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HS Code |
481579 |
| Product Name | Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate |
| Molecular Formula | C10H15NO2S |
| Molecular Weight | 213.30 g/mol |
| Appearance | Solid (exact color may vary from off-white to light yellow) |
| Purity | Typically ≥ 95% (as provided by most suppliers) |
| Solubility | Soluble in organic solvents such as ethanol, methanol, and DMSO |
| Smiles | CC(C)(C)c1cc(N)sc1C(=O)OC |
| Inchi | InChI=1S/C10H15NO2S/c1-10(2,3)7-5-8(11)14-9(7)6(12)13-4/h5H,11H2,1-4H3 |
| Storage Temperature | Store at 2-8°C, protected from light and moisture |
As an accredited Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass vial with a tamper-evident cap and labeled for laboratory use only. |
| Shipping | Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate is securely packaged in sealed containers to prevent moisture and contamination. Shipped under ambient conditions unless otherwise specified, it is labeled according to chemical safety regulations and complies with all transport guidelines for handling organic compounds. Expedited or temperature-controlled shipping is available upon request. |
| Storage | **Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep at room temperature and protect from moisture. Ensure that the storage area is equipped for handling organic chemicals and has appropriate spill containment measures. |
Applications of Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate in Industrial ManufacturingAs a producer, we supply Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate directly for advanced specialty applications in pharmaceutical synthesis, agrochemical intermediates, electronic material production, and specialty polymer modification. Below we outline the main downstream use cases, addressing regulatory requirements, typical incorporations, industry-specific integration points, and finished product forms. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisMany pharmaceutical manufacturing operations employ this compound as a key intermediate in the synthesis chain of thiophene-based API structures, especially within central nervous system (CNS) and anti-inflammatory drug research pipelines. The compound undergoes downstream amidation and cyclization reactions during multi-step synthesis; it requires tight compliance and batch traceability. Clients establish production campaigns based on the regulatory approval stage of the related API molecule, scaling up under Good Manufacturing Practice frameworks. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide Active Ingredient PrecursorsAgrochemical manufacturers use this thiophene derivative as a functional intermediate in the creation of selective herbicide actives. Its amino and ester functionalities allow flexible ring modification and side chain extension for structure-activity optimization. Downstream processing often involves chlorination, side-chain introduction, and final formulation under controlled industrial environments to ensure result consistency. Industry compliance standards
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3. Advanced Electronic Materials – Organic Semiconductors SynthesisElectronic material producers employ this compound for the design and synthesis of advanced organic semiconductors, particularly in the development of thiophene-based field-effect transistors (OFETs) and organic photovoltaic (OPV) materials. Its tert-butyl group and amino placement enhance solubility and electronic modulation, supporting fine-tuning of mobility and on/off characteristics during device prototyping and scale-up. Industry compliance standards
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4. Specialty Polymer Modification AdditiveManufacturers of advanced engineering plastics and specialty copolymers integrate this thiophene material as a chain modifier to impart targeted electrical conductive properties and photo-reactivity. The unique combination of amino and bulky tert-butyl functions allows chemical grafting into polymer backbones, improving material response in optoelectronic and specialty film markets. Processing involves melt blending or solution grafting, depending on the desired polymer matrix and application. Industry compliance standards
Typical usage ratio
Downstream process integration
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