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HS Code |
417996 |
| Cas Number | 2345-28-0 |
| Molecular Formula | C7H8O2S |
| Molecular Weight | 156.20 g/mol |
| Iupac Name | Methyl 2-(thiophen-2-yl)acetate |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 111-113°C at 17 mmHg |
| Density | 1.164 g/mL at 25°C |
| Refractive Index | n20/D 1.536 |
| Melting Point | -20°C |
| Flash Point | 104°C |
| Smiles | COC(=O)Cc1cccs1 |
As an accredited Methyl 2-Thienylacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with a screw cap, labeled "Methyl 2-Thienylacetate, 100 mL," includes hazard and handling information. |
| Shipping | Methyl 2-Thienylacetate should be shipped in tightly sealed containers, protected from moisture, direct sunlight, and extreme temperatures. It must be labeled according to local and international transport regulations for chemicals. Store and transport upright, in a well-ventilated area, and handle with appropriate personal protective equipment to prevent leaks or spills. |
| Storage | Methyl 2-Thienylacetate 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 separate from strong oxidizers, acids, and bases. Ensure proper labeling and use secondary containment to prevent leaks or spills. Access should be restricted to trained personnel wearing appropriate protective equipment. |
Applications of Methyl 2-Thienylacetate in Industrial ManufacturingMethyl 2-Thienylacetate plays a specialized role in select chemical manufacturing sectors where its unique aromatic and functional properties support precise formulation requirements and regulated product development. Our production controls for this material ensure consistent quality and traceability, meeting the needs of professional downstream formulators and processors worldwide. 1. Fine Fragrance and Perfume CompoundingPerfume manufacturers utilize methyl 2-thienylacetate as a specialty aroma ingredient to impart a subtle, sweet, herbal-thiolic note and act as a key modifier in high-end fragrance creations. Its olfactory character enables fine-tuning of complex accords, particularly in chypre, green, and fougère profiles. Perfumers adjust the dosage carefully to balance projection and longevity while adhering to regulatory thresholds, using it primarily during the blending stage alongside other aldehydic and floral components. Industry compliance standards
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2. Flavors Development for Food and Beverage ApplicationsFood and beverage flavor houses incorporate methyl 2-thienylacetate as a trace component to create authentic mushroom, savory, and roasted profiles, particularly in flavor systems for soups, snacks, and processed foods. Its delicate sulfurous and fruity undertones offer subtle complexity, responding well to matrix interactions and thermal stability during product finishing. Precise dosing ensures legal compliance while avoiding over-flavoring or off-notes. Industry compliance standards
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3. Pharmaceutical Intermediate SynthesisChemical and pharmaceutical companies employ methyl 2-thienylacetate as a building block in the synthesis of certain heterocyclic active pharmaceutical ingredients (APIs) and specialized intermediates. The compound’s thienyl moiety and ester group facilitate regioselective alkylation, condensation, and cyclization steps within multi-stage organic synthesis. The material’s traceability and batch purity suit cGMP environments for regulated production workflows. Industry compliance standards
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4. Agrochemical Active Ingredient ManufacturingAgrochemical companies utilize methyl 2-thienylacetate as a core reactant during the synthesis of thienyl-based fungicides and pest control agents. Its controlled chemical reactivity and compatibility with established chlorination or esterification sequences support the generation of potent active ingredients. Producers adhere to pesticide regulatory submissions while monitoring carry-over into formulated products throughout multi-step factory processes. Industry compliance standards
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5. Specialty Polymer and Resin SynthesisChemical manufacturers utilize methyl 2-thienylacetate for introducing thienyl moieties into functional polymer backbones during the synthesis of conductive polymers and specialty resins. This enables materials engineers to realize specific electronic or surface-active properties in end-use applications for advanced coatings or electronics. Strict process control and raw material verification support the achievement of defined polymer structures and consistent performance characteristics for downstream conversion and application. Industry compliance standards
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We see a lot of chemicals pass through our reactors, but few are as distinctive in both smell and behavior as Methyl 2-Thienylacetate. Over years of scaling up batch sizes, refining the crystallization stages, and tracking feedback from perfumers and pharmaceutical folks, certain characteristics stand out. Straight from our own synthesis line, this ester wears its sulfur signature on its sleeve. If you handle a fresh dribble or open a container, you catch an unmistakable aroma—sweet, slightly earthy—with a soft fruity backbone. That's the distinctive fingerprint sulfur-based aromatics bring.
Our current standard batches land between 98% and 99.5% purity by GC. Years ago, we struggled to identify whether that half percent of impurity really mattered for key uses, but after debriefs with seasoned formulators and side-by-side testing in fragrances and flavors, it became clear—cleaner product doesn’t just raise the olfactive intensity, it cuts noise. That makes the jobs of blending masters easier since they don’t have to chase down off-notes or compensate for batch variability.
