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2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid

    • Product Name 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid
    • Alias 2-Methyl-4-thiazoline-5-thioglycolic acid
    • Einecs 259-208-6
    • 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

    767975

    Cas Number 13437-22-8
    Molecular Formula C6H7NO2S2
    Molecular Weight 189.25 g/mol
    Appearance White to off-white powder
    Melting Point 205-207°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature 2-8°C (Refrigerated)
    Smiles CC1=NC(=S)SC1CC(=O)O
    Inchikey KONGYTLPTIWCEG-UHFFFAOYSA-N

    As an accredited 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a secure screw cap, clearly labeled with hazard symbols and product details.
    Shipping 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid is shipped in tightly sealed containers, protected from moisture, light, and incompatible substances. It should be transported according to applicable regulations for hazardous chemicals, with labeling and documentation. Store in a cool, dry place, and handle with proper personal protective equipment to ensure safety during transit.
    Storage 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature or as specified by the manufacturer. Always follow proper laboratory safety protocols and keep the container clearly labeled.
    Application of 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid

    Applications of 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid in Industrial Manufacturing

    As a dedicated manufacturer of specialty thiazole derivatives, we focus on the precise industrial roles of 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid across multiple downstream sectors. This compound finds targeted use primarily in advanced pharmaceutical intermediates, corrosion inhibition formulations, specific rubber vulcanization systems, and custom synthesis for specialty agrochemical precursors. Below, we detail the authentic manufacturing application scenarios, with technical details relevant for industrial and formulation professionals.

    1. Pharmaceutical Intermediate for Cephalosporin Synthesis

    Our material supports the synthesis of advanced cephalosporin side-chains, including key intermediates required for third-generation cephalosporins. This thiazole acid acts as a nucleophile in acylation steps, enabling selective formation of thiazole side arms that confer strength to the β-lactam core in regulated production environments. Quality assurance teams routinely validate this process according to established monographs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • Pharmacopeia: USP, EP, ChP monographs for raw ingredients and finished antibiotics
    • FDA DMF registration and quality documentation
    • EU REACH pre-registration for pharmaceutical grade intermediates

    Typical usage ratio

    • 0.8 – 1.2 molar equivalents relative to β-lactam core, adjusted depending on target cephalosporin derivative

    Downstream process integration

    • Compound is introduced during the acylation of aminothiazole subunits in multi-step synthesis reactors; validated in batch and semi-continuous processes under inert atmosphere

    Final product types

    • Cefepime bulk API
    • Cefpirome API
    • Cephalosporin injectable intermediates
    • Semi-synthetic β-lactam antibiotic powder

    2. Corrosion Inhibitor in Oilfield Water Treatment

    This thiazole derivative performs as a sulfur-donor corrosion inhibitor additive in oilfield and refinery recirculating water systems. It disrupts electrochemical corrosion at the steel/water interface, particularly in systems containing chlorides and sulfides, and can be formulated into multi-component inhibitor packages with nitrites and phosphonates, subject to industrial water treatment certification.

    Industry compliance standards

    • API RP 574, API RP 932-B on corrosion control
    • REACH classification for oilfield additives
    • ASTM D2688 (Corrosion Inhibitors in Water)
    • OSHA Process Safety requirements for chemical handling

    Typical usage ratio

    • 10–150 mg/L in recirculating cooling and injection water, optimized per corrosion rate and water chemistry profiles

    Downstream process integration

    • Batch-dosed or continuously metered into oilfield water circulation system reservoirs or downstream from demulsifiers; compatible with scale inhibitors, dispersants, and oxygen scavengers

    Final product types

    • Multi-function oilfield water treatment packages
    • Blended corrosion inhibitor concentrates
    • Closed-loop refinery water system chemicals
    • Custom-formulated pipeline protection fluids

    3. Vulcanization Accelerator in Rubber Manufacturing

    The compound serves a role in HSV and EVA rubber compounding as a delayed-action vulcanization accelerator. It supports cross-linking reactions for specialty elastomers, where precise mechanical and aging properties are required, particularly in technical rubber for automotive, conveyor belts, and anti-vibration mounts. Compliance with rubber formulation safety and environmental standards is monitored throughout the production workflow.

