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1,3-Thiazole-2-Carbaldehyde

    • Product Name 1,3-Thiazole-2-Carbaldehyde
    • Alias 2-Formylthiazole
    • Einecs EINECS 211-519-9
    • 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

    992029

    Chemical Name 1,3-Thiazole-2-carbaldehyde
    Molecular Formula C4H3NOS
    Molecular Weight 113.14
    Cas Number 3586-55-8
    Appearance Pale yellow to yellow liquid or solid
    Boiling Point 84-87 °C at 17 mmHg
    Melting Point 36-38 °C
    Density 1.295 g/cm3
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Purity Typically ≥97%
    Smiles C1=CSC(=N1)C=O
    Inchi InChI=1S/C4H3NOS/c6-3-4-5-1-2-7-4/h1-3H
    Refractive Index 1.608
    Storage Conditions Store at 2-8 °C, away from light and moisture
    Synonyms Thiazole-2-carboxaldehyde

    As an accredited 1,3-Thiazole-2-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mg of 1,3-Thiazole-2-carbaldehyde is packaged in a sealed amber glass vial with a printed chemical label for identification.
    Shipping 1,3-Thiazole-2-Carbaldehyde is shipped in tightly sealed containers, protected from light and moisture, and labeled in accordance with hazardous material regulations. The chemical is typically transported under ambient conditions, with packing designed to prevent leaks or contamination. Compliance with local, national, and international shipping guidelines is required for safe handling and transport.
    Storage 1,3-Thiazole-2-carbaldehyde should be stored in a cool, dry, and well-ventilated area, tightly sealed in its original container. Keep it away from sources of ignition, direct sunlight, and incompatible substances such as oxidizing agents. Ensure that storage conditions prevent moisture ingress. Use in a fume hood and follow all applicable safety and chemical handling protocols for aldehydes.
    Application of 1,3-Thiazole-2-Carbaldehyde

    Applications of 1,3-Thiazole-2-Carbaldehyde in Industrial Manufacturing

    As an experienced manufacturer of 1,3-Thiazole-2-Carbaldehyde, we supply this specialty intermediate to key sectors that demand rigorous process control, precise formulation, and adherence to international regulatory standards. Proven applications extend across pharmaceutical APIs, advanced agrochemicals, dye intermediates, and specialized flavor synthesis, each requiring dedicated technical solutions and traceable quality systems.

    1. Pharmaceutical Active Ingredient Synthesis

    Innovators in pharmaceutical manufacturing use 1,3-Thiazole-2-Carbaldehyde as a core building block for synthesizing thiazole-based APIs, including antifungals, antivirals, and metabolic disorder treatments. Its aldehyde group enables targeted condensation and cyclization steps, making it integral for molecular skeleton construction in several patented and generic medicines. Synthesis lines require traceable purity, batch reproducibility, and close alignment with international pharmacopoeia monographs, particularly when scaling from preclinical to cGMP pilot and full production.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU Pharmacopoeia (Ph. Eur.) relevant monographs
    • United States Pharmacopeia (USP)–residual solvent, heavy metal, and impurity limits
    • FDA 21 CFR Part 211 process and batch controls

    Typical usage ratio

    • 0.5–3.5 molar equivalents per API synthesis batch, adjusted according to target yield and reaction pathway
    • The ratio depends on stoichiometry of condensation or ring-closing reactions

    Downstream process integration

    • Integrated into initial condensation stage for thiazole ring formation
    • Used in small- and large-scale reactors under nitrogen or argon blanketing
    • Monitored via HPLC for accurate conversion and impurity profile control

    Final product types

    • Oral and injectable antifungal APIs
    • Antiviral lead compounds
    • Metabolic disorder drug intermediates
    • Novel thiazole-based research chemicals

    2. Agrochemical Intermediate Manufacturing

    Producers in the crop protection sector leverage 1,3-Thiazole-2-Carbaldehyde as a strategic intermediate for constructing heterocyclic scaffolds in selective herbicides and fungus-resistant seed treatments. The aldehyde moiety reacts readily with amines or hydrazines, enabling formation of key agrochemical functional groups under mild reaction conditions. Detailed process optimization addresses scale, safety, and downstream formulation requirements specific to each agrochemical’s mode of action.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius pesticide residue limits
    • Regulation (EC) No 1107/2009 for plant protection product registration in the EU
    • ISO 9001:2015 for quality management and batch traceability
    • Local GHS/REACH safety labeling for hazardous raw materials

    Typical usage ratio

    • 0.8–2.0 molar equivalence per active ingredient synthesis batch, modulated by desired functionalization and yield targets
    • Adjustment based on route of heterocycle construction and cost-of-goods optimization

