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HS Code |
649142 |
| Chemical Name | 2-Methylformanilide |
| Synonyms | o-Tolylformamide |
| Molecular Formula | C8H9NO |
| Molecular Weight | 135.16 g/mol |
| Cas Number | 614-30-2 |
| Appearance | Solid or liquid (depending on temperature), colorless to pale yellow |
| Boiling Point | 276 °C |
| Melting Point | 34-36 °C |
| Density | 1.09 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 147 °C |
| Structure | A benzene ring with a methyl group at the 2-position and a formamide group (–CONH2) at the 1-position |
As an accredited 2-Methylformanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Methylformanilide, 500g, supplied in a sealed amber glass bottle with a secure screw cap, labeled with hazard and handling information. |
| Shipping | 2-Methylformanilide should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport in accordance with local, national, and international regulations for chemicals. Handle with care, using appropriate labeling and documentation. Avoid physical damage and ensure containers remain upright to prevent leaks or spills during transit. |
| Storage | 2-Methylformanilide should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, strong oxidizers, and incompatible materials. Protect from moisture and direct sunlight. Use chemical-resistant storage cabinetry if available. Ensure appropriate labeling and keep away from food and drink. Safety measures should be observed to avoid accidental spills or exposure. |
Applications of 2-Methylformanilide in Industrial ManufacturingAs a specialized producer of 2-Methylformanilide, we supply this high-purity material to a select range of established downstream industries. Below are the key sectors and scenarios in which our product supports precise manufacturing goals, with details covering regulatory compliance, formulation, integration stage, and end product categories. 1. Agrochemical Synthesis – Herbicide IntermediateIn the crop protection segment, 2-Methylformanilide functions as a targeted intermediate for the synthesis of certain phenyl-substituted urea herbicides. Agrochemical manufacturers employ it to achieve controlled reactivity and side-chain customization, particularly to optimize selectivity and degradation kinetics under field conditions. Its distinctive reactivity toward isocyanates supports the creation of actives with specified weed control profiles, while minimization of impurities requires strict adherence to formulation parameters and batch QC routines. Industry compliance standards
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2. Dye and Pigment Manufacturing – Solvent and Modifying AgentIndustrial dye and pigment manufacturers use 2-Methylformanilide as a polar aprotic solvent and coupling agent in the synthesis of select azo and anthraquinone dyes. Its controlled solubility profile enhances dyeing uniformity and process throughput, especially in processes where reaction kinetics strongly depend on solvent parameters. The material facilitates color shade adjustment and impurity extraction steps in both batch and continuous colorant production lines and promotes stability during downstream formulation. Industry compliance standards
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3. Pharmaceutical Intermediate Production – Specialty Synthesis Building BlockPharmaceutical fine chemical manufacturers utilize 2-Methylformanilide to synthesize key building blocks for APIs, especially in the creation of substituted anilines and related heterocycles. Its selective reactivity enables tight control over molecular purity during multi-step active ingredient production. Due to regulatory scrutiny, ingredient traceability and in-process verification remain critical, necessitating confined batch records and validated process controls when this material is used. Industry compliance standards
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4. Polymer Additive and Modifier Synthesis – Engineering PlasticsProducers of engineering plastics and specialty resins apply 2-Methylformanilide in the synthesis of specific chain extenders and as a functionalizing reagent for performance polymers. By introducing methylformyl groups under controlled reaction conditions, manufacturers achieve improved polarity, adhesion, or processing stability of polyamide, polyurethane, and copolymer systems. The process must comply with sectoral standards on residual solvent content and additive migration, requiring precise dosing and rigorous in-process controls. Industry compliance standards
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