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Methyl 4-Chloro-3-Methylbenzoate

    • Product Name Methyl 4-Chloro-3-Methylbenzoate
    • Alias Methyl 4-chloro-m-toluate
    • Einecs EINECS 258-939-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    559652

    Chemicalname Methyl 4-Chloro-3-Methylbenzoate
    Casnumber 16821-04-0
    Molecularformula C9H9ClO2
    Molecularweight 184.62
    Appearance White to off-white crystalline solid
    Meltingpoint 44-48°C
    Boilingpoint 277°C
    Density 1.22 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and ether
    Purity Typically ≥98%
    Smiles CC1=CC(=C(C=C1)C(=O)OC)Cl
    Inchi InChI=1S/C9H9ClO2/c1-6-5-7(10)3-4-8(6)9(11)12-2/h3-5H,1-2H3

    As an accredited Methyl 4-Chloro-3-Methylbenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, sealed with a plastic cap, features hazard labels and a white chemical label displaying name, formula, and warnings.
    Shipping Methyl 4-Chloro-3-Methylbenzoate should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be labeled according to chemical regulations and transported in compliance with relevant safety and environmental guidelines. Ensure cushioning and proper documentation to minimize risk during transit and for prompt identification upon arrival.
    Storage Store Methyl 4-Chloro-3-Methylbenzoate in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and use secondary containment to prevent leaks or spills. Follow all relevant health, safety, and environmental regulations.
    Application of Methyl 4-Chloro-3-Methylbenzoate

    Applications of Methyl 4-Chloro-3-Methylbenzoate in Industrial Manufacturing

    As a direct manufacturer, we supply Methyl 4-Chloro-3-Methylbenzoate to diverse industrial sectors where its unique structure supports high-value synthesis. Below we detail key downstream applications, including specific industry compliance requirements, formulation ratios, processing stages, and the nature of end-use products. Each section is focused on real-world integration by downstream manufacturers using our material as a key intermediate or functional additive.

    1. Pharmaceutical Intermediate for Antihypertensive Sartan Synthesis

    Downstream pharmaceutical manufacturers use Methyl 4-Chloro-3-Methylbenzoate as a protected aromatic acid derivative in the multi-step synthesis of Sartan-class antihypertensive active pharmaceutical ingredients (APIs) such as Losartan and Valsartan. Its defined reactivity and substituent pattern support selectivity in acylation and subsequent heterocycle-forming reactions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monographs for APIs
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • China Pharmacopeia requirements for registered intermediates

    Typical usage ratio

    • 0.85–1.1 molar equivalents per API synthesis batch; adjusted based on yield optimization and final step purification requirements

    Downstream process integration

    • Introduced during Stage 2–3 of multi-step reaction sequencing; employed as a key acylating building block, followed by hydrolysis and condensation with biphenyl-tetrazole or other functional cores

    Final product types

    • Losartan potassium tablets
    • Valsartan capsules
    • Irbesartan dry APIs for further formulation

    2. Agrochemical Intermediate for Fungicide & Herbicide Synthesis

    Agrochemical plants utilize this material as an intermediate for the synthesis of specific benzoic acid-based fungicides and pre-emergent herbicides, where selective halogenation and methylation patterns influence bioactivity towards fungal cell membranes or weed seedling enzymes.

    Industry compliance standards

    • FAO/WHO Guidelines on Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical production management
    • China ICAMA registration guidelines
    • EU Regulation (EC) No 1107/2009 for plant protection product approval

    Typical usage ratio

    • 5–12% by weight in intermediate reaction charge; determined by synthetic route and scale of output batches for final active ingredient formation

    Downstream process integration

    • Condensation and hydrolysis steps after halogen-methyl benzoate introduction, enabling functional group access critical for target molecule assembly

    Final product types

    • Azole-class fungicides (e.g., triazole benzoates)
    • Benzoic acid herbicide technical powder
    • Emulsifiable concentrate or wettable powder pesticide formulations

    3. Dye and Pigment Intermediate

    Dye manufacturers leverage Methyl 4-Chloro-3-Methylbenzoate as a precursor for synthesizing specialty azo and anthraquinone dyes. The specific halogen-methyl substitution delivers controlled chromophore formation and influences shade as well as fastness properties in final colorants for textiles and industrial coatings.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 on Registration, Evaluation and Authorization of Chemicals
    • OEKO-TEX Standard 100 (for textile dyes)
    • ZDHC MRSL v2.0 (Zero Discharge of Hazardous Chemicals for textile manufacturing)
    • ISO 9001 management systems in dye synthesis

    Typical usage ratio

    • 1.0–3.5 molar equivalents relative to base aromatic amine or phenol condensation partners; adjusted by chromophore target and solubility profile

    Downstream process integration

    • Introduced during coupling step to modify core dye structure, with downstream oxidation or sulfonation forming the final dye molecule

    Final product types

    • Anthraquinone dyes for polyester and nylon
    • Azo dyes for cotton textiles
    • Custom pigments for industrial coatings and plastics coloration

    4. Fine Chemicals: Fragrance Ingredient Precursor

    Producers of aroma chemicals employ this raw material as a niche intermediate in the synthesis of select benzoic acid ester derivatives. These act as foundational blocks for perfumery compounds, allowing for molecular modifications that provide nuanced volatility and unique olfactory notes in finished fragrance concentrates.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Amendments
    • EU Regulation No 1223/2009 on Cosmetic Products (for fragrance usage)
    • ISO 9001 in aroma chemical production
    • FDA 21 CFR Part 182 (GRAS substances, when fragrance is used in foods)

    Typical usage ratio

    • 0.3–0.8 equivalents per fragrance ester batch; dependent on reaction specificity and purity requirements dictated by customer olfactory profile

    Downstream process integration

    • Added during esterification and transesterification reactions to yield functionalized benzoates, followed by fractional distillation and blending with core aroma bases

    Final product types

    • High-purity perfume blend intermediates
    • Specialty fragrance esters for luxury consumer goods
    • Flavor and fragrance additive concentrates

    5. Specialty Polymer & Resin Intermediate

    Advanced material manufacturers make use of Methyl 4-Chloro-3-Methylbenzoate as a monomer precursor to engineer functional polyesters and specialty resins. The material imparts specific chain branching and halogen functionality, affecting film-forming, adhesion, and barrier properties in technical coatings and electronic encapsulants.

    Industry compliance standards

    • RoHS 2011/65/EU for electronic material inputs
    • UL 94 flammability standards (for resins used in electronics)
    • ISO 14001 environment management in polymer production
    • ASTM D256 and D638 for polymer mechanical testing

    Typical usage ratio

    • 2–6% wt in copolymerization recipe; tuned for film properties, final resin hardness, or electronic encapsulation needs

    Downstream process integration

    • Introduced during pre-polymerization feeding; reacted with glycols, diacid halides, or anhydrides prior to polymerization or curing

    Final product types

    • Specialty polyesters for technical films
    • Epoxy-modified resin systems for PCB encapsulation
    • High-barrier coatings for electronic devices
    Free Quote

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