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HS Code |
612919 |
| Productname | 3,5-Dichloro-4-Methylbenzoic Acid |
| Casnumber | 2905-62-6 |
| Molecularformula | C8H6Cl2O2 |
| Molecularweight | 205.04 g/mol |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 165-169°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in ethanol and methanol |
| Density | 1.47 g/cm³ |
| Smiles | CC1=C(C=C(C=C1Cl)Cl)C(=O)O |
| Inchi | InChI=1S/C8H6Cl2O2/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3H,1H3,(H,11,12) |
| Synonyms | 4-Methyl-3,5-dichlorobenzoic acid |
As an accredited 3,5-Dichloro-4-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a secure screw cap, clearly labeled with "3,5-Dichloro-4-Methylbenzoic Acid" and safety information. |
| Shipping | 3,5-Dichloro-4-Methylbenzoic Acid is shipped in tightly sealed, chemically resistant containers, clearly labeled with hazard information. The package should be protected from moisture and direct sunlight, and comply with local and international regulations for shipping hazardous materials. Appropriate documentation, including safety data sheets (SDS), accompanies each shipment for safe handling and transport. |
| Storage | Store 3,5-Dichloro-4-Methylbenzoic Acid in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Clearly label the container, and ensure appropriate chemical spill containment and proper access to safety equipment such as eyewash and safety showers. |
Applications of 3,5-Dichloro-4-Methylbenzoic Acid in Industrial ManufacturingAs a direct manufacturer, we supply 3,5-Dichloro-4-Methylbenzoic Acid for specialized use in advanced chemical industries where fine control over synthesis and compliance is essential. Below we detail key downstream applications and the technical context required for productive integration into manufacturing processes. 1. Agrochemical Synthesis for Wheat HerbicidesAgrochemical manufacturers utilize this material as an essential intermediate in the multi-step synthesis of post-emergence herbicides targeting broadleaf weeds in wheat fields. The compound participates in specific condensation and chlorination reactions unique to phenoxyacetic acid-type herbicide production, demanding strict feedstock purity controls and traceability to comply with regulatory limits on secondary contaminants. Industrial users optimize the input ratio based on reaction efficiency and downstream purification, adapting process parameters to crop protection regulatory requirements in export markets. Industry compliance standards
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2. Synthesis of Pharmaceutical IntermediatesWithin API manufacturing, process chemists employ this acid as a specialized carboxylic precursor in assembling complex molecular scaffolds for certain non-steroidal anti-inflammatory drug intermediates. Regulatory agencies require traceable use of such benzoic acid derivatives due to potential carry-over of chlorinated impurities. Production processes stipulate tight input controls and batch record documentation, with active ingredient manufacturers scaling the inclusion rate based on reaction stoichiometry and final process validation results. Industry compliance standards
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3. Specialty Polymer Processing for High-Performance CoatingsManufacturers of specialty polymers integrate this benzoic acid derivative in the synthesis of high-molecular-weight polyesters and modified polyamides used in protective industrial coatings. The chlorine substitution and methyl group guide polymer structure toward chemical resistance and controlled surface reactivity. Operators dose the additive based on polymer chain growth rate and desired end-use mechanical characteristics, verifying raw material quality under industry-specific standards for polymers intended for industrial equipment and machinery. Industry compliance standards
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4. Advanced Dye and Pigment ManufacturingProducers of specialty colorants use this compound as a building block in the design of halogenated azo and anthraquinone dyes. The unique substitution pattern affects electronic delocalization, enabling color tuning for specific textile and leather applications. Batch chemists carefully regulate the addition rate during the diazotization and coupling phases, considering downstream application regulations for exported dye goods. Industry compliance standards
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