|
HS Code |
598009 |
| Chemical Name | 2-Thiopheneacetonitrile |
| Molecular Formula | C6H5NS |
| Molecular Weight | 123.18 g/mol |
| Cas Number | 2275-18-5 |
| Appearance | Colorless to yellow liquid |
| Boiling Point | 237-239 °C |
| Melting Point | -8 °C |
| Density | 1.13 g/cm3 |
| Refractive Index | n20/D 1.567 |
| Flash Point | 110 °C |
| Solubility | Slightly soluble in water |
| Synonyms | 2-(Thiophen-2-yl)acetonitrile |
| Pubchem Cid | 33189 |
| Inchi | InChI=1S/C6H5NS/c7-4-6-2-1-3-8-6/h1-3H,4H2 |
As an accredited 2-Thiopheneacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Thiopheneacetonitrile (25g) is an amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2-Thiopheneacetonitrile is shipped in tightly sealed containers to prevent moisture and air exposure. It should be handled as a hazardous material, complying with local, national, and international shipping regulations. Protective packaging and accurate chemical labeling are required to ensure safety during transit. Store in a cool, dry, and well-ventilated area. |
| Storage | 2-Thiopheneacetonitrile should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight. It should be isolated from incompatible substances such as strong oxidizing agents. Proper chemical storage protocols, including clear labeling and secondary containment, are recommended to prevent accidental release or exposure. Always follow safety guidelines and regulatory requirements. |
Applications of 2-Thiopheneacetonitrile in Industrial Manufacturing2-Thiopheneacetonitrile serves as a critical intermediate in several specialized chemical sectors. Its selective reactivity and compatibility with strict quality management enable reliable downstream manufacture of active pharmaceutical ingredients, dyestuffs, agrochemicals, advanced electronic materials, and polymer additives. Below, we outline industrial application scenarios based on real user segments and standardized process protocols. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use 2-Thiopheneacetonitrile as a building block in the multi-step synthesis of heterocyclic APIs, such as anti-inflammatory and anti-hypertensive drugs. Its thiophene moiety introduces specific molecule functionalities required for drug efficacy, particularly in active structures where sulfur-containing aromatic rings increase bioactivity. During the synthetic process, the material participates in nucleophilic substitution and cyclization steps under controlled reaction conditions. QC teams routinely monitor the reaction profiles for compliance with impurity thresholds and consistency in compound structure. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate ProductionMajor agrochemical firms select 2-Thiopheneacetonitrile to initiate synthesis of crop protection agents, such as selective herbicides and systemic fungicides, where thiophene derivatives improve biological selectivity and environmental stability. The compound enters key alkylation and coupling protocols under continuous flow conditions to meet high-volume batch requirements. Quality control validates each lot for residual solvents and trace metals to comply with national pesticide regulations before moving to the formulation stage. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Dyestuff and Pigment SynthesisPigment and dye manufacturers utilize 2-Thiopheneacetonitrile as a core intermediate for making sulfur-heterocyclic chromophores, which deliver enhanced thermal stability and unique color properties in textile and plastics applications. The chemical supports condensation reactions with aromatic aldehydes and amines, forming extended conjugated systems essential for high-performance dyes. Batch processes feature pH and temperature optimization to regulate hue intensity and dye solubility for end-use standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Electronic and Organic Semiconductor MaterialsManufacturers specializing in organic electronics select 2-Thiopheneacetonitrile to synthesize π-conjugated monomers for optoelectronic devices such as OLED displays, photovoltaic modules, and organic field-effect transistors (OFETs). The compound participates in Suzuki and Stille coupling reactions to extend electronic delocalization and tune bandgap properties for specific device architectures. High-purity supply and trace contaminant management remain essential throughout, as even minor impurities may disrupt charge mobility or film morphology in final semiconductor structures. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Polymer Additive and Modifier SynthesisAdvanced materials producers employ 2-Thiopheneacetonitrile to generate specialty monomers and functional additives that adjust polymer conductivity, UV resistance, and antistatic properties. It initiates modification or copolymerization steps with acrylates, maleimides, or styrene under free-radical or ionic polymerization protocols. Analytical QC spans NMR, FTIR, and GPC to confirm successful additive incorporation and block contaminants that impact downstream extrusion or molding steps. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Thiopheneacetonitrile prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Producing 2-Thiopheneacetonitrile requires grit and precision on the shop floor. In our experience, any deviation at the raw material stage, especially with thiophene or acetonitrile sources, creates headaches in both yield and purity. Hands-on involvement with each batch teaches the importance of managing reaction temperatures and maintaining oxygen exclusion during synthesis. The process produces an off-yellow to pale brown liquid, and the sharp, pungent odor always signals its chemical backbone—no sweet or floral notes, just honest chemical intensity.