    Industry compliance standards

    • ISO 9001, ISO 14001 for chemical and rubber processing
    • REACH Annex XVII compliance (candidates for restricted substances in finished goods)
    • European Tyre and Rubber Manufacturers Association (ETRMA) guidance
    • ELV Directive 2000/53/EC (for automotive-grade components)

    Typical usage ratio

    • 0.2 – 1.0 phr (parts per hundred rubber), adjusted for specific polymer matrix and curing temperature

    Downstream process integration

    • Compound is weighed into the rubber mixing stage, typically on high intensity open mills; dispersed before addition of sulfur and zinc oxide, under tightly controlled time/temp protocols

    Final product types

    • Elastic seals for automotive engineering
    • Technical conveyor belts
    • Anti-vibration rubber bushings
    • Custom industrial rubber gaskets

    4. Intermediate for Thiazole-based Agrochemical Synthesis

    2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid finds a defined use as a nucleophilic intermediate for the construction of thiazole rings in modern agrochemical actives, especially where resistance to photodegradation and metabolic deactivation are desired. Industrial producers employ this material in closed synthesis environments to meet prevailing regional agrochemical notification and registration systems.

    Industry compliance standards

    • FAO Specifications for plant protection products
    • EPA 40 CFR Part 180 (Tolerances and exemptions for pesticide chemicals in or on food)
    • OECD Principles of Good Laboratory Practice (GLP) for pilot synthesis data
    • REACH or China IECSC notification for import and production

    Typical usage ratio

    • 1.0 – 1.3 molar equivalents regarding pyridine or haloalkylation substrates; final ratio fine-tuned for yield optimization per specific actives

    Downstream process integration

    • Introduced during the heterocycle-forming condensation stage under controlled pH and temperature, supported by in-process HPLC or GC monitoring

    Final product types

    • Thiazole-based fungicide active ingredients
    • Selective herbicide intermediates
    • Pesticide technical concentrate production
    • Prepared pre-formulations for crop protection use
    Free Quote

    Competitive 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Deep Dive: 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic Acid in Modern Synthesis

    Chemical manufacturing rewards precision and honesty. Through years of working with 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid, certain things become clear only after running pilot runs, scaling up, fixing real-world bugs during QC, and tracking batches from raw material intake to finished packaging. This compound draws steady interest from pharmaceutical labs, agrochemical developers, and specialty formulation scientists who call in looking for reliable quality and answers beyond sales talk.

    The Chemistry Behind Our Process

    Producing 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid requires careful attention right from sourcing thiazole intermediates. In our plant, the biggest challenge crops up in managing the mercapto group – its reactivity means trace amounts of oxygen or heavy metals throw reactions off balance, affecting purity and yield. The thiazole ring comes together only when temperature and pH hold to a narrow band; one slip in solvent choice or timing clogs up downstream steps. Any shortcut in purification brings extra sulfurous odors, or even worse, inconsistent melting points. Our reactors run with inline monitoring to keep these risks in check and clamp down on batch variation.

    Finished product typically comes as a light yellow to tan powder, easily distinguishable from its close relatives by a sharper, slightly pungent scent. We lock our drying procedure tightly to avoid residual solvents which often cause headaches during regulatory checks down the road. Typical batch scale ranges from kilos to several hundred, with continuous quality checking to detect any early drift in spectral profiles or moisture uptake.

    What Makes This Compound Stand Out

    A quick glance through catalogues suggests many thiazole-based molecules look similar on paper. Our 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid brings a combination that solves certain design obstacles others don’t. The mercapto group sits, not at the ring position, but out on the acetic acid side chain, which opens doors for both solid-phase and solution-phase coupling strategies. Pharmas ask about this feature because it lets them graft the molecule onto resin backbones in peptide synthesis. The methyl group at the 4-position also gives a noticeable difference – it adds a level of hydrophobicity, altering how the molecule behaves in organic syntheses compared to non-methylated analogs.

    Over the years, small differences in structure have proven to make or break custom reactions. Some buyers try generic 2-Mercaptothiazole or 2-Mercapto-4-methylthiazole for coupling and get stuck with poor yields or side reactions. We’ve run in-house comparisons with our acetic acid variant; the extra carboxyl gives both added solubility in polar aprotic solvents and a convenient point for further derivatization. In real terms, this has shaved weeks off custom route development or analytical validation in at least three of our recent customer partnerships.

