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HS Code |
830349 |
| Chemical Name | 3-Methylthiophene-2-Carbonitrile |
| Molecular Formula | C6H5NS |
| Molecular Weight | 123.18 g/mol |
| Cas Number | 55921-65-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 236-238°C |
| Melting Point | -8°C (approximate) |
| Density | 1.122 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Flash Point | 97°C |
| Refractive Index | 1.553 |
| Smiles | CC1=CSC(=C1)C#N |
As an accredited 3-Methylthiophene-2-Carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-Methylthiophene-2-Carbonitrile, tightly sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 3-Methylthiophene-2-Carbonitrile is shipped in tightly sealed containers under ambient conditions, protected from moisture and extreme temperatures. It is labeled in compliance with chemical safety regulations and transported according to international guidelines for hazardous materials, ensuring safe handling, storage, and delivery to the specified destination. |
| Storage | 3-Methylthiophene-2-carbonitrile should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed when not in use. Store separately from strong oxidizing agents. Use only with adequate ventilation, and avoid exposure to moisture. Recommended storage temperature is typically at room temperature, protected from direct sunlight. |
Applications of 3-Methylthiophene-2-Carbonitrile in Industrial ManufacturingAs an established producer, we supply 3-Methylthiophene-2-Carbonitrile to key industrial sectors that rely on strict quality control, precise integration into downstream synthesis, and proven end-use value. The following application areas reflect real commercial use and industry-driven formulation guidelines. 1. Advanced Pharmaceutical Intermediate SynthesisLeading API manufacturers utilize 3-Methylthiophene-2-Carbonitrile as an advanced intermediate in the multi-step synthesis of anti-inflammatory, antiviral, and anti-tumor actives, including specialty thiophene-containing drugs under clinical and commercial phases. The compound’s nitrile and methylthiophene functionalities allow for selective hydrolysis, cross-coupling, and further heterocycle elaboration. In GMP-oriented pharmaceutical manufacturing, this raw material is carefully measured and introduced at specific stages to ensure downstream target molecule formation, batch traceability, and impurity profile control. Industry compliance standards
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2. Electronic Materials and OLED Intermediate ManufacturingDownstream producers in the electronics sector employ 3-Methylthiophene-2-Carbonitrile as a functional building block for synthesizing organic light-emitting diode (OLED) intermediates and advanced semiconducting materials. The electron-rich thiophene ring structure supports the formation of donor-acceptor conjugated systems that enhance charge mobility and optical performance. Incorporation takes place under strictly controlled solvent choices and inert atmospheres to avoid contamination of high-purity electronic-grade feedstocks. Close monitoring at every reaction stage ensures batch-to-batch uniformity and device reliability. Industry compliance standards
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3. Agrochemical Active Ingredient DevelopmentMajor agrochemical research and production companies integrate 3-Methylthiophene-2-Carbonitrile into the synthesis of innovative sulfur-containing crop protection agents. Its thiophene structure and nitrile group facilitate the construction of high-activity pesticide scaffolds through controlled substitution and cyclization reactions. In pilot and commercial scale settings, technicians adjust the input ratio to match efficacy, residue, and cost targets based on seed or foliar application requirements and environmental safety profiles. Industry compliance standards
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4. Specialty Dye and Pigment Intermediate SynthesisLeading dye manufacturers incorporate 3-Methylthiophene-2-Carbonitrile as a controlled intermediate in the preparation of novel conjugated pigment systems for high-performance inks, coatings, and textile dyes. The unique molecular structure enables targeted modifications to absorption, solubility, and substrate adhesion, enhancing color fastness and process stability. Industrial chemists optimize addition rates and processing conditions to maximize pigment yield while meeting strict end-user application and regulatory requirements. Industry compliance standards
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Over the years, manufacturing heterocyclic chemicals like 3-Methylthiophene-2-Carbonitrile has shown us the importance of purity, consistency, and supply chain transparency. From raw material sourcing to small-batch synthesis, we see how much every variable matters to our partners in pharmaceuticals, agrochemicals, and material science. Our 3-Methylthiophene-2-Carbonitrile, CAS number 55910-95-9, doesn’t just appear on a shipment manifest—it represents careful process controls, robust quality metrics, and a focus on supporting real innovation in downstream chemical applications.
Producing thiophene derivatives, particularly those carrying sensitive nitrile groups at the 2-position, isn’t a basic exercise for chemical plants. The sulfur-containing ring system asks for specialized handling and inert conditions throughout. Over time, we have invested in closed-system reactors, tailored distillation columns, and continuous monitoring systems because thiophene analogs can degrade or polymerize when exposed to air, moisture, or trace impurities. Keeping methyl substitution at the 3-position integral and minimizing contamination with isomeric byproducts has called for tight process control and decades of know-how in heterocycle chemistry.
Most inquiries focus on assay values, physical appearance, melting point, and trace impurity limits for a reason. Engineers and scientists expect a fine yellowish liquid or, sometimes, a pale solid, with a distinct, neutral scent, indicative of minimal sulfurous contaminants. Our typical offerings reach purity levels above 98%, often surpassing custom thresholds. Close attention to trace water content and final filtration pushes color clarity beyond basic expectations.
Handling a compound like 3-Methylthiophene-2-Carbonitrile requires lab familiarity and respect for its reactivity. Storage under argon or nitrogen, in containers designed for air-sensitive materials, preserves shelf life. Our clients demand transparency about batch-to-batch variance—not just a paper guarantee, but genuine statistical evidence from independent tests. We routinely provide GC-MS traces, HPLC chromatograms, and sometimes NMR spectra, reflecting the routine scrutiny informed customers have learned to expect.
There isn’t a one-size-fits-all approach to production. New model development asks for kilogram-scale R&D runs with tight analytical feedback. We build pilot batches around feedback loops—what worked, what gummed up lines, what extended lead time. When demand ramps up, our facility can shift to multi-ton volumes, supported by supply chains that go back to sulfur and cyanide precursors we’ve sourced for decades. Difficulties in scaling up don’t catch us off guard. The process behind 3-Methylthiophene-2-Carbonitrile tolerates scaling because we’ve tweaked variables like solvent cycles, temperature ramps, and work-up protocols based on real observations rather than blind repetition of published literature.
This compound won’t sit on the shelf for long. Agrochemical researchers pursue it for its potential as a synthetic intermediate in herbicide and fungicide discovery. Medicinal chemists sketch structures that leverage the electron-rich thiophene core coupled with a versatile nitrile substituent, mapping out analog libraries in search of new therapeutics. Our teams field frequent requests for documentation backing up claims about impurity profiles, because one stubborn contaminant can sink a medicinal chemistry project before it starts.
Organic materials labs look to 3-Methylthiophene-2-Carbonitrile for conjugated polymer projects and as a building block in specialty dye synthesis. Those running hydrogenation or cross-coupling reactions demand evidence that the methyl and nitrile groups sit exactly where they’re expected. We’ve seen even a subtle isomeric impurity create headaches with reaction sequence planning, which pushes us to maintain rigorous, reproducible chemistry.
Not every thiophene carbonitrile behaves the same. For instance, 2-Methylthiophene-3-Carbonitrile and 2-Thiophenecarbonitrile diverge sharply from 3-Methylthiophene-2-Carbonitrile in reactivity and downstream compatibility. Our customers in pharmaceutical or agrochemical sectors share that, in their hands, backbone methyl placement influences binding affinities and biological activity, not to mention synthetic utility. Isomeric mixtures muddy results, making pathway optimisation much harder. We’ve pared laboratory and pilot protocols so the methyl sits only at the 3-position, not wandering to the 2- or 5- position, aiming at more than just regulatory acceptance: it’s about reliable results at every scale.
Comparing strictly against plain thiophene-2-carbonitrile, adding a methyl group in the 3-position changes solubility, boiling point, and reaction selectivity. Chemists who explore Suzuki or Heck coupling, for instance, feedback that regioselectivity and yield profiles differ—sometimes substantially—depending on minor changes in the aromatic core. A trader might take those differences for granted, but as the operator running columns and collecting fractions, we’ve lived those details. RAW inventory control and loss during purification have taught us that not all regioisomers are created equal, either in physical properties or market demand.
Regular suppliers often underestimate just how much downtime a single off-spec batch can cause. As manufacturers, we stay close to the realities of GMP and non-GMP production alike. Our batch records go deeper than compliance—extensive internal documentation captures shift operator notes, maintenance logs, and subtle seasonal effects (humidity, for example, shifts the product’s behavior during distillation).
This direct investment in data isn’t just for audits. Chemists—ours and our customers’—rely on rigorous traceback and sample retention, because a month or even a year down the line, a single oddball impurity may need to be explained. We have built redundant quality assurance structures, not because standards demand it, but because our customers call for it. Real relationships mean responding to more than order forms—we regularly troubleshoot alongside our contacts, offering technical know-how, and troubleshooting roots of anomalies whether the cause is a shipping delay, supplier issue, or weather-driven process fluctuation.