Most users want to know what they can expect the moment they unscrew the drum or break the ampoule seal. Ours comes as a clear, pale-yellow to colorless liquid. Part of that clarity comes from our choice of purification route—careful distillation using a stainless steel setup that’s never touched by other thienyl derivatives or halogenated raw materials. This decision keeps cross-contamination at bay, which matters for companies tracing every note in a fragrance or running registers in a pharma QC lab.
We run every lot past a simple but effective analysis: Gas Chromatography for purity and residual solvents, Karl Fischer for moisture, and a straightforward color check. There’s no ambiguity. You see what you get, and you can track the numbers from batch history. Our partners in the EU and Asia now ask for these printouts as a matter of habit, and our local technical people have the documentation on hand before shipping any drum out.
A big advantage of Methyl 2-Thienylacetate lies in its reliable chemical profile. Unlike higher homologs in the thienylalkyl ester family, this ester holds steady under typical processing temperatures for both food and cosmetics. Users aiming for consistent tonality in perfumes—from delicate florals to woody blends—find this predictability saves time during reformulations.
In fine fragrance and flavor, this molecule often pulls double duty. It’s not a front-row star the way certain storied aldehydes or musks might be. Instead, it acts as an enhancer, smoothing rough edges and rounding out top notes. It lends an elusive, fruity-wine nuance when diluted, and in higher concentrations brings an amber warmth, thanks to the sulfur ring. Our blending clients have noted it helps marry tobacco, leather, and gourmand accords—no surprise to any nose with experience in traditional European blending techniques.
From the pharmaceutical perspective, Methyl 2-Thienylacetate serves mainly as a building block. The alpha position opens a world of derivatives, and we’ve fielded requests ranging from prodrug synthesis to thienylalkyl amide production. In our own experience, nothing drags down a synthesis more than supplier inconsistency. So, we use a fixed-mass, low-metal catalyst protocol for the main esterification step. Consistency here isn’t about theory—it’s what keeps mid-process failures off the report sheet and minimizes waste.
Over the years, comparative trials have pitted Methyl 2-Thienylacetate against its close cousins: ethyl 2-thienylacetate, benzyl thienylacetate, and even branched esters. Solubility is a primary separator. Our methyl ester dissolves readily in both polar and non-polar solvents, from ethanol to DPG to many silicones used in cosmetics. During pilot production, filtration rates and crystallization curves stay predictable, so bottlenecks rarely pop up downstream.
On the sensory side, this specific ester outperforms both the ethyl and butyl variants in subtlety and blendability. Ethyl 2-thienylacetate delivers a greener, sharper profile—sometimes pushing an unpleasant sweetness in confectionery and drinks. Methyl’s edge comes in its modesty; instead of dominating, it enhances, which allows formulators to coax out more tonality from other notes. We watched perfumers select the methyl over the ethyl repeatedly during in-house panel tests, especially for tobacco and honey bases.
An important handling difference comes up during storage. Unlike benzyl 2-thienylacetate, which can thicken or even partially solidify in chilly climates, the methyl ester remains liquid and pourable well below standard room temperature. Shippers, especially those working through central Asian routes in winter or the northern US early in the year, tell us this saves headaches and reduces drum wastage.
We started sourcing raw thienylacetic acid years ago from a handful of smaller producers. In the early days, yields bounced around and by-products crept in. Our team rebuilt the process—switching from aluminum to glass-lined reactors, dialing in the acid/catalyst balance, omitting chlorinated solvents—because experience taught us that shortcuts showed up as defects downstream. Customer feedback signaled what mattered most: fewer color bodies, zero trace metals, and absolutely no extraneous odors. Meeting these points took time. Each improvement in isolation and wash steps shows up at QC every week.
We’ve since grown into in-house synthesis of both the acid and the ester. Working from basic thiophene derivatives gives us tailored control over lot traceability and cuts out many supply headaches. These shifts let us guarantee clean ester content and ensure buyers—whether they make a fine French liqueur or a restorative skin cream—see batch reports that mean something. There’s no need to translate between suppliers or chase down missing COAs.
Chemistry always chases purity, but some end-users care more than others. For those mixing fragrance compounds, spec purity speaks not only to regulatory compliance but also to the blend’s stability over time. We have watched R&D teams check for color drift, off-notes developing after six months, and performance changes after heating. Methyl 2-Thienylacetate’s clarity and low impurity content hold up in these long-term trials.
We have learned through our pharma partners that impurity content above 2% often throws off analytical methods downstream. Baseline coelution drags out audits and burns hours in corrective action. Our tighter fractionation has shrunk client troubleshooting, especially for those sensitive endpoints, where even a trace oxidized thienyl contaminant can interfere.
Feedback from flavorists, perfumers, and pharma labs comes regularly. Those working on flavor ingredients want to avoid solvent residues and carryover from processing aids. That’s why every batch receives both internal and third-party testing for residual solvents, even though we control the process start to finish.
