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Thiazolidine-2-Carboxylic Acid

    • Product Name Thiazolidine-2-Carboxylic Acid
    • Alias Thiazolidine-2-carboxylate
    • Einecs 214-989-6
    • 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

    280892

    Chemical Name Thiazolidine-2-Carboxylic Acid
    Molecular Formula C4H7NO2S
    Molar Mass 133.17 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 134-138 °C
    Boiling Point Decomposes before boiling
    Solubility In Water Soluble
    Cas Number 502-92-5
    Pka 2.13 (carboxylic acid)
    Density 1.367 g/cm3
    Smiles C1CSCN1C(=O)O
    Storage Conditions Store at room temperature, tightly sealed
    Synonyms Thiazolidine-2-carboxylate; 2-Thiazolidinecarboxylic acid
    Application Intermediate in organic synthesis and pharmaceuticals

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

    Packing & Storage
    Packing Sealed 25g amber glass bottle with tamper-evident cap, labeled "Thiazolidine-2-Carboxylic Acid," purity, hazard symbols, and batch details.
    Shipping Thiazolidine-2-Carboxylic Acid is typically shipped in tightly sealed containers to prevent moisture ingress, under ambient conditions unless otherwise specified. It is packed according to standard regulations for non-hazardous chemicals, ensuring safe transit. Appropriate labeling and documentation accompany the consignment, and handling instructions are provided to avoid exposure and degradation.
    Storage **Thiazolidine-2-carboxylic acid** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store at temperatures below 25°C and protect from moisture and light to maintain stability and prevent degradation of the compound.
    Application of Thiazolidine-2-Carboxylic Acid

    Applications of Thiazolidine-2-Carboxylic Acid in Industrial Manufacturing

    As a chemical raw material manufacturer, we supply thiazolidine-2-carboxylic acid to customers across multiple sectors. Below, we outline major application routes based on current industrial demand, compliance frameworks, and formulation practices. This section details genuine downstream uses, integration into manufacturing processes, and the nature of final products in each specific field.

    1. Pharmaceutical Intermediate for Beta-Lactam Antibiotics

    Pharmaceutical producers utilize thiazolidine-2-carboxylic acid as a critical intermediate in the synthesis of certain beta-lactam antibiotics, most notably penicillins and cephalosporins. The compound forms part of the core structure during side-chain assembly and ring closure steps, contributing directly to molecular integrity and biological activity. Manufacturers select this material for its high purity and suitability in large-scale synthesis, adhering to strict quality and traceability regimes in regulated pharma production.

    Industry compliance standards

    • EU GMP (EudraLex Volume 4, Part II: Basic Requirements for Active Substances)
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia (ChP, relevant monographs)

    Typical usage ratio

    • 0.9 – 1.1 molar equivalents relative to aminopenicillanic acid or 7-aminocephalosporanic acid starting materials
    • Adjusted according to process yield optimization and impurity profile control

    Downstream process integration

    • Direct addition during side-chain formation or cyclization stages of antibiotic synthesis
    • Followed by purification through crystallization, solvent extraction, or preparative chromatography

    Final product types

    • Pharmaceutical-grade penicillins (e.g., ampicillin, amoxicillin)
    • Cephalosporin antibiotics (e.g., cefadroxil, cefalexin)
    • Intermediates for further antibiotic modification

    2. Chiral Synthesis Auxiliary in Agrochemical Manufacturing

    Producers in agrochemical sectors apply thiazolidine-2-carboxylic acid as a chiral auxiliary during stereoselective synthesis of crop protection agents. Its ring structure enables precise control during asymmetric alkylation or condensation, supporting industrial-scale manufacture of fungicides and herbicides that demand strict enantiomeric purity. Proper handling, documentation, and removal protocols ensure final products comply with global crop protection regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (Plant Protection Product) and REACH Registration
    • ISO 9001:2015 Quality Management Systems
    • China GB 20700 Safety Guidelines for Pesticide Production

    Typical usage ratio

    • 0.8 – 1.2 molar equivalents against key substrate
    • Optimized for the desired chiral ratio and yield-maximization in production batches

    Downstream process integration

    • Introduced at the stereocenter development stage or for transient protection of reactive groups
    • Usually removed or recycled after target molecule formation by standard hydrolysis or extraction

