Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales6@sinochem-nanjing.com
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Thiophene

    • Product Name Thiophene
    • Alias Thiolan
    • Einecs 205-328-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    202298

    Chemical Name Thiophene
    Molecular Formula C4H4S
    Molar Mass 84.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 84°C
    Melting Point -38°C
    Density 1.051 g/cm³
    Odor Pleasant, similar to benzene
    Solubility In Water Slightly soluble
    Flash Point 4°C
    Vapor Pressure 80 mmHg (20°C)
    Refractive Index 1.528 (20°C)
    Cas Number 110-02-1

    As an accredited Thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Thiophene is supplied in a 500 mL amber glass bottle with a tightly sealed cap, labeled with hazard warnings and product details.
    Shipping Thiophene should be shipped in tightly sealed, properly labeled containers, away from sources of ignition due to its flammable nature. Transport must comply with relevant local, national, and international regulations. Use of UN-approved packaging and placement in well-ventilated vehicles is recommended. Keep separate from oxidizing agents and strong acids during transit.
    Storage Thiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Use tightly sealed containers made of compatible materials to prevent leaks. Keep away from strong oxidizing agents and acids. Proper labeling and grounding of containers are essential to minimize fire risk, as thiophene is flammable and volatile.
    Application of Thiophene

    Applications of Thiophene in Industrial Manufacturing

    Our thiophene production supports advanced industrial processes globally. Across several high-value chemical sectors, thiophene provides critical molecular building blocks in customer formulations and synthesis protocols.

    1. Synthesis of Pharmaceutical Intermediates

    Thiophene serves as a key aromatic precursor in the manufacture of advanced pharmaceutical intermediates, enabling the construction of heterocyclic scaffolds for drug discovery and API (active pharmaceutical ingredient) synthesis. Customers rely on its controlled reactivity and high purity to produce cardiovascular, anti-inflammatory, and CNS-active agents. We supply thiophene that is suitable for stringent pharmaceutical elaboration, ensuring batch-to-batch reproducibility and compliance with regulatory-driven specifications throughout the downstream process.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF Monographs (where applicable to end-use APIs)
    • EU EudraLex Vol. 4 (GMP Guidelines)
    • 21 CFR Part 210/211 (US FDA regulations)

    Typical usage ratio

    • 0.5–2.5 moles per mole of target intermediate, adjusted to route-specific yield and conversion efficiency
    • Stoichiometry may shift for acylation or oxidative coupling protocols

    Downstream process integration

    • Thioether introduction step in heterocycle synthesis
    • Grignard or metal-catalyzed cross-coupling at early intermediate stage
    • Precursor input for selective sulfonation or halogenation
    • Support for multi-step synthetic routes under GMP environmental controls

    Final product types

    • Antihypertensive agent intermediates
    • Pain management pharmaceuticals
    • Antidepressant and CNS drug scaffolds
    • Custom-built drug discovery libraries

    2. Production of Conjugated Polymers and Conductive Materials

    Formulators and engineers in the electronics sector require thiophene as a direct monomer for the synthesis of polythiophene and related conductive polymers. Its aromatic structure provides the electroactive backbone crucial for optoelectronics, OLED layers, and antistatic coatings. Tight control over monomer purity and inhibitors supports customer requirements for predictable polymerization kinetics and high electronic performance in finished devices.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • IEC 62679-2-1 for electronic display component manufacturing
    • RoHS (Restriction of Hazardous Substances) compliance for electronic materials
    • REACH Regulation for monomers and polymer products

    Typical usage ratio

    • 100 mol% as a principal feedstock in oxidative polymerization
    • Blend ratios of 5–40% with comonomers for copolymer tuning
    • Loading based on film thickness (20–200 nm) and device design

    Downstream process integration

    • Direct loading into chemical vapor deposition (CVD) reactors
    • Feed for in situ solution or electropolymerization units
    • Monomer blending stage for custom polymer precursor solutions
    • Integration with connectivity and patterning lines in PCB and display fabrication

