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2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid

    • Product Name 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid
    • Alias TTC
    • Einecs 619-608-5
    • 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
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    Specifications

    HS Code

    289781

    Product Name 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid
    Cas Number 129458-45-3
    Molecular Formula C8H7NO2S2
    Molecular Weight 213.28 g/mol
    Appearance White to off-white solid
    Melting Point 180-185°C
    Purity Typically ≥ 98%
    Solubility Soluble in DMSO and methanol, slightly soluble in water
    Storage Temperature 2-8°C
    Iupac Name 2-(thiophen-2-yl)-1,3-thiazolidine-4-carboxylic acid
    Smiles C1C(NC(S1)C2=CC=CS2)C(=O)O
    Synonyms 2-(2-Thienyl)thiazolidine-4-carboxylic acid

    As an accredited 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 25 grams of 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid, labeled with chemical name and hazard warnings.
    Shipping 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid is shipped in secure, sealed containers to prevent contamination and degradation. Packages are clearly labeled and handled according to standard chemical transport regulations, including protection from moisture and extreme temperatures, and dispatched via certified carriers for safe, compliant, and prompt delivery.
    Storage Store 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Label the container clearly and avoid prolonged exposure to air. Follow standard laboratory safety protocols and local regulations for chemical storage.
    Application of 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid

    Applications of 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid in Industrial Manufacturing

    Our company supplies 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid as an advanced intermediate for multiple high-value, regulated industrial sectors. The following sections detail real downstream usage scenarios, specifying compliance, formulation, integration, and finished product types for each application area.

    1. Active Pharmaceutical Ingredient Synthesis for Antimicrobial Agents

    Pharmaceutical manufacturers employ 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid as a core intermediate in multi-step syntheses of new-generation beta-lactam antimicrobial APIs. This thiazolidine derivative forms a key building block for penem and carbapenem structures, crucial for Gram-negative bacterial coverage. Our clients utilize this material following strict cGMP protocols, ensuring full traceability and batch consistency. Process chemists incorporate it in amidation and cyclization steps, optimizing yield and minimizing impurity profile to meet international registration dossiers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directive 2003/94/EC for medicinal substance production
    • USP/EP/BP monograph expectations for final APIs
    • FDA 21 CFR Part 211 controls in US-regulated facilities

    Typical usage ratio

    • Usage typically ranges from 0.18 to 0.35 mol per mol of target API, based on coupling efficiency and desired yield.
    • Process scale can vary from kilo-lab up to several hundred kilograms batch size depending on target commercial volumes.

    Downstream process integration

    • Introduced after initial condensation stages, participating in cyclization to form the heterocyclic core of the pharmaceutical agent.
    • Followed by downstream hydrolysis, purification, and crystallization for bulk API isolation.
    • Subjected to in-process HPLC and NMR analysis for impurity and identity confirmation at each stage.

    Final product types

    • Sterile injectable beta-lactam antibiotics (penems, carbapenems)
    • Oral solid dose tablets for hospital and prescription markets
    • Finished bulk APIs for secondary formulating partners
    • Development-stage investigational drug substances

    2. Advanced Agrochemical Building Block for Fungicide Formulations

    Producers of crop protection agents incorporate this thiazolidine acid for constructing heterocyclic fungicide actives. This intermediate contributes to synthesis routes for thiophene-modified thiazolidine derivatives, required in formulations targeting cereal and rice blight diseases. Agrochemical formulation teams closely monitor process conditions and impurity specifications to comply with global pesticide registration and export market requirements.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • ISO 9001:2015 certified QC and traceability
    • China ICAMA registration for agricultural chemicals
    • REACH (EC 1907/2006) registration for European exports

    Typical usage ratio

    • Employed at 0.12–0.24 mol per mol of final actives, adjusted based on specific molecular architecture and synthesis efficiency.
    • Scalable between lab pilot (10 L reactor scale) and commercial bulk (1–5 tonne) batches dependent on annual campaign volumes.