    Specifications That Matter in Day-to-Day Work

    Many labs lay out tables claiming “purity >99% HPLC” and “moisture <0.5%,” but what sticks out after hundreds of kilogram lots is how stability shifts during storage and shipping. At our factory, we seal material directly after drying and test for sulfur content, carboxylate integrity, and chromatic impurities. UV-Vis spectra and LC-MS back up every outgoing lot, and our scale-up chemists track every spectral deviation. We've found that small spectral shoulders or minor IR peaks tell more about hidden byproducts than most certificate-of-analysis templates show. It’s easy for low-level metal catalysts to creep in during thiazole ring closure steps, but diligent controls clamp these into the single-digit ppm range every time.

    We recommend our lots for pharmaceutical research and functionalization studies where residual solvents would skew analytical methods or biological test results. Some clients have commented that generic offerings from unverified suppliers leave behind a persistent sulfury note, which lingers during formulation blending or causes baseline instability in chromatograms. Having faced this issue ourselves during the early years, we set up extra filtering and double distillation for raw mercapto intermediates. This investment adds days to production but pays off in consistent signals on NMR, HPLC, and DSC profiles.

    Handling and Packaging in Production Environments

    Working with thiazole compounds challenges both operators and logistics teams. Dust control makes a difference since the sulfurous nature of the material means even a small spill leaves a strong, lingering scent that neighboring lines soon notice. We run sealed transfer systems and have engineered powder charging to minimize open handling. Feedback from regular users confirms that tightly sealed HDPE drums and double-bagging prevent caking and odor escape over multi-month storage. Shipment during muggy summers tends to risk moisture gain, so we add desiccant canisters and ship everything on pallets, wrapped against sudden temperature swings.

    Autumn and spring bring sharp humidity shifts at our plant. This taught us early on to sample for weight changes after storage as extra insurance against unseen problems. By tracking these details, we’ve headed off several potential complaints about clumping before they ever leave our dock. Labs that keep this compound for peptide conjugation or drug discovery recognize the advantage of opening each drum and finding the same free-flowing consistency, batch after batch.

    End Use: Real Applications Drive Product Evolution

    Direct feedback from the field has always guided our process tweaks. Early in our production years, small pharma startups put in requests for customization – sometimes asking for specific particle sizes, or wanting the material in moisture-proof vials for easy weighing at glovebox stations. We responded by redesigning some of our packaging lines and offering both drum-scale and pre-weighed sample formats. Feedback loop to R&D is tight, which means every quality issue or application snag is discussed during weekly production meetings.

    Our material has taken part in early-stage synthesis screens, antithyroid agent design, and basic research into cysteine mimicry. The mercapto group in this compound acts as a versatile handle for disulfide formation and surface modification, letting researchers graft the thiazole ring onto biological, inorganic, or polymeric backbones. Several customers testing thiol-ene click chemistry and site-specific bioconjugation found our product delivered cleaner results than others – confirming the value of purity and lot-to-lot reliability. Some reports point out unique reactivity patterns for the methyl group, which sometimes improves coupling efficiency in aqueous-organic hybrid systems designed in modern peptide or oligonucleotide syntheses.

    Years of observation show that regular users develop trusted protocols around established supply chains. Any disruption in phase purity or handling creates ripple effects in their downstream processes. This keeps us honest in maintaining not just paper specs, but predictable batches that integrate smoothly into even the most demanding analytical methods or reaction conditions. It takes extra work to keep up with evolving needs, so we stay in regular communication with research chemists and scale-up teams, noting their practical concerns.

    Why Purity and Consistency Move the Industry Forward

    Not all research chemical suppliers use the same diligence during manufacture, and over time, even small inconsistencies add up in productivity losses or missed regulatory registrations. A compound like 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid doesn’t always show immediate visible impurities, but persistent users learn to spot subtle differences in chromatographic baselines, trace elemental content, or reaction reproducibility. Tight feedback from our long-term customers proves that small investments in purification, documentation, and process tuning yield substantial value.

    Our batch records stretch back many years, and we welcome customer audits on site. QC teams are equipped not only with standard HPLC and GC but also with ICP-OES, Karl Fischer titration, and microbalance setups dedicated to this product. Tracking these details might seem overkill to some, but in regulated industries, they’re often the difference between getting an IND submission approved or facing weeks of rework. Analytical chemists using our lots send in performance data, confirming retention times and baseline noise remain within tight ranges, regardless of production scale or seasonality.

