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HS Code |
553384 |
| Chemical Name | 3-Hydroxy-4,5-Dimethoxybenzoic Acid |
| Molecular Formula | C9H10O5 |
| Molecular Weight | 198.17 g/mol |
| Cas Number | 1163-60-6 |
| Appearance | White to off-white solid |
| Melting Point | 209-211°C |
| Solubility | Soluble in DMSO, methanol |
| Synonyms | 3-Hydroxy-4,5-dimethoxybenzoic acid; 4,5-Dimethoxy-3-hydroxybenzoic acid |
| Smiles | COC1=C(C=C(C(=C1)C(=O)O)OC)O |
| Inchi | InChI=1S/C9H10O5/c1-13-7-4-5(9(11)12)6(10)8(14-2)3-7/h3-4,10H,1-2H3,(H,11,12) |
As an accredited 3-Hydroxy-4,5-Dimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 3-Hydroxy-4,5-Dimethoxybenzoic Acid, tightly sealed with a screw cap and labeled. |
| Shipping | The chemical **3-Hydroxy-4,5-Dimethoxybenzoic Acid** is shipped in a tightly sealed container, protected from light, moisture, and incompatible substances. It is packaged according to regulatory guidelines for laboratory chemicals. The package includes relevant safety documentation and is clearly labeled to ensure safe handling during transit. Temperature control may be applied if required. |
| Storage | 3-Hydroxy-4,5-Dimethoxybenzoic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the container tightly closed to prevent moisture absorption. Store at room temperature and avoid heat sources. Ensure appropriate labeling and use suitable personal protective equipment when handling the chemical. |
Applications of 3-Hydroxy-4,5-Dimethoxybenzoic Acid in Industrial Manufacturing3-Hydroxy-4,5-Dimethoxybenzoic Acid serves as a key intermediate in multiple specialized chemical industries. Its unique molecular structure supports targeted downstream synthesis where strict regulatory, formulation, and process control standards apply. Below outlines four focused industrial application fields supported by proven manufacturing integration and compliance practices. 1. Pharmaceutical Intermediate for Antihypertensive APIsThis raw material plays a critical role in producing select antihypertensive active pharmaceutical ingredients (APIs), particularly in the synthesis of methyldopa derivatives. Manufacturers utilize this compound in the multi-step reaction pathway to introduce precise hydroxy and methoxy substitutions. Purity and traceability are closely regulated, with the pathway monitored under controlled batch conditions to fulfill endpoint API quality and pharmacological activity profiles required by regulatory bodies. Industry compliance standards
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2. Specialty Dye and Pigment SynthesisMany colorant manufacturers apply this compound in advanced dye chemistry. The dual methoxy positioning imparts color fastness and improved solubility to azo, anthraquinone, and specific reactive dye classes. Feedstock selection follows strict batch identity management, and the compound enters as a building block during diazotization, coupling, and subsequent sulfonation or mordant fixation stages, supporting tailored pigment synthesis for textile and paper finishing. Industry compliance standards
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3. Food Contact Resin ModifierProducers of specialty polyesters and epoxide-based resins for food packaging applications employ 3-Hydroxy-4,5-Dimethoxybenzoic Acid as a modification agent. Its controlled introduction improves flexibility and acid resistance of the final resin matrix. Compliance with food safety regulations is essential, with manufacturers monitoring migration limits and residual levels at each batch release. The compound enters the esterification stage, contributing to polymer structure uniformity without compromising regulatory compositional thresholds. Industry compliance standards
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4. Agrochemical Intermediate for Selective HerbicidesSynthesis of certain selective phenoxy herbicides depends on precise aromatic substitutions achieved using this compound as an advanced intermediate. Manufacturers deploy it as a starting material for generating ether or ester-linked molecules with activity against broadleaf weeds. Stringent process documentation, effluent control, and toxicological assessment steps ensure batch-to-batch reproducibility and alignment with agrochemical safety requirements. Industry compliance standards
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