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HS Code |
796968 |
| Cas Number | 102-08-9 |
| Molecular Formula | C5H5N3O3S |
| Molecular Weight | 199.18 g/mol |
| Iupac Name | N-(5-nitro-1,3-thiazol-2-yl)acetamide |
| Appearance | Yellow crystalline powder |
| Melting Point | 183-186°C |
| Solubility In Water | Slightly soluble |
| Density | 1.61 g/cm³ (calculated) |
| Pubchem Cid | 11645 |
As an accredited 2-Acetamido-5-Nitrothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, labeled "2-Acetamido-5-Nitrothiazole, 25g", chemical hazard and handling instructions clearly displayed. |
| Shipping | 2-Acetamido-5-Nitrothiazole is shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and heat. Packaging complies with transport regulations for hazardous materials. Proper labeling and documentation ensure safe handling. During transit, the chemical is kept secure to prevent leaks, spills, or contamination, in accordance with safety and regulatory standards. |
| Storage | 2-Acetamido-5-Nitrothiazole should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Proper labeling and adherence to safety guidelines, including wearing suitable protective equipment, are essential during handling and storage. |
Applications of 2-Acetamido-5-Nitrothiazole in Industrial Manufacturing2-Acetamido-5-Nitrothiazole serves as a specialized intermediate for advanced manufacturers operating in the pharmaceutical and veterinary sectors, supporting large-scale synthesis of products where strict quality, formulation, and compliance requirements define market viability. Our factory-direct supply integrates seamlessly into validated processes, supporting downstream innovation and operational reliability. 1. Antiprotozoal Drug SynthesisThis material functions as a core intermediate in the batch production of nitrothiazole-based antiprotozoal pharmaceuticals, particularly for human and veterinary applications targeting intestinal protozoan infections. Its integration into controlled synthesis lines under cGMP conditions enables the precise development of finished APIs, with consistent purity essential for regulatory approval and therapeutic reliability. Industry compliance standards
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2. Veterinary Antidiarrheal PreparationsLivestock medication manufacturers employ this compound in the formulation of water-soluble veterinary antidiarrheal agents. Its reliable nitro group reactivity ensures targeted inhibition of protozoal pathogens in aqueous solutions, supporting efficient livestock disease management in accordance with international animal health guidelines. Industry compliance standards
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3. Intermediate for Active Pharmaceutical Ingredient (API) Custom ManufacturingCustom synthesis providers in the small molecule drug development sector utilize this reagent for constructing complex heterocyclic scaffolds, particularly in pilot and commercial scale processes registered under regulatory dossiers. Its controlled reactivity under multi-step organic syntheses yields high-purity intermediates necessary for forming bioactive molecules used in clinical trials and eventual mass production. Industry compliance standards
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4. Analytical Reference Standard SynthesisThis compound serves as a precursor in the synthesis of traceable analytical reference materials. QC laboratories and certified reference material (CRM) producers rely on its batch-to-batch consistency for re-crystallizing ultra-high purity standards, supporting accurate pharmacopoeial method validation and ongoing quality control of related nitrothiazole APIs. Industry compliance standards
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Working at a chemical manufacturing plant offers a unique perspective into the world of heterocyclic compounds. Day in and day out, 2-Acetamido-5-Nitrothiazole remains a product we handle with both respect and diligence. This compound, known by its formula C5H5N3O3S, carries a thiazole ring with a nitro and an acetamido group attached, giving it properties distinct from simpler thiazole derivatives.
We produce this compound in a crystalline, light yellow powder form, which provides two immediate benefits during handling and downstream processing. The powder’s coloration comes straight from its nitro group—a feature appreciated among chemists who track such characteristics for identification and purity checks. At our site, routine spectroscopic and chromatographic analyses confirm the purity exceeds 98%, which matters a great deal because anything lower risks introducing unknown variables into the synthesis pipeline.
Years of manufacturing have shown that subtle variations in quality directly impact batch reproducibility for pharmaceutical intermediates. Many clients in both academic and industrial settings require this compound for their specific lineage of nitrothiazole-based pharmaceuticals and research chemicals. Our experience tells us a sharp melting point—typically around 224–228°C—signals a clean product. If the melting point range drifts, it's a sign to reinvestigate the process, whether that means the nitration step or acylation.
Not all 2-Acetamido-5-Nitrothiazole is made equal. It isn’t just about the base chemical structure; several manufacturers cut corners, skipping advanced purification or using impure recrystallization solvents. From a manufacturing point of view, the knock-on effects could include lower yield or the formation of side-products further downstream. We choose pharmaceutical-grade solvents and control pH closely during synthesis, limiting degradation and giving users more consistent results batch after batch. Chemists counting on consistent HPLC traces notice the reliability, whether they're assembling new drug molecules or studying reconjugation reactions.