At the bench, the chemistry is straightforward but leaves no room for shortcuts. Stirring potassium cyanide, working around the hazards, and dealing with waste management keep the entire operation grounded in responsibility, not desk-bound theorizing. Controlling the sulfur impurities coming off the thiophene ring remains the most consistent challenge. Even a small slip shows up in the final GC trace, and that hits both downstream quality and customer trust. We keep detailed records because regulations tighten each year, especially for nitrile handling. Anything less feels reckless.
Every lot receives careful spectrometric analysis, primarily GC and NMR, to confirm a purity north of 98%. Moisture, color, and acid-base properties get checked before signing off. The physical nature of 2-Thiopheneacetonitrile makes it unforgiving; spill a little in the workspace, and the smell lingers for hours. This is not a hypothetical concern—it’s the day-to-day atmosphere in production. Our scale-up process prioritized removing residual cyanide and sulfur-containing byproducts, since these can disrupt further synthesis steps or damage catalysts downstream. Everything depends on the diligence and experience of the operators, not just machine settings.
Stability comes down to dry storage, capped metal drums, and frequent checks on seal integrity. If air enters, hydrolysis isn’t far behind, threatening the reliability of the material customers rely on for their reactions. Over the years, we've learned that small actions—checking pallets, monitoring warehouse temperature, enforcing first-in, first-out—pay off in avoided complaints. Years ago, a batch stored poorly picked up enough water to ruin a customer’s key pharmaceutical intermediate yield. Since then, we keep a pulse on every lot, meeting regulatory requirements while doing right by customers’ ambitions and anxieties.
Our largest orders go to pharmaceutical research groups and specialty chemical producers. Chemists value the reactive nitrile group, especially for constructing thienopyridines and other heterocycles where sulfur atoms play a crucial role. Once, a major agrochemical client used our material to build a platform molecule for a next-generation fungicide. Even undergraduate researchers, with creative synthesis projects, come searching for a few grams to enable C–C coupling on thiophene rings. A common thread runs through every project: requiring confidence in the chemical backbone and impurity profile.
The comparison to similar alternatives such as 3-thiopheneacetonitrile or thiophene-2-carboxaldehyde is instructive. With 2-thiopheneacetonitrile, reactivity leans strongly toward nucleophilic substitution at the benzylic position, making it a favorite for direct functionalization. The nitrile group is robust enough to survive strong basic or anhydrous acidic conditions, striking the right balance between reactivity and stability. In contrast, aldehydes often react too quickly, and substitution patterns on the thiophene ring matter more than textbooks suggest—every process engineer learns this the hard way. We settled on producing the 2-substituted variant after extensive feedback from the field, where reliability trumped theoretical versatility.
In head-to-head reactions, 2-thiopheneacetonitrile tends toward higher yields in Suzuki and Heck coupling, thanks to its electronic properties. Many find that the electron-withdrawing nitrile at the 2-position boosts selectivity. For sulfonation reactions or Grignard additions, steric bulk also remains manageable, particularly compared to more hindered ring systems. Synthetic organic chemists often mention that 3-thiopheneacetonitrile, with its altered electron density, misses the mark for several pharmaceuticals of interest. Recognizing these nuances means more than quoting literature values—it comes out of hundreds of hours spent troubleshooting on the line and listening to customer complaints about missed targets.
As for storage and shipping, the market offers countless resins, acids, and solvents with laxer requirements, but our handling of 2-thiopheneacetonitrile includes custom container sealing and padded shipment. This shields the product from airborne moisture and temperature swings that can degrade sensitive material. Bulk clients ordering drums receive smaller sample vials as a standard practice, so analytical teams can measure the quality before opening full containers. It’s a lesson from the years when minor batch-to-batch differences led to wasted time and material on their end. We keep channels open with clients to smooth over supply chain irregularities or changing purity requirements.
Pumping out tons of 2-thiopheneacetonitrile takes more than raw horsepower. The work brings exposure to caustic substances and toxic vapors—not glamorous, but undeniably impactful. Health monitoring, specialty ventilation, and regular staff rotation became part of process improvement through necessity. Some engineers suggested automating transfer steps with remote monitoring, but we found a balance with manual intervention still key when scaling up unfamiliar reactions. This flexibility prevented costly downtime from equipment fouling or unpredicted reaction side products. From the earliest steps, every synthesis run gets an unvarnished report—our team knows nothing gets glossed over, because cutting corners always finds a way to catch up.
On days when things run smoothly, it’s tempting to forget the dozens of interlocking safety and quality measures. Fires, spills, or minor cyanide exposure have left their mark in lessons learned, shaping our current protocols. What remains unchanged is the pride felt in producing material that underpins major synthetic projects—whether it’s a university group trialing new anti-cancer molecules or an agrochemical leader working on green pesticide alternatives.