Over several years, customer expectations and use cases for 3-Methylthiophene-2-Carbonitrile have grown more sophisticated. Early requests were limited to purity tests; now, compliance staff ask about residual solvents, stability under stress conditions, and particle size distribution for solid forms. Analytical and regulatory staff often visit our site, check product storage, and share feedback about how our methods support their own product development cycles. They don’t just want a drum or flask. They want shared risk—a supplier who genuinely understands how small changes in process or handling could impact their work downstream.
Our facility doesn’t function in a vacuum. Every specification update comes from direct conversations with researchers and plant engineers. Process tweaks sometimes cut yields in exchange for superior control over impurity classes that consistently show up as regulatory targets or patent-blocking side products. We treat this feedback loop as central, not as an afterthought. Open data, QA transparency, and readiness to adapt batch processes all flow from understanding these collaborations aren’t optional for anyone who manufactures specialized chemicals in a changing world.
Real stories come from the lab benches and pilot suites, not sales scripts. We once worked with a specialty pigment company that found a chromophore shift in their final product traceable to a single low-level impurity in a thiophene intermediate. The trouble started out with inconsistent color standards over several months, traced back through extensive documentation. Tightening purification and tracing back to a maintenance incident solved the problem and improved repeatability—not just for them, but down our entire product line.
End-users sometimes notice subtle changes in crystallization behavior, particularly in kilogram lots transferred between sites or after prolonged warehousing. These shifts have sparked process tweaks, such as adopting stricter inerting during transfer and adapting packaging to shorten transit exposure. A focus on root-cause analysis, rather than surface fixes, brings stability, and that approach scales whether a client sources liters or hundreds of kilos.
In recent years, fluctuations in raw material markets have demanded vigilance. Volatility in sulfur markets, changes in synthesis-scale cyanide regulatory landscape, and shifting international transportation all introduce potential bottlenecks. Developing backup suppliers for key inputs isn’t a gimmick; it’s a survival tactic. Our facility has doubled down on forward contracts and quality-assured sourcing strategies. Close tracking of every consignment—down to trace metals and lot-level certificates—matters all the way up the supply chain.
Shipping conditions can play just as strong a role. On occasions, hot summers have triggered slight shifts in physical state for heat-sensitive shipments, prompting us to overhaul container specs and rethink warehouse temperature standards. It didn’t happen overnight, but experience dealing with reclaimed shipments or customer complaints became a catalyst for retooling logistics alongside manufacturing.
Continual updates in chemical regulations drive us to rethink process and QA at a granular level. Shifting environmental standards touch not only emissions but also packaging waste, spill preparedness, and even labeling. Direct engagement with regulatory bodies, not just reading updates, keeps us ahead. Changing a documentation system, for instance, may not seem like chemistry, but small investments in barcoding and batch tracking have paid off in fewer lost containers and tighter lot management.
Third-party audits have moved from sporadic to routine, and our facility actively encourages open access for responsible partners. This introduces more paperwork, but also more trust. Whether dealing with REACH compliance, US EPA registrations, or local environmental health and safety officers, our responses stay rooted in our understanding of not just our own operation, but in direct awareness of our partners’ obligations.
Collaboration remains the center of everything. Developing analytical methods with clients, troubleshooting new reactions, or simply sharing technical notes on what’s worked (and what failed) keeps us sharp. As academic groups push into new reaction technologies—flow chemistry, for example—we adapt with them, modifying throughput and mitigating new operational hazards.
Sometimes our best process tweaks come from outside our own team. Customer process feedback pinpoints improvements no in-house pilot run revealed. We’ve upgraded condenser hardware, altered cleaning protocols, and added secondary containment based on shared knowledge. The intersection of manufacturing and user experience turns problems into progress. It supports our belief that a supplier in tune with real-world labs and the shifting currents of science becomes something more than a vendor.
Turning out 3-Methylthiophene-2-Carbonitrile isn’t the end of the story; it marks the start of practical, collaborative applications for our partners. Each drum, bottle, or sample reflects a production anchored in decades of technical refinement, analytics, data transparency, and collaborative spirit. We put our own data to work, not just to satisfy internal targets, but so that those developing the products and solutions of tomorrow can rely on a material—and a partnership—that meets more than the minimum.
As regulation, demand, and research directions evolve, our factory shifts as well—never losing sight of the simple truth that meaningful chemical manufacturing relies on feedback, adaptation, and deep attention to detail. All those insights come not from abstraction, but from hands-on engagement with the process, the product, and above all, the people who count on us to deliver.