Weight | 240.431 g/mol |
---|---|
Formula | C16H32O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 14 |
hexadecanal (629-80-1)
palmitaldehyde · palmitoyl aldehyde
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- Metabolism of sphingosine bases. IX. Degradation in vitro of dihydrospingosine and dihydrospingosine phosphate to palmitaldehyde and ethanolamine phosphate. (Biological Chemistry, 1968)
- Metabolism of palmitaldehyde-1-14C in the rat brain. (Biochemistry, 1967)
- Inelastic electron tunnelling spectroscopy (IETS) of carboxylic acids and related systems chemisorbed on plasmagrown aluminium oxide. Part 3.Propanoic acid, butanoic acid and butanal, octanoic acid, dodecanal, hexadecanal and octadecanal (Journal of the Chemical Society, Faraday Transactions, 1979)
- Potential of hexadecane-utilizing soil-microorganisms for growth on hexadecanol, hexadecanal and hexadecanoic acid as sole sources of carbon and energy. (Chemosphere, 2008)
- Support for (Z)-11-Hexadecanal as a Pheromone Antagonist in Ostrinia nubilalis: Flight Tunnel and Single Sensillum Studies with a New York Population (Journal of Chemical Ecology, 2007)
- Conversion of dihydrosphingosin to palmitaldehyde and palmitic acid with cell-free preparations of guinea pig intestinal mucosa. (Acta Chemica Scandinavica, 1970)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - palmitaldehyde
- palmitoyl aldehyde
-
SMILESCCCCCCCCCCCCCCCC=O
-
InChIKeyNIOYUNMRJMEDGI-UHFFFAOYSA-N
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