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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 | 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). |
Applications of Methyl 2-Hydroxy-3-Methylbenzoate in Industrial ManufacturingAs 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 SynthesisMethyl 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
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2. Fine Fragrance Ingredient ManufacturingMethyl 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
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3. UV-Absorber Precursor in Polymer AdditivesIn 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
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4. Dye Intermediate for High Fastness PigmentsThis 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
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5. Agrochemical Intermediate in Fungicide SynthesisIn 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
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