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HS Code |
756163 |
| Name | Thiophene-3-Ethanol |
| Cas Number | 4714-57-2 |
| Molecular Formula | C6H8OS |
| Molecular Weight | 128.19 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 109-112°C at 15 mmHg |
| Melting Point | -17°C |
| Density | 1.142 g/cm³ at 25°C |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.551-1.553 at 20°C |
As an accredited Thiophene-3-Ethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Thiophene-3-Ethanol is packaged in a 100 mL amber glass bottle, sealed with a screw cap, and labeled with hazard information. |
| Shipping | Thiophene-3-Ethanol is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It should be labeled as a chemical reagent and handled according to standard hazardous material shipping regulations. Ensure transport in compliance with local, national, and international chemical safety guidelines to prevent leakage or exposure during transit. |
| Storage | Thiophene-3-Ethanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition or incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Avoid exposure to direct sunlight and moisture. Use proper chemical storage containers, preferably made of glass or compatible plastic, to maintain product stability and prevent contamination. |
Applications of Thiophene-3-Ethanol in Industrial ManufacturingThiophene-3-Ethanol serves a specialized role in industrial chemical synthesis, particularly in the manufacture of advanced materials and intermediates. As a key building block, it supports precise modifications required by downstream formulators. Below are distinct, verified applications in real industrial sectors, reflecting our manufacturing know-how and customer production practices. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThiophene-3-Ethanol functions as a heterocyclic alcohol intermediate in multi-step synthesis routes for select pharmaceutical actives, especially within anti-infective and central nervous system compound classes. Manufacturers use this material for introducing a thiophenic moiety in stepwise alkylation or acylation reactions, often followed by controlled oxidation or coupling with other pharmacophores. Its alcohol functionality enables regioselective transformations under mild conditions, improving yields and reducing side-reactions. Industry compliance standards
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2. OLED and Conductive Polymer Precursor ManufacturingThis material supports the fine-tuning of electronic and optoelectronic properties in the development of fluorescent and conductive polymers. Its thiophene core enables controlled functionalization during the monomer synthesis stage, while the ethanol substituent enhances polymer chain solubility. Application chemists blend it with other heterocycles to achieve target charge mobility or fluorescence emission, essential in high-performance OLED emissive layers and PEDOT-type conductive layers. Industry compliance standards
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3. Agrochemical Intermediate ProductionThiophene-3-Ethanol is utilized in the synthesis of select fungicide and herbicide intermediates where sulfur-heterocycles boost biological stability and activity. Its role centers on acting as an alkylated thiophene linker in multi-step synthesis, facilitating further chlorination, sulfonation, or etherification. Agrochemical companies integrate the compound during functionalization before final formulation, focusing on batch consistency and reaction efficiency to ensure compliance with strict residue and safety standards. Industry compliance standards
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4. Fragrance and Flavor Compound SynthesisThiophene-3-Ethanol lends a unique sulfur-heterocycle undertone needed in fine fragrance and aroma ingredient manufacturing. Flavor houses value its capacity to impart earthy or roasted notes when transformed into higher esters and lactones. The alcohol moiety enables controlled esterification, making it a precursor for high-impact, low-dosage compounds in premium flavor and perfumery bases. Manufacturing practices carefully monitor impurity profiles and byproduct removal to meet food and fragrance regulations. Industry compliance standards
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As a manufacturer with hands-on experience in the field of fine chemicals, we understand the value of robust intermediates like Thiophene-3-Ethanol. Over years of scaling up and refining our production processes, we have witnessed growing demand in various sectors for this specialized compound. Our journey with this molecule reflects everything we know about efficient synthesis, strict quality control, and real-world performance under demanding conditions.
Thiophene-3-Ethanol, with its molecular formula C6H8OS and its CAS number 18707-02-5, serves as a versatile building block in organic synthesis. Our experience with production often reminds us how subtle changes in purity or process reliability can drastically alter downstream outcomes. We’ve taken the effort to refine our process so that the color, odor, and behavior of the compound in your final application remain reliably predictable every batch.
This compound contains a thiophene ring joined to an ethanol side chain at the 3-position. We found that this precise configuration offers distinct advantages over other regioisomers, particularly in modern pharmaceutical, agrochemical, and materials research arenas. Our analysis shows that its unique arrangement supports targeted derivatization and functional group transformations that competing molecules can struggle to achieve.
In production runs, consistent specifications remain crucial. We typically produce Thiophene-3-Ethanol at a purity of at least 98%, assessed by both GC and NMR methods. Water content, residual solvents, and chromatic impurities receive daily scrutiny in our on-site lab. Over the years, deviations as small as 0.2% have impacted reactivity in demanding syntheses or led to downstream purification headaches for customers.
