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2-Cyanothioacetamide

    • Product Name 2-Cyanothioacetamide
    • Alias 2-cyano-2-thioacetamide
    • Einecs EINECS 224-338-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    760726

    Cas Number 14047-28-0
    Molecular Formula C3H4N2S
    Molecular Weight 100.14
    Appearance White to off-white crystalline powder
    Melting Point 152-154°C
    Solubility Slightly soluble in water
    Synonyms 2-Cyanoethanethioamide
    Smiles C(C#N)C(=S)N
    Inchi InChI=1S/C3H4N2S/c4-2-1-3(5)6/h1H2,(H2,5,6)
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Purity Typically ≥98%

    As an accredited 2-Cyanothioacetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Cyanothioacetamide is packaged in a tightly sealed, amber glass bottle, 25 grams, labeled with hazard symbols and chemical identification.
    Shipping 2-Cyanothioacetamide should be shipped in tightly sealed containers under cool, dry conditions. It must be protected from moisture and incompatible materials, following all applicable regulations for hazardous chemicals. Proper labeling, packaging, and documentation are required to ensure safe and compliant transport. Handle with care to prevent spills or exposure.
    Storage 2-Cyanothioacetamide should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed when not in use, and protect from moisture and direct sunlight. Store in a labeled, chemical-resistant container and follow all relevant safety and regulatory guidelines for hazardous chemicals.
    Application of 2-Cyanothioacetamide

    Applications of 2-Cyanothioacetamide in Industrial Manufacturing

    As the manufacturing originator, we support multiple downstream industries with high-purity 2-Cyanothioacetamide, meeting strict quality benchmarks. Below, we outline several specialized industrial applications, providing detailed compliance, recommended ratios, integration details, and resulting products.

    1. Pharmaceutical Intermediate Synthesis

    2-Cyanothioacetamide functions as a key intermediate in manufacturing certain active pharmaceutical ingredients, especially for thiazole and thiadiazole derivatives. Pharmaceutical producers carry out ring-closure reactions, condensation, and further functionalization steps, integrating 2-Cyanothioacetamide to generate targeted medicinal molecules. The compound’s high purity is critical for downstream process yields and regulatory filings. Segregated production, validated analytical controls, and traceability of batch records are required for global pharma supply.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia quality monograph references for intermediates
    • DMF support documentation upon request for regulatory submission

    Typical usage ratio

    • 0.95–1.10 mole equivalents per target API intermediate, altered per route optimization data and process scale

    Downstream process integration

    • Introduced as a starting substrate for heterocycle-forming condensation step in multi-stage synthesis
    • Requires pre-dissolving in compatible solvent, typically ethanol or DMF, under nitrogen atmosphere
    • Incorporation monitored by in-process HPLC/GC to control unreacted material

    Final product types

    • Thiazole-based API precursors
    • Thiadiazole derivatives for antimicrobial or anti-inflammatory medications
    • Nitrogen- and sulfur-containing heterocyclic drug candidates

    2. Agrochemical Synthesis

    Major agrochemical companies use 2-Cyanothioacetamide as a sulfur-nitrogen donor for synthesis of fungicide and pesticide intermediates. The compound enables cost-effective construction of bioactive scaffolds such as 1,3,4-thiadiazoles, used in plant protection agents. Formulation must follow both environmental impact studies and international standards for pesticide manufacturing.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH Regulation (EC) No. 1907/2006 for handling and safety
    • ISO 9001:2015 quality management systems for batch consistency
    • GLP (Good Laboratory Practice, OECD) for toxicology studies

    Typical usage ratio

    • 0.75–1.05 mole per target heterocycle, depending on conversion yield and downstream purification demands

    Downstream process integration

    • Added in the cyclization phase with hydrazine and other nitrogen reagents
    • Process conditions: 20–40°C, monitored for byproduct control and impurity removal
    • Critical parameter: pH maintained between 7.5–8.5 during reaction

    Final product types

    • 1,3,4-Thiadiazole-based fungicides
    • Precursor intermediates for insecticidal formulations
    • Crop protection agents for cereal and vegetable seeds

