Legend: toxin field target field
| Version | 1.0 |
| Creation Date | 2009-07-30 17:58:33 |
| Update Date | 2010-03-18 22:00:34 |
| Accession Number | T3D3470 |
| Name | Vinyl acetate |
| Compound Type |
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| Description | Vinyl acetate is an organic compound and industrial chemical. It is used mainly for the production of other industrial chemicals, such as polyvinyl acetate, an important polymer for which it is the precursor. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. Vinyl acetate is also used as a coating in plastic films for food packaging and as a modifier of food starch. (S883, S885) |
| Synonyms |
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| Chemical IUPAC Name | ethenyl acetate |
| Chemical Formula | C4H6O2 |
| Chemical Structure | |
| CAS Registry Number | 108-05-4 |
| InChI Identifier | InChI=1S/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H3 |
| InChI Key | InChIKey=XTXRWKRVRITETP-UHFFFAOYSA-N |
| PubChem Compound ID | 7904 ![]() |
| KEGG ID | Not Available |
| UniProt ID | Not Available |
| OMIM ID | Not Available |
| ChEBI ID | 46916 ![]() |
| BioCyc ID | Not Available |
| SuperToxic ID | Not Available |
| CTD ID | Not Available |
| Stitch ID | Vinyl acetate ![]() |
| DrugBank ID | Not Available |
| PDB ID | Not Available |
| ACToR ID | 1463 |
| Wikipedia Link | Not Available |
| Monoisotopic Mass | 86.036779 |
| MOL File | Show |
| PDB File | Show |
| SDF File | Show |
| SMILES | CC(=O)OC=C |
| Appearance | Not Available |
| Melting Point | -93.2 oC |
| Solubility | 20 mg/mL at 20 oC [RIDDICK,JA et al. (1986)] |
| Predicted LogP | 0.4272 |
| Route of Exposure | Oral (R885) ; inhalation (R885) ; dermal (R885) |
| Mechanism of Action | One of the metabolites of vinyl acetate, acetaldehyde, is a known animal carcinogen. Acetaldehyde can form adducts with DNA, causing damage such as cross-links. (S885, S891) |
| Metabolism | Vinyl acetate may be absorbed following ingestion, inhalation, or dermal exposure, and distributes throughout the body. It is rapidly hydrolyzed by esterases in the blood to acetate and the unstable intermediate, vinyl alcohol. Vinyl alcohol is then rapidly converted to acetaldehyde, which in turn is metabolized to acetate in the liver. This in turn is incorporated into the "2 carbon pool" of normal body metabolism and eventually forms carbon dioxide as the major breakdown product, which is expired. (S885) |
| Toxicity Values | LD50: 2.92 g/kg (Oral, Rat) (R603) LC50: 2511 ppm over 4 hours (Inhalation, Rabbit) (R285) |
| Lethal Dose | Not Available |
| Carcinogenicity (IARC Classification) | 2B (R264) |
| Uses/Sources | Vinyl acetate is used mainly for the production of other industrial chemicals, such as polyvinyl acetate, an important polymer for which it is the precursor. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. Vinyl acetate is also used as a coating in plastic films for food packaging and as a modifier of food starch. (S883, S885) |
| Minimum Risk Level | Intermediate Inhalation: 0.01 ppm (R260) |
| Health Effects | Vinyl acetate may affect the immune system. It may also be a carcinogen. (S885) |
| Symptoms | Inhalation of vinyl acetate irritates the eyes, nose, and throat. Skin contact causes irritation and blisters. (S885) |
| Treatment | Not Available |
| General References |
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