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HS Code |
870727 |
| Chemical Name | 3-Thienylmethanol |
| Cas Number | 1603-56-7 |
| Molecular Formula | C5H6OS |
| Molecular Weight | 114.17 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 223-225°C |
| Density | 1.162 g/cm3 |
| Flash Point | 95°C |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.592 |
| Smiles | C1=CSC=C1CO |
As an accredited 3-Thienylmethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Thienylmethanol is supplied in an amber glass bottle, 25g quantity, with a screw cap, tamper-evident seal, and hazard labeling. |
| Shipping | 3-Thienylmethanol is shipped in tightly sealed containers under ambient conditions. It should be protected from light, moisture, and incompatible substances. The container must be clearly labeled and comply with all applicable regulations for handling and transport of chemicals. Appropriate safety documentation, such as Safety Data Sheets (SDS), accompanies each shipment. |
| Storage | 3-Thienylmethanol should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. It should be protected from light and moisture. Proper chemical storage procedures and labeled containers are essential to ensure safety and maintain the compound’s stability. |
Applications of 3-Thienylmethanol in Industrial ManufacturingAs a direct manufacturer of 3-Thienylmethanol, we support a range of advanced downstream industrial applications, focusing on sectors that gain added value from the compound’s thiophene-based structure. The use scenarios outlined below reflect real, quality-driven adoption by commercial manufacturing and development partners worldwide. Each section addresses regulatory guidelines, formulation ratios, critical process steps, and the specific types of finished products produced within each industry. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers integrate 3-Thienylmethanol as a key synthon during the assembly of targeted heterocyclic drugs, most commonly for active pharmaceutical ingredients with thiophene cores. Its alcohol group enables focused derivatization, including etherification, esterification, and further functional group installs that define the pharmacological properties of the final molecule. Adoption relies on purification and traceability controls in batch records to meet international regulatory expectations. Industry compliance standards
Typical usage ratio
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2. Organic Electronic Material ProductionManufacturers of organic semiconductors and optoelectronic materials use 3-Thienylmethanol to synthesize conjugated polymers and oligomers with thiophene motifs, directly impacting film-forming properties and electrical characteristics. Controlled reactivity at the methylol position supports precise chain extension and functionalization, which is critical during process scale-up for device-grade material production. Industry compliance standards
Typical usage ratio
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3. Agrochemical Active Ingredient ManufacturingAgrochemical producers utilize 3-Thienylmethanol as a specialty intermediate when constructing certain pest control actives containing fused or substituted thiophene structures. The compound’s reactivity supports efficient coupling in multi-component syntheses, contributing to desired target specificity and bioavailability in the finished formulation. Stringent production documentation and impurity profiling ensure product consistency and regulatory compliance. Industry compliance standards
Typical usage ratio
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4. Dye and Pigment Synthesis for Specialty InksProducers of technical dyes and advanced pigments incorporate 3-Thienylmethanol to introduce heteroatom functionalities within custom colorant structures, particularly for inks engineered for security printing, anti-counterfeiting features, and specialty coatings. Its use enables tailored solubility and electronic properties, facilitating strong chromophore performance under strict batch reproducibility requirements imposed by inkjet and flexographic printing systems. Industry compliance standards
Typical usage ratio
Downstream process integration
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Years ago, our team began producing 3-Thienylmethanol because researchers and process chemists kept running into sourcing headaches with heterocyclic alcohols. In the lab, you quickly see limitations in supply and quality for even modestly specialized building blocks. Drawing from work in both electronics and pharmaceuticals, we noticed a steady pattern: even a trace of by-product or excess moisture could spoil expensive, late-stage work. 3-Thienylmethanol, with the CAS number 33315-05-2 and formula C5H6OS, answered plenty of those recurring demands.
