage practices play a direct role: airtight drums, buffer gases, and cool, stable warehouses all prove their worth in the finished product’s shelf life and handling safety. In the line, we learned that static charge from rapid bulk transfer promotes airborne dust—never an issue in small labs, but a safety risk and headache when producing multiple tons a month.
Process purification steps influence the downstream workability of each batch. Recrystallization solvents and drying technologies create tiny differences in crystal habit, which feed back into customer mixing performance. Listening to feedback from clients, whether in pharmaceutical labs or material science departments, closes the loop in production optimization.
Shipping stability makes a bigger difference than many realize. Freight exposure to humidity, heat, or rough handling causes oxidation and caking. Corrugated fiber drums with custom liner bags became our industry standard, outlasting plain barrels every time. Temperature logging, especially for longer haul exports, adds a layer of assurance to customers who see product performance change with unseen, unnoticed transport conditions.
In some regional markets, local regulatory filings and customs paperwork for thiol compounds become tedious and time-consuming. Close attention to label accuracy, hazard classification, and batch certification protects both the customer and the supply chain—mistakes here mean more than just paperwork delays; they put whole project timelines at risk. We saw the need for clear regulatory compliance over time, as tightening environmental and workplace safety rules set higher standards.
Maintaining consistency across continents becomes a trust issue. In some climates, humidity eats away at drum liners and subpar packaging melts in transport heat. Finding the right bulk container — heavy-walled, moisture-proof, and sealable—cut down rejections and complaints more than any process tweak inside the plant.
Direct discussions with buyers, lab managers, or production staff reveal what’s working and what’s not. One printed electronics lab flagged a subtle drop in surface binding efficiency, traced back to a minor change in our drying protocol. Interviews with researchers in dye labs led to a process revision that lowered an off-odor impurity not caught by standard tests. These stories shape production decisions more than datasheets.
Supply chains today demand resilience—COVID-19 disruptions, raw material fluctuations, and new chemical regulations have changed sourcing for goods like 4-Aminothiophenol. By maintaining stocks of intermediate products and establishing redundant packaging contracts, manufacturing delays drop, and end users avoid sudden shortages. Transparency about these precautions reassures process engineers and purchasing agents who rely on uninterrupted supply for their workflow.
Trust gets earned over many orders and years. When a biomedical company found unexpected product discoloration after opening a drum, we performed a full root-cause analysis and updated packaging—a step beyond just replacing the product, which builds lasting relationships in research-driven industries.
Manufacturing aromatic thiols poses environmental and workplace safety risks. Over years, our attention to closed-loop handling and real-time detection systems reduced both spillage and worker exposure. Monitoring air quality inside and outside the facility became routine, and continuous operator training lowered incident rates. Sulfur compounds carry a strong odor, making leak identification both urgent and unmistakable in the workplace.
Waste neutralization and responsible disposal receive constant scrutiny. Process residues and mother liquors run to full-scale treatment, not just token neutralization. Auditor feedback led to new scrubber installations and periodic updates to hazard communication systems. In markets with stringent chemical registration laws, thorough documentation and long-term records matter. End users often seek reassurance not just about “pure” product but also about ethical sourcing and handling safety—a demand we meet through both process and transparency.
Technological change in electronics and material science will influence demand for 4-Aminothiophenol in the coming years. Miniaturization of sensor platforms, flexible electronics manufacturing, and new colorants in medical diagnostics all call for functional molecules like this one. Synthetic routes may evolve to reduce waste and energy consumption; green chemistry initiatives offer both challenges and chances for becoming more sustainable.
Collaboration with downstream users shapes how these materials get produced. Device makers push for next-level purity, even as regulatory scrutiny grows stricter. By building direct feedback loops from the lab bench to the plant floor, the manufacturing process stays nimble, adapting to meet requirements with each new application.
Expansion in global markets comes with unique technical and logistical hurdles. As research teams discover new uses for thiol-functionalized aromatics, manufacturers must offer not only high-quality products but also flexible, reliable supply chains. Combining chemical manufacturing know-how with real-world responsiveness to customer needs keeps production viable in changing markets.
Producing 4-Aminothiophenol is about far more than a chemical catalog entry. It involves a web of experience—from running clean synthesis and safe packaging, to working alongside scientists developing next-generation devices. Attention to process detail, regulatory adaptation, ongoing dialogue with users, and a continual focus on both product and environmental safety keep quality high and support innovation. The molecule’s dual functionality, reactive sulfur and amine groups, opens paths in research and industry applications not easily filled by substitutes. Through careful manufacturing, diligent feedback, and forward-looking production strategies, the goal remains: reliable, high-performance 4-Aminothiophenol ready for the next wave of challenges in science and technology.