    Final product types

    • Enantio-pure fungicides
    • Selective herbicides
    • Intermediates for further agrochemical modification

    3. Precursor in Specialty Polymer Synthesis

    Thiazolidine-2-carboxylic acid finds application in specialty polymer production, particularly as a nucleating or crosslinking agent for sulfur-containing polymers and copolymers. Industrial polymer formulators select this compound to introduce sulfur-based functionality, modify physical properties, or create biodegradable resin backbones for advanced materials, coatings, and medical device components. Specifications for purity and residual solvents remain critical to ensure end-use performance and legal compliance.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for polymer manufacturing process control and environmental management
    • REACH (EC) No 1907/2006 Registration for chemical safety in Europe
    • RoHS Directive 2011/65/EU (for electronics and electrical product components)

    Typical usage ratio

    • 0.1 – 2.5 wt% depending on the resin system type and desired modification properties
    • Adjusted based on chain length and degree of crosslinking required per batch

    Downstream process integration

    • Used in pre-polymer blending prior to polymerization or extrusion steps
    • Introduced during in situ functionalization for enhanced polymer matrix compatibility

    Final product types

    • Sulfur-containing polymers (medical device grade, electronics-grade)
    • Functionalized copolymers for specialty coatings
    • Biodegradable packaging films

    4. Analytical Reagent in Laboratory and Quality Control Testing

    Laboratories specializing in amino acid analysis and protein sequencing employ thiazolidine-2-carboxylic acid as a derivatization reagent for aldehydes and ketoacids. Its specific reactivity ensures the reproducible formation of stable derivatives, facilitating high-sensitivity quantitation by HPLC and LC-MS. QC managers and analytical chemists depend on material integrity, documentation, and traceability from suppliers manufacturing under validated analytical reagent protocols.

    Industry compliance standards

    • ISO/IEC 17025 Accreditation for testing and calibration laboratories
    • USP General Chapter <621> Chromatography – system suitability in pharmaceutical testing
    • GLP (Good Laboratory Practice) OECD Principles

    Typical usage ratio

    • 5–50 mM in reaction mixture for derivatization, depending on target analyte concentration
    • Adjusted by analytical method, matrix, and instrument calibration requirements

    Downstream process integration

    • Preparation of reaction solutions for sample derivatization prior to chromatographic analysis
    • Batch documentation in laboratory record systems and certificate of analysis validation

    Final product types

    • Derivatized analytical standards for amino acid and protein analysis
    • Validated HPLC method kits
    • Research and diagnostic reagents

    5. Precursor in Cosmetic Ingredient Manufacturing

    Cosmetic ingredient manufacturers use thiazolidine-2-carboxylic acid during the synthesis of certain bioactive complexes and peptides for use in anti-aging and skin conditioning formulations. It facilitates the formation of thiazolidine derivatives that display targeted physiological interactions with skin cells. For regulatory and commercial acceptance, suppliers must provide documentation for purity, low contaminants, and manufacturing practices aligning with cosmetic-grade safety standards.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • China GB 7916 Cosmetic Safety Technical Specification
    • ISO 22716 GMP for Cosmetics

    Typical usage ratio

    • 0.05 – 1.0% in final cosmetic ingredient synthesis formulations
    • Adjusted by batch scale and target peptide length

    Downstream process integration

    • Reacted during peptide chain assembly or complexation stages
    • Purification by ultrafiltration or chromatography to meet cosmetic ingredient limits

    Final product types

    • Anti-aging peptide complexes
    • Skin conditioning agents
    • Cosmetic grade bioactive additives
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    Certification & Compliance
    More Introduction

    Thiazolidine-2-Carboxylic Acid: Experience from the Manufacturer’s Bench

    From Our Process Line: What Sets Thiazolidine-2-Carboxylic Acid Apart

    Every shift, our teams handle the full route from raw material to finished batch, so we know exactly how Thiazolidine-2-carboxylic acid takes shape. There’s a unique confidence that comes from seeing the crystalline product at multiple points in production. Repeated filtration, purification, and analysis allow us to spot quality markers that go well beyond a certificate. We intend not simply to meet a specification, but to keep consistency batch after batch—because anyone using this compound in their process depends on no surprises, no hidden variability.

