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2-Naphthalenethiol

    • Product Name 2-Naphthalenethiol
    • Alias 2-Naphthalenethiol
    • Einecs 205-355-5
    • 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
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    Specifications

    HS Code

    807816

    Name 2-Naphthalenethiol
    Cas Number 91-60-1
    Molecular Formula C10H8S
    Molecular Weight 160.24 g/mol
    Appearance Yellow to brown crystalline powder
    Melting Point 47-50 °C
    Boiling Point 194-196 °C (15 mmHg)
    Density 1.22 g/cm3
    Solubility In Water Insoluble
    Smiles C1=CC=C2C(=C1)C=CC=S2
    Inchi InChI=1S/C10H8S/c11-10-6-5-8-3-1-2-7-9(8)4-6/h1-5,7,11H
    Synonyms beta-Naphthalenethiol; 2-Naphthyl mercaptan
    Refractive Index 1.71 (at 71 °C)
    Pka 6.15 (of thiol group)

    As an accredited 2-Naphthalenethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 2-Naphthalenethiol (25g) is a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 2-Naphthalenethiol is shipped in tightly sealed containers under cool, dry, and well-ventilated conditions, away from sources of ignition, heat, and incompatible materials. Proper labeling and hazardous material documentation are mandatory. Standard packaging includes glass or plastic bottles, compliant with transport regulations for flammable and toxic chemicals. Handle with appropriate safety precautions.
    Storage 2-Naphthalenethiol should be stored in a tightly sealed container, away from light, heat, and moisture. Store it in a cool, well-ventilated area, separate from oxidizing agents, acids, and strong bases. Proper labeling and secure storage help prevent accidental exposure. Use chemical-resistant containers, and ensure access to appropriate spill containment and emergency equipment.
    Application of 2-Naphthalenethiol

    Applications of 2-Naphthalenethiol in Industrial Manufacturing

    We supply 2-Naphthalenethiol directly from manufacturer facilities, supporting a range of specialized industrial sectors where this compound’s thiol reactivity and aromatic structure are essential for advanced downstream applications. The following overview details verified end-use scenarios, with a strict focus on sectors leveraging 2-Naphthalenethiol as a functional intermediate, process aid, or synthesis raw material.

    1. Agrochemical Intermediate Synthesis

    2-Naphthalenethiol serves as a sulfur donor in the customization of pesticides and fungicide molecules, especially for creating heterocyclic thioether motifs found in certain crop protection agents. Agrochemical manufacturers integrate this molecule during structure elaboration to introduce site-specific sulfur functionality, critical for bioactivity against target pests and fungal strains. Customized synthesis routes demand defined purity levels for regulatory submissions, and the addition percentage depends on the targeted synthesis step to maximize yield without process impurity buildup.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH Annex XVII (EU)
    • US EPA 40 CFR Part 158 (Toxicology Data Requirements for Pesticide Registration)
    • Good Agricultural Manufacturing Practice (GAMP) protocols for intermediates

    Typical usage ratio

    • 0.5–2.5% w/w, fine-tuned by process chemists to match target molecule conversion and downstream impurity control

    Downstream process integration

    • Introduced in sulfur functionalization or cyclization steps during multi-stage synthesis of thiolated agrochemicals

    Final product types

    • Systemic fungicides (e.g., benzenesulfonyl-containing triazoles)
    • Thioether-class insecticides
    • Seed treatment chemical actives
    • Custom crop-specific protection agents

    2. Dye and Pigment Intermediate Manufacturing

    Manufacturers of organic pigments and specialty dyes incorporate 2-Naphthalenethiol as a thiolating agent and aromatic modifier during the assembly of sulphur and azo dye intermediates. This application relies on the precise introduction of mercapto groups to achieve the desired colorfastness and brilliance in the final pigment structure, particularly for high-performance applications in plastics, fibers, and ink formulation. Process engineers control addition strictly to maintain bath composition and downstream purification efficiency.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Dye Safety)
    • ISO 9001:2015 Quality Management for colorants
    • EN 71-3 (Toy Safety – Migration of Certain Elements)
    • US FDA 21 CFR Parts 74/82 (Color Additives)

