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HS Code |
820992 |
| Productname | Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate |
| Casnumber | 54160-14-4 |
| Molecularformula | C10H10N2O2S |
| Molecularweight | 222.27 g/mol |
| Appearance | Light yellow to brown crystalline powder |
| Meltingpoint | 146-150°C |
| Solubility | Slightly soluble in water; soluble in organic solvents (e.g., DMSO, ethanol) |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8°C |
| Synonyms | Ethyl 6-carboxy-2-aminobenzothiazole |
| Smiles | CCOC(=O)c1ccc2nc(sc2c1)N |
| Inchikey | NPZSVBMLDQZJJP-UHFFFAOYSA-N |
As an accredited Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle with a tamper-evident seal, labeled with hazard information and CAS details. |
| Shipping | Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate is shipped in tightly sealed containers, protected from moisture and light. It is typically transported as a solid, under ambient or cool conditions, with appropriate hazard labeling. Handling and shipping comply with relevant safety regulations for laboratory chemicals, ensuring safe and secure delivery to the destination. |
| Storage | Store **Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, incompatible substances (such as strong oxidizers), and moisture. Keep the container properly labeled. Use appropriate personal protective equipment when handling and ensure storage under recommended laboratory chemical storage guidelines. |
Applications of Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate in Industrial ManufacturingAs a specialized manufacturer of Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate, we support industries with consistent quality and supply for precise downstream integration. Our expertise ensures the raw material performs efficiently across key segments requiring purity, stability, and strict conformity with sectoral standards. Below, we outline the primary downstream industrial applications where this compound is established in actual production and provide targeted technical details for each segment. 1. Active Pharmaceutical Ingredient (API) Intermediate for Antimicrobial AgentsThis compound functions as an essential building block for the synthesis of several benzothiazole-based antimicrobial pharmaceuticals. Formulators and process chemists incorporate the material as a core intermediate during multi-step organic synthesis routes, where structural integrity is critical for the targeted antimicrobial activity in finished drugs. API manufacturers rely on rigorous analytical verification and regulated manufacturing practices to ensure batch consistency and traceability. Industry compliance standards
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2. Organic Synthesis Intermediate for Agrochemical Active CompoundsIn crop protection product manufacturing, this compound serves as a synthetically valuable intermediate for the construction of heterocyclic scaffolds present in many modern fungicides and insecticides. Agrochemical formulators integrate this raw material during the targeted functionalization step to introduce amino and ester groups, critical for biological activity and target specificity in field applications. Industry compliance standards
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3. Luminescent Ingredient in Dyes and Optical BrightenersSpecialty dye and optical brightener manufacturers employ this compound for the creation of luminescent benzothiazole derivatives. Its inclusion enhances fluorescence properties required for textile, plastics, and paper applications. Technicians monitor the material’s reactivity profile to optimize shade, intensity, and durability under different processing temperatures and pH conditions during bulk dyeing or coating operations. Industry compliance standards
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4. Chemical Intermediate for Specialty Polymer SynthesisManufacturers of advanced functional polymers utilize this compound as a key monomeric precursor in the synthesis of benzothiazole-modified polymer chains. Its chemical structure permits precise control over the resulting polymer’s thermal properties, mechanical resistance, and electronic performance, making it valuable in high-end coatings and engineered thermosets for electronics and automotive applications. Formulation chemists focus on consistency in purity and molecular weight impact. Industry compliance standards
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Direct experience in manufacturing specialty chemicals brings an appreciation for the significance of each intermediate. Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate shows up again and again as a lynchpin for many downstream products. In our production environment, tight control in every synthesis step makes a difference—starting from how we manage raw materials, through to purification and characterization. Diverse clients—from pharmaceutical innovators to agricultural product formulators—rely on consistent, reliable deliveries for their own internal R&D and production schedules.
Every batch reflects a convergence of careful process monitoring and attention to supply chain realities. We have seen how the wrong grades of starting materials or inaccurate moisture content throw off reaction yields or mess with downstream purification. To solve this, we use dedicated storage for moisture-sensitive intermediates, and for Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate we limit exposure to air, which helps preserve its appearance and minimize degradation before it reaches formulation or coupling reactors.
Having a precise handle on what makes this compound unique can mean success or failure in target synthesis pathways. The benzothiazole core, with its ethyl ester and amino group substitutions at the 2 and 6 positions, plays well in a variety of condensation and cyclization reactions. In drug synthesis projects, chemists value the electron-donating amino moiety and the reactivity of the carboxylate segment for stepwise modifications and ring-closure strategies. For some, it's an intermediate leading toward anti-microbial candidates, fluorescent probes, or dyes with notable stability.