    Downstream process integration

    • Added post-initial thiophene coupling to form key heterocycle structure of fungicidal active.
    • Followed by one-pot or staged oxidation and chlorination, then formulation blending with safeners and carrier excipients.
    • End-of-line analysis by GC-MS and HPLC for regulatory dossiers.

    Final product types

    • Emulsifiable concentrate fungicides (EC)
    • Wettable powder actives for field mixing
    • Granular systemic crop treatments for rice, wheat, and barley
    • Technical grade intermediates for offshore formulation

    3. Specialty Monomer for High-Performance Polythiazolidine Polymer Resins

    Industrial polymer manufacturers utilize this thiazolidine acid as a specialty monomer in synthesis of high-performance, electrically conductive polymer resins. The material provides thiophene-thiazolidine conjugation essential for anti-static coatings, flexible printed circuit substrates, and OLED encapsulation sheets. Operators maintain tight process control on monomer purity and reactivity, adhering to downstream application safety and material performance standards.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for quality and environmental controls in polymer synthesis
    • RoHS Directive 2011/65/EU for electronic device component manufacture
    • REACH Annex XVII substance restriction verification
    • UL 94 flammability testing for electronic-grade polymers

    Typical usage ratio

    • Incorporated at 1.5–8 wt% of total monomer batch, depending on targeted electrical conductivity and polymer matrix.
    • Higher loading for conductive films, lower ratios for blend reinforcement.

    Downstream process integration

    • Charged into pre-polymerization vessel with solvent carrier and other functional monomers.
    • Polycondensation proceeds at controlled temperature (80–160°C), initiated via radical or acid catalysis.
    • Product isolated by solvent removal and extrusion, followed by post-polymerization curing for mechanical optimization.

    Final product types

    • Anti-static floor coatings for electronics manufacturing
    • Flexible circuit board base films
    • EMI shielding materials for telecom
    • OLED and flexible display encapsulation sheets

    4. Chemical Intermediate in Diagnostic Reagent Synthesis

    Manufacturers of in vitro diagnostics use 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid to synthesize specialty chromogenic and fluorogenic probes. The thienyl-thiazolidine core allows targeted derivatization, enabling sensitive detection methods for biomedical analytes in immunoassays and enzymatic screening platforms. Production requires stringent batch release and traceability, with rigorous impurity and performance checks to satisfy regulatory demands for clinical testing materials.

    Industry compliance standards

    • ISO 13485:2016 for medical device component manufacturing
    • US FDA QSR 21 CFR Part 820 for in vitro diagnostics
    • EU IVDR (Regulation 2017/746) for diagnostic reagent approval
    • CLSI guideline-based batch QC for clinical laboratory use

    Typical usage ratio

    • Ranging from 0.02–0.09 mol per mol in probe precursor synthesis, tailored to desired probe yield and labeling efficiency.
    • Scalable from gram-level research syntheses to commercial kilogram lots.

    Downstream process integration

    • Used in nucleophilic substitution and amide coupling stages to introduce fluorescent or chromogenic signal groups.
    • Purified by recrystallization or preparative HPLC to remove byproducts before labeling conjugation.
    • Subsequent integration into bulk diagnostic reagent blending and lyophilization packaging.

    Final product types

    • Enzyme-driven colorimetric test kits (clinical diagnostics)
    • Fluorescent immunoassay tracers
    • Chromogenic marker panels for biochemical analyzers
    • Research-use-only (RUO) kit markers for academic and industrial labs
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    Certification & Compliance
    More Introduction

    2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid: Practical Value from a Manufacturer’s Eye

    Understanding 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid in Real Work

    Years on the shop floor and in the lab have taught us that every molecule has a story. 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid isn’t just a name on an order sheet. This compound, shaped by its thiazolidine and thienyl units, gets chosen by people solving difficult synthesis and research tasks. When you work day in and day out with heterocyclic compounds, you notice details that don’t hit the catalog pages: stability under pressure, ease of purification, performance in condensation and coupling steps.

    We started producing this acid when colleagues in pharmaceutical research described their headaches with similar building blocks. Many complained about batch inconsistency — awkward melting behaviors, discoloration, unreliable reactivity — coming from the pickup points in global supply. These add up to lost time and wasted funding for scientists running tight experiments. So we looked into process design, batch monitoring, and analytical feedback to nail down reproducibility.