Specification sheets rarely tell the whole story. Years ago, a batch with “spec-compliant” levels of inorganic salt content led to unsolvable precipitates for a client scaling up a lab process. The recognized safe limits for related thiazole impurities—such as unreacted nitrothiazole or over-acylated byproducts—don’t always address the unpredictable nature of real-world reactivity. A supplier might offer a 98% assay, but seldom describe how remaining 2% affects shelf stability or compatibility with lab techniques like column chromatography.
We commit to producing 2-Acetamido-5-Nitrothiazole in environments segregated from compounds with interfering functional groups. Cross-contamination may seem rare in theory, but after witnessing a ruined kilo-scale run due to minor nitrocontaminants, we doubled hygiene procedures. Open communication with our clients revealed that chemists often use our material for multi-step biotransformation experiments or as a substrate for targeted synthesis of antibacterials. In these cases, even small inconsistencies can derail research schedules or regulatory approval timelines.
Usage defines expectations. Many clients focus on its role as an intermediate for nitrothiazole antimicrobial agents. The nitro group, placed critically at the 5-position, proves especially useful for medicinal chemists seeking to modify activity or reduce toxicity of existing drugs. Our partners in custom synthesis ask not just for material, but for flexibility—like packaging smaller or strictly sealed lots to reduce exposure to humidity and light, which otherwise causes slow degradation.
In our plant’s R&D labs, 2-Acetamido-5-Nitrothiazole enables novel derivatization work. Advanced research teams develop derivatives by selectively reducing the nitro group or adjusting the acetamido substituent, which opens paths to compounds with improved therapeutic profiles. This wouldn’t be possible if we didn’t maintain high purity and stability. Early in our production, issues with minor acid residues caused rapid decomposition in some derivatives. Adjusting the neutralization step and extending drying times solved the problem, saving both resources and time.
Outside medicinal chemistry, some agrochemical developers use this thiazole derivative as a scaffold for synthesizing experimental herbicides or bactericides. The compound’s stability and nucleophilic character make it well suited for coupling reactions, even under robust reaction conditions. Without stable intermediates, yields drop, and predictive modeling in pilot runs falls apart.
Manufacturers face a stream of changing demands—stringent regulatory environments, tighter tolerances, new testing standards. Chemists ordering kilogram or multi-ton lots of 2-Acetamido-5-Nitrothiazole look for transparency about how a batch is made and what analytical tests are in place. Our team spends time tracing raw material lots and records every synthesis batch step-by-step. Small changes in acetic anhydride batches or lot-to-lot differences in thiazole can sometimes shift conversion efficiency, so every new run starts with small-batch pilot verification. Although some may see this as delay, for us these checks reduce returns, minimize complaints, and keep long-term partnerships steady.
Trace metal analysis is another step that grew in importance after feedback from electronics researchers who found catalytic interference when trace iron got above 15 ppm. Today, our ICP-MS testing identifies heavy metals below 5 ppm, and if we see a spike, we hold shipment. From our point of view, downtime for testing trumps the cost of flawed research or product recalls.
Safety is not just a regulatory point; production staff see firsthand how dust control, correct filter selection, and regular storage inspections reduce incidents. The fine powder form means static and airborne particles are a real concern. Process rooms feature grounded equipment, and all staff receive specific handling training. Any manufacturer can list an MSDS page, but practical procedures in daily work matter more. Emergency drills and rapid-response protocols catch small spills before they threaten broader facility safety or product integrity.
Some clients ask how 2-Acetamido-5-Nitrothiazole compares to structurally related thiazole derivatives or less-complex nitroaromatic intermediates. From a synthetic perspective, the presence of the acetamido group limits unwanted side reactions in subsequent steps. This group blocks specific reactive sites, streamlining regioselective modifications and reducing purification stages down the road.
Contrast this with 5-nitrothiazole itself: in trial runs lacking the acetamido substituent, results skewed due to competitive side-chain modifications. Higher waste, lower yield. Adding acetamido not only cleans up later stages, but increases solubility in select polar solvents, which laboratory groups appreciate during workup and crystallization.
Another distinction: compared to common nitro-substituted aromatic compounds, 2-Acetamido-5-Nitrothiazole remains less prone to redox degradation under standard storage. Some related nitroaromatic molecules drop purity as they oxidize further in typical glass or plastic packaging, creating problems for months-long research. Our thiazole-based intermediate stays stable under dry, cool conditions for up to twenty-four months—no need for exotic preservation or inert atmosphere storage.
Clients sometimes ask about substituting this intermediate with other acetylated heterocycles. In our experience, unless the research goal involves totally re-engineering the final product, this substitution leads to unpredictable results and threatens reproducibility. The thiazole core and specific group orientation are key to precise transformations needed for many medicinal and fine chemical syntheses. The effort, time, and cost of re-optimizing every subsequent step discourage easy replacement, especially where established regulatory or patent frameworks already recognize this exact scaffold.
