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HS Code |
720763 |
| Cas Number | 547-20-0 |
| Molecular Formula | C4H6O2 |
| Molar Mass | 86.09 g/mol |
| Iupac Name | 3-butenoic acid |
| Synonyms | Vinylacetic acid, Crotonic acid beta |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 187 °C |
| Melting Point | -50 °C |
| Density | 1.029 g/cm3 |
| Solubility In Water | Miscible |
| Flash Point | 86 °C (closed cup) |
| Refractive Index | 1.428 |
| Smiles | C=CC(=O)O |
| Pubchem Cid | 10998 |
| Odor | Pungent |
As an accredited Vinylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Vinylacetic Acid is packaged in a 500g amber glass bottle, sealed with a screw cap, and labeled with hazard warnings. |
| Shipping | Vinylacetic acid should be shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. It must be handled as a hazardous material, avoiding heat, sparks, and sources of ignition. Proper labeling and documentation in compliance with relevant regulations such as DOT, IATA, and IMDG are required during transportation. |
| Storage | Vinylacetic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers and bases. Protect from direct sunlight and moisture. Properly label the container and keep it away from food and drink. Use secondary containment to prevent accidental spills or leaks. |
Applications of Vinylacetic Acid in Industrial ManufacturingVinylacetic Acid is an established intermediate in several demanding chemical manufacturing sectors. Our plant produces high-purity material with stable supply for direct incorporation by formulators and large-scale processors. The following use cases reflect real, quality-critical downstream channels. 1. Synthesis of Pharmaceuticals (Active Pharmaceutical Ingredients and Intermediates)Pharmaceutical manufacturers employ Vinylacetic Acid as a precursor in the synthesis of key heterocyclic intermediates, specifically in the production of pyrrolidone and pyrrolidine derivatives utilized in active pharmaceutical ingredients (APIs). Its controlled reactivity supports side-chain functionalization in nitrogenous compounds, ensuring selectivity in multi-step organic transformations. Typical use includes Grignard reactions or Michael additions to install vinyl or carboxylate functional groups, integral in the assembly of nootropic, anticonvulsant, or psychotropic compounds. Production personnel tune charge ratios for process yield and regulatory compliance at every batch. Industry compliance standards
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2. Production of Agrochemical Active CompoundsAgrochemical synthesis facilities utilize Vinylacetic Acid for constructing key moieties in pesticide and herbicide intermediates, especially where insertion of a vinyl group enhances biological activity. It is often esterified or amidated during the synthesis of proprietary diazinone-type or phenoxycarboxylic herbicide molecules. Batch formulation experts control input volume to prevent overfunctionalization, leveraging the acid's reactivity for regioselective functional group installation. Industry compliance standards
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3. Polymerization for Specialty Resin ModificationSpecialty resin manufacturers integrate Vinylacetic Acid to introduce reactive carboxyl or vinyl groups into polymer backbones, enhancing crosslinking sites and adhesion properties in acrylic and hybrid resins. Feed control is critical: operators add the monomer at calculated stages for copolymer grafting and to adjust final product molecular weight. Batch polymerization remains sensitive to the proportion of acid to monomer, directly impacting glass transition temperature and end-use surface characteristics. Industry compliance standards
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4. Fine Chemical and Flavoring Intermediate ManufactureProducers of fine and specialty chemicals select Vinylacetic Acid to prepare intermediates in fragrance and flavor compounds, where precise control of functional group content tailors volatility and olfactory profile. Chemists use it as a building block for constructing acylated heterocycles, unsaturated acids, and lactones with applications in aroma production. Control of acid concentration and purity is critical, with point-of-use analytics confirming residual solvent and isomer content to meet food additive regulations. Industry compliance standards
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