Long-term partners push for higher volume consistency. A drink flavor house using 30 kilos a month doesn’t want surprises batch-to-batch. They expect drum one to drum ten to behave identically. Those years where we saw variance in minor impurity fingerprints drove us to refine our finishing techniques. Having a process reproducible across five-ton, one-ton, and 200-liter batches took time, but the outcome is practical trust—a concrete advantage in the industrial world.
Cosmetic clients angle for purity, but also low odor contamination and ease of blending. For color cosmetic forms and fine fragrance, unpredictability in even faint animalic or plasticic notes becomes unacceptable. That’s why we carry out a final organoleptic panel before packaging. Those with keen noses ensure product matches the benchmark before drums get sealed.
Anyone scaling from beaker to batch sees where theoretical chemistry meets industrial practice. Early on, we saw a 0.5% water content result in hydrolytic cleavage at pilot ran at higher temp. Adjustments came—vacuum drying before storage, cool room barrels, moister jars swapped for high-bar barrier flasks. Step changes like this didn’t come from a textbook, but from days spent cleaning gummed-up lines and tossing test lots.
During filtration, finer mesh choices provided clearer product. Non-standard batches let us experiment with tighter cut points in distillation, so customers with ultra-high standards in flavors—such as Japanese beverage companies—could take direct shipments, knowing the chances of haze, color, or off-taste were minimal.
Every chemical shows a personality during storage and shipping. For Methyl 2-Thienylacetate, two main concerns come up: oxidation and polymerization. Left in sunlight or exposed to damp air, you see slight color creep and eventual viscosity rise. We keep nitrogen blanketing on every larger storage tank, and smaller vessels use tight-seal closures, never standing open longer than necessary.
Back in the early days, drum stoppers and gaskets were standard black rubber. We found, through customer complaints and our own long-term studies, that sulfur compounds like this ester can leach color and minor odors from standard stoppers. Stainless and high-grade fluoroelastomer shifted that problem off the table. It’s another example where hands-on experience rewrites best practice over time.
Big distillation runs mean minor issues become big headaches in downstream filling. Any lag in temperature or vacuum control shows up as compositional drift in the finished product. That’s why we have a dedicated technician for process monitoring and automated tracking. Years of missed batches taught us running “good enough” never works for these sulfur-rich esters.
We work inside a framework shaped by REACH, IFRA, and assorted national food safety standards. Our documentation doesn’t just exist for paperwork’s sake—it’s the backbone that keeps products moving through customs and into the hands of multinational buyers. Batches register through electronic tracking, so if a QA question arises, full traceability sits a click away.
Deliveries into pharmaceuticals, especially APIs, means every solvent, catalyst, and even shipment container leaves a digital paper trail. We share this willingly with our clients; there’s value in knowing your product’s pedigree is clear at all stages. It builds trust, especially when customers depend on lot-to-lot reproducibility and regulatory compliance.
Every year we revisit not only cost and yield, but also the external footprint of our manufacturing practice. For Methyl 2-Thienylacetate, solvent selection and energy optimization have drawn the most focus. Swapping out high-HAP solvents for greener equivalents trimmed emissions and reduced post-processing headaches. In-house solvent recovery now pays for itself in both savings and environmental reports. Adding digital metering on reactors and distillation columns turned what once were paper logs and handwritten corrections into a system where deviations reveal themselves in real time.
Raw material sourcing also reflects environmental scrutiny. Long ago, thienylacetic acid came from multi-step chemical streams known for by-product waste and challenging disposal. Our current thiophene feedstocks flow from more efficient catalytic routes, which cut unwanted output and tighten overall yield. Meeting client expectations for responsible sourcing isn’t just a marketing point. It keeps regulatory eyes in agreement and ensures long-term access to demanding, high-standard markets.
At the end of the day, supplying Methyl 2-Thienylacetate goes further than just filling drums and sending invoices. Years of customer interaction, QA failures, and little process tweaks have honed every batch to what it is now—livable, reliable, and quietly elegant in application. Whether ending up in a fine Eau de Parfum, acting as an elusive flavor enhancer, or backing up a pharma synthesis, every drop brings a pedigree shaped by genuine shop-floor experience.
This compound stands apart from its cousins—softer and more adaptive in fragrance, more consistent on the line, and better behaved in storage and transit. We’ve learned what matters from hands-on trials, feedback loops, and troubleshooting headaches that shape a product customers can reliably build on. If you ask why people return to this particular ester, it comes down to this blend of chemical precision, predictable behaviour, straightforward documentation, and the steady improvements born from years at the bench.
Chemistry lives at the intersection of laboratories, production floors, and end-use creativity. Our product development approach keeps both process repeatability and user outcomes front and center. Every reformulation, every QA review, every feature request—these shape not just the product specifications, but the way the whole team approaches quality and service. Methyl 2-Thienylacetate might never claim the center stage of flashy product launches, but its value plays out in quiet reliability, practical efficiency, and trusted support for every innovative formulator who depends on clean, sulfur-rich performance with no surprises in the pot.