Structure of propanone

We are working on a new version of ChemSpider — if you structure of propanone to try the new interface go to beta. Simple Structure Advanced History. Comment on this record. Featured data source.

Acetone 2-propanone or dimethyl ketone is an organic compound with the formula CH 3 2 CO. It is a colorless, highly volatile and flammable liquid with a characteristic pungent odor. Acetone is miscible with water and serves as an important organic solvent in industry, home, and laboratory. About 6. It serves as a solvent in household products such as nail polish remover and paint thinner. Acetone is produced and disposed of in the human body through normal metabolic processes. It is normally present in blood and urine.

Structure of propanone

.

Retrieved EC Number.

.

Drinking methanol is harmful, not because of the CH 3 OH molecules themselves, but rather because the human body converts these molecules into methanal formaldehyde molecules by combination with oxygen:. Formaldehyde, H 2 CO, is very reactive—in the pure state it can combine explosively with itself, forming much larger molecules. Consequently it is prepared commercially as a water solution, formalin, which contains about 35 to 40 percent H 2 CO. It is used as a preservative for biological specimens, in embalming fluids, and as a disinfectant and insecticide—not a very good substance to introduce into your body. The biggest commercial use of formaldehyde is manufacture of Bakelite, melamine, and other plastics. The functional group found in formaldehyde is called a carbonyl group. Two classes of compounds may be distinguished on the basis of the location of the carbonyl group. In aldehydes it is at the end of a carbon chain and has at least one hydrogen attached. In ketones the carbonyl group is attached to two carbon atoms. Some examples are.

Structure of propanone

We are working on a new version of ChemSpider — if you want to try the new interface go to beta. Simple Structure Advanced History. Comment on this record. Featured data source. Dimethyl formaldehy de. Dimethyl ketone. Ketone, dimethyl-.

Get get down

For the musical instrument company, see Ace Tone. Journal of the American Chemical Society. Journal of Breath Research. MLD , Revision No. Skin cancer management : a practical approach. It is normally present in blood and urine. Molecules detected in outer space. Download as PDF Printable version. Acetone is however an irritant, causing mild skin and moderate-to-severe eye irritation. Industrial organic chemicals.

Acetone 2-propanone or dimethyl ketone is an organic compound with the formula CH 3 2 CO. It is a colorless, highly volatile and flammable liquid with a characteristic pungent odor.

The carbonyl compounds, J. Chemical Safety Data. Waltham, MA: Focal Press. SRI consulting. Hordeum vulgare subsp. Gas-chromatographische Charakterisierung organischer Verbindungen. Environmental Protection Agency June 16, NIST Spectra nist ri Hazard statements. Miscible [10]. Fragaria vesca subsp. The conversion of acetone to a polyketal PKA would be analogous to the formation of paraformaldehyde from formaldehyde , and of trithioacetone from thioacetone. One litre of acetone can dissolve around litres of acetylene at a pressure of 10 bars 1.