    From a technical ground, Thiazolidine-2-carboxylic acid presents a stable, white crystalline appearance that survives rigorous transit and handling. Those tuning their process sensitivity can rest easy seeing how our in-house HPLC consistently verifies purity above 99%. Our staff pay close attention to trace contamination limits, especially amines and sulfur, which show up during certain reaction stages. Years of operational experience have taught us which adjustments in pH, filtration mesh, and temperature stabilize the process when scaling from small runs to industrial tanks. That know-how doesn’t show up on a spec sheet, but it prevents a cascade of costly chain-reaction issues during downstream use.

    Understanding Our Model and Specifications—Why They Matter

    We manufacture this product to a single, well-established molecular model: C4H7NO2S. Both alpha and beta crystalline forms have turned up in literature samples, but we commit to the form demanded by the broadest segment of the industry, which ensures downstream compatibility. Each lot comes with full traceability back to raw input: an approach grounded in years of customer feedback. Water content can matter in final applications, so our team dries the product to <0.5% moisture by controlled vacuum—a decision traced to lessons from mishandled drying stages years ago, where higher moisture skewed analytical readings and gummed up certain reactors.

    Our production line hits a melting point close to 164°C with a ±1°C margin on calibrated apparatus. We’ve seen end-users rely on this narrow melting range—both as a quick indicative check for batch acceptance and as proof against cross-contaminated stock. Our QC floor runs parallel tests for chloride and heavy metals using established wet chemistry, not shortcut strips, because trace metallics can disrupt subtle synthetic pathways. These operational details, part of our day-to-day work, might get overlooked in hands-off distribution networks but anchor the reliability of each shipment.

    Key Uses Informed by Field Experience

    Years of direct feedback from formulators and process chemists have shown us where Thiazolidine-2-carboxylic acid stands out. Many clients in pharmaceutical synthesis treat this material as a chiral building block, especially for constructing beta-amino acids and prodrugs. They value the product’s chemical stability even when faced with strong bases or temperature shifts during multi-step synthesis. Peptide chemistry platforms, in particular, appreciate the way our product avoids racemization, a concern that kept resurfacing early in our operational history with less tightly controlled batches.

    Food and feed supplement manufacturers regularly purchase this compound in bulk, using it as a source of bioavailable sulfur and non-starch amino precursors. We keep a dedicated filling line for food-grade batches to avoid cross-exposure with technical reagents. This practice grew out of repeated audits by inspectors and requests from regular clients who experienced delays and compliance headaches from commingled packing elsewhere.

    Our agricultural partners reach out to us for thiazolidine-2-carboxylic acid as a plant growth stimulant. Through field feedback, we learned early on that fine particle sizing improves miscibility with carrier sprays. Over the years, our plant upgraded hammer-milling and sieve steps to reach a median particle size below 120 microns, a measure checked every lot to fulfill contract promises—not as an afterthought, but as part of how we build trust shipment after shipment.

    What Experience Teaches About Product Differences

    Thiazolidine-2-carboxylic acid falls into a family with a few close analogs, including thiazolidine derivatives with altered carboxylic, methyl, or hydroxyl substitutions. Some market offerings rebrand analogs, which can confuse dosing or reactivity in sensitive applications. Clients have sent us competitors' lots that turned out to be blends of thiazolidine analogs. Performance and yields suffer in pharmaceutical and biochemical settings when using these substitutes. For this reason, we developed a consistent fingerprint using FTIR and NMR analysis: not only to answer consultant inquiries, but to back up any client who needs analytical confirmation, especially for regulatory audits or patent filings.

    In food and nutrition, experienced clients spot adulteration quickly. Higher sulfur content signals thiazolidine-4-carboxylic acid, which alters flavor and metabolite release. Our experience has shown conscious buyers prefer a single, authenticated isomer for tighter control in both supplements and livestock feed. No certificate replaces repeated test results—and we keep records stretching years back for any query.

