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2-(2-Naphthoxy)Ethanol

    • Product Name 2-(2-Naphthoxy)Ethanol
    • Alias beta-naphthoxyethyl alcohol
    • Einecs 239-312-7
    • 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

    638611

    Chemicalname 2-(2-Naphthoxy)Ethanol
    Casnumber 612-16-8
    Molecularformula C12H12O2
    Molecularweight 188.23 g/mol
    Appearance White to off-white solid
    Meltingpoint 58-62 °C
    Boilingpoint 357.1 °C at 760 mmHg
    Density 1.18 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractiveindex 1.594

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

    Packing & Storage
    Packing Amber glass bottle, tightly sealed, labeled with hazard symbols. Contains 100g of 2-(2-Naphthoxy)Ethanol for laboratory use.
    Shipping 2-(2-Naphthoxy)Ethanol is typically shipped in tightly sealed containers to prevent moisture ingress and contamination. Containers should be clearly labeled and handled according to chemical safety regulations. The chemical should be shipped at ambient temperature, away from incompatible substances, with appropriate hazard documentation included. Compliance with local, national, and international transport regulations is essential.
    Storage 2-(2-Naphthoxy)ethanol should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances like strong oxidizers. Protect the chemical from light and moisture. Appropriate chemical safety practices and labeling should be followed. Store at room temperature unless specified otherwise by the manufacturer or Safety Data Sheet (SDS).
    Application of 2-(2-Naphthoxy)Ethanol

    Applications of 2-(2-Naphthoxy)Ethanol in Industrial Manufacturing

    2-(2-Naphthoxy)Ethanol is a specialty intermediate widely applied in chemical synthesis across diverse industrial sectors. Its structural compatibility and reactive functionality make it valuable for precise molecular adaptation in downstream manufacturing. Below we highlight recognized application areas, integrating technical use requirements and regulatory frameworks with practical process guidance.

    1. Synthesis of Optical Brightening Agents for Textiles

    Major textile chemical producers incorporate this material during the multi-step synthesis of stilbene- and naphthalene-based fluorescent whitening agents. It reacts in alkoxylation or etherification stages, typically before sulfonation and condensation. The compound’s naphthoxy moiety ensures high brightness and washfastness essential in quality textile optical brighteners. Only select derivatives meet ecolabel and product safety requirements enforced by large textile brands.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • REACH Annex XVII for restricted substances
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 14024 Type I ecolabels for textile chemicals

    Typical usage ratio

    • Initial reactions dose 2-(2-Naphthoxy)Ethanol at 0.5–1.5 molar equivalents versus core diaminostilbene or naphthalene substrates.
    • Higher ratios (up to 2:1) used in specialty high-saturation brightener grades or for end uses demanding extra UV resistance.

    Downstream process integration

    • Charged as a primary reactant in alkoxylation or etherification vessels.
    • Monitored for complete conversion on in-process HPLC systems, prior to sulfonation sequence.
    • Any unreacted content recovered for solvent fractionation and recycling.

    Final product types

    • Fluorescent brighteners for cellulosic textile finishing
    • Optical whitening agents for detergent applications
    • Brightener masterbatches for synthetic fiber spinning
    • Formulated textile auxiliaries compatible with direct/acid dyeing lines

    2. Intermediate in High-Performance Liquid Crystal Material Synthesis

    Specialty chemical firms use this naphthoxy ethanol as a building block in the manufacture of liquid crystal compounds for flat-panel displays. Its aromatic ether linkage enables tailored mesogenic structure formation. The compound enters the etherification or esterification sequence under inert conditions, precisely controlled for purity to avoid contamination in electronics end-use.

    Industry compliance standards

    • IEC 61249-2-21 (halogen-free criteria for display chemicals)
    • IPC-4101D for copper-clad laminate material compatibility
    • RoHS Directive (2011/65/EU) for hazardous substances
    • ISO 9001:2015 certified QMS for electronic chemicals production

    Typical usage ratio

    • Added at 0.25–0.9 molar ratio during intermediate synthesis depending on mesogen chain length requirement.
    • Adjusted based on desired thermal and optical properties of the resultant nematic or smectic liquid crystal formulation.

    Downstream process integration

    • Pre-dried and charged in anhydrous reaction vessels under nitrogen or argon atmosphere.
    • Transformation monitored by GC-MS and FTIR to ensure full conversion and product selectivity.
    • Integrated into downstream mixing stages for final liquid crystal compound assembly.

    Final product types

    • Display-grade liquid crystal monomers
    • Processed LCM blends for LED/OLED applications
    • Reactive mesogen additives for touch panel coatings
    • Specialty pre-polymers for electronic substrate films

    3. Building Block in Pharmaceutical Intermediate Synthesis

    API manufacturers employ this compound as a critical intermediate during the assembly of select naphthalene-based pharmaceutical molecules, especially non-steroidal anti-inflammatory drug (NSAID) precursors. The raw material enters O-alkylation or nucleophilic substitution reactions, subject to stringent QC. Purity, moisture, and trace solvent residues get tightly controlled following global pharmacopeia guidelines.

    Industry compliance standards

    • ICH Q7A GMP for active pharmaceutical ingredients
    • USP-NF (United States Pharmacopeia)
    • Ph. Eur. (European Pharmacopoeia)
    • 21 CFR Part 211 (current Good Manufacturing Practice)

    Typical usage ratio

    • Charged at 1.0–1.5 molar equivalent to the targeted aromatic base molecule in O-alkylation synthesis steps.
    • Adjusted for yield and side-product minimization; optimization performed at lab and pilot scale phases.

    Downstream process integration

    • Fed in solvent system alongside base and coupling agents.
    • Process controls include in-line Raman or NMR for impurity profiles.
    • The resultant intermediate undergoes purification before final API synthesis.

    Final product types

    • Naphthalene-derived anti-inflammatory intermediates
    • Custom-synthesized building blocks for drug discovery
    • Precursors for analgesic and antipyretic drug candidates
    • Semi-synthetic naphthol derivatives for central nervous system APIs

    4. Component in High-Performance Polymer Additive Formulations

    Polymer compounders and additive manufacturers use 2-(2-Naphthoxy)Ethanol in molecularly engineered UV absorbers and stabilizers for engineering plastics. Its chemical structure improves absorption in the 280–340 nm region, supporting weatherability and color fastness in outdoor plastics. Formulators incorporate the compound during melt blending or solution mixing, where precise dispersion and compatibility matter.

    Industry compliance standards

    • ASTM D3424 (UV exposure evaluation)
    • ISO 4892-2 (Plastics—methods of exposure to laboratory light sources)
    • RoHS Substance Restriction (if used in E&E plastics)
    • REACH SVHC compliance statements

    Typical usage ratio

    • Used at concentrations of 0.1–0.5% by polymer weight for UV absorber packages in ABS, PC, or PET blends.
    • Higher end (up to 1%) adopted where extended weatherability or outdoor exposure resistance is required.

    Downstream process integration

    • Premixed in masterbatch or melt compounded directly with polymer resins.
    • Dispersed during twin-screw extrusion or in pre-polymer mixing tanks for solvent-based systems.
    • QC evaluates dispersion effectiveness and absorption curve in final plastic article.

    Final product types

    • Weather-resistant automotive plastics panels
    • Outdoor electrical housings
    • High-transparency window glazing films
    • Specialty films and sheets for agricultural applications
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