3-Thienylmethanol stands apart because of its thiophene ring—five carbons and one sulfur—fused to a single methanol (-CH2OH) group at the 3-position. That slight tweak on the thiophene structure, adding a methanol, opens new chemistry doors. Chemists regularly point out how crucial this building block becomes during coupling reactions, protective-group manipulations, and even polymer work. We learned early that the impact isn’t just about availability; it comes down to consistency in the finer details: low trace impurities, minimal residual solvents, and batch-to-batch color stability. Most mainstream providers treat this as a commodity, but if you run a pilot batch and something’s off, you pay the price in wasted time and troubleshooting.
When groups reach out with questions, purity tops the list. From experience, a GC purity of at least 98% unlocks reproducible results, especially in scale-up or regulated environments. HPLC can confirm even tighter specs, but if you look at what actually matters in routine use, it comes back to the side-products: isomeric by-products, unreacted starting material, and traces of higher-boiling thiophenes. The model we follow in-house starts with a careful, moisture-controlled reaction—no open-vessel shortcuts—giving transparent traceability from starting raw materials right through production.
Another area users ask about: water content. Anyone doing organometallic or Grignard chemistry shudders at high moisture. So, we focus on keeping Karl Fischer readings under 0.2%, and certificate records bear that out for routine lots. If someone needs lower, we can further dry under vacuum; we’ve done that for specialty electronics work, especially OLED material R&D. Packaging also plays a role—we’ve switched from low-grade HDPE bottles to amber borosilicate for certain grades, limiting light exposure that could yellow the product.
Melting and boiling points weigh into downstream planning. 3-Thienylmethanol melts around 29–32°C (just above room temperature on a summer day), and boils at roughly 217–218°C. That means you handle it as a crystalline solid for most of the year, but it can liquefy if your warehouse gets warm. We found early on that caking can pose challenges in shipping during hot seasons, so we adapted bulk packs to minimize fused clumps. End-users appreciate these little changes, especially those transferring by automated weighing or robotics.
Real-world uses of 3-Thienylmethanol stretch from the lab bench to kilo-scale process synthesis. The largest users are typically in pharmaceutical discovery, where thiophenes crop up in antifungal, antiviral, and CNS-active drug candidates. The -CH2OH group delivers straightforward derivatization—everything from esters to halides, and oxidative transformations, flows from there. In agrochemical labs, you often see it in fungicide and herbicide scaffolds. The electronic materials sector picks it up for conductive polymer development, especially in polythiophene variants used as hole-transport layers or sensor films.
On the custom synthesis side, we provide 3-Thienylmethanol for intermediate synthesis in patent-protected programs. It’s not only about the core molecule; clients sometimes request isotopic labeling or specific metal-catalyst residues under defined ppm thresholds, often driven by sensitive downstream applications or regulatory filings. We’ve run batches under tailored process conditions, and customers rely on transparent communication for project-critical timelines.
Over time, we’ve collaborated on a few surprising projects: solar cell R&D teams exploring new organic photovoltaics, flavor and fragrance manufacturers blending heterocycles for specialty notes, and polymer chemists aiming for anti-static coatings. Each application has brought new requirements for handling, shipping, and documentation. It’s clear that success depends on anticipating those evolving needs.
One of the things that sets our 3-Thienylmethanol apart is control at every step. We never use outdated glassware or tolerate corners cut in distillation. Modern reactor setups, backed by in-line monitoring, keep reaction conditions consistently tight, which in turn preserves the purity profile. Quality isn’t about what a label says, it shows up in repeat results, from the first gram to the hundredth kilo.
We don’t race to the cheapest source of starting thiophene; instead, we rely on long-term partners who deliver on both specification and documentation. We regularly hear from labs that tried cheaper alternatives, then struggled with trace sulfur by-products or off-colors that crept into NMR spectra, delaying whole projects. By managing raw material sourcing with audits and lot traceability, we catch these quality shifts before they reach the end-user.
Small improvements in handling also add up. We switched to low-oxygen headspace filling for select pharmaceutical clients, which kept both purity and appearance stable through transcontinental shipping. After experimenting with tamper-evident seals and robust secondary containers, we saw a drop in complaints about caking or contamination. The lessons came from real troubleshooting on the ground, not theory.
Clients often compare 3-Thienylmethanol with other substituted thiophenes or simple benzyl alcohols. The differences are tangible. 3-Thienylmethanol, unlike 2-thienylmethanol or ring-unsubstituted variants, shows different reactivity. The position of the hydroxymethyl group (at the third carbon on the ring) alters both steric and electronic properties. In cross-coupling or directed ortho-lithiation, even small shifts in substitution make or break synthetic routes. We’ve seen side-by-side trials where a misplaced methyl or an extra sulfur led to poor yields or failed purifications.
Compared to benzyl alcohol, the thiophene ring brings aromatic sulfur into play, changing not only electronic properties but also odor, volatility, and solubility. In sensor development or material science, these differences drive performance. Chemists tell us they can’t substitute benzyl alcohol or even 2-thienylmethanol and achieve the same outcome. In fact, one electronics group shared data showing increased sensitivity in organic transistor performance because of the 3-thienyl motif.
We also field questions on batch-to-batch reproducibility. Some suppliers blend or re-distill material from diverse origins, risking light or thermal decomposition, and this introduces subtle impurities—something you spot on careful GC analysis. We focus on closed-loop process management, using dedicated packaging chains for moisture-sensitive lots. And every drum or bottle carries clear lot information, so customers can track performance over time.
There are also key differences in scalability. Some labs buy fine chemicals from catalog houses, but for anything above gram scales, pain points emerge. Traditional sources package in low volumes, and their documentation rarely hits the standards needed for GMP or ISO audits. By comparison, our procedures anticipate those needs from the outset. Batch records, validated test methods, and regular risk reviews support researchers and formulators working under heavy regulatory scrutiny.
Anyone working in chemical manufacturing knows synthesis rarely goes exactly as planned. Our earliest 3-Thienylmethanol campaigns showed bottlenecks in purification, from column fouling to build-up in collection receivers. Some of these problems stemmed from older glassware and outdated atmospheric distillation, which couldn’t deliver the necessary purity after repeated runs. Room for improvement meant investing in new fractional distillation gear and humidity-monitored storage, lifting both overall yield and finished product quality.
Disposal of sulfur-containing residues also proved to be more complex than simple aromatic alcohols. Adhering to proper waste treatment keeps the plant compliant and avoids environmental headaches. We worked out separation and recycling solutions for certain process streams, minimizing hazardous output and creating lower-cost, sustainable operations. On top of regulation, our clients benefit from stable long-term pricing without sudden upcharges for unplanned hazardous waste handling.
Getting samples to customers safely was another early lesson. Thiophenes can sometimes take on off-odors during long storage, especially if packaging fails. We shifted to tighter-sealed containers, and now include humidity and oxygen scavengers for long-haul shipments. Each improvement came from practical feedback in the field; every solution built trust over time.
Direct conversation with scientists over the years shaped our outlook. A university group in organic synthesis once tracked an unexpected side-reaction back to a trace impurity—less than 1%—in a sample from another provider. Switching to our product cut their time spent on troubleshooting, and their project progressed along the planned path. In another case, an R&D team working on dye-sensitized solar cells faced repeated batch failures until we shared modified handling protocols and offered a tailored, light-protected grade of 3-Thienylmethanol.
Pharma clients report less variation in NMR and MS spectra, thanks to our attention to process stability. Earlier, one group faced reproducibility problems when scaling from bench to pilot plant. Engaging with their chemists, we uncovered subtle impurities stemming from differences in reaction scale and cleaning procedures. Jointly, we ironed out the issues, leading to a process they could scale up for regulatory submissions.
We’ve also heard from electronics engineers working on conductive polymers. They pointed out that even microgram differences in sulfur content impact the electrical properties of finished films. Our multi-step distillation, with ongoing analysis of metal ion and halogen residues, kept their R&D results within spec. These outcomes came through hands-on troubleshooting, open technical dialogue, and a willingness to re-tool the process.