    Direct-From-Plant Experience Shapes the Product Model

    Fresh runs of 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid come off our reactors at volume, using controlled thermal cycling and timing to drive the formation of the five-membered thiazolidine ring with its carboxylic acid corner. Batch by batch, adjustments to solvent ratios and temperature curves made a real difference. Final product forms into a fine, pale solid, easily handled without clumping and reliably stable even after months in sealed packaging.

    We run purity checks with both HPLC and IR, mapping out the fingerprint stretches so customers know what to expect. Over time, we’ve recorded typical purity in the 98-99% range, and rarely find ourselves below that. Moisture content stays low: process-side drying and rapid packing lets us ship with controlled water levels, avoiding complications in downstream coupling or acylation. These details separate what rolls out of our production lines from generics circulating without documentation or quality tracking.

    Typical Applications: Stories from the Field

    2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid plays a real role in new molecule construction. Many teams in medicinal chemistry use it as the backbone for designing small molecule ligands or intermediates, as the thienyl structure can add unique electronic and spatial properties. Some researchers describe how the compound’s profile – combining aromatic sulfur with the thiazolidine motif – leads to better selectivity in binding screens. Others point out how it forms clean intermediates for making thiazolidine-linked peptides or analogs, helping streamline their workflow.

    Our experience matches theirs: it dissolves cleanly in DMF and DMSO, allows for predictable coupling reactions, and the thiazolidine ring holds up through mild acid or base treatment. More than a few of our customers order in series, testing structure-activity relationships (SAR) across panels of thiazolidine carboxylic acids. Consistent performance in coupling and functionalization reactions helps develop drug candidates quickly. We’ve also heard anecdotes about its use in agrochemical and specialty polymer research, though the largest volume moves to pharmaceuticals and chemical biology.

    Why Our Process Makes a Difference

    We manufacture at scale, starting from thienyl aldehyde and cysteine derivatives, using reliable condensation reactions. Process optimization, including the tuning of pH, temperature, and solvent polarity, plays a real role in ensuring a high yield and avoiding byproduct formation. We monitor batches for off-color products or unreacted starting materials and quickly adjust protocols based on analytical data. For us, the challenge always lies in scaling without losing control over fine reaction details.

    Our plant layout grants us close oversight. Operators watch critical points, and every step — from filtration to drying — happens under one roof. This avoids delays that can let product degrade or attract impurities. Fielding questions from formulation chemists, we can give clear explanations about the synthesis path, solvent system, and residual impurity profile, down to specific peak areas. This transparency, built into our workflow, lets research partners model risk and plan their critical steps with more confidence.

    Comparing 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid to Similar Compounds

    Not all thiazolidine carboxylic acids act the same in labwork. Substitutions on the thiazolidine or the aromatic ring change solubility, reactivity, and downstream compatibility. 2-(2-Thienyl) substitution sets this material apart: the thienyl group shifts polarity and ring electronics, giving researchers a way to modulate interactions in active site design or material modification. We’ve compared its performance side-by-side with analogous phenyl and non-aromatic thiazolidines. Our internal screens and customer feedback show tighter melting points, improved shelf-stability, and reliable reactivity profiles. This impacts real-world tasks — from easier purification to cleaner endpoint reads in assay development.

    Customers sometimes ask why one wouldn’t simply use a 2-phenyl or an unsubstituted analog. In many projects, a thienyl ring tightens binding or improves selectivity. Oxygen and sulfur play distinct roles in hydrogen bonding and stacking behavior; deploying a thienyl thiazolidine changes a molecule’s interaction with both proteins and surfaces in unexpected ways. Over years of direct support for structure optimization campaigns, we’ve seen researchers reach for our compound when phenyl analogs stalled due to low efficacy or poor stability.