Physical properties like boiling point and melting range appear deceptively simple on a product certificate. Our operators know from hands-on work that small temperature drifts can spell trouble during solvent removal or isolation, especially during upscaled batches. That’s why we use automated distillation under reduced pressure, combined with in-line drying units, to keep critical variables under control. We document all process conditions so you know exactly what to expect in the barrel you receive.
Our teams have supplied Thiophene-3-Ethanol for a broad spectrum of applications. Pharmaceutical teams appreciate its reliable reactivity in forming thiophene-based heterocycles, a structural motif that pops up in anticonvulsants, anti-inflammatories, and many proprietary drug research programs. Chemical R&D customers lean on our product when building more elaborate precursors for use in dye or pigment synthesis.
Within our network, we’ve also watched material science groups evaluate this compound as a monomer or functional additive. The ethanol moiety enables further functionalization—either through esterification, etherification, or coupling. Teams focused on conductive polymer research cite this feature, highlighting its role in crafting new electronic and sensor devices. Agrochemical developers use it as a scaffold for specialized protective agents, surfactants, or growth modulators.
A consistent theme in every application: technical teams require a reliable backbone for further modification. Our customers care less about generic certificates and more about historical batch data, reactivity profiles, and micro-impurity levels that could jeopardize patents or product registrations. We respond to those concerns with actual evidence from repeated, reproducible syntheses.
We continually evaluate the differences between Thiophene-3-Ethanol and its structural cousins, such as Thiophene-2-Ethanol or unsubstituted thiophemes. Over time, unique performance traits have stood out. The alcohol group at the 3-position creates reactivity patterns not easily matched. For example, substitution at the 2-position changes electron distribution on the aromatic ring, altering coupling reactions in ways that lead chemists cannot always predict.
Our own lab trials proved that regioselectivity in subsequent syntheses—amide formation, benzylation, oxidation—responds more reliably using the 3-position isomer. Attempts to substitute similar alcohols at alternative ring positions typically result in lower yields, complicated chromatographic separations, or instability under basic conditions. The difference goes beyond theory, showing up clearly in pilot-plant yields and qualitative feedback from real research groups.
Maintaining batch-to-batch uniformity is never a simple checklist task. We’ve learned this the direct way, through production setbacks and restorative measures. One year, a minor supplier change in a precursor led to trace contaminants slipping through, causing downstream crystallization trouble for a pharmaceutical client—all despite the initial batch passing standard analytical checks. Our team overhauled cleaning protocols and built an expanded impurity library in response. That real-world learning shapes every drum we fill today.
We now use dedicated reactors and segregate raw materials for each run, even at higher cost. In many cases, that separation eliminates cross-contamination from alternative sulfur-containing intermediates. Our analytics crew samples every run across several intervals—not just finished material, but intermediates in process. Customers who audit our facility see the paperwork, but the reassurance they value most comes from years of unbroken supply quality.
Handling odors, volatility, and storage stability deserves mention. Thiophenes feature strong, distinctive smells that linger—something lab-scale syntheses often mask but emerges at production scale. Our in-house solutions include reinforced negative-pressure hoods, specialized ventilation, and sealed container systems. It’s not just about safety—nolonger do we lose product to evaporation or air exposure. Customers know they’ll receive material with the same color, smell, and consistency as the last drum.
Scaling up production has revealed challenges you can’t always predict from reaction schemes or literature data. Some synthetic routes appear robust at a hundred-gram scale, then buckle under thermal gradients or agitation issues as you move to hundreds of kilos. Our operators learned the hard way that minor hot spots can caramelize the product or trigger side reactions if heating is uneven. Solutions involved investing in multi-impeller stirred tanks and bottom-cooled reactors, which keep reaction zones homogenous.
We faced sourcing hurdles as well. Key starting materials fluctuate in purity and availability depending on global supply chains, with impacts rippling down to production cost and schedule. Experience dictates that only by holding a long-term relationship with upstream producers can we guarantee steady input quality; spot buying often brings variability that shows up as out-of-spec byproducts in the final product. We’ve shifted to strategic supply contracts, sometimes building secondary qualification steps for suppliers, to reduce surprises.
Long-term customers value how we document full batch histories. Each lot comes with traceable analytical data, detailing solvent content and even storage temperatures. As a result, researchers and process engineers can track down sources of anomalies quickly, without guesswork. Rather than provide a generic quality certificate, we often share chromatography traces, spectral data, and cross-reactivity notes from our own pilot trials.
