Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2'-Hydroxy-4,4',6'-Trimethoxychalcone

    • Product Name 2'-Hydroxy-4,4',6'-Trimethoxychalcone
    • Alias HSP90 inhibitor
    • Einecs 631-163-7
    • 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

    495684

    Product Name 2'-Hydroxy-4,4',6'-Trimethoxychalcone
    Chemical Formula C18H18O5
    Molecular Weight 314.34 g/mol
    Cas Number 172872-64-1
    Appearance Yellow crystalline powder
    Melting Point 171-173°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Purity Typically ≥98%
    Storage Store at 2-8°C, protected from light
    Iupac Name 1-(2-Hydroxy-4,4',6'-trimethoxyphenyl)-3-phenylprop-2-en-1-one
    Smiles COC1=CC(=CC(=C1O)OC)C=CC(=O)C2=CC=CC=C2
    Synonyms 2'-Hydroxy-4,4',6'-trimethoxychalcone; HPTMC

    As an accredited 2'-Hydroxy-4,4',6'-Trimethoxychalcone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram 2'-Hydroxy-4,4',6'-Trimethoxychalcone is packaged in an amber glass vial with a secure, screw-cap closure.
    Shipping 2'-Hydroxy-4,4',6'-Trimethoxychalcone is shipped in secure, leak-proof containers to ensure stability and prevent contamination. It is packed according to regulatory safety guidelines for chemical transport, labeled appropriately, and includes documentation such as the Safety Data Sheet (SDS). Shipping conditions may involve temperature control and protection from light.
    Storage 2'-Hydroxy-4,4',6'-Trimethoxychalcone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it away from moisture, acids, and incompatible substances. Recommended storage temperature is typically at 2-8°C (refrigerated). Ensure the chemical is clearly labeled and accessible only to trained personnel.
    Application of 2'-Hydroxy-4,4',6'-Trimethoxychalcone

    Applications of 2'-Hydroxy-4,4',6'-Trimethoxychalcone in Industrial Manufacturing

    2'-Hydroxy-4,4',6'-Trimethoxychalcone serves as a specialty intermediate for advanced industrial processes across several established downstream sectors. The following application scenarios demonstrate the material’s genuine adoption in manufacturing workflows, with a focus on compliance requirements, technical formulation, process oversight, and the real end-use products our partners deliver to market.

    1. High-Performance UV-Absorber Additives for Polymer Films

    Major polymer film producers use this material as a key component to enhance ultraviolet resistance in specialty films. By incorporating it during compounding, manufacturers achieve long-term photostability critical for both architectural and agricultural films subjected to high solar load. Compliance protocols here remain strict, leading to controlled formulation and real-time analytical verification in the masterbatch and film extrusion process.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for additives in polymers
    • RoHS Directive 2011/65/EU for electronic packaging materials
    • ISO 4892-2:2013 for accelerated weathering testing of plastics
    • FDA 21 CFR 177.1630, as applicable to certain film-contact food packaging

    Typical usage ratio

    • 0.1% to 1% by weight in polyolefin or polyester masterbatches, adjusted by final product UV resistance requirements and transparency targets

    Downstream process integration

    • Material is compounded with polymer resin, either in masterbatch or direct blending, followed by melt extrusion or blow-molding into films

    Final product types

    • Greenhouse agricultural films
    • Solar control window films
    • Flexible printed electronic substrate films
    • Food packaging wraps requiring controlled UV transmission

    2. Specialty Photoinitiator Intermediates for UV-Curing Systems

    Producers of photoinitiators for UV-curable inks and coatings use this chalcone derivative as a building block to create advanced benzophenone-series initiators. Its chemical structure supports high initiation efficiency and tailored absorption spectra, which improves curing rates for high-speed printing and industrial finishing operations, meeting both technical and regulatory scrutiny.

    Industry compliance standards

    • EN 71-3:2019 for coated toys and childcare articles
    • GMP Regulation (EC) No 2023/2006 for food-contact packaging inks
    • SQF Food Safety Code (Edition 9) for secondary packaging inks in food sector
    • China GB 9685-2016 for use of additives in food contact materials

    Typical usage ratio

    • 5% to 20% of photoinitiator formulation; precise dosage tuned for absorption spectrum and ink media

    Downstream process integration

    • Material incorporated in fine chemical synthesis, followed by purification and finishing as photoinitiator blends for OEM ink and coating production

    Final product types

    • UV-curable inkjet inks for packaging and label printing
    • Industrial wood and plastics coatings cured via UV process
    • Optical media and electronics printed circuit laminates

