|
HS Code |
637608 |
| Cas Number | 1193-02-8 |
| Molecular Formula | C6H7NS |
| Molecular Weight | 125.19 g/mol |
| Appearance | Light yellow to brown crystals or powder |
| Melting Point | 38-42 °C |
| Boiling Point | 273 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.18 g/cm³ |
| Purity | Typically ≥98% |
| Smiles | c1ccc(cc1S)N |
| Inchi | InChI=1S/C6H7NS/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2 |
As an accredited 4-Aminothiophenol/4-Aminobenzenethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled **4-Aminothiophenol/4-Aminobenzenethiol**, 25 grams, with hazard symbols and safety information, securely sealed. |
| Shipping | 4-Aminothiophenol (4-Aminobenzenethiol) should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled as a hazardous chemical, following all relevant local, national, and international transport regulations (such as DOT, IATA, or IMDG). Appropriate protective packaging and documentation for toxic substances are required during shipping. |
| Storage | 4-Aminothiophenol (4-Aminobenzenethiol) should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Store under inert atmosphere (e.g., nitrogen or argon) if possible, to minimize oxidation and degradation. |
Competitive 4-Aminothiophenol/4-Aminobenzenethiol prices that fit your budget—flexible terms and customized quotes for every order.
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Experience matters in chemical production. In our facility, the synthesis of 4-Aminothiophenol, also called 4-Aminobenzenethiol, comes from decades of focused work with aromatic thiols and amines. Our job does not end at meeting a molecular formula; it depends on producing true consistency batch after batch. We manage all the fine points from raw material choice, precise reaction conditions, purification, to the practical packing and dispatch. Every step calls for skill, patience, and respect for the properties that make 4-Aminothiophenol a staple in research and industry.
In the bench and in manufacturing, few aromatic thiols come close to the functional utility of 4-Aminothiophenol. Long-time users know the value of the para-positioned amino and thiol groups on the benzene ring. This arrangement brings a rare combination of reactivity, selectivity, and downstream versatility in organic transformations and advanced material synthesis.
Historically, industries chose 4-Aminothiophenol for its unique dual-functionality. That combination doesn’t show up in general substitutes or act-alikes such as aniline or benzenethiol. These lack either the strong nucleophilicity of the para-amino group or the high binding affinity that the thiol sulfur delivers. By having both on one molecule, users unlock routes in surface chemistry, nanotechnology, dye intermediates, and sensor applications that demand both electron-donating and binding capabilities at once.
Many buyers focus on the purity stated on a spec sheet. From the inside of manufacturing, we know that controlling trace impurities shapes outcomes far more than a number on paper. Even at 99%, a slight presence of oxidized disulfides or residual solvents can derail sensitive catalysis or surface assembly work. Our technicians manage tight controls over reaction quenching, distillation, and inert storage—not just to clear a purity checkbox but to protect downstream process stability.
Stubborn odors and discoloration in shipments reveal uncontrolled side reactions in the supply chain. Our reactors and lines see regular validation, and we watch for not only HPLC purity but also the subtler clues: color, spectral fingerprints, and simple handling characteristics that signal product stability. This gives assurance not only to QC teams but also to lab researchers who need reliable, repeatable building blocks.
Users in the field treat 4-Aminothiophenol as much more than a reagent. This molecule bridges fundamental research and advanced commercial processes. Surface modification is a prime area—self-assembled monolayers on noble metals wouldn’t reach the robustness needed for biosensors and nanoelectronic devices without the strong Au–S bonds offered by the thiol end, joined with an exposed amino group for peptide or dye conjugation. In practice, clean, mono-layer formation draws directly from careful control of product volatility and impurity profile; manufacturing mistakes show up as monolayer inconsistency or unpredictable desorption rates in finished sensors.
Organic synthesis makes heavy use of the ortho/para directing effects of the amino and thiol rings. Custom dye intermediates start here, where the right functionalization order can mean high or low conversion and avoid costly protecting group switches. Some of our oldest industrial customers rely on the strong nucleophilicity of the para-amino for diversification in azo dyes, while medicinal chemistry groups value the molecule’s facility in constructing sulfur-bridged scaffolds for lead molecule development.
Analytical chemistry and materials science each leverage the molecule in their own ways. As a Raman probe, 4-Aminothiophenol presents unique, recognizable peaks thanks to its conjugated system, helping detect trace substances at extreme sensitivity. Researchers have referenced these properties again and again in published sensor builds, smart surfaces, and even nonlinear optics. These high-tech outcomes depend on a deep bench of experience to ensure every batch arrives performing as expected.
Chemists debate the differences among manufacturing sources for good reason. We see the practicalities: crystal morphology, handling loss, and even glassware memory effects can vary wildly with minor shifts in process. Those running scaled functionalizations find that minor levels of precursor carryover or oxygen load can produce side products that resist bulk separation. After facing these headaches firsthand, we rebuilt our production sequence to favor strict batch traceability, tightly controlled nitrogen handling, and exhaustive post-synthesis checks. Only then does the final material reach its familiar, free-flowing pale-yellow solid form that chemists expect.
Some producers target volume over specificity. That trade-off often shows in batch reproducibility failures when the molecule appears to “work” in one analytic run, but disappoints in application trials or after storage. By overseeing all details from raw aniline derivatives through organosulfur management, our team delivers a product whose melting point, odor, and color spectrum do not surprise at scale-up. For us, these are not minor issues—lab managers often share stories of lost weeks to inconsistent reagent batches. The best results begin with raw material discipline at the manufacturing stage.