    Manufacturing Challenges and Our Solutions

    Over decades, we have encountered and solved specific production problems with Thiazolidine-2-carboxylic acid. Sulfurous odors, while natural to the synthesis, created persistent headaches during scale-up. Activating extra fume extraction and refining condensation allowed us to reduce exposure for staff and trim workplace complaints. Incomplete reaction conversion showed up as dark tints in early batches—so we optimized reactant ratios and switched to higher-purity amino acid starting materials. Small operational choices, like shifting the order of reagent addition or extending specific heating periods, built cumulative improvements into our methods.

    Solid-liquid separation in this synthesis can be notoriously finicky. Most issues trace back to incorrect agitation speed or inconsistent cooling rates. Our plant standardized batch cooling with digital controllers after a string of batches a decade ago showed filtration stalls and increased labor. Staff now monitor real-time viscosity to avoid filter overload and stop losses before they build up. Downtime has dropped, and batch-to-batch reproducibility has risen.

    Waste minimization shapes our plant layout and process design. Thiazolidine-2-carboxylic acid accuracy in stoichiometry trims both unwanted side products and aqueous discharge. Years ago, our team tackled effluent treatment head-on by recovering sulfur and neutralizing spent acids through an external licensed handler instead of venting or dumping. Costs dropped and local compliance investigations ended. Through these actions, we have seen investment in environmental control pay lasting business and community dividends.

    The Role of Operator Judgment

    Even with modern sensors and automated dosing, operator skills remain critical to achieving reliable product quality. New hires shadow veterans to learn subtle visual cues—crystal shape, sheen, fluid dynamics in mixing tanks—that signal proper conversion. These human observations provided real warnings of hidden issues that benches filled with statistical control charts sometimes missed. Many process upsets got caught and corrected through vigilant hands-on attention, keeping contaminated batches from reaching customers.

    Routine pre-ship inspection offers another layer of protection. Our teams select at least three cross-section samples from each major lot for blended re-testing and hold these as long-term retention. This practice often uncovers storage or packing defects a week or two before delivery—helping us fix issues before they ever reach a customer’s dock.

    End-User Feedback Shapes Operational Focus

    Chemical manufacturers can easily overlook how end-users actually interact with the product. We learned this lesson the hard way. Years ago, a bio-lab partner reported crystallization and sticking during high-humidity storage. Our QA managers started tracking caking resistance and packaging permeability, introducing vacuum-sealed, foil-lined sacks for sensitive orders. As a result, complaints dropped and our repeat business increased.

    In another case, pharmaceutical developers faced inconsistent reactivity due to micro-impurities. We committed to raising the frequency of batch analytics and providing breakdowns down to parts-per-million. This added transparency let their chemists adapt protocols much faster than before—and increased their trust in collaborating with us as opposed to single-use suppliers.

    Direct transportation experience counts for a lot too. A few years back, we saw that bulk shipments during summer months absorbed ambient heat, risking product softening at the bottom of large containers. Since then, we ship with insulated liners and temperature recorders during hot spells. These efforts grew straight from field experience, not by following someone else’s checklist. Customers can see the practical results, not just paperwork.

    The Importance of Process and Analytical Transparency

    Internally, we put significant resources into methodically documenting our operational techniques and improvements over time. Not all manufacturing sites do this, but we see it as insurance against mistakes and a means for keeping long-term customer trust. Our daily journals record which reactor ran which lot, note ambient conditions, operator in charge, and even small hiccups quickly resolved. Whenever a downstream customer finds an issue—the rare off-odor, clumping, or deviation from expected performance—we track back through hundreds of points of information to find root causes.

    Our analytical methods include tailorable HPLC, mass spectrometry, and chiral column access. These capabilities did not come out of a box: successive technical staff built and refined them over the course of projects for pharma clients with specialized needs. Regulatory filings for this compound benefit directly from transparency—since our records trace each lot from plant gate to packaged drum. This has helped clients avoid setbacks with authorities or in-house audits.

    We have learned that sharing supporting analytical data with partners on request speeds up approvals and brings clarity during technical discussions. Many clients have returned with urgent requests for chromatograms or batch syntheses records when facing regulatory challenges. This transparency, built into our standard practice, breaks down doubts and builds collaborative relationships that last beyond the single transaction.