    3. Fine Chemical & Dye Intermediate

    Manufacturers of specialty dyes and pigments utilize 2-Cyanothioacetamide to construct sulfur- and nitrogen-containing chromophore systems. The compound undergoes condensation with aromatic aldehydes and diazo components, tailoring optical properties for advanced applications. Material quality and trace metal residues are tightly controlled to meet downstream performance requirements such as color stability and solubility.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys—migration of certain elements, for end-use pigments
    • ISO 13320:2020 Particle size analysis—compliance for dispersibility
    • Oeko-Tex Standard 100 for textiles dyeing agents (where applicable)
    • Customer-specific restricted substance lists (RSL) for coatings & ink industry

    Typical usage ratio

    • 5–15% w/w in pigment precursor batch, adjustable per color intensity requirements and batch scale

    Downstream process integration

    • Introduced during initial mixing phase (aqueous or solvent-based medium)
    • Sequential addition to maximize conversion to desired dye or pigment backbone
    • QC by UV/Vis spectroscopy for completed chromophore structure

    Final product types

    • Sulfur-rich azo dyes for textiles
    • Custom pigments for industrial coatings
    • Organic dye intermediates for inkjet inks and plastics coloration

    4. Flotation Agent Precursor for Mining Industry

    Producers of mineral flotation reagents employ 2-Cyanothioacetamide as a chemical precursor for synthesizing sulfur-nitrogen flotation agents, which enhance selectivity in sulfide ore processing. The compound’s consistency and sulfur content allow precise formulation of collectors, modifying mineral surface properties during ore concentration steps. All batch documentation and test data must support environmental release and downstream residue minimization targets for global mining operations.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • Global Mining Guidelines Group (GMG) for reagent characterization
    • National and local mining water discharge limits for reagent residues
    • Internal QC validation per customer flotation performance labs

    Typical usage ratio

    • 7–12% w/w as a precursor for collector synthesis, adjusted for targeted ore type and flotation kinetics

    Downstream process integration

    • Feeds into collector synthesis via reaction with alkali and amines
    • Final flotation agent blended into aqueous slurry during ore separation
    • Monitoring of reagent stability and decomposition under process conditions

    Final product types

    • Sulfur-nitrogen flotation collectors
    • Selective sulfide ore separation additives
    • Specialty mining chemicals for mineral concentration systems
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    Certification & Compliance
    More Introduction

    2-Cyanothioacetamide: Our Commitment to Reliable, High-Purity Chemical Synthesis

    Introduction to 2-Cyanothioacetamide

    Chemists know the pain of inconsistent reagents. Our 2-Cyanothioacetamide stands out for long-term reliability and straightforward handling in both R&D and manufacturing. Over the years, production challenges and market shifts have shown us the importance of a consistent process. This compound, bearing CAS number 7585-39-9, remains a valuable building block across several industries. Its molecular formula, C3H4N2S, with a molar mass of 100.14 g/mol, lends itself to a versatile role in organic synthesis.

    A Closer Look at Purity and Handling

    Our production team pays attention to details that others sometimes overlook. From raw material selection to crystallization and packaging, we have refined and stress-tested every step over years on the shop floor. Laboratory feedback confirmed a recurring issue from other sources: inconsistent particle sizes and varying impurity levels would create headaches downstream. We addressed this directly with more rigorous intermediate filtration and precise temperature controls. Current batches reach purity consistently above 99 percent by HPLC, with no dust or unknown specks that could result in side reactions later. Even under heavy demand, the process runs at scale without deviation from the original specs.

    How End-Users Leverage 2-Cyanothioacetamide

    2-Cyanothioacetamide finds its way into countless research programs and manufacturing setups. During visits with industrial clients, we’ve seen it transform intermediates that ultimately shape medicines, agrochemicals, and colorants. Its reactivity results from the juxtaposition of cyano and thioacetamide groups, which brings unique possibilities in heterocyclic chemistry and pharmaceutical lead compound design.

