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Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate

    • Product Name Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate
    • Alias 3-Amino-5-tert-butyl-2-thiophenecarboxylic acid methyl ester
    • Einecs 642-124-5
    • 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

    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 & Storage
    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.
    Application of Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate

    Applications of Methyl 3-Amino-5-(Tert-Butyl)Thiophene-2-Carboxylate in Industrial Manufacturing

    As 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) Synthesis

    Many 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals where applicable)
    • European Pharmacopoeia monographs by drug target
    • US DMF (Drug Master File) referencing for regulatory submission

    Typical usage ratio

    • 3–10 mol% relative to total API precursor; adjusted based on molecular weight and yield
    • Batch size from 1 kg lab scale to 500 kg production scale with validated scalability

    Downstream process integration

    • Integrated as the primary amination building block
    • Participates in the condensation or cyclization step post-ester protection adjustment
    • Undergoes quality release before reaction charge-in

    Final product types

    • Thiophene-based small molecule APIs
    • Central nervous system (CNS) disorder treatment APIs
    • Non-steroidal anti-inflammatory drug (NSAID) molecules
    • Advanced research-grade pharmaceutical intermediates

    2. Agrochemical Synthesis – Herbicide Active Ingredient Precursors

    Agrochemical 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

    • ISO 9001:2015 for chemical production management
    • FAO/WHO Specification for Pesticides
    • REACH pre-registration & safety data dossier for EU distribution
    • China GB/T 1600–2018 for agricultural chemicals

    Typical usage ratio

    • 5–15 wt% as intermediate in multi-step herbicide synthesis
    • Adjusted by crop target and desired herbicidal spectrum

    Downstream process integration

    • Initial coupling to core structure during route scouting
    • Chlorination or alkylation for final active composition
    • Intermediate QC for identity and impurity profile

    Final product types

    • Triazole-thiophene herbicide technical concentrates
    • Granular and liquid herbicide formulations
    • Pre-emergent agricultural herbicides

    3. Advanced Electronic Materials – Organic Semiconductors Synthesis

    Electronic 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

    • ISO 9001:2015 certified production & traceability
    • RoHS Directive (2011/65/EU) compliance for electronic material restrictions
    • IEC 62690 for organic electronic device materials

    Typical usage ratio

    • 0.5–2 mol equivalents relative to total semiconductor monomer input
    • Batch adjustments based on desired charge transport behavior

    Downstream process integration

    • Enters monomer pool in Stille or Suzuki coupling polymerizations
    • Post-reaction purification using preparative LC or recrystallization
    • In-line QC for purity/structure

    Final product types

    • Organic FET (OFET) substrate layers
    • Active layers for organic solar cells
    • Printed electronic sensor films

    4. Specialty Polymer Modification Additive

    Manufacturers 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

    • ISO 14001 for environmental management systems in chemical processing
    • ASTM D638 test method for polymer material properties
    • REACH compliance for batch documentation

    Typical usage ratio

    • 0.1–3 parts per hundred resin (phr) in base polymer formulation
    • Ratio adjustment per product performance testing and electrical specification

    Downstream process integration

    • Fed into extruder during melt blending
    • Alternatively introduced via solution mixing for specialty films
    • Quality monitored by spectroscopic and thermal analytics

    Final product types

    • Antistatic polycarbonate blends
    • Photoresponsive polymer films
    • Electrically conductive engineering plastics
    • Flexible printed circuit substrates
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