Our technical staff has learned that purity above 98%—with attention to-off isomeric forms and trace metal content—removes roadblocks in downstream pipelines. By conducting NMR and LC-MS quality checks in-house, we edge out the unpredictable downstream failures that can hit when dealing with suppliers focused primarily on commodity throughput. There's a visible difference in how products perform in real-world synthesis laboratories: reduced side products, higher conversions, and simpler workup processes save valuable project hours. These are not abstract improvements but real gains our own team depended on in developing process validations.
The reality with Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate is that not all material labeled with the same name behaves alike. Different production sites leave distinct fingerprints—residual solvents, minor process impurities, or microscale particle size differences. We recall a case in partner labs where trace acetic acid left over from esterification led to unexpected transesterification later in a multistep process, underlining the necessity of clear analytical data, not just a certificate to tick a box.
Continual improvement in our own analytical methods—adding HPLC trace impurity detection and updating drying protocols—has resulted in reliable stocks that withstand extended transport and storage without forming lumps or yielding unpredictable results. Staff investments in cross-training mean multiple sets of eyes on routine data, not just at batch release but also over the product’s shelf life. These lived details translate to shipments with consistent particle size and composition, reducing downstream rework.
Within the family of benzothiazole compounds, subtle changes in functional groups lead to dramatic differences in physical handling, reactivity, and safety data. We have handled derivatives with methyl, ethoxy, or amide substitutions at the 6 position, or where the amino group is shifted or replaced. Each brings its own set of handling and process requirements. In our workshops, the ester form, Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate, provides much softer material at room temperature and dissolves smoothly in most common polar organics. This fluidity stands in contrast to the carboxylic acid analog, which clumps with moisture and gives poor reproducibility for direct esterification steps.
Compared to the methyl ester, the ethyl variant delivers lower volatility and greater compatibility in slow-heating protocols—an edge for users seeking tighter thermal control. The amino substitution at the 2-position also affords greater engagement in peptide coupling chemistry, an observation our lab staff made in side-by-side test syntheses. These nuances do not just define lab process yields—they also reflect back in product shelf life, shipping cost, and even on environmental health and safety reporting for downstream users.
Production teams that deal with this compound daily come to appreciate the way it holds up under varying storage conditions. By implementing humidity-monitored storage and using nitrogen sparge tanks for bulk transfers, we have reduced the risk of hydrolysis and discoloration. In multi-ton batches, small lapses in storage protocol show up as reduced purity on the back end. Addressing these, we enforce a logistical discipline from weighing to bottling. Employees receive regular refresher training in personal protection, spill protocol, and correct decanting to preempt skin and eye exposure—practices that came about from direct lessons with older, less stable analogs.
As our own site moved away from small batch glassware to jacketed stainless reactors, we learned to avoid hot spots and minimize decomposition by integrating real-time temperature and pH controls. These upgrades produced more uniform quality and opened up the door to larger, more reliable batch sizes while keeping post-production blending and sampling transparent. Each iteration is driven by lessons logged from previous cycles—sometimes mistakes, sometimes customer feedback, always pushing toward better product stewardship.
Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate has proven versatility for research and production groups. The basic platform supports a diversity of end uses: as a building block in heterocyclic drug synthesis, as a precursor for specialty dyes, and even within agricultural innovation projects. When our technical service team fields questions from formulation scientists, the common theme is reliability over multiple cycles—not just purity on day one. Our own hands-on tests with derivatization reactions have reinforced its reputation as a predictable performer: reproducible melting points, clean isolation, and minimal need for multiple washes.
Some long-term relationships with buyers grew out of joint resolution of tough process issues—such as unwanted dimerization owing to improper solvent selection, or handling protocols that led to static build-up and lost material. We’ve addressed these by refining flow rates, suggesting more robust anti-static packaging, or consulting direct on blend ratios. In one example, a client kept running into discoloration in stored intermediates; after visiting their facility, we shared modified secondary containment methods, which cut their issues almost entirely. This collaborative attitude spreads from our own plant, where production, QC, and customer teams are just as likely to swap notes on tough batches as they are to record new best practices.
Transitioning from kilogram quantities for bench-scale synthesis to hundreds of kilograms for commercial runs introduces pressure points. Heat transfer, mixing uniformity, and containment requirements change as batch sizes grow. Our chemists learned to anticipate challenges like incomplete mixing or phase separation, even with subtle differences in solvent composition. The solution came through installing new inline blending systems and recalibrating agitation speeds for different vessel geometries.