    For example, several synthetic routes to pyrimidine and thiazole derivatives use 2-Cyanothioacetamide as a key C-N-S donor. Researchers cite shorter steps and cleaner conversions compared to using separate cyanide or thioamide components. Over time, this has reduced costs and waste in plants running at industrial volumes. Labs working on antimicrobial or antifungal compounds report higher consistency and fewer rework cycles. Production yields benefit directly. Students in academic labs tell us they waste less time troubleshooting impurities—reaction mixtures simply behave more predictably.

    In the Plant: Lessons Learned in Scale-Up

    Scaling specialty chemicals presents daily surprises. Most synthetic chemistries look neat in the textbook or bench top, but running several kiloliters per shift exposes hidden flaws. Early in our experience, we battled instability during the solidification stage—the choice of solvents, cooling rates, and holding times all created variability in the final product. After a few years, we discovered that strict humidity controls in the crystallization room and a switch to stainless steel containment eliminated several chronic failures.

    Today, we rely on monitored nitrogen blanketing to keep oxidation away. Every lot is checked onsite for free thiol and amide impurities before shipment. Our QA supervisor once caught a suspicious brown tint in a sample, which traced back to an upstream supplier’s contaminated ammonia. That day reminded us that vigilance pays off, as colored impurities wreak havoc in sensitive photoreactive applications downstream.

    What Sets Our 2-Cyanothioacetamide Apart

    Having supplied grams to tons for decades, we reserve some pride in the subtle engineering behind this product. Our process achieves a stable crystalline powder with low residual solvent levels and virtually no detectable moisture by KF (Karl Fischer titration). The substance transitions easily between powder, suspension, or solution; this gives formulators much-needed flexibility. Some competitors in the market bring in material that tends to clump or cake, especially in humid storage. We never shy away from discussing how we tackle this issue—adding a minor step to guarantee batch-to-batch free-flowing physical form.

    Quality control is more than a checklist for our team. Routine IR and NMR fingerprinting sounds mundane, but we have caught minor process shifts before they caused downstream problems. Manufacturers who ignore small stepwise chromatogram drifts often pay in returns or scrap. By investing in regular staff training and keeping instrumentation current, our deviations remain close to zero. As a result, our clients, from pharma API pilot plants to dye and pigment blenders, count on our batches to behave the same with each shipment.

    Feedback from process chemists guided us to lower the sodium and chloride content, which previously complicated organometallic syntheses. This reduction helps in those labs that follow GMP guidelines, as fewer downstream solvents are required for washing. We've also reduced the detectable range of heavy metals far below common technical grade suppliers through double recrystallization methods. These improvements did not come from market pressure, but from long-standing relationships with researchers and engineers frustrated by poorly controlled intermediates.

    Applications Highlighted by Real-World Use

    Those on the synthesis side recognize how a better intermediate streamlines innovation. In agricultural chemistry, 2-Cyanothioacetamide serves as a linchpin for preparing new herbicide scaffolds. We support agricultural R&D houses testing for efficacy and environmental breakdown, which demand tight analytical reports and repeatable results. In fine chemicals, several pigment and dye producers rely on our material as a reliable sulfur-nitrile source; their engineers have told us clean, pale crystals prevent color contamination at source.

    Therapeutics also rely on this compound. Process optimizations in beta-lactamase inhibitors and similar drug candidates often revolve around C-N-S couplings and ring construction. Chemists prefer predictable reaction profiles, and our product delivers batch-to-batch. Sometimes the difference between a smooth scale-up and lost weeks comes down to ridding trace contaminants and knowing granulation won’t change overnight. For older catalogues of peptides, nucleotides, and specialty APIs, we have supported teams by sharing years of stability data under different storage and shipping conditions. That institutional memory cuts project risk measurably.

    Ongoing Challenges and Further Improvements

    No chemist will claim perfection. Every cycle, our team reviews yield data, impurity profiles, and customer feedback. A recurring request from some long-term clients is for customizable particle size distributions for specific reactors. While tight protocols are in place, specialty orders sometimes require equipment retooling and manual sieving. We make these accommodations, knowing that collaboration often leads to new process insights for us as well as our customers.