Each passing year tightens compliance around nitrile manufacturing, especially in Europe and North America. Documentation piles up, and ongoing site audits now play a regular part in the landscape. We made hard choices to invest in overhead air scrubbers, real-time sensor arrays, and tighter digital batch tracking, finding it pays off in clean compliance records and staff retention. Training new staff for safe, efficient handling takes several months; no quick fixes exist here. Nitriles remain flagged as potential precursors for controlled substances, which means periodic coordination with customs agencies and regular paperwork. Those measures can feel cumbersome in the moment, but they have kept production running smoothly during periods that brought new scrutiny after international incidents or regulatory updates.
Waste handling is a perennial concern—thiophene byproducts often come with a sulfur punch, complicating incineration or solvent recovery. Partnering with specialty waste management firms, we process all effluents and regularly test output streams to keep compliance in check. Years of open communication with local agencies built trust, proving vital during crisis events or when scaling up after successful pilot runs.
Clients present ever-evolving requirements—traces of water below 0.1%, specific maximums for sulfur content, or unique packaging needs to accommodate automation on their end. Feedback from one major pharma customer prompted us to revamp drying procedures, ending up with batch quality that passed their high-throughput screening tests and led to repeat orders. Requests for eco-friendly alternatives or green manufacturing spurred us to tweak process chemistry, minimizing solvent use with each run. Facts speak louder than marketing—we’ve logged real reductions in carbon emissions and improved batch yields, passing those savings along without diluting product integrity.
Markets are sensitive to interruptions—natural disasters, port slowdowns, or raw material shortages all leave their traces. Our supply chain strategy rests on robust vendor relationships and holding buffer stocks to ride out turbulent months. Where global shipping falters, air freight steps in, although at far higher cost. The lesson always plays out the same: clients don’t tolerate excuses, only reliable delivery and a material that works in their syntheses.
Our lab and technical team field countless questions: reactivity with metallic sodium, behavior under hydrogenation, or stability in specific solvents. Over the years, we heard stories about plenty of competitor products—some worked in test reactions, others gummed up filters or left odd side-color in final products. Our own learning curve wasn’t flat; early runs of 2-thiopheneacetonitrile tarnished by sulfur or trace base cost time and trust. Only by logging test outcomes, collaborating with client labs, and running our own side-by-side assays did we find pathways to meaningful improvements.
A recurring request—differential scanning calorimetry data for thermal decomposition and expanded impurity panel analyses—shows the demands of modern synthesis and regulatory frameworks. Laboratory scale customers care less about drum shipping or moisture titrations, but we scale services to match, always chasing the intersection where production volume, purity, and analytical transparency meet usable, real-world material.
Our commitment to 2-thiopheneacetonitrile production stretches beyond routine batch runs. Serving the interface between chemical manufacturing and world-changing research offers lessons on the importance of reliability and accountability. With competition pressing from every corner, consistency remains our main edge. The market for specialized heterocycles grows as new pharmaceuticals, materials, and diagnostics rely on adaptable building blocks. Each year brings announcements for molecular electronics, new molecular imaging agents, or crop-protection platforms, all requiring new takes on old chemistry.
New challenges such as circular economy goals and increased product stewardship are no longer theoretical debates. We regularly participate in industry consortia to advance process optimization or environmental impact reduction. Years spent refining purification not only improve our bottom line, but also shrink our waste footprint, reflecting a true partnership with downstream users and the broader community.
Our approach to 2-thiopheneacetonitrile distillation, recovery of side streams, and minimizing off-gas aligns with a practical mindset: reduce risk, increase output, and keep environmental concerns front and center. Each plant operator holds direct responsibility over critical control points. Discussions about reaction bottlenecks, rework options for borderline specs, and design of safer loading docks pepper the daily meetings. Sometimes solutions arise from trial, error, and failure—cataloged and memorialized so newer staff avoid repeating old mistakes.
For current and prospective clients, our experience runs deeper than order forms. We encourage plant visitors to walk through the process, ask direct questions, and review documentation. Trust, over time, prevents misunderstandings and catch bottlenecks before they ripple down the supply chain. We remain transparent about capacity constraints and shifting regulatory frameworks, providing updates and alternatives where necessary—even partnering with customers on pilot projects to prove a new concept.
The chemical industry changes fast, pressuring every manufacturer to keep pace or fall behind. 2-Thiopheneacetonitrile occupies a unique niche: small in volume compared to bulk commodities, but mighty in its role building the next generation of molecules. Our experience in manufacturing it has shown the value of paying close attention at every step, from sourcing to end use. Building relationships with upstream vendors and downstream laboratories protects product quality and fosters resilience in the face of uncertainty. Every kilo shipped tells its own story of detail, vigilance, and adaptation—a sum of hard-won lessons from the factory floor to the client lab bench.
We take pride knowing our 2-thiopheneacetonitrile continues to help scientists make strides in pharmaceuticals, materials, and agricultural chemistry. Success rests on open communication, evidence from actual production, and earned trust, not marketing gloss. As we refine our processes and expand capacity, our focus remains steady: provide genuine value through reliable material, keep environmental impacts minimal, and always collaborate with customers—because their outcomes and our progress advance together.