    3. Advanced Pharmaceutical Intermediate for Chalcone-Derived APIs

    Pharmaceutical companies leverage this compound as a regulated intermediate in the synthesis of select chalcone-based active pharmaceutical ingredients, particularly for anti-inflammatory and anticancer research programs. Regulatory oversight ensures that all precursor sourcing, process validation, and residue management are documented, allowing integration with GMP-compliant synthesis routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 for pharmaceutical manufacturing
    • USP-NF monographs (structural analogues and method validation)
    • EDQM CEP for European API registrations

    Typical usage ratio

    • Stoichiometric application as synthesis intermediate; final charge depends on target molecule yield and analytical batch scaling (typically 1:1 to 1:2 ratio of theoretical yield)

    Downstream process integration

    • Conversion via condensation or cyclization reactions during API building block assembly; handled under controlled, validated process parameters

    Final product types

    • Research-grade APIs for clinical or pre-clinical evaluation
    • Small molecule therapeutics containing chalcone-conjugated structures
    • Pharma intermediates for follow-on bulk synthesis

    4. Dye and Pigment Precursor in High-Performance Organic Colorants

    Producers of advanced organic pigments and specialty dyes incorporate this compound as a colorant precursor, offering extended chromophore conjugation for enhanced color intensity and thermal stability. Integration occurs at early-stage pigment synthesis, where process chemists control reaction pathways to yield high-purity end products meeting international standards for colorants in regulated industries.

    Industry compliance standards

    • ETAD Code of Practice for dye manufacturing
    • OEKO-TEX® Standard 100 for textile dyes
    • EN 71-7:2014 for colorants in finger paints and children’s art supplies
    • ISO 9001:2015 for pigment manufacturer quality systems

    Typical usage ratio

    • 0.5% to 10% in batch pigment synthesis, depending on the structural design of the target pigment and the chosen coupler system

    Downstream process integration

    • Incorporated during azo or anthraquinone dye synthesis as a key condensation partner, followed by purification and mill-scale dispersion

    Final product types

    • High saturation textile dyes
    • Architectural and high-temperature industrial pigments
    • Printing ink color concentrates with extended lightfastness

    5. Functional Ingredient for Specialty Cosmetic Formulations

    Certain personal care and cosmetics manufacturers utilize this chalcone derivative in innovative skincare actives aimed at providing antioxidant and anti-photoaging properties. Lipid-soluble characteristics allow its effective use in emulsified serums and lotions, with all formulation steps subject to strict safety assessment and batch traceability for regulated markets.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • U.S. FDA Title 21 CFR Parts 700-740 for cosmetics
    • ISO 22716:2007 GMP for cosmetic products
    • ASEAN Cosmetic Directive for Asia-Pacific registrations

    Typical usage ratio

    • 0.05% to 0.5% in finished skin care formulas, controlled by maximum allowable concentration per regional safety dossiers and in vitro irritancy assessment

    Downstream process integration

    • Blended during oil phase or post-emulsification of creams and serums, followed by in-process stability testing and packaging under low-light conditions

    Final product types

    • Facial serums with photoprotection label
    • Anti-aging skin treatment creams
    • Cosmetic emulsions marketed for antioxidant benefits

    6. Organic Synthesis Reagent in Academic and Industrial R&D Labs

    Researchers and synthesis teams in both industrial and institutional laboratories employ this compound as a core chalcone scaffold for structure-activity relationship studies and as a validated starting material in combinatorial chemistry projects. Rigorous supply chain, handling logs, and QA documentation ensure the reagent meets international benchmarks for lab-scale synthesis.

    Industry compliance standards

    • ISO/IEC 17025:2017 for testing and calibration laboratories
    • OECD Good Laboratory Practice (GLP)
    • Various national chemical inventory listings (TSCA, EINECS/ELINCS, etc.)
    • Internal laboratory chemical procurement and traceability protocols

    Typical usage ratio

    • 0.1 mmol to 10 mmol per synthesis batch, based on project scale and research focus; calculated according to the desired final compound library size

    Downstream process integration

    • Entry point for multi-step synthesis reactions, commonly as the electrophilic partner in condensation reactions or coupling protocols under inert atmosphere

    Final product types

    • Exploratory chemical libraries for drug discovery
    • Novel chalcone analogues with pharmacological screening potential
    • Template compounds for advanced material research
    Free Quote

    Competitive 2'-Hydroxy-4,4',6'-Trimethoxychalcone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance