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HS Code |
965924 |
| Product Name | Methyl 4-Chloro-3-Nitrobenzoate |
| Cas Number | 14389-43-0 |
| Molecular Formula | C8H6ClNO4 |
| Molecular Weight | 215.59 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 64-67°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Density | 1.54 g/cm³ (approximate) |
| Purity | Typically ≥ 98% |
| Smiles | COC(=O)C1=CC(=C(C=C1)Cl)[N+](=O)[O-] |
| Inchi | InChI=1S/C8H6ClNO4/c1-14-8(11)5-2-3-6(9)7(4-5)10(12)13/h2-4H,1H3 |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited Methyl 4-Chloro-3-Nitrobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with secure screw cap, labeled "Methyl 4-Chloro-3-Nitrobenzoate," hazard symbols, and batch details. |
| Shipping | **Shipping Description:** Methyl 4-Chloro-3-Nitrobenzoate should be shipped in tightly sealed containers, protected from light and moisture. Handle with care as it may be harmful if inhaled, ingested, or upon skin contact. Transport according to regulations for hazardous chemicals, with appropriate labeling and documentation. Store in a cool, dry, well-ventilated area. |
| Storage | Methyl 4-Chloro-3-Nitrobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and sources of ignition. Protect from direct sunlight and moisture. Keep separate from incompatible materials such as strong oxidizing agents and reducing agents. Label the container clearly and handle with appropriate personal protective equipment (PPE). |
Applications of Methyl 4-Chloro-3-Nitrobenzoate in Industrial ManufacturingMethyl 4-Chloro-3-Nitrobenzoate finds critical use as a key intermediate in specialized sectors of industrial chemical synthesis, including advanced pharmaceutical APIs, crop protection formulations, dyes, and specialty polymer additives. By integrating this compound into diverse downstream operations, manufacturers achieve precise customization in high-value product lines under strict regulatory guidance. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisOur clients in the pharmaceutical sector rely on this material for the targeted synthesis of several advanced APIs, including non-steroidal anti-inflammatory drugs (NSAIDs) and select antihypertensive agents. As a precursor in multi-step organic syntheses, it is essential for introducing specific electron-withdrawing and halogen-substituted aromatic groups, which are key for final molecule activity. We ensure strict lot traceability and purity thresholds according to customer route requirements, facilitating reproducibility in reaction yields and impurity profiles. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingThis compound serves as a core precursor in the synthesis of several modern selective herbicides and fungicides. With its reactive chloro and nitro functional groups, it enables halogenated benzoic acid derivative formation, critical in developing actives for broadleaf weed control and crop disease resistance. End users benefit from consistent impurity profiles and the capability to scale synthesis to multi-ton production, meeting regulatory residue and specification limits. Industry compliance standards
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3. Dye and Pigment IntermediateColorants producers utilize this compound as a selective coupling intermediate in azo, anthraquinone, and nitro dye synthesis. The chloro and nitro functionalities enable strong chromophoric system development, allowing manufacturers to control wavelength absorption, mordant compatibility, and wash fastness properties in textile dyeing and specialty pigment blends. Tight batch reproducibility is maintained to ensure color consistency for high-spec end-use demands. Industry compliance standards
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4. Specialty Polymer Additive SynthesisSpecialty polymer manufacturers use this compound to create functionalized monomers or cross-linkers. Its electron-deficient aromatic ring is valuable in building halogenated, nitro-substituted polymer blocks, especially for flame retardant and chemical-resistant applications. Its integration contributes to key performance properties in engineering plastics and adhesives, where precise functionalization levels are required for regulatory and performance certification. Industry compliance standards
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