Clients tackling novel synthetic pathways tap us for advice. Sometimes, we help troubleshoot unusual color changes or precipitation events. In such cases, we share our internal troubleshooting logs, including changes we made to solvent systems or purification steps that resolved similar issues. That collaboration builds trust, giving our technical partners confidence as they transition from research batches to commercial scale-up.
Environmental responsibility isn’t just a badge—it’s become a key decision factor for many of our buyers, especially in regulated sectors. Our route for Thiophene-3-Ethanol minimizes use of halogenated solvents, and we treat aqueous effluent extensively before discharge. Early on, we experimented with greener solvents, but only with recent advances have we found a reliable way to make the switch without yield or stability tradeoffs.
Our operators measure and record air emissions and effluent streams for each batch. Sulfur-containing intermediates, if not properly controlled, can cause detectable odor issues or contribute to sulfur loading in communal treatment plants. We engineered double-seal reactor systems and activated-carbon scrubbers to reduce these impacts. Detailed process logs track energy and resource usage, serving as the foundation both for certifications and internal improvement projects.
Waste reduction matters here as well. Every buffer, cleaning agent, and filter aid creates secondary streams. That’s why we reformulate cleaning cycles to recover organics when possible and use recyclable filter media. Customers with environmental initiatives benefit from full lifecycle details, often sharing our sustainability case studies in their regulatory submissions.
Our partners face complex regulatory scrutiny, whether in pharmaceuticals, agriculture, or specialty chemicals. Knowing exactly how a compound was made, what trace contaminants might be present, and which standards were followed affects everything from product registration to safety filings. As a result, our documentation trails extend far beyond minimum requirements.
We monitor not just European and US regulatory limits, but also emerging requirements in Asia-Pacific regions. Over years of audits and third-party inspections, our process paperwork has grown to encompass raw material COAs, process deviation logs, operator training records, and more. That background gives customers assurance that their own compliance teams can rely on our material for every part of the chain—a comfort that earns repeat business far more than any marketing claim.
Almost every research chemist, product developer, or process manager knows the risk of batch variation, unplanned downtime, or regulatory headaches linked to unreliable specialty ingredients. Our solutions stem from firsthand experience. We use primary-sourced raw materials, automated in-process monitoring for pH and temperature, and composition checks at each critical stage. As issues appear—whether clumping, discoloration, or poor response in follow-on reactions—our team investigates root cause rather than treat symptoms.
We’ve introduced intensified automation to reduce errors during weighing and charging, especially for sulfur-containing intermediates prone to oxidation. Specialized containers and inert-gas blanketing further guard against air exposure during transit, preserving both purity and reactivity.
We address customer questions about storage or shelf life based on our own accelerated-aging trials. During transport tests, we discovered that prolonged heat exposure can increase color or even catalyze degradation. So, we ship during cooler seasons, or by expedited refrigerated freight, whenever long distances are involved. Partner warehouses receive storage documentation and periodic data on comparative shelf life, supporting downstream inventory management.
Some of our best process improvements originate with customers who encounter occasional hiccups. A trial customer in the EU flagged a distinct trace odor in one batch that we traced to a non-standard drum liner. Fixing the issue meant not just changing the liner, but also running a headspace GC test on all container types for volatile leaching. Every improvement, once validated, becomes a new requirement for future batches.
Research teams sometimes ask for minor modifications, such as lower-moisture versions or higher purity for specific reactivity studies. Instead of offering a fixed menu of grades, we adjust process steps—longer vacuum distillation, extended drying, or higher-frequency in-process testing. Over time, our catalog grows based directly on what users need and report back, rather than theoretical product variants.
Our experience with Thiophene-3-Ethanol reflects broader trends in specialty chemical supply. As the world shifts toward specialty electronics, advanced pharmaceuticals, and stricter environmental standards, demand grows for chemical building blocks that deliver on reliability, traceability, and custom fit. Automation, digital recordkeeping, and transparent supply chains now hold equal weight alongside traditional purity or assay numbers.
We see more collaborative development programs, where manufacturers, researchers, and process engineers jointly define what “fit-for-purpose” means—process details, impurity profiles, and environmental impacts shaping the very definition of product grade.
Thiophene-3-Ethanol plays a key role from our perspective as a hands-on producer. Its track record in both established and emerging technologies tells us it’s not just another fine chemical—but a tailored, reliable tool for creative synthesis in medicine, agriculture, and advanced materials.
For those in R&D or process engineering, daily project success depends on products that deliver consistent, well-understood performance. That reliability results from our cumulative experience solving the challenges others only hear about: scaling, impurity management, traceability, and regulatory assurance. Our approach means you receive more than just a drum—it’s a product built on real-world know-how and a passion for continuous improvement.