    Final product types

    • Antistatic layers for transparent displays
    • Organic solar cell active films
    • OLED and flexible display modules
    • Printable electronic circuitry

    3. Agrochemical Intermediate and Pesticide Manufacturing

    Chemical formulators in agricultural protection utilize thiophene as a heterocyclic starting material for synthesizing a range of fungicide and insecticide intermediates. Our production enables custom substitutions on the thiophene ring, driving the development of high-activity, selective agents. Customers require analytical-grade purity to guarantee crop safety, environmental compliance, and successful regulatory submissions for new molecule registrations.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Ingredients
    • OECD Guideline 106 (Adsorption/Desorption for environmental fate)
    • ISO 17025 for analytical characterization in quality control
    • EU Reg. 1107/2009 (Plant Protection Product regulatory framework)

    Typical usage ratio

    • 0.2–1.2 equivalents per target intermediate, based on core reaction pathway
    • Adjustment depending on desired substitution and functionalization pattern

    Downstream process integration

    • Early-step input to heteroaromatic building block synthesis
    • Coupling agent for sulfonamide or carboxyl derivative formation
    • Ring basis for bioactive moiety attachment in pilot or full-scale reactor trains
    • QC validation for maximum residual solvent or impurity controls

    Final product types

    • Broad-spectrum fungicide precursors
    • Insecticide and acaricide active agent cores
    • Synergist building blocks for agro formulations
    • Registered crop protection active substances

    4. Synthesis of Dye and Pigment Precursors

    Customers in specialty chemicals manufacture use thiophene as a precursor molecule to synthesize high-performance dyes and pigments, especially for technical textile applications and ink systems. Its ring structure enhances chromophores' electron delocalization, translating to improved stability and color retention in processed fibers and coatings. Precise thiophene dosing, alongside strict purity standards, ensures batch consistency and compliance with global ecolabel specifications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • ISO 9001:2015 for specialty colorant production
    • REACH registration for intermediates
    • GOTS (Global Organic Textile Standard) chemical input compliance

    Typical usage ratio

    • 1–10% of total chromophore mass, depending on final pigment shade or dye performance specification
    • Dosage adjustment driven by intended lightfastness and application coverage

    Downstream process integration

    • Precursor charging in coupling or diazo synthesis steps
    • Incorporation into condensation or cyclization reaction stages
    • Combined blending in pigment dispersion or granulation units
    • Quality gate at spectral color matching and migration testing labs

    Final product types

    • Reactive and disperse textile dyes
    • High-durability pigments for automotive coatings
    • Printing ink dye precursors
    • Functional color additives for plastics and films

    5. Production of Flavor and Fragrance Intermediates

    Synthesizers in the flavor and fragrance industry turn to thiophene as a sulfur-containing aromatic to build vital aroma compounds. Its volatiles contribute characteristic earthy, roasted, or woody notes, providing depth in roasted food flavors and tobacco blends. We produce food-grade thiophene suitable for subsequent transformation under closely managed reaction environments with high traceability, supporting downstream FSSC 22000 or ISO 22000 certified facilities.

    Industry compliance standards

    • FEMA GRAS Status for flavoring substances (No. 3247 for thiophene)
    • IFRA Code of Practice for fragrance usage
    • Food Chemicals Codex (FCC) for purity and residue limits
    • ISO 22000:2018 for food safety management systems

    Typical usage ratio

    • 0.05–0.4% by weight in aroma concentrate formulation
    • Limits based on product outcome and odor threshold testing

    Downstream process integration

    • Direct introduction in aroma compounding reactors
    • Alkylation and oxidation steps to generate higher-order aroma chemicals
    • Blending in topnote or trace additive stages
    • Finished concentrate QC for residual solvent and organoleptic profiling

    Final product types

    • Roasted nut and coffee flavorings
    • Tobacco blending aroma agents
    • Complex fragrance bases for perfumery
    • Food-grade aroma extracts
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