    Comparison Versus Other Thiazole Derivatives

    There’s no shortage of thiazole derivatives available. What sets this one apart often comes down to the attached acetic acid group, combined with the methyl substituent. We’ve tested numerous variants like 2-mercaptothiazole or 2-mercapto-4-methylthiazole in similar applications, but none match the handle for further modification offered by the side-chain carboxyl. This proves critical in peptide, polymer, and surface science work where direct covalent attachment is needed without extra activation or protection steps. In solution, differences become obvious: the methylated, acid-functionalized thiazole offers slightly higher solubility, better handling in buffer solutions, and again, fewer sulfury byproducts in downstream reactions.

    Drawing from real project data, at least two clients switching from basic mercaptothiazole to our acetic acid analog achieved both shorter reaction times and better coupling efficiency under identical conditions. That’s not a claim, but measured lab performance after well-documented side-by-side comparisons. We shared detailed technical support to help optimize their purification protocols, noting any deviations in recovery yields or side product formation.

    Supporting Responsible Chemistry

    Our factory environment prizes safety and compliance. Each stage of producing 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid meets global requirements for responsible handling of sulfurous raw materials, solvent recycling, and air emissions. The downside of thiazole chemistry lies in its distinctive smell, but our emission capture, scrubbing, and filtering equipment work overtime to keep plant air fresh and neighbors happy. New operators train for months before supervising final packaging, learning to spot even minor off-odors or color shifts.

    We support responsible downstream use by offering detailed handling advice, SDS sheets, and technical consultations—tailored from our own learning curve. We don’t pitch “green” chemistry without real process data, but our focus remains on minimizing waste, maximizing raw material conversion, and sharing smarter use guidelines built from batch-level experience. Regular plant audits and third-party environmental reviews keep us up to industry standards and ready for unexpected challenges as market needs evolve.

    Potential Growth and Research Pathways

    2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid holds promise for new applications almost every year. Evidence from the last two decades shows continued focus on sulfur-based modifications in discovery chemistry. Each time a new client requests an off-spec variant—smaller crystalline fraction, higher dryness, special packaging for inert atmosphere work—our response involves trial runs, then scaling up successful approaches for regular supply. This keeps our technical team sharp and in tune with academic as well as commercial research targets.

    Recent years brought requests for bioconjugation, especially site-directed labeling of peptides and oligos. Feedback revealed this molecule behaves cleaner in mixed-phase reactions, likely thanks to both the acid group and the subtle hydrophobic balance set by the 4-methyl substitution. Polymer and materials scientists approach us looking for unique disulfide linkages, stable anchoring groups, and sometimes photoactive site modifications. Each new field application brings more data and process know-how, which feeds back into our core QC and process development teams.

    Building Trust in Every Shipment

    Listening to the end user has shaped how we make and supply this compound. Too many suppliers stop at the spec sheet, but we look for issues in each shipment—caking, moisture shifts, subtle color drifts—and troubleshoot these before product ships. Customers often report smoother blending, stable analytical performance, and better results in high-throughput screens. This track record reflects years of attention to detail.

    Trust grows with transparency and consistency. Through audits, shared analytical runs, and open dialogue, clients gain the confidence that their hard science rests on solid material, not just high-level purity numbers. We believe that giving both process details and honest answers solves more long-range problems than glossy catalogs ever could. Operating as an actual manufacturer inspires a tangible responsibility to the science and business of every client, and this outlook drives continuous improvement with each production cycle.

    Moving Forward: Bridging Research and Manufacturing

    As chemical needs shift, real-world feedback keeps the production method nimble and reliable. This means constantly monitoring trends, sharing performance data from ongoing lab work, and encouraging dialogue with users ranging from graduate students to process engineers scaling up in GMP settings. Long experience shows that small tweaks made today pay off in reproducible, world-class results next year and beyond.

    Our approach to making and supplying 2-Mercapto-4-Methyl-1,3-Thiazol-5-Yl-acetic acid stays grounded in practical results, open communication, and detailed attention through each production stage—never just ticking boxes, but striving for genuine compatibility with the next big breakthrough. The result: a thiazole compound that stands apart, developed by real hands-on chemists for others who demand the same reliability and depth in every gram delivered.