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2,4,6-Trihydroxybenzoic Acid

    • Product Name 2,4,6-Trihydroxybenzoic Acid
    • Alias Phloroglucinol carboxylic acid
    • Einecs 202-027-8
    • 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

    421415

    Name 2,4,6-Trihydroxybenzoic acid
    Synonyms Phloroglucinol carboxylic acid
    Cas Number 610-94-6
    Molecular Formula C7H6O5
    Molecular Weight 170.12 g/mol
    Appearance White to off-white solid
    Melting Point 217-220°C
    Solubility In Water Slightly soluble
    Pka 3.39
    Boiling Point Decomposes before boiling
    Density 1.693 g/cm³
    Smiles OC(=O)c1cc(O)cc(O)c1
    Inchi InChI=1S/C7H6O5/c8-3-1-4(9)6(7(11)12)5(10)2-3/h1-2,8-10H,(H,11,12)
    Pubchem Cid 11839

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled with the chemical name "2,4,6-Trihydroxybenzoic Acid," hazard symbols, and lot number.
    Shipping 2,4,6-Trihydroxybenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. Packaging complies with safety regulations, clearly labeled with hazard information if applicable. The product should be stored and transported in a cool, dry place, away from incompatible substances, and handled according to standard chemical safety procedures.
    Storage 2,4,6-Trihydroxybenzoic acid should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances like strong oxidizers and bases. Store at room temperature or as specified by the manufacturer, and ensure proper labeling. Use standard laboratory safety measures to prevent inhalation or direct contact.
    Application of 2,4,6-Trihydroxybenzoic Acid

    Applications of 2,4,6-Trihydroxybenzoic Acid in Industrial Manufacturing

    2,4,6-Trihydroxybenzoic acid serves as a specialty intermediate in several technically advanced manufacturing chains. As an original manufacturer, we supply this compound to globally established production lines, supporting rigorous quality needs and regulatory frameworks in target sectors. The following sections detail its established industrial applications, summarizing downstream compliance, dosage principles, process stages, and realized end-products.

    1. Pharmaceutical Intermediate for Flavonoid Synthesis

    This raw material plays a critical role in synthesizing select flavonoid-based APIs, including those used in vascular health and anti-inflammatory formulations. Producers rely on its unique hydroxyl arrangement for building specific glycosylated flavones. Use occurs during fine chemical stage synthesis, where tight specification adherence is essential for subsequent cGMP steps. Flavonoid APIs containing this scaffold undergo extensive quality checks for impurity, residual solvents, and heavy metals prior to formulation into finished dose medications.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monographs on relevant APIs
    • EMA Guideline on the chemistry of active substances
    • Ph. Eur. standards (as applicable to APIs synthesized from this building block)

    Typical usage ratio

    • Input range: 0.8–1.2 molar equivalents relative to target flavonoid, adjusted for purity and target molecular yield

    Downstream process integration

    • Introduced during the condensation or glycosylation stage of small-molecule API synthesis; followed by isolation, purification, and characterization routines

    Final product types

    • Bulk pharmaceutical ingredients (e.g., diosmetin, baicalin)
    • Oral tablets for vascular support
    • Injectable formulations for clinical studies
    • API reference standards for pharmaceutical QC labs

    2. Antioxidant Additive in Cosmetic Formulations

    Leading cosmetic houses adopt this ingredient for its polyhydroxyl structure, which supports free radical scavenging and product stabilization, especially in formulations targeting skin brightening and anti-aging. The material is included at specific stages in emulsion and serum production, with close monitoring for regulatory limits on skin-contact substances and preservation of antioxidant capacity after high-shear mixing or heating.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • Cosmetic Ingredient Review (CIR) Safety Assessment Guidelines
    • ISO 22716: Cosmetics Good Manufacturing Practices
    • China National Medical Products Administration (NMPA) Cosmetic Safety Technical Standards