It’s tempting for buyers to view structurally similar chemicals as adequate substitutes. In practice, using benzenethiol or aniline in place of 4-Aminothiophenol leads to missed reactivity and increased complexity. Benzenethiol lacks the electron-rich amino group, so it underperforms in condensation and coupling reactions, with lower yields or selectivity drops. On the other hand, plain aniline does nothing for gold surface coverage in assembly work and stumbles in applications that demand strong Au-S interactions for immobilization.
4-Aminothiophenol stands apart by letting users bridge these gaps in one step. Both ends of the molecule contribute, so process engineers and bench researchers bypass synthetic detours, avoid unstable intermediate handling, and manage direct functionalization. This isn’t just a structural difference—it’s a time, resource, and process efficiency benefit.
Sourcing matters for real-world process reliability. Even the most high-profile research projects can grind to a halt due to bottlenecks or impurities in 4-Aminothiophenol supply. As upstream producers, we watch the market move and see the temptation to cut corners mid-stream. Our infrastructure lets us buffer against price swings for key aniline and thiol feedstocks, so production remains steady even when market dynamics threaten delays or shortages. Repeatedly, labs share that analytical performance and reproducibility rise or fall based on these supply-side realities, much more than on catalog numbers or glossy marketing.
Downstream, the biggest winners are those who integrate our 4-Aminothiophenol into large-scale sensor platforms, custom surface treatments, or as a cornerstone of new molecule libraries. Every gram carries years of bench-tested quality, trusted by customers who need one less experiment lost to doubtful raw materials. We also support partners by offering insights gained on the line—suggesting solvent handling to maximize product longevity, or sharing details about trace impurity management for high-sensitivity electronic work.
Users share a few major concerns across industries: product shelf life, batch-to-batch predictability, and ease of use without hazardous surprises. 4-Aminothiophenol can be sensitive to oxidation and light, leading to slow color changes and degraded reactivity. Decades back, this caused frustration in sensitive reactions or storage. Through close control of reaction conditions, thorough exclusion of air and light, and careful drying, we consistently deliver a stable product that preserves reactivity.
No batch ever leaves our site without confirmation on purity—not just through standard HPLC or melting point, but also through practical application checks. These sometimes spot imperfections before they cost users time and money down the line. For research teams scaling up, knowing that every package aligns with the last lets them skip needless troubleshooting.
Today, material buyers encounter a flood of intermediaries, each promising “authentic” product. Our customers, after experience with trading house inconsistencies, always return to the manufacturers that show real technical background and transparency. The ability to discuss exact process details, batch records, and even failure cases with us reassures process engineers who want more than paperwork or empty marketing.
Direct connections also smooth integration. Many times, we adjust particle size, packaging, or handling protocols for large-scale clients or precise R&D use. That isn’t practical with commodity brokerage, where product origin shifts and technical knowledge sits far from actual synthesis steps. Some users require documentation to meet country-specific standards or new regulatory scrutiny—our long history in direct production means we can provide data, origin assurance, and controlled samples on demand.
As production specialists, we see responsibility as more than a slogan. 4-Aminothiophenol requires strict adherence to environmental, safety, and health standards due to its reactive amine and thiol groups. Our facility does not treat these obligations lightly. Every worker on our line trains in safe handling, emergency spill response, and hazard minimization. We track waste streams carefully to ensure no unwanted emissions or residues enter the environment, in line with both external regulations and our own values.
This attention pays off in safer product for the user as well. We offer technical guidance reflecting hard-earned experience: always store sealed, in the original container, away from strong oxidizers, and use an efficient local exhaust in open operations. Small changes, from leak-proof closures to anti-static drums, prevent many headaches that users face with uncontrolled or reprocessed materials.
The best chemical manufacturing does not happen by formula alone. In the real world, products like 4-Aminothiophenol see shifting requirements—new application challenges, more demanding process specs, and pressure for greater safety or sustainability. Our technical support team works side-by-side with researchers, engineers, and purchasing managers to troubleshoot issues from solubility questions in process scale-up, to selection of appropriate solvents for storage or use, to impurity spikes that could threaten analytical outcomes.
Open conversations with users spark most improvements. For example, we altered finishing steps based on feedback about stubborn product residue in glassware, improving both clean-out and product transfer. Some customers want larger crystal fractions for easier transfer in automated dispensing, others need micro-scale packages for high-throughput screening. Our approach—listening closely, experimenting at bench scale, and scaling up successful tweaks—sets us apart from traders who have never actually run or adjusted a reactor.
The world of specialty chemicals is always changing, and 4-Aminothiophenol continues to prove itself in new technology frontiers. Emerging uses in bio-conjugation, advanced Raman probes, flexible electronics, and responsive coatings push the boundaries of what small organic molecules can accomplish. Our relationship with researchers and engineers at these frontiers informs how we improve process steps, quality assurance, and even new grades of product for special use cases.
Manufacturing is never static. In our workshops and pilot plants, we work relentlessly to tighten controls, reduce waste, and find ways to make our 4-Aminothiophenol even more dependable for the next round of scientific and industrial innovation. Those doing real work in the lab, the plant, or the field recognize the difference—the respect for science, materials, and partnership.
Every bottle of 4-Aminothiophenol carries more than a product specification—it delivers years of practical problem-solving, built by people who know what it takes to keep research and industry on track. Those who depend on accuracy, performance, and full support recognize the difference that comes from a manufacturer’s care and long-term vision, not just a supply chain’s reach. By focusing on reliability, technical dialogue, and safe, responsible manufacturing, we let this essential building block drive new results across chemistry’s fastest-moving fields.