Other vendors occasionally treat 3-Thienylmethanol as an afterthought or specialty footnote. That attitude never flies for clients facing critical project deadlines or scale-ups. What we bring, beyond the molecule itself, is direct insight from a decade of producing, shipping, and troubleshooting. We know the pinch points clients run into because our own team faced them, too.
From the ground up, our operators—some with 10 or more years running this line—learned why small details matter, from monitoring heat input to making quick decisions at the filtration stage. Technical staff maintain close links with R&D customers; that feedback loop shapes not only each lot but decisions about process upgrades. Whether an agrochemical team calls with cleaning questions or a pigment formulator needs bulk packaging, the answers come from boots-on-the-ground, not from a generic script.
For labs planning to use 3-Thienylmethanol, there are tips we pass along from years of hands-on experience. Always check certificate of analysis (COA) details closely—don’t assume older specs keep up with your application, especially for sensitive pharmaceuticals or electronics work. Ask about real, recent impurity profiles. We give actual chromatograms from the last lot, not hand-me-down historical data. If you need a unique grade—anhydrous, light-stabilized, or low-metal—you’ll get honest timelines and transparent discussion about achievable specs.
Watch for seasonal changes, too; bulk users should plan for hot-weather shipping shifts, or get tailored advice on repacking. We help coordinate documentation and test method sharing with quality teams, so you won’t lose time on regulatory record requests.
Some teams require stability studies, extended shelf-life, or advice on solid-to-liquid handling. We share our own SOPs and lessons learned, helping your staff avoid common pitfalls. For kilo-scale runs, we offer pre-packed sample lots and batch splits, so you can qualify new sources without risk.
Over the past several years, more researchers moved away from simple benzene rings, turning to heterocycles for new properties in drug and material development. With sustainability on everyone’s mind, the drive for less toxic, more efficient coupling partners only grows. 3-Thienylmethanol, with its versatile functional group and manageable regulatory profile, now lands in the toolkit of not just academic labs but multinational formulators and startups, too.
Regulatory expectations keep climbing, especially for pharmaceutical and electronic uses. We continually update traceability, analytical methods, and waste handling to meet stricter client and government demands. In some markets, end-users request certified conflict-free sourcing or extended environmental documentation, which we provide upon request. By anticipating these shifts, we help our customers stay ahead of the regulatory curve.
A rising opportunity shows up in fine chemicals and specialty polymers: customer requests for made-to-order derivatives, such as halogenated thiophenes or longer-chain alcohols. We’ve taken on custom synthesis and contract manufacturing that stems from our core know-how on the parent molecule. In an era where “off the shelf” no longer keeps pace, flexibility and technical depth make a measurable difference.
Working as the actual manufacturer, our commitment goes further than just shipping bottles. False economies appear when teams chase the cheapest option and later face delays from off-grade material, incomplete documentation, or technical support that evaporates after the first sale. Anyone responsible for a big project understands the value of reliability. By being on the ground—in the labs and the plant—we’re ready to answer detailed questions, share troubleshooting steps, and adapt our process to future-proof your work.
Our track record isn’t built on faceless transactions or third-party markups. We keep relationships direct and open, whether for routine lots or complex, regulated projects. The knowledge gained producing, storing, and shipping each drum or bottle flows right back into boosting your success.
Chemical manufacturing runs on more than reactors and bottles—the heart of it comes from dedicated teams who solve challenges, learn from every lot run, and adapt to the shifting needs of innovators everywhere. 3-Thienylmethanol isn’t rare in theory, but finding reliable, deeply-supported sources still proves tricky. We’ve made it our business to focus on the details that matter, delivering quality that moves projects forward and knowledge that saves real time for end-users. Our perspective stays grounded in what we learn together with our clients—because in the end, the chemistry isn’t only in the molecules, but in the partnership itself.