    Typical usage ratio

    • Added at 0.05–0.25% by weight, adjusted based on formulation type and skin compatibility tests

    Downstream process integration

    • Dispersed in water phase or pre-solubilized for emulsion, gel, serum, and lotion manufacture; incorporated prior to final homogenization to maintain antioxidant activity

    Final product types

    • Brightening face serums
    • Anti-aging creams
    • Protective day lotions
    • Night repair essences

    3. Intermediate in Food Additive Production (Natural Preservatives)

    Food additive producers employ this raw material during synthesis of polyphenolic antioxidants used as natural preservatives. Its multi-hydroxylated aromatic structure is vital for constructing plant-based preservatives with reduced toxicity and strong oxidative stability. Incorporation occurs early in controlled esterification or glycosylation processes, linked to downstream applications in minimally processed foods and beverages.

    Industry compliance standards

    • FSMPs and food additive guidelines under GB 2760-2022 (China)
    • Food Chemicals Codex (FCC) specifications for polyphenol-derived antioxidants
    • EFSA guidance on natural food preservatives
    • CFR Title 21 FDA regulations for food additives

    Typical usage ratio

    • Raw input: 2–5% by mass relative to other reactants; final preservative dosage in food products must comply with additive limits per region

    Downstream process integration

    • Introduced during precursor assembly for polyphenolic preservative synthesis, followed by chemical transformation and subsequent purification prior to blending with final food-grade excipients

    Final product types

    • Natural antioxidant blends for beverages
    • Preservative-enriched snack coatings
    • Polyphenol-based food additives for bakery applications
    • Low-temperature processed ready meals

    4. Dye and Pigment Intermediate for Specialty Ink Manufacturing

    This compound functions as a precursor in synthesizing lake pigments and azo dyes tailored for specialty inks, particularly where intense coloration and lightfastness are critical. Commercial ink producers introduce this raw material at defined steps in organic pigment synthesis, with reactive control for shade consistency and migration resistance in commercial printing systems. Final formulations are tested for regulatory conformance, print permanence, and zero-hazard classification for intended substrates.

    Industry compliance standards

    • DIN EN 71-3: Migration of certain elements (for printing on toys)
    • ISO 2846: Color and transparency of printing ink sets
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ASTM D4236 (Labeling for art materials)

    Typical usage ratio

    • Used at 1–4% (w/w) in dye synthesis feedstock, with adjustment for color depth and final product stability

    Downstream process integration

    • Utilized during early reaction steps to generate color precursor, followed by coupling or metal complexation, filtration, and dispersion in ink vehicles

    Final product types

    • Water-based printing inks
    • Specialty artist inks
    • Food packaging-safe pigments
    • Archival-grade inkjet cartridges

    5. Research-Grade Chemical for Analytical Reference Standards

    Analytical laboratories and reference material producers incorporate this compound as a calibration standard in polyphenol method development. Certifying bodies require precise purity and traceability when preparing CRM (Certified Reference Materials) and QC standards for high-performance liquid chromatography and related techniques. These applications demand full documentation, stability data, and compliance with mandatory laboratory accreditation requirements.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for the competence of reference material producers)
    • ISO/IEC 17025:2017 (Testing and calibration laboratories)
    • USP General Chapter <11> (Reference Standards)
    • FDA Good Laboratory Practices GLP 21 CFR Part 58

    Typical usage ratio

    • Prepared as 0.1–10 µg/mL methanolic standards for instrument calibration; actual concentration adjusted to detector sensitivity and required quantification range

    Downstream process integration

    • Dissolved, filtered, and aliquoted during preparation of primary and secondary calibration standards for routine use in analytical laboratories

    Final product types

    • Certified reference materials (CRMs) for chromatography
    • Polyphenol test kits for quality control
    • Analytical standards for validation of food, pharma, and environmental tests
    • HPLC calibration solutions
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    Tel: +8615371019725

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