    Downstream process integration

    • Feeding into first or second synthesis step depending on target herbicide or pesticide
    • Reactor dosing synchronized with catalyst addition and solvent selection for environmental compliance
    • Intermediates isolated for final formulation as liquid or wettable powder

    Final product types

    • Systemic triazole herbicides
    • Seed coating fungicides
    • Thiazole-based nematicides
    • Intermediate stock solutions for toll formulation

    3. Dye and Pigment Intermediate Production

    Specialty dye and pigment manufacturers incorporate 1,3-Thiazole-2-Carbaldehyde for coloring agents used in high-performance textiles and printing inks. Key processes exploit the reagent’s reactivity to introduce thiazole chromophores, greatly improving shade intensity and fastness. Strict control over the aldehyde’s input quality and its percentage in condensation reactions ensures consistent coloration and resistance properties in the final dye lots.

    Industry compliance standards

    • OEKO-TEX Standard 100—restricted substance lists and safety verification
    • REACH (EC) No 1907/2006—registration and authorization for dye intermediates
    • ISO 1833—standardized dye content determination
    • ZWH Textile Standard for color fastness and environmental protection (where applicable)

    Typical usage ratio

    • 5–15% by weight in relation to total chromophore-forming reactants
    • The ratio is determined by desired chromatic strength and compatibility of the end dye system

    Downstream process integration

    • Blended in batch-wise at azo-coupling or condensation reaction stage
    • pH, solvent, and temperature tightly monitored for maximum color yield
    • Post-reaction purification by recrystallization or filtration for pigment preparation

    Final product types

    • Reactive textile dyes for cotton and blends
    • Disperse dyes for polyester applications
    • Thiazole orange pigments for specialty coatings
    • High-stability printing inks

    4. Flavor and Fragrance Ingredient Synthesis

    Manufacturers of specialty flavors and aroma chemicals apply 1,3-Thiazole-2-Carbaldehyde to synthesize sulfur-containing thiazole notes found in roasted, meaty, or savory accords. The compound typically enters controlled cyclization and subsequent alkylation steps, with analytics performed to ensure food-contact grade purity and organoleptic profiles. Batch tracking and documentation support compliance with food safety requirements and end-user transparency in flavor concentrate production.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association—Generally Recognized As Safe) status for constituent thiazoles
    • EU Regulation 1334/2008 for flavoring substances and source materials
    • ISO 22000/HACCP certified food safety systems for ingredient processing
    • US FDA 21 CFR 172 for food additive specifications

    Typical usage ratio

    • 0.02–0.1% by weight in conversion to finished aroma compounds
    • Precise dosage set after GC-MS quantification and sensory panel validation

    Downstream process integration

    • Dosed during early cyclization steps to obtain volatile sulfur notes
    • Purified via distillation before use in liquid flavor blending
    • Quality control includes GC-MS profiling for residuals and purity

    Final product types

    • Roasted/umami flavoring concentrates
    • Meat and snack flavor bases
    • Sulfurous aroma ingredients for savory and processed foods
    • Flavor chemicals for beverage enhancement
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    Certification & Compliance
    More Introduction

    1,3-Thiazole-2-Carbaldehyde: A Manufacturer’s Perspective

    Trusted Production, Measurable Purity

    Years spent on the factory floor have shown us what labs and research teams value most—consistency, reliability, and transparency. 1,3-Thiazole-2-Carbaldehyde (CAS 2717-40-8) comes to our customers not just as a finished chemical, but as the result of careful process control and ongoing improvement in thiazole chemistry.

    We prepare this aldehyde with sharp attention to raw material handling, temperature regulation, and moisture management across every step. Finished lots display a pale yellow to light orange appearance, characteristic of high-purity thiazole derivatives. GC analysis typically shows main-content purities above 98%, with low water and negligible secondary impurities. Each production batch enters rigorous quality checks—often tighter than the minimal requirements for thiazole intermediate sourcing.

    Applications Driven by Precision

    Our biggest volumes move towards pharmaceutical building blocks, where customers demand batch-after-batch uniformity. 1,3-Thiazole-2-Carbaldehyde’s reactive aldehyde group invites incorporation into complex molecular scaffolds. Medicinal chemistry teams, custom synthesis operations, and early-stage drug developers reach for this compound to create rings, linkages, and exploratory candidates for further derivatization.

    We do not just serve pharma. Crop protection R&D taps this molecule for the design of novel fungicides and pesticide candidates. Universities, contract research labs, and custom chemical houses use it to expand their thiazole collections, often modifying the core for new bioactive compounds. Thiazole derivatives show promise in anti-infective research, and we see interest from labs exploring flavin analogs, sulfur-heterocycle-modified ligands, and flavor chemistry too.

    Process Choices That Set Us Apart

    Manufacturing experience matters. Thiazole aldehydes pose synthetic and isolation challenges if moisture or temperature fluctuate. Years of investment into reaction setup and workup—especially in the transition from lab scale to multi-ton output—make a difference in how customers rank supply partners. We source our starting materials direct from vetted upstream producers, not random local brokers, eliminating much of the batch-to-batch variability seen elsewhere.

    We prefer reaction kinetics that avoid over-oxidation and side-product formation, even if this lowers overall throughput. Maintaining a nitrogen or argon blanket keeps aldehydic functionalities from oxidizing, while fractionating distillates at controlled pressures helps capture the narrow boiling range required for quality product. By sticking with time-tested workup and filtration practices, we minimize both thiazole ring opening and unwanted polymerization.

    We also avoid solvent residues by using customized drying cycles and distillation columns cleaned between runs. Product handling staff receive regular refresher training, reinforcing correct sampling, label management, sealing, and storage protocols. Each bottle, drum, or tote is not just an inventory item, but proof of process reliability built on years of validation and small but crucial improvements.

    What Sets Our 1,3-Thiazole-2-Carbaldehyde Apart?

    Specifications tell only part of the story. Technical buyers and end-users look for differences hiding behind the certificate of analysis. We compete with routine suppliers by focusing on several make-or-break factors:

    Usage Experience: Working Directly With the Builders

    A manufacturer sees unexpected usage trends before reports show up in the supply journals. Over the years, we have watched 1,3-Thiazole-2-Carbaldehyde transition from a largely niche chemical to a more standard intermediate. Requests come from big-name pharma, but smaller, specialized research houses now make up much of the recurring volume.

    Chemists searching for new thiazole-based motifs often start with simple aldehyde introduction. The molecule’s electron-poor ring and reactive carbonyl carbon enable access to imines, hydrazones, oximes, and even Grignard additions for side-chain extension. In practice, this compound’s specific reactivity helps generate benzothiazoles, carboxamide derivatives, and more complex thiazole-linked structures. Flavors and fragrances teams sometimes leverage the mild odor profile for proprietary mixes, though the main draw remains in targeted molecular construction.

    Many users appreciate our willingness to customize aliquots, provide stability data from real storage conditions, or coordinate packing compatible with automatic dosing equipment. While price per kilo remains important, most teams report that process confidence—knowing they will not have to repeat failed syntheses due to off-spec supply—means the most in the hectic world of commercial labs and research runs.

    Beyond Commodity: Supporting Innovation in Real Environments

    True value emerges when partners collaborate. Many customers come to us with questions: which solvents delay degradation, how does light affect stability, what packaging lengthens shelf life, and how to minimize olfactory impact at scale. Being an actual producer means we do not just forward the MSDS, but run trials, set up long-term stability studies, and test shelf-life claims in real, variable production settings.

    One recurring lesson—each application draws out slightly different requirements. Teams doing kilogram-scale combinatorial chemistry push for maximum throughput and simplified delivery, while those in analytical labs ask for ultra-high purity, corrected for trace solvent and moisture. Agrochemical and pharma clients put a premium on regulatory documentation, impurity profiling, and traceable batch genealogy.

    We maintain a tight feedback loop with end users. Our technical services staff have chemistry backgrounds, not just call center scripts. Customers with novel syntheses or complex downstream conversions often send us unique technical requirements. Sometimes, these stem from unexpected pH sensitivity, solubility requirements, or specific reaction conditions. We integrate these findings into our continuous improvement, resulting in a product closely matched to real-world needs.

    Challenges and Practical Solutions in Thiazole Aldehyde Manufacturing

    Problems can occur even in mature manufacturing setups. Thiazole aldehydes like this one require careful management of humidity, oxygen, and short-term stability under storage. Our process engineers monitor each lot for moisture ingress, even during short-term holding, which can cause container pressure flux or promote unwanted transformations.

    Another challenge involves downstream contamination. Most customers require material sparkled for both purity and homogeneity. Cross-contamination with other thiazoles, oxidized byproducts, or non-thiazole sulfur species can throw off analytical readings or downstream conversion rates. We adopt tank and line-dedicated cleaning protocols, use closed transfer systems, and validate cleaning results with multi-point chromatography.

    Transporting aldehydes raises separate risks—temperature excursions, UV exposure, or accidental mixing with incompatible materials. Over several years, we have strengthened our approach: weather-resistant courier handlers, insulated shipment during hot summers, and morning-only dispatches from high-humidity warehouses.

    Customers in regulatory-heavy industries sometimes worry about global differences in chemical legislation. We keep an internal compliance team up-to-date with the latest REACH, TSCA, and Asian substance notification requirements, simplifying the process for larger batch releases. Up-to-date labeling and documentation keep audits hassle-free and reduce hold-ups at borders.

