|
HS Code |
398556 |
| Chemical Name | 2-(2-Thienyl)phenol |
| Cas Number | 17469-38-6 |
| Molecular Formula | C10H8OS |
| Molecular Weight | 176.24 g/mol |
| Appearance | Off-white to yellow solid |
| Melting Point | 96-100°C |
| Solubility | Soluble in organic solvents |
| Smiles | C1=CC=C(C(=C1)O)C2=CC=CS2 |
| Inchi | InChI=1S/C10H8OS/c11-10-5-2-1-4-9(10)8-6-3-7-12-8 |
| Purity | Typically >97% |
As an accredited 2-(2-Thienyl) Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 2-(2-Thienyl) Phenol, tightly sealed, labeled with hazard warnings, supplier, and CAS number. |
| Shipping | 2-(2-Thienyl) Phenol is shipped in tightly sealed containers, protected from light and moisture, and kept at room temperature. Packages comply with chemical safety regulations, including labeling for hazardous materials. Transported by authorized carriers, it requires handling precautions to avoid spills, breakage, and exposure during transit. Appropriate documentation accompanies all shipments. |
| Storage | 2-(2-Thienyl) phenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and secondary containment to prevent leaks. Store at room temperature, following all safety guidelines and local chemical storage regulations. |
Competitive 2-(2-Thienyl) Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Years of experience in specialty intermediates taught us that the right structure impacts more than chemical yield—it opens up new synthetic pathways and brings efficiency to downstream formulations. Our 2-(2-Thienyl) Phenol, with a molecular formula C10H8OS, stands apart from standard phenolic compounds because it introduces a sulphur-containing heterocycle directly linked to the phenolic ring. This nuanced change serves chemists aiming for either electronic effects or unique sterics in advanced organic synthesis.
We manufacture this material in crystalline form with a purity typically above 98%. Every batch meets strict analytical standards using HPLC and NMR, so project chemists don’t waste time with laborious pre-purification or worrying about batch-to-batch variability. Early on, we saw a need for consistent color and fluorescence profiles; our in-house QC tracks slight hue changes, which sometimes hint at trace impurities that could impact sensitive catalytic or pharmaceutical applications.
In-house conversations with customers center on what makes this molecule compelling: the fusion of phenol’s reactivity with thiophene’s electron-rich ring structure. Several synthetic teams, particularly in pharmaceutical R&D and electronics, keep files of transformations streamlined by using our material. It functions as a versatile intermediate in the synthesis of more elaborate heterocycles and conjugated systems, particularly for medicinal chemistry libraries, OLED matrix development, and ligand construction for transition metal catalysis.
Some research groups told us that the ortho-thienyl arrangement enables cyclization routes or C-H activation work that plain phenol or para/thienyl substitutions cannot provide. In ligand chemistry, these subtle differences in positioning directly affect binding affinities when building out organometallic complexes. From firsthand feedback, chemists noted yields improved when the product didn’t require extra recrystallization—an advantage that emerges from our process control, right down to how we cool each crystallization batch.
Working closely with R&D labs, we observed that off-spec melting point or solubility affects everything from chromatography protocols to reaction scalability. Our 2-(2-Thienyl) Phenol consistently melts between 102–105°C and dissolves predictably in various organic solvents—ethyl acetate, dichloromethane, and acetonitrile. Water solubility remains negligible, a feature desired for most organic synthesis.
Odor, often overlooked, yields clues about trace sulfur compounds; our product avoids the typical sharpness of impure thiophenes. Every shipment features tamper-proof packaging and includes a certificate with chromatograms for each batch, offering transparency and saving researchers planning time. We ship both kilogram and multi-ton lots, since needs change from pilot investigations to full-blown commercial production.
Most practicing chemists have access to an array of phenols and simple heteroaromatics. What they lack is a reliable source for more complex, fused-structure materials like 2-(2-Thienyl) Phenol. This compound offers a distinct path compared with 2-phenylphenol or plain thiophenol: the placement of the thiophene ring at the ortho position changes the electronic character and opens doors for selectivity in cross-coupling, oxidative dearomatization, or as a building block for polymers with finely tuned optical or conductive properties.
Historically, alternatives such as 2-(4-thienyl) phenol or other positional isomers present either synthetic hurdles or produce less consistent intermediates for high-purity electronic applications. Consulting with technical teams and end-users, it became clear that alternative isomers lead to lower performance in OLED and photoactive material applications, due to differences in conjugation and molecular planarity.
Production-scale chemistry rarely lines up perfectly with small-lab methods. During scale-up, our team tracked by-products using in-line GC to control parameters so downstream users deal with fewer purification steps. Post-reaction handling also matters—we saw several customer protocols improve when using our material because they could streamline extraction and minimize silica gel usage. That influences not just cost and workflow, but reduces the overall solvent and energy input per kilogram of finished molecule.
Our direct relationships with R&D and commercial production chemists reveal the importance of particle size uniformity for batch consistency. Granule size distribution, controlled during drying and packaging, prevents sampling biases and boosts reproducibility, especially when automated weighing or liquid handling systems are employed. We developed SOPs around this feedback—by keeping our production lines responsive, we help chemists scale promising reactions straight from screening to pilot batch without recalibrating conditions for a new lot.
