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The TLV value for 3-pentanone is 200 ppm (705 mg/m 3). [4] 3-pentanone can be hazardous if it comes in contact with the skin or eyes, and can cause irritation of the skin and redness, watering, and itching of the eyes. This chemical can also cause nervous system or organ damage if ingested.
3-Pentanone; This page was last edited on 25 March 2021, at 20:13 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional ...
Pentanone may refer to the following ketones containing five carbon atoms: 2-Pentanone (Methyl propyl ketone, MPK) 3-Methyl-2-butanone (Methyl isopropyl ketone, MIPK)
3-Penten-2-one occurs naturally in the berries of two species of Aronia melanocarpa. [7] It has also been found in other plants and foods such as tomatoes, cocoa, tea, and potato chips. [5] 3-Penten-2-one can be used for the synthesis of other compounds such as the alkaloids senepodine G and cermizine C, for example. [7]
Burn rate (typically expressed in mm/s or in/s) is the sample length over time at a given pressure and temperature. For solid fuel propellant, the most common method of measuring burn rate is the Crawford Type Strand Burning Rate Bomb System [3] (also known as the Crawford Burner or Strand Burner), as described in MIL-STD-286C. [4]
1 See also. 2 References. ... In organic chemistry, pentanonide is a functional group which is composed of a cyclic ketal of a diol with 3-pentanone. [1]
1 cup (2 sticks) unsalted butter, at room temperature. 2 large eggs. 2 3/4 cups flour. 1/4 cup instant vanilla pudding mix. 1 teaspoon cream of tartar1 teaspoon baking soda. 1 teaspoon salt.
N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.