Quality teams don’t just sign off based on initial purity. They double-check retention times, look for trace impurities, and test storage stability under simulated transport conditions. Our policy came out of direct feedback from end users who suffered losses—not only from flawed deliveries, but from batches that arrived out of specification due to storage mishaps. As a manufacturer, we have resources that many traders or third-party packagers do not: real-time access to raw and finished inventory, knowledge of every upstream and downstream sample history, and the ability to respond at the earliest symptoms of deviation. This trust—earned, not declared—anchors repeat relationships.
Manufacturing Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate safely means more than tuning a reaction and collecting product. Years ago, regulations on emissions and solvent disposal grew tighter. Rather than look for shortcuts, we redesigned solvent recovery systems and adopted stricter controls over nitrogen and volatile organic compound (VOC) handling. By capturing, condensing, and reusing organic vapors, we lowered plant costs and brought emissions well below current guidelines.
On-site, spill and containment protocols use lessons from near-miss incidents as well as formal HAZOP reviews. Operators know firsthand how quickly a minor leak can escalate into real risk, so we keep all storage and transfer operations under continuous monitoring and train staff in fast incident reporting. Our documentation reflects candid self-assessments, and our public disclosures on environmental performance have validated investments in process safety upgrades. Responsibility doesn’t just appease regulations—it keeps our community safer and builds real-world trust.
Open communication with the technical and sourcing teams of our partners shaped several innovations in this product line. Some requests focused on tighter control of residual esterification agents, or batch-to-batch color matching for demanding dye applications. Others asked for particle size modification to suit high-throughput reactors, or more accurate water content reporting to drive closed-system operations. Rather than pushing off these requests for “standard grades,” we re-tooled small parts of our production, sometimes re-testing older processes or revisiting filtration methods.
Access to technical staff who understand not just paperwork but practical process chemistry makes a difference. Staff follow up on every support request—sometimes with a sample shipment, sometimes with a troubleshooting call to study the user’s process directly. Over time, these exchanges built the knowledge base that later forms the core of both our production improvements and our new product development. With the global spread of researchers and technology partners, expectations stretch further, so adapting to bespoke demands for cloud point, purity, or trace element content became part of our continuous improvement program.
Over the last few years, global supply pressures occasionally squeezed raw material flows and extended lead times, especially for fine chemicals derived from niche feedstocks. Real flexibility comes from investments in diverse sourcing, advance purchase agreements with upstream partners, and inventory practices that absorb shocks without cascading into production stops or risky substitutions. Communication with our logistics partners identifies possible delays ahead of time, and we keep alternate shipping channels on hand to avoid customs or port bottlenecks.
Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate rarely wins headlines in global commodity reports, but it’s built into the supply-risk models we use for both long-term contracts and new product rollouts. Knowing exactly how much product is held in cold storage, how quickly material can be released for rush orders, or where strategic reserves live, provides reassurance down several layers of the value chain.
The most rewarding part of manufacturing is seeing real products, real yields, and real improvements in a client’s hands. Across years of production, our team encountered every scenario—from idealized R&D conditions to hard-edged commercial realities—so every jar leaving our site leverages those lessons. Unlike generic distributors, we know the quirks that come with this compound: the way moisture can creep into open containers, the difference in filterability against similar analogs, or the method to rescue a partially caked batch without loss of quality.
A competitive advantage lies in tackling issues at the origin—focusing on repeatable processes and investing in people who care about both detail and scale. Customers need more than a shipment; they seek partners able to respond, adapt, and explain. Whether the discussion concerns adoptability in a new solvent regime, extending product shelf life for heat-sensitive formulations, or uncovering the root cause behind inconsistent crystal morphology, real-world answers come from hands-on manufacturing experience.
Manufacturing fine chemicals means carrying responsibility from start to storage, from process tweaks to end-user support. Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate does more than supply a functional group—it enables a range of complex syntheses and innovation projects. Each container, as it ships from a trusted production floor, reflects the everyday discipline of process improvement, analytical testing, and the adaptations made to meet evolving customer needs.
What stands out across all challenges and changes in the industry is a straightforward truth: dedicated manufacturing delivers more than purity on paper. Our years with this compound—tracking, tweaking, and troubleshooting—gave us proof that details matter, and that real value also comes from honest communication and support. For every development goal, research cycle, or scale-up trial, having reliable, consistent Ethyl 2-Amino-1,3-Benzothiazole-6-Carboxylate in hand gives researchers and producers the confidence to focus on what they do best, sure that their foundation is sound.