    Continuous Improvement Builds Value Over Time

    The market for Thiazolidine-2-carboxylic acid has grown more competitive, but our approach centers on experience-based improvement rather than simple price cutting. Years of hands-on work with synthesis and purification have led us to refine solvent choices, switch to upgraded filtration materials, and test new drying techniques. Any one change might only shave five or six minutes off a batch cycle, but compounded across hundreds of runs, this reduces cost, resource usage, and workplace fatigue.

    While we keep tabs on competitors, we invest twice as much energy in learning from each production trial and end-user report. Occasional customer pushback on color or odor prompted us to review and upgrade cleaning protocols for both lines and storage vessels. By pursuing thorough root-cause analyses instead of blaming exterior “outsiders,” we have built a plant and culture focused on steady, daily improvement.

    Supporting Innovation with Reliable Material

    As new research directions emerge in pharmaceutical chemistry and agricultural biostimulants, a reliable source of thiazolidine-2-carboxylic acid provides stability for R&D teams. We understand the pressure our customers face—tight timelines, budget ceilings, and the need to impress regulatory examiners. Many of our largest, most loyal customers began with small evaluation lots for feasibility studies. Because their chemists achieved success in scaling up with consistent, predictive behavior from our material, they expanded both the project scope and their orders.

    In addition, collaborative pilot runs with downstream partners have enabled us to further tailor particle size and purity profiles—not through speculative marketing, but by walking through each process step with their technical teams. Our willingness to send technical experts on-site to troubleshoot and provide sample-based studies has led to enduring partnerships and two-way learning. This investment in field relationships outweighs short-term savings from less involved manufacturing approaches.

    Unique Perspective: Handling, Safety, and Compliance

    Direct handling of chemicals on a daily basis informs our understanding of safety and compliance. Each worker receives training not only in procedural matters but also in practical, experience-shaped caution. Through this culture, we have successfully lowered both minor incidents and near misses—critical for a compound containing sulfur, as it can form irritating gases under heat. Our facility stores thiazolidine-2-carboxylic acid under controlled, dry, and properly ventilated conditions, and we work with logistic partners we have personally vetted for both product protection and regulatory paperwork.

    Local environmental and safety authorities review and visit our site regularly, providing another set of expert eyes. Our team approaches these audits as opportunities for learning, not as hurdles. We fund safety upgrades proactively—personal air monitors, modernized packaging systems—based on years of detailed incident logs and frontline staff suggestions. This real-world vigilance has fostered a low-turnover workforce, reinforcing institutional memory and reliable process execution.

    Markets Served—Adapted for Each Sector

    Our scope of supply has evolved over the years to suit a variety of customer bases. Pharmaceutical synthesis leads in both technical demand and volume, with strictest purity and documentation requirements. Our teams provide detailed batch records and responsive technical backup for these partners, drawing on our facilities' continuously updated analytical toolkit.

    For food, feed, and agricultural end-users, the emphasis falls on both purity and adaptability. We prioritize segregated production runs, unique labeling, and certification support for audits and certification renewals. Years of on-site visits and industry dialogue showed us that paperwork and real traceability matter as much to these partners as the physical product.

    Custom blends and research-scale orders get equal attention. Research institutions and biotech incubators often reach out for small-volume, high-precision batches or custom isomeric forms. These niche clients give feedback that circles back into how we refine our core offering. Our staff feel personal pride in seeing products developed, papers published, or crops improved using the material they have prepared.

    Looking Ahead: The Manufacturer’s Commitment

    Over decades of evolving with this molecule, our company’s team has seen quick solutions rise and fall, trends come and go, and products cycle through supply chains. Beneath it all, the core value remains reliability rooted in hands-on manufacturing experience. Each lot of Thiazolidine-2-carboxylic acid reflects thousands of cumulative improvements, continuous operator training, and direct response to real-world application demands.

    Future process upgrades will continue to be shaped by what works under full-scale conditions, and by operational details only visible from our vantage point inside the plant gates. Open communication with our customers, readiness to share data, and experience-driven innovation keep us aligned with both near-term market shifts and long-term sector stability.

    Our story with Thiazolidine-2-carboxylic acid is grounded in daily practical engagement—not just chemistry but also customer communication, logistics, and the unglamorous but vital work of plant maintenance and iterative improvement. Our customers benefit not only from a product but also from a partnership built on direct manufacturing expertise.