    Typical usage ratio

    • 1.0–3.0% by formulation batch weight, optimized for targeted pigment shade and solubility; exact ratio subject to pigment structure complexity

    Downstream process integration

    • Added during condensation or coupling reactions to introduce naphthylthio units into pigment molecules or dye intermediates

    Final product types

    • Pigments for plastics (e.g., modified azo dyes)
    • High-stability textile dyes
    • Colorants for printing ink concentrates
    • Industrial coating pigments

    3. Pharmaceutical API Intermediate Production

    Several pharmaceutical synthesis routes rely on 2-Naphthalenethiol as a sulfurating intermediate, particularly in the manufacture of molecules containing naphthylthio or related functional groups. Trusted by API producers to ensure regioselective thioetherification and introduce aromatic sulfur atoms, this intermediate enters schemes submitted under regulated filings, where material traceability, impurity profile, and process reproducibility are paramount. QC teams set addition rates based on target API pathway and impurity mapping.

    Industry compliance standards

    • cGMP (ICH Q7)
    • European Pharmacopoeia (EP)
    • US Pharmacopeia (USP)
    • FDA DMF (Drug Master File) submission requirements

    Typical usage ratio

    • 0.3–1.2 molar equivalents relative to pharmaceutical precursor, controlled per synthesis stage and API end-group requirement

    Downstream process integration

    • Participates in aromatic thioetherification, nucleophilic substitution, or sulfur bridge formation steps in multi-stage API intermediate assembly

    Final product types

    • Active pharmaceutical ingredient precursors with naphthylthio substituents
    • Specialty small-molecule drugs featuring thionaphthalene units
    • Chiral drug intermediates for CNS and anti-infective APIs
    • Sulfur-containing process control standards

    4. Rubber Vulcanization Accelerator Additive

    Specialty elastomer compounds—especially those based on naphthalene-extended rubber formulations—employ 2-Naphthalenethiol as a secondary accelerator to fine-tune cure rate and crosslink structure. It enters the compounding phase to improve network formation, thermal stability, and aging resistance, particularly for industrial-performance rubber and technical seals. Compounders adjust addition based on specific vulcanization profile, balancing speed with finished article durability.

    Industry compliance standards

    • ASTM D2000 (Standard Classification System for Rubber Products)
    • ISO 9001:2015 (Rubber Processing QC)
    • RoHS Directive (2011/65/EU) for restricted substances
    • PAH content according to GS Mark (product safety)

    Typical usage ratio

    • 0.2–1.0 phr (parts per hundred rubber), dependent on base elastomer type and desired crosslink density

    Downstream process integration

    • Dispersed during masterbatch mixing as a co-accelerator before vulcanization press and curing step

    Final product types

    • High-performance industrial hoses
    • Vibration damper rubber components
    • Technical seals and gaskets
    • Wear-resistant conveyor belts

    5. Organic Electronic Material Precursor

    Producers of organic semiconductors and luminescent materials use 2-Naphthalenethiol during precursor synthesis to introduce sulfur motifs that enhance device charge mobility and tune electro-optical properties. Integration occurs at the building-block assembly stage, where rigorous material traceability and functional group consistency guarantee downstream film uniformity and device lifespan, especially important for OLED layers and sensor substrates.

    Industry compliance standards

    • IEC 62899 (Printed Electronics Standards)
    • ISO 14001:2015 (Environmental Management for electronic materials)
    • RoHS Directive (2011/65/EU)
    • UL 94 (Flammability of Plastic Materials)

    Typical usage ratio

    • 0.8–2.5% w/w, varied by target precursor chain length and functionalization density based on device application (e.g., OLED display or organic transistor)

    Downstream process integration

    • Participates in building-block synthesis for thiolated naphthalene monomers before post-polymerization or thin-film deposition

    Final product types

    • Organic light-emitting diode (OLED) layers
    • Organic field-effect transistor (OFET) materials
    • Photoconductive polymer sensor substrates
    • Printable organic semiconductors
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