Experience producing 2-Acetamido-5-Nitrothiazole, year over year, teaches manufacturers to balance consistency, responsiveness, and technical know-how. Each new order presents its own challenges: whether large multinational projects or a small lab startup’s first kilogram. Open communication with chemists, quality managers, and purchasing agents offers insight into changing trends, bottlenecks, or regulatory shifts. Periodic technical exchanges help us adapt process screens, introduce new in-process analytics, or modify purification to improve our process and product.
Feedback from end users often goes beyond what technical datasheets predict. For example, an academic medicinal chemistry group once ran into solubility problems when scaling up their protocol; our technical team consulted directly, suggesting changes to their workup water pH based on how our material handled in similar plant settings. Real-world solutions come out of such direct exchanges rather than relying on generic product literature.
Smaller startup clients sometimes run into cashflow issues, prompting them to request split shipments or alternative payment schedules. By understanding the pressure points for young companies or research institutions, we adapt our batch scheduling and logistics. This flexibility means both sides build trust, and, more often than not, we see these clients grow and return for larger orders. Their success fuels our own longevity and strengthens relationships across multiple industries.
Producing any nitro compound involves naturally tricky chemistry, chiefly due to safety risks and environmental burden. Our plant’s wastewater treatment treats nitro effluent with specialized reduction steps before discharge, protecting local water sources. Evaporative losses and air handling keep workplace exposure and community emissions to a minimum. These practices don’t merely tick regulatory boxes; workers live near the plant, so our commitment to safety and sound environmental performance is personal as well as professional.
Newest investments focus on solvent recovery to further reduce environmental load. Acetic acid reclaimed from acylation steps is purified and recycled back into batch processing—less waste leaves the site, and raw feedstock volumes drop. This approach benefits the business as well as the environment. Tracking emissions and chemical release inspires tweaks in daily process parameters, often leading to both cost savings and improved batch reproducibility.
Emerging regulations in some markets require increasingly specific documentation, from detailed impurity profiles to shipment carbon footprints. Meeting these evolving standards calls for continuous investment in analytical equipment and process tracing, not just for external compliance, but also to preempt failures and inefficiencies that interrupt reliable product delivery. By making traceability and analytics part of our daily work, we future-proof our plant as well as our client supply chains.
Having compounded, tested, and shipped 2-Acetamido-5-Nitrothiazole for years, it’s clear why demand remains high. The blend of selectivity, reactivity, and relative stability under standard storage stands out for teams tackling complex synthesis. Medicinal chemists look for intermediates that don’t break down unexpectedly or contaminate downstream products. Our material’s shelf life and batch consistency support these goals, enabling quicker turnarounds and deeper trust in collaborative projects.
Regular feedback from users suggests that practical support—such as providing technical background during scale-up or helping troubleshoot purification—matters as much as a certificate of analysis. Quality alone doesn't win long-term customers if a partnership lacks transparency or responsiveness. Whether a partner asks about solvent compatibility or regulatory documentation, those conversations guide how we update and refine our production playbooks.
In the chemical industry, progress stems from listening, adapting, and investing in both people and technology. As users diversify their applications—developing new pharmaceuticals, investigating antibacterial coatings, or testing agricultural actives—we keep modifying our production routines to meet specifics of each use case. Lab automation, more precise temperature control, and faster analytics mean purer output at scale. Regular training and safety reviews keep staff prepared for any production surprises that inevitably crop up in complex chemistry.
With supply chains tightening and global markets demanding precise lead times, maintaining a reliable track record grows more valuable. Long-term relationships with suppliers of thiazole and acetic acid ensure steady input quality. Routine review of purification techniques weeds out subtle new impurities before they affect larger batches. Consultants and visiting scientists sometimes walk through our plant, ask questions about process control or quality checks, and their insight sharpens our own.
Emergency preparedness—a lesson drawn from both real and near-miss incidents—now integrates into each shift handoff and site inspection routine. Production and logistics teams coordinate with regulatory and technical staff to keep shipments compliant and documentation up-to-date, letting our partners focus on their research without endless back-and-forth over missing paperwork or inconsistent labeling.
Producing and supplying 2-Acetamido-5-Nitrothiazole isn’t just about following a chemical recipe. Success comes from understanding where small changes create big ripple effects in downstream research and manufacturing. Real-world experience—learning from setbacks, improving process with every batch, listening to user feedback—shapes how reliable, high-quality product makes it from plant to lab and beyond. As needs evolve and chemistry grows more complex, keeping standards high and communication open means users keep coming back, which drives all of us to refine what we do, every day.