Chemical manufacturing faces ever-evolving regulatory requirements concerning residual solvents, byproduct screening, and trace metals content. We update our analysis panel based on customer and regulatory body feedback, not just internal preference. Most recently, one electronics manufacturer requested expanded heavy metal testing down to ppb scale for new photonic device compliance. As a result, we added ICP-MS to the routine workflow, improving data certainty for every customer, not just those in regulated markets.
In pharmaceutical lead synthesis, trace contaminants from starting materials or solvents risk regulatory setbacks later in development. Our lot approval hinges on multi-point certification—from raw material traceability through final NMR fingerprinting—giving chemists and compliance officers confidence they won’t hit surprises during scale-up or validation.
Turning theory into practice is a story that plays out each week at our site. Early on, we found routine issues scaling lab methods to 100-liter reactors: exotherms during thienyl addition required retooling agitation and cooling. Fielding questions from customers, we shared our own experience redesigning the reactor jacket and staging base addition to avoid hot-spots and side-product formation. Later, customers remarked on improved yields and smoother filtrations—a win for both sides.
We see real consequences from small formulation changes: tiny increases in purity can reduce downstream purification time, letting scientists focus effort on innovative chemistry, not triaging inconsistent raw materials. Our technical service team frequently works in tandem with clients to troubleshoot side-reactions or optimize workflows, aiming for less waste and greater reliability with each batch.
Requests for custom runs led us to invest in multi-purpose reactors and flexible purification setups. Some clients require higher-than-standard purity or exceptionally tight particle size ranges. We adapt drying times and fine-tune crystallization cycles to meet these demands without compromising material stability. More than once, adjusting mother liquor concentration trimmed several hours from downstream steps for our partners.
Demand for green chemistry drove us to trial alternative oxidant and solvent recovery systems. We worked out protocols combining safer, recoverable solvents with targeted process water purification. Our operational data showed waste volumes dropped, giving both environmental and cost savings over a cycle of several thousand kilos.
Over the years, regulations and end-user requirements have shifted, prompting us to stay agile in both formulation and reporting. More customers now request additional documentation—impurity profiles, RSI/R&D samples, transport compliance—so we tightened up our data systems and product tracking. This also led to implementing blockchain-backed certificates of analysis, ensuring the documentation trail keeps pace with product movement.
Unexpected challenges often arise: new analytical techniques sometimes reveal trace byproducts invisible to previous generation equipment. Our technical staff stays proactive, updating screening methods and collaborating with customers to set investigation thresholds that make sense for their own QC environments. Responding to these needs takes both technological investment and hands-on experience, since the implications affect not only batch consistency but regulatory compliance and downstream patent or formulation claims.
Growth areas for this compound extend beyond early synthetic intermediates. Recently, interest spiked in advanced materials research and custom electronics applications. Researchers focus on structure-property relationships, and the unique electronic traits of 2-(2-Thienyl) Phenol make it attractive for organic photovoltaics and semiconductors. We onboarded several academic and industrial partners eager to leverage the compound’s ability to fine-tune bandgap and improve processability in polymer blends.
Compared to other phenol or thiophene derivatives, our product’s consistent structure and electronic properties underpin advances in organic electronics and next-generation optoelectronic devices. Some teams adopted it as a standard for benchmarking new catalyst development, appreciating its predictable reactivity and well-documented impurity profile. In the polymers field, the molecule’s specific connectivity delivers enhanced thermal stability and unique dopant possibilities, broadening its use beyond traditional synthesis roles.
Every stage, from purchasing raw thiophene and hydroxybenzene to isolating and packing finished crystals, shapes final quality. Tight process control, real-time monitoring, and rapid feedback cycles keep production in step with our customers’ needs. By investing in skilled staff and updated analytics, we deliver not only the compound itself but the assurance of a supply partner who understands both industry and bench-scale chemistry intricacies.
The value of 2-(2-Thienyl) Phenol, as seen in customer labs, comes not just from its reactivity, but from the reliability and transparency that back each order. We keep lines open—both for routine queries and for those times when projects change direction suddenly. Chemistry is a field where every detail matters; by ensuring quality and flexibility at every step, we aim to play a supporting role in turning bright ideas into tangible breakthroughs.
Trust builds through action and experience. Over time, open dialog with customer labs has shaped improvements large and small, from modifying drying schedules to developing new shipment formats. We learned that even packaging choices—foil liners versus high-density PE—make a difference for users with sensitive downstream setups. Listening to feedback drives us to recognize industry trends early and keeps us responsive in a fast-changing landscape.
Our approach centers around collaboration—sharing our own bench and plant-floor lessons alongside technical data. Whether troubleshooting crystal growth issues or supporting new research targets, our team views each kilo shipped as part of a bigger project that goes further than a simple sales transaction.
This industry never stands still. Regulatory change, shifting market demands, and new frontiers in organic and materials chemistry mean 2-(2-Thienyl) Phenol continues to evolve as a product and as a solution for tomorrow’s challenges. Ongoing dialogues with universities, startups, and established multinationals shape the upgrades we make to analysis, packaging, and process design.
Our commitment runs deeper than the molecular structure itself—it comes from decades spent advancing process control, listening to those on the research front lines, and investing in technology that drives precision. The synthesis journey involves more than just chemical conversion; it’s about aligning purity, reliability, and partnership so that innovative research doesn’t get held back by supply or quality issues. In every batch of 2-(2-Thienyl) Phenol, customers receive more than a compound—they gain a connection to the accumulated knowledge and hands-on problem solving that only comes from genuine, long-term manufacturing experience.