    Real Problems Faced in Sourcing and Solutions from Manufacturing

    People working in chemical research live with the reality of supply interruptions, off-spec product, and rising costs. Having worked both at the bench and in the plant, we know how frustrating it gets. Labs buying from traders or intermediates often stumble into hidden costs — such as inconsistent melting ranges, informal documentation, and unknown contaminants. The real test comes when a single 5 grams of off-spec material derails weeks of labor.

    Production in-house gives us a grip that middlemen can’t match. We batch-release every lot after direct QC by trained analysts — not just spot checks, but full analytics with retention samples and historical tracking. Communicating batch-specific data to researchers gives teams at the receiving end the information to troubleshoot or replicate results. We control our raw material pipeline, vetting suppliers and maintaining buffer stocks for continuous output, instead of getting caught by market swings or delays in foreign shipments.

    Shipping practices matter, too. Moisture management, temperature exposure, and packaging integrity all affect how a material performs after weeks in transport. Humidity exposure can ruin sensitive heterocycles; so, we moved toward double-sealing and vacuum packing, especially for larger orders. Our team has worked with researchers to investigate failed reactions, finding trace moisture or foreign fibers from poor handling as culprits. Supplying directly from the source, with robust storage protocols, limits these risks.

    Supporting Innovation with Consistent, Transparent Product

    Synthetic chemistry moves on trust and repeatability. A single unreliable batch breaks down experiment chains and eats up lab budgets. From experience, we know that getting a clean, true-to-label 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid helps research groups work faster and propose bolder projects. We regularly get feedback about how a switch to our material cleaned up analytical traces in reaction monitoring or cut down on troubleshooting. It’s not about being a hero — just about steady, transparent communication around what leaves the factory.

    Our philosophy puts data up front. Every batch travels with a full report: spectral overlays, chromatograms, lot-specific storage guidance. This means if a researcher notices a deviation, we can dig up batch details, storage logs, or process notes to resolve questions. Open, frequent dialogue with people at the bench closes the loop — we learn where real headaches happen and tweak production to address them.

    This transparency adds value beyond the product. When a researcher reaches out about an unexpected TLC spot or an outlier in reactivity, we treat those moments as learning opportunities. Process tweaks, like adjusting final wash conditions or switching from glass to lined steel drums, have come directly from feedback. Many improvements in durability and performance stem from communication and a willingness to challenge the status quo. This culture of responsiveness makes a difference: more reliable product, greater customer confidence, and, ultimately, research that runs smoother from start to finish.

    Improvement Never Stops: Feedback and Forward-Looking Steps

    Even with established methods, unexpected challenges still appear. Weather shifts, raw material impurities, and equipment aging play their part in production realities. We review each run in post-batch meetings, analyzing not only the yield and analytic scans but also operator logs and customer reports from previous lots. Trends like small yield drops or minor shifts in IR peaks prompt us to dig into reactor maintenance or evaluate new suppliers for precursors.

    Trace contamination and subtle side reactions make all the difference to a pharmaceutical formulation chemist. Our staff regularly review published literature, connect with research partners, and monitor broader trends in heterocyclic compound use. By keeping an eye on academic and industrial feedback, we spot rising analytical needs or changing purity standards and try to adjust before issues ripple through the supply chain. With 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid, we’ve updated our filtration media and drying protocols just because a colleague pointed out faint off-odors in solid state material under certain storage conditions.

    Change isn’t just about fixing faults — it’s about improvement in response to evolving uses. Some teams moving to solid-supported synthesis need larger, dust-free particle sizes. Others working in microfluidic platforms want fast-dissolving, fine powders. Our production line can tailor material form, but only because we invested in flexible drying, milling, and sieving equipment based on real user needs. Over time, we’ve listened to formulating chemists and iterated on the product to match workflows, rather than forcing a one-size-fits-all solution.

    Fact-Based Quality: What We’ve Learned from Decades in the Business

    Sourcing quality 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid goes beyond price tags or purity certificates. From hundreds of production cycles and real-world troubleshooting, we see how minute shifts in synthesis protocol lead to large changes in final use. Early on, missing a drying step or cooling too quickly produced clumpy material that wouldn’t dissolve on the customer’s workbench. It took process control — and a willingness to test, re-test, and solicit feedback — to get batches running right.