    Comparing 1,3-Thiazole-2-Carbaldehyde to Other Building Blocks

    Chemists frequently ask what sets this thiazole aldehyde apart from similar compounds in the laboratory reagent market. Structure and electronic properties set it apart from saturated or benzene-based aldehydes. The thiazole ring imparts electron withdrawal, which affects both reaction rates and selectivity in condensation and addition reactions.

    We see customers weighing 1,3-Thiazole-2-Carbaldehyde against alternatives like 2-formylthiazole, 4-methylthiazolecarboxaldehyde, or benzaldehyde derivatives. Our observations show that 1,3-Thiazole-2-Carbaldehyde’s balance of reactivity and stability drives many in medicinal chemistry to prefer it for initial screening, scaffold elaboration, or SAR (structure-activity relationship) studies. The position of the aldehyde functional group on the thiazole ring shifts both regiochemistry and downstream pathway outcomes.

    Sourcing makes a practical distinction as well. Some products—especially those made via less controlled upstream processes—vary wildly in minor impurity content. Unreacted starting thiazoles, poly-thiazyl residues, and even chloride or nitrate carryover can impact both downstream chemistry and analytical reproducibility. By controlling inputs and process settings, we deliver a profile matched to tightly specified needs.

    Supporting Reliable R&D Scale-Up

    Lab-scale chemistry often depends on materials produced with care, but scaling up reveals new weak points. Unstable intermediates, minor isomerization, or slow degradation—issues that barely register at the flask scale—become major headaches in pilot runs. Our own chemists have worked through these transitions, dialing in purification steps, adjusting bottling size, and counseling customers about the risks of changing suppliers mid-project.

    Many clients come to us with scale-up requests just as discovery chemistry hands off viable leads to process teams. We support them by producing multi-kilogram lots under tightly recorded conditions, providing all supporting QA documentation, and adding post-batch analysis. Each kilogram that leaves our facility reflects the lessons of ongoing collaboration, repeated optimizations, and transparent incident reporting.

    For scale-up customers, flexibility rarely means cutting corners. Instead, it means running stability testing at different temperatures and moisture levels, sending reference standards alongside bulk deliveries, or agreeing on customized labeling and repackaging. We have solved logistical challenges by adding batch reservation systems, so regular buyers receive product from familiar lots, with full tracking of updates in process setting or raw material sources.

    Real Supply Chain Reliability, Not Just Paper Promises

    A good aldehyde answers only half the need—the other half lies in reliability under real-world sourcing conditions. We have fielded emergency requests from researchers facing unexpected project acceleration, or industry teams left in the lurch by inconsistent global shipping. Our in-house inventory and tracking systems can typically address urgent requirements with same-day release for common package sizes.

    Transport delays, logistics bottlenecks, or country-specific import restrictions never disappear entirely, but we have built redundancies into supply planning, documentation, and warehousing. Over-capacity storage and staggered holdings reduce risk from shutdowns or transit snags. We communicate realistic timelines as soon as issues arise, helping customers in turn adjust their own production windows.

    Because we produce at scale and handle upstream raw material contracts directly, we can ride out regional shortages or price surges without passing every fluctuation onto the buyer. This stability means more focus on R&D and less time lost chasing elusive “spot” inventory.

    Continuous Learning, Real Conversations

    As both chemical producers and daily operators, our direct interactions with users steer product improvement and lead to workable solutions. We learn from customer troubleshooting—what quality standards are insufficient, which packing sizes frustrate end users, which documentation eases regulatory approvals. Active relationships with research groups, QA teams, and industrial buyers keep us on our toes, validating each improvement in the next batch or process tweak.

    Above all, we value the chance to discuss genuine technical issues, learn user preferences, and adapt offerings as scientific work evolves. 1,3-Thiazole-2-Carbaldehyde has taught us that chemical manufacturing depends not just on molecular formulae, but on responsiveness, listening, and shared expertise.

    The Road Ahead

    Producing specialty intermediates takes more than just a reactor and a set formula. Business as usual in chemical manufacturing can lead to stagnation and missed opportunities for improvement. Regular collaboration with customers and practical engagement in product use environments yield a cycle of process advancement and user benefit. Our ongoing mission is to provide not only 1,3-Thiazole-2-Carbaldehyde of reliable quality, but also to supply the kind of trusted relationships and technical support that move chemistry forward.

    We do not see our job as finished with each successful batch. New project demands emerge, legal and quality frameworks tighten, and research goals shift to new targets. Thanks to the thousands of practical observations and user interactions built over years, we approach production not as a commodity task but as a long-term partnership with scientific creators ready to shape the next set of discoveries.