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HS Code |
914074 |
| Product Name | 3-Chloro-4-Methylbenzoic Acid |
| Synonyms | 3-Chloro-p-toluic acid |
| Molecular Formula | C8H7ClO2 |
| Molar Mass | 170.60 g/mol |
| Cas Number | 17833-43-7 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 167-171°C |
| Solubility In Water | Slightly soluble |
| Density | 1.37 g/cm³ |
| Pka | 3.98 |
| Smiles | CC1=CC(=C(C=C1)Cl)C(=O)O |
As an accredited 3-Chloro-4-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle, tightly sealed, labeled "3-Chloro-4-Methylbenzoic Acid," with hazard warnings and lot number displayed. |
| Shipping | 3-Chloro-4-Methylbenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. It is handled according to standard chemical shipping regulations, with clear hazard labeling. Packages are cushioned to prevent breakage, and a safety data sheet (SDS) accompanies each shipment to ensure safe handling during transport and delivery. |
| Storage | 3-Chloro-4-Methylbenzoic Acid should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid extremes of heat. Use appropriate chemical storage cabinets if available, and clearly label the container for safety and easy identification. |
Applications of 3-Chloro-4-Methylbenzoic Acid in Industrial ManufacturingAs a direct manufacturer of 3-Chloro-4-Methylbenzoic Acid, we provide this specialty aromatic carboxylic acid for several advanced downstream industries. Our technical grade meets the demands of differentiated production scenarios, with each sector having specific process requirements, compliance considerations, and performance criteria. The following sections outline how this material integrates into four major application chains, detailing practical deployment in industrial environments. 1. Agrochemical Active Ingredient SynthesisManufacturers of pre-emergent and post-emergent herbicide actives rely on this intermediate in the synthesis pathway for targeted benzoyl derivatives used in selective weed control. The compound is directly incorporated in multi-step organic synthesis, often via acylation or halogenation reactions, to construct key agrochemical cores while maintaining regulatory-compliant impurity profiles. Downstream players adjust the charge to match the conversion rate in batch or continuous reactors, factoring in catalyst compatibility and residual solvent control for regulatory approval. Industry compliance standards
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2. Pharmaceutical Intermediate ProductionSpecialty API manufacturers utilize this material as a key benzoic acid derivative for producing advanced pharmaceutical intermediates, especially for non-steroidal anti-inflammatory APIs and select cardiovascular drug syntheses. It typically supports side-chain modification reactions and facilitates halogen-substituted scaffold development. Process engineers calibrate addition volumes based on route selectivity, monitoring residuals to meet ICH Q3A impurity thresholds. Industry compliance standards
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3. Polymer Additives and Monomer SynthesisProducers of functional polymers and specialty resin systems incorporate this compound as an intermediate for synthesizing custom monomers or chain modifiers, where its aromatic and halogenated functionalities provide desired compatibility and reactivity. It enters condensation reactions with diols and diamines, contributing to tailored thermal and physical properties in resins used for advanced coatings and engineering plastics, especially where controlled halogen content is specified for insulation or flame resistance. Industry compliance standards
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4. Dyes and Pigment Intermediate ManufacturingSpecialty dye and pigment formulators use this compound to build precise halogenated aromatic structures in high-performance organic pigment molecules. The acid group serves as a reactive handle for azo coupling and other arylation chemistries, while chlorinated and methyl substituents regulate hue and stability. The formulation chemist specifies the charge based on required chromophore intensity and end-use application, whether for technical inks or specialty plastics coloration. Industry compliance standards
Typical usage ratio
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