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Methyl 2-Hydroxy-3-Methylbenzoate

    • Product Name Methyl 2-Hydroxy-3-Methylbenzoate
    • Alias Methyl o-cresotate
    • Einecs 244-810-0
    • 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

    628907

    Iupac Name Methyl 2-hydroxy-3-methylbenzoate
    Molecular Formula C9H10O3
    Molar Mass 166.18 g/mol
    Cas Number 6068-76-6
    Appearance White to off-white solid
    Boiling Point 310 °C (estimated)
    Melting Point 53-56 °C
    Density 1.23 g/cm3 (estimated)
    Solubility In Water Slightly soluble
    Structure Type Aromatic ester
    Smiles CC1=CC(=C(C=C1)C(=O)OC)O
    Inchi InChI=1S/C9H10O3/c1-6-4-3-5-7(10)8(6)9(11)12-2/h3-5,10H,1-2H3
    Logp 2.0 (estimated)
    Refractive Index 1.563 (estimated)

    As an accredited Methyl 2-Hydroxy-3-Methylbenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of Methyl 2-Hydroxy-3-Methylbenzoate, securely sealed with a plastic screw cap, labeled with hazard information.
    Shipping Methyl 2-Hydroxy-3-Methylbenzoate is shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. Packages comply with relevant safety regulations, including proper labeling and documentation. During transit, the chemical should be kept at ambient temperatures and handled according to standard chemical transport guidelines to prevent leaks or accidental exposure.
    Storage Methyl 2-Hydroxy-3-Methylbenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated place away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and avoid exposure to moisture. Store at room temperature, ideally between 15–25 °C (59–77 °F).
    Application of Methyl 2-Hydroxy-3-Methylbenzoate

    Applications of Methyl 2-Hydroxy-3-Methylbenzoate in Industrial Manufacturing

    As a specialized manufacturer of Methyl 2-Hydroxy-3-Methylbenzoate, we directly supply this intermediate to downstream producers who demand reliability in formulation and regulatory traceability. Below are recognized industrial segments where our material plays a critical role, informed by in-market utilization and downstream quality standards.

    1. Pharmaceutical API Intermediate Synthesis

    Methyl 2-Hydroxy-3-Methylbenzoate acts as a benzene ring-modified precursor in the synthesis of active pharmaceutical ingredient (API) intermediates, predominantly where controlled hydroxy substitution on the aromatic structure improves biological selectivity or bioavailability. Major drug manufacturers leverage its structural attributes to enhance reactivity control during multi-step synthetic transformations, particularly for non-steroidal anti-inflammatory and antimicrobial APIs, optimizing their process efficiency under stringent quality systems.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. standards relating to precursor quality for API synthesis
    • FDA 21 CFR Part 210/211 (for US-bound formulations)
    • Qualified supplier status per customer-specific audit protocols

    Typical usage ratio

    • Ranging from 0.8% to 3% of the total batch weight, adjusted based on targeted downstream transformation yield and impurity threshold controls

    Downstream process integration

    • Entry at the condensation or esterification step, forming part of the core skeleton for final API structures, followed by sequential functionalization reactions

    Final product types

    • Pharmaceutical grade intermediates for anti-inflammatory, antipyretic, and antimicrobial API categories

    2. Fine Fragrance Ingredient Manufacturing

    Methyl 2-Hydroxy-3-Methylbenzoate supports aromatic compound blends in the fine fragrance sector, where its methylated ester structure contributes both subtle top-note characteristics and stability to olfactory formulations. Perfumers and compounders select this material to extend shelf-life and modulate volatility in high-end eau de parfum, ensuring the fragrance profile persists after application and during storage, while conforming to IFRA safety and purity standards.

    Industry compliance standards

    • IFRA Standards and Amendments for Fragrance Ingredients
    • EU Cosmetic Regulation (EC) No 1223/2009 (Restricted Substances Lists)
    • ISO 9235:2013 for Aroma Chemicals
    • REACH Substance Registration (when shipped to the EU)

    Typical usage ratio

    • Used at 0.05%–0.8% in concentrated fragrance bases, adjusted for batch size and targeted olfactory intensity

    Downstream process integration

    • Added during the aroma blending and fixative introduction phase, prior to solubilization and ethanol dilution

    Final product types

    • Eau de parfum concentrates, luxury fine fragrances, personal care scent blends

    3. UV-Absorber Precursor in Polymer Additives

    In polymer modification and plastic compounding, Methyl 2-Hydroxy-3-Methylbenzoate functions as a building block for synthesizing benzotriazole and salicylate-based UV absorbers. Leading plastic processors select this intermediate where traceability and consistent purity across lots contribute to reliable reaction yields and inhibitor performance, especially in outdoor-use polymers that require proven photostability and long-term color retention under solar exposure.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics and electrical polymer parts
    • REACH Annex XVII restrictions for additive purity and byproduct content
    • FDA 21 CFR 177.1520 (for indirect food-contact plastics, if applicable by end use)
    • ISO 9001:2015 QMS for documented supply traceability

    Typical usage ratio

    • 0.3%–1.5% in masterbatch or direct compounding, varying by final UV absorber loading and compatibility with host resin

    Downstream process integration

    • Undergoes ester exchange, cyclization, or coupling reactions to yield the final UV-absorbing additive, which is then blended into polyolefin, PVC, or engineering plastic resins

    Final product types

    • UV-stabilized masterbatches, outdoor films, automotive plastic trim, high-end coatings additives

    4. Dye Intermediate for High Fastness Pigments

    This material provides a hydroxy-methyl benzoate backbone essential in the diazo coupling process, integral to manufacturing azo and anthraquinone pigments for textile and plastics coloration. Pigment producers utilize it to enhance molecular stability and ensure pigment hues maintain their vibrancy under heat and light, demanding precise control over intermediate purity to exceed OEM color consistency targets and satisfy regulatory frameworks, both within textile and consumer goods segments.

    Industry compliance standards

    • OEKO-TEX Standard 100 Certification for textile colorants
    • EN 71-3:2019 Toy Safety (Migration of certain elements, relevant to pigmented plastics)
    • ZDHC MRSL for chemical input management
    • ISO 787-2 Methods of test for pigments and extenders

    Typical usage ratio

    • Dosage between 1.0% and 2.5%, subject to target color strength and pigment particle engineering

    Downstream process integration

    • Applied in the diazotization or condensation stage prior to pigment isolation, serving as a core chromophore precursor

    Final product types

    • High fastness textile dyes, polymer-compatible pigments, printing ink colorants

    5. Agrochemical Intermediate in Fungicide Synthesis

    In the agrochemical sector, the compound serves as a structural intermediate for constructing benzoic acid-derived fungicides, where functional group selectivity directly correlates with biological activity on target crops. Agrochemical formulators prioritize batch homogeneity and impurity management to maintain product registration compliance across export markets, integrating our material to ensure reaction specificity and downstream toxicity predictability for both field trials and commercial formulations.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • China GB 2763 Maximum Residue Limits for pesticides (where applicable)
    • ISO 9001:2015 and ISO 14001:2015 for quality and environmental management
    • REACH pre-registration (if exported to the EU)

    Typical usage ratio

    • Varies between 2.0% and 4.5% by process, depending on synthesis route and fungicide concentration targets

    Downstream process integration

    • Introduced during the acylation or ester modification steps, prior to active ingredient finalization and formulation blending

    Final product types

    • Technical-grade and formulated fungicidal agents for cereals, horticultural crops, and specialty produce
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