    By charting each lot’s analytic profile, we’ve built a repository of reference data that lets us anticipate questions before orders even ship. This approach means a chemist can request previous lot data, overlay spectra, or drill into process notes when troubleshooting. Hearing about a failed peptide coupling or color change triggers us to pull retention samples and rerun tests. We want scientists to spend less time fighting with raw materials and more time advancing their projects.

    Long-term relationships – not one-off sales – matter. We’ve seen groups stick with our products for years, designing entire research pipelines around the characteristics of our material. As a manufacturer, we take that seriously. Investments in plant upgrades, analytical equipment, and staff training all feed back into product quality and reliability. The up-front effort pays off when researchers send us re-order after re-order, sharing publications and discoveries that started with a request for "the same 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid" they’ve come to trust.

    Why Reliability and Direct Supply Win Over Repackaged Alternatives

    Production-side experience gives a grounded view of what makes a specialty chemical dependable. Ordering from repackers or non-producers far from the supply chain puts a barrier between the researcher and the facts: little transparency about shelf life, uncertain storage, and limited traceability if problems crop up. We’ve received plenty of samples labeled with vague “equivalents” that failed to match the stated specifications. In our factory, any deviation — from melting point to subtle discoloration — triggers a batch stop, investigation, and, if needed, reformulation.

    Researchers choose from dozens of suppliers for each project, but they quickly learn which products repeat. The true differentiator isn’t just purity percentage or a lower price per gram. Success builds on clear, honest communication of how the batch was made, shipped, and stored. Having a direct line to the producer means that a tech question gets a technical answer, not a scripted reply. Our QC team has answered late-night emails and reviewed process logs for a single mysterious impurity — and followed up with changes to seal it out next time.

    The comfort level knowing that batch data, process notes, and documentary trail all live in the same company that produced and packed the compound can’t be overstated. This also shortens lead times; we hold inventory ourselves and release lots as they pass final inspection. Labs pushing for grant deadlines or scaling up preclinical candidates need that reliability. In the end, success turns on repeatability, transparency, and open lines of feedback, not just a shipping label or a scanned COA.

    Listening to the Market, Serving the Real Users

    Years of serving advanced labs have shown us that needs evolve faster than standard product lines. Researchers shift from old methods to new ones, try bold combinations, and often spot effects in molecules that no manufacturer predicted at launch. We’ve been contacted about unexpected binding patterns, new synthetic pathways, and even environmental remediation studies. The best part of manufacturing 2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid sits in the ongoing relationship with scientists and developers building the next breakthrough.

    We’re not just filling orders. Each batch shipped stands as an answer to a challenge faced by a government lab, hungry startup, or established pharmaceutical leader. Our process emphasizes feedback loops, traceability, and the willingness to adapt as use cases change. If a synthetic route opens up new chemistry for a group in Boston or Shanghai, we look at how our process can evolve to support them. Sometimes that means changing particle size, other times it’s about packaging, or even cGMP adoption for customers heading into clinical use.

    Upstream knowledge, control over supply, and respect for the researcher’s time all combine to turn a specialty compound into a reliable tool. We know the consequences if a batch fails or an impurity derails a deadline. That’s why the effort to communicate, document, and improve never takes a back seat in our operation.

    Designing Chemistry for Collaboration

    Open lines between manufacturing and end users create better products. Whether solving a stubborn condensation, debugging an NMR spectrum, or scaling to pilot production, communication matters. Our staff answer technical inquiries from troubleshooting failed assays to assisting with scale-up adaptation. This feedback not only sharpens our own methods — it supports the broader community of researchers pushing into new territory. Moving beyond a product line and seeing our material in scientific articles, grant reports, and patents validates the effort that goes into every gram we produce.

    2-(2-Thienyl)-1,3-Thiazolidine-4-Carboxylic Acid isn’t a commodity. Its performance stems from careful control, user feedback, and a dedication to transparency. That approach, grounded in years of operational learning, guarantees that ideas born in the lab come alive in practice.