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HS Code |
123165 |
| Cas Number | 4282-31-9 |
| Molecular Formula | C6H4O3S |
| Molecular Weight | 156.16 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 105-110 °C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CSC(=C1)C(=O)C(=O)O |
| Synonyms | Thiophene-2-glyoxylic acid |
| Storage Temperature | Store at 2-8 °C |
| Pka | Expected around 2.5-3.0 |
As an accredited 2-Thiopheneglyoxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Thiopheneglyoxylic Acid, 25g: Supplied in an amber glass bottle with a secure screw cap, labeled with hazard and handling information. |
| Shipping | 2-Thiopheneglyoxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It is packaged according to safety regulations for chemicals, typically in glass or plastic bottles inside cushioned, labeled boxes. Standard shipping includes documentation such as Safety Data Sheets (SDS) and complies with relevant hazardous material transport guidelines. |
| Storage | 2-Thiopheneglyoxylic Acid should be stored in a tightly sealed container, protected from moisture and light. Store in a cool, dry, and well-ventilated area, away from sources of heat and incompatible materials such as strong oxidizers. Keep the storage area clearly labeled and restrict access to trained personnel. Proper storage helps prevent decomposition and ensures safety. |
Applications of 2-Thiopheneglyoxylic Acid in Industrial ManufacturingAs the direct producer of 2-Thiopheneglyoxylic Acid, we support large-scale industrial clients who require precise control over synthesis, compliance, and integration for high-value downstream products. The following examples illustrate accepted industrial applications, compliance requirements, processing guidelines, and targeted end-uses across differentiated manufacturing sectors. 1. Pharmaceutical Intermediate for Anticonvulsant Drug SynthesisPharmaceutical manufacturers use 2-Thiopheneglyoxylic Acid as a core building block in the multistep synthesis of thiophene-based anticonvulsants, notably within the process routes of complex API development. Its reactivity, selectivity, and stability enable pharmaceutical-grade condensation with amines, driving the formation of molecular scaffolds for regulated therapeutic compounds. The intermediate is subject to intensive analytical QC, strict impurity profiles, and lot traceability throughout cGMP production streams, with all batch records retained for regulatory inspection. Industry compliance standards
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2. Agrochemical Synthesis—Herbicide Active Ingredient ManufacturingMajor agrochemical processors employ 2-Thiopheneglyoxylic Acid in the manufacture of specific thiophene-derivative herbicide actives. The raw material supports the electrophilic condensation steps with nitrogen or sulfur nucleophiles, delivering targeted activity profiles and adaptation to environmental regulations. Careful monitoring ensures low sulfoxide byproduct and conformance to industrial purity standards for downstream formulation and field registration. Scale-up facilities utilize closed-system reactors for environmental and personnel safety. Industry compliance standards
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3. Organic Electronics—Functional Material PrecursorIn advanced materials chemistry, electronic component manufacturers utilize 2-Thiopheneglyoxylic Acid as a core precursor in the synthesis of conjugated thiophene-polymers and small molecules targeted for organic semiconductors. Its integration within cross-coupling reactions forms essential building blocks for improved charge transport and flexibility—crucial for the next-generation OLED, OFET, and photovoltaic devices. Strict control over moisture, impurities, and S-containing residues underpins the consistency needed in high-value electronics fabrication. Industry compliance standards
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4. Specialty Dye Intermediates—Synthesis for Textile and Ink IndustriesDye and pigment manufacturers use 2-Thiopheneglyoxylic Acid to introduce sulfur- and heteroaromatic structures in complex dye intermediates. It is charged at controlled process points in order to achieve extended chromophore systems within specialty dyes, supporting requirements for high colorfastness and resistance to light, washing, and oxidants. Quality assurance emphasizes batch purity, heavy metal absence, and absence of restricted amines to meet downstream textile and ink standards. Application also mandates documentation of residual sulfur compounds in compliance with EU and international standards for eco-friendly dyes. Industry compliance standards
Typical usage ratio
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We have handled countless raw materials over the years, but few specialty acids pique as much attention as 2-Thiopheneglyoxylic Acid. Our facility produces this compound with a focus sharpened by practical understanding of its place within research and industrial settings. This acid emerges from a methodical synthesis in which every step—not only those guided by protocol—receives careful hands-on monitoring. You need more than routine paperwork when working with reactive intermediates; you need process intuition garnered through years on the floor and repeated quality testing.
Our main model for 2-Thiopheneglyoxylic Acid balances reliable yield with high purity, minimizing impurities such as halide or sulfurby-products. From raw thiophene stock, a controlled oxidation gives the glyoxylic sidechain, usually yielding a fine crystalline powder. We do not just look at purity in black and white terms; we track residual solvents and actual elemental composition because reactions—even microscale—respond sensitively to “hidden” anomalies.
Typical specifications: bright off-white appearance, melting point close to 110-115°C, and assay above 98% by HPLC. Handling batches ourselves, we see the connections between subtle shifts in synthesis (like altering oxidant concentration) and downstream product performance. These specifications did not originate in a vacuum; years of feedback from users in medicinal chemistry, polymer development, and material science shaped this detailed picture.
In the lab, 2-Thiopheneglyoxylic Acid plays a role far more compelling than stated in a catalogue entry. Academic groups pursue new heterocyclic drugs, finding that the thiophene ring, with its electronic twist, often brings biological relevance. Production-scale users request the acid for step-up reactions, especially those building blocks where a carboxylic acid adjacent to an aromatic sulfur ring offers a direct synthetic handle. People use it for coupling with amines or alcohols, forming esters or amides—scaffolds that go back into libraries for biological or physical testing.
We often field requests from teams pushing beyond classic pharmaceuticals. Some are exploring the acid as a precursor to custom ligands in catalysis. Others rely on its structure to influence conductivity or thermal characteristics in new materials. Our experience producing and shipping this acid has taught us that reliable characterization and clean crystalline form directly impact reproducibility in their work. Even the consistency of particle size cannot be underestimated: uneven grains cause metering errors, splash, and delayed reaction completion—every operator at our plant knows the headaches caused when physical quality drops half a grade.
Customers often ask: what makes 2-Thiopheneglyoxylic Acid unique compared to other arylglyoxylic acids, like phenylglyoxylic or 2-furylglyoxylic acids? Our perspective is rooted in months and years of side-by-side processing. The answer involves more than structural diagrams: direct experience shows real synthetic advantages. The thiophene ring imparts both greater electron density and sulfur ability to delocalize charge, making downstream reactions—in particular, nucleophilic attacks at the glyoxylic carbonyl—more tractable in many heterocycle-forming steps. This feature helps when you need to finely tune selectivity, especially in systems prone to unwanted side-reactions.
Phenylglyoxylic acid delivers strong utility in basic aromatic settings yet misses opportunities for extended conjugation and electron modification. The furan analog, with an oxygen heteroatom, brings its own subtle behaviors, sometimes making certain final compounds overly reactive to degradation. 2-Thiopheneglyoxylic Acid sits between these options, striking a balance that appeals to synthetic chemists after months spent troubleshooting yields or avoiding product instability. You see these lessons in the design of drug candidates and advanced materials: sulfur rings withstand harsher conditions yet do not hinder reactivity at the glyoxylic group.
Practically, this acid often enters reactions at lower activation energies. We trace this to the electron-donating character of the sulfur adjacent to the carboxylate. Feedback from material chemists backs this up: polymer modifications respond smoother, and small-molecule targets incorporate the acid with fewer side-products than with basic aromatic analogs.
Consistency is not just a checkmark on a certificate. Each batch of 2-Thiopheneglyoxylic Acid carries a signature defined by the subtle, accumulated habits in our production line. We watch not only for correct melting point and purity by testing, but also look for color changes, flowability, and dryness. Simple factors—like how many hours the product spends in final vacuum drying—mean the difference between a stable, easily soluble powder and a stubborn, sluggish mass. Analysts from pharmaceutical or research settings tell us a poor batch creates days of extra troubleshooting. Cost or delay, from incomplete dissolution, offsets any savings found in generic supplies.
We keep our 2-Thiopheneglyoxylic Acid under nitrogen in moisture-controlled rooms. Past experience tells us even trace humidity kicks off hydrolysis and slight yellowing. In one instance, a transport delay led to several barrels arriving with caked clumps near the edge—small issue, yet over weeks the off-color and microimpurities showed up in client HPLC traces. After adjustments, tighter regulations on sealing and desiccant use have paid off. End users recognize the extra care since their own purity checks match ours. We never claim zero deviations, but every incident feeds back into training for our storage staff and field team.
We also date every shipment with real manufacture and drying times—not just “lot” numbers, but true origin so that clients can trace performance shifts. These small markers have allowed teams to correlate analytical hiccups to a specific shipping date and environment, not only batch formula.
Our work does not end at dispatch. We often consult with chemists debugging a stuck amidation or an unexpected side product. Many stories repeat: optimization efforts fail because an off-brand acid didn’t dissolve predictably, or an impurity derailed a sensitive step. In those cases, honest dialogue reveals the need for better testing or even altering the way we finish each batch.
One research team encountered variable crystal shapes that altered solubility in DMSO, throwing off assay reproducibility. We responded by tweaking our crystallization solvent system, producing a consistently more manageable powder morphology. Such incidents build trust, but—more importantly—they remind us that specification sheets only go so far. What happens on the bench or production line drives our iterative process.
Our collaborations with university labs and industrial R&D often uncover new uses. Some clients use 2-Thiopheneglyoxylic Acid’s unique ring system to probe mechanisms in photochemical switches. Others test its suitability as a sulfur source in layered materials research. We learn as much from failed experiments as from successes, especially when feedback points to issues in stability or unexpected reactivity. Every cycle of insight leads to small refinements—sometimes barely noticeable in a paperwork sense, but critical for actual results.
As new customers enter the field, we notice a greater emphasis on provenance and responsible chemistry. Our supply chain for 2-Thiopheneglyoxylic Acid now includes measures ensuring our thiophene feedstock comes from reputable, transparent sources, minimizing environmental risks from the upstream process. Many clients—especially those pursuing regulatory approval—query the sourcing as much as the purity.
We have adopted periodic audits and share summaries with long-term buyers. Where older models focused only on end purity, our plant now measures energy use, solvent recovery, and waste neutralization with each run. Chemical manufacturing is evolving, and adoption of green chemistry principles fits naturally with the improvements demanded by researchers and manufacturers alike.
2-Thiopheneglyoxylic Acid keeps finding new homes outside its traditional applications. In organic electronics, researchers are leveraging the sulfur-rich ring to increase charge mobility in thin films and polymer blends. Each year, new patents and papers cite its ability to anchor functional groups for advanced electronics. Several of our contacts in France and Japan have shifted some aromatic carboxylic acid purchases to the thiophene variant, drawn by its combination of thermal stability and chemical accessibility in device fabrication.
In the synthesis of bioactive molecules, optimization stories sometimes seem routine—but using 2-Thiopheneglyoxylic Acid spurs creative strategies that wouldn’t work with more inert options. The electron-rich backbone allows precise control over coupling sites, influencing biological compatibility and metabolic resilience once compounds enter cell-based assays.
Scaling up production of this specialty acid brings hurdles more complicated than toggling between batch sizes. At smaller scales, reaction parameters and product form remain under tight watch. On larger lines, even modest changes—like flow rate of oxidizers or dwell time in filtration—change crystalline form as well as the impurity profile. Our plant underwent several cycles of troubleshooting when larger glass-lined reactors brought new types of sticking and localized overheating. Adjusting agitation speed and jacket cooling improved process control.
We encountered unique clumping in some large-scale drying units. The root cause: minor residue in the condenser line offset solvent removal rate, allowing wet pockets to coalesce and resist drying. Now, we double-check this area before each production cycle, and log any observed drift in drying curves. Routine, yes, but every plant operator can recount a costly delay caused by overlooking these “minor” technical fixes.
Customers who attempt in-house synthesis often express frustration at similar hurdles. Their feedback validates our observation that mastering the details—consistent feeding, careful monitoring of temperature, precise addition sequences—determines the outcome more than any single “recipe.” In supporting them, we do not hold back know-how: we share our process tweaks where possible, helping their scale-up or lab prep perform as expected. These exchanges sustain an ecosystem of reliable chemical development.
Experience on the plant floor has taught our staff to respect both the strengths and hazards of 2-Thiopheneglyoxylic Acid. Although less noxious than aggressive acyl chlorides or peroxides, prolonged exposure or poor ventilation can exacerbate respiratory or skin sensitivity in certain users. We invest in regular training, reinforced procedures, and prompt substitution of worn-out PPE.
Direct transfer from reaction vessel to containment by staff trained to recognize early signs of cross-contamination means end-users rarely report off-batches linked to manual error. This vigilance—born of practical mistakes over decades—has led to a reduction in product loss and downstream customer complaints.
Safe, reliable product handling across continents, seasons, and customs inspections marks a mature operation. Moisture control, as mentioned, stays a top priority, but so does ensuring staff turnover never leads to knowledge loss. Documenting each nuance of the prep, transfer, and testing safeguards not only our output but also our role as supply partner rather than mere bulk vendor.
Our business reflects more than volume shipped. We recognize that every gram of 2-Thiopheneglyoxylic Acid represents experimental investment by clients worldwide. By anchoring our production in documented results and ongoing dialogue, we keep refining not only our product but also our readiness to support entirely new syntheses as science advances.
We welcome partnerships, whether troubleshooting a tricky coupling, fine-tuning a batch for solubility, or reviewing upstream feedstock to meet new regulatory expectations. Every successful project, every lesson from a batch that fails to meet an ambitious spec, adds to the knowledge underlying our product.
Years of focused manufacture taught us that real quality comes not from an isolated certificate, but from thousands of small, sometimes unseen adjustments. Beyond the certificate and the checklists, experience-driven manufacturing roots each vial and drum firmly in the practical needs of real-world chemists. Our commitment holds steady as applications expand, and we continue to see new directions emerging for 2-Thiopheneglyoxylic Acid across research and industry.