    Logistics sometimes present bigger hurdles than the chemistry itself. International shipping calls for compliance with changing regulatory rules, safe labeling, and temperature control. Adapting to stricter transport thresholds for thioamide substances, we proactively reached out to technical agencies and now offer sealed, double-bagged drums for intercontinental loads. This extra step minimizes contamination risk and meets heightened scrutiny from customs agencies in high-regulation markets. Engaging in pre-shipment technical assessments with partners helps reduce return rates, a pain no manufacturer wants to experience twice.

    Occasionally, researchers propose scaling to volumes where offgassing of volatile impurities could risk plant safety. To mitigate, we invested in stronger vapor traps and pressure checks in our granulation section. Open communication with plant safety officers at client sites ensures that new uses or experimental processes are matched by tweaks in our packaging and documentation.

    Comparing 2-Cyanothioacetamide to Other Specialty Intermediates

    Navigating the crowded field of chemical intermediates has taught us that surface similarities don't guarantee interchangeable function. Specialty nitriles and thioacetamides often overlay in catalogs, but cross-use in the plant wipes away the paper similarities. For example, regular thioacetamide lacks the additional activation delivered by the cyano group in this compound. That extra functionality opens up synthetic options that would otherwise require multiple steps or harsh conditions.

    Compared to other cyano-bearing compounds, 2-Cyanothioacetamide introduces a softer reaction profile for S-substitution and cyclization reactions, avoiding the sudden side reactions that make batch scaleup unpredictable. Many teams migrating from separate nitrile and thioamide feeds see immediate benefits in simplified inventory and lower risk when handling toxic or waste-prone reagents. Our own records show reduced on-site hazardous waste volume over the years after such process switches. These operational improvements compound into bottom-line benefits that matter to both plant managers and sustainability auditors.

    Some new customers ask about substituting higher-purity technical or analytical thioamides, only to discover that the extra process steps do not offset the improved cleanliness and predictable reactivity of our product. With 2-Cyanothioacetamide, yields stand stronger across a range of reaction types and volumes, minimizing wasted time and material. Scientific journals may focus on the theoretical yields, but plant chemists see the advantages in real throughput and less downtime.

    Supporting Innovation and Training

    Chemistry is ultimately about sharing hard-won knowledge. We believe in supporting the next generation. We offer tailored support to universities and research institutes, not just by supplying material but also by sharing process notes and troubleshooting insight that comes from years on the line. During training sessions for new hires, we use our own experiences with 2-Cyanothioacetamide to illustrate the pitfalls and problem-solving approaches necessary for routine and novel synthetic work alike.

    As new fields arise—beyond pharmaceuticals and agrochemicals, like advanced materials and functional dyes—our team engages actively with innovators who aim to push boundaries. Cross-discipline conversations help us spot upcoming demand well before textbook routes appear in the literature. Our continuous feedback loop with customers and academic collaborators allows us to maintain production flexibility while sustaining quality standards you rarely see from short-term traders or importers.

    By staying hands-on with batch process improvements and taking customer problems seriously, we continue to evolve. Our improvements reflect more than just profit motives—they build trust with every researcher, process engineer, and plant manager who relies on our intermediate to meet ambitious project goals.

    Conclusion: Why 2-Cyanothioacetamide Remains a Go-To Choice

    Chemical manufacture is a field where long-term commitments matter. We've devoted years to looping back every bit of feedback from plant, lab, and product teams into the heart of our 2-Cyanothioacetamide process. The difference is tangible: higher purity, faster dissolution or blending, traceable supply, and reliable documentation at every stage from synthesis to delivery.

    Choosing a specialty intermediate should never come down to price or a slick catalog photo. Performance in the real world, backed by detailed technical support and a culture of continuous improvement, puts us where clients need us. As new challenges and industry needs surface, we pledge to remain close to those on the frontlines doing the chemistry—offering insight, hard-earned experience, and a product that simply works as promised.