Palmitic acid

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Palmitic acid
Image:Palmitic acid.png
Chemical name	Hexadecanoic acid
Other names	Palmitic acid hexadecylic acid cetylic acid
Chemical formula	C₁₆H₃₂O₂
Molecular mass	256.42 g/mol
CAS number	[57-10-3]
Density	0.853 g/cm³ at 62 °C
Melting point	63-64 °C
Boiling point	215 °C at 15 mmHg
SMILES	CCCCCCCCCCCCCCCC(=O)O
Disclaimer and references

Palmitic acid, or hexadecanoic acid in IUPAC nomenclature, is one of the most common saturated fatty acids found in animals and plants. As its name indicates, it is a major component of the oil from palm trees (palm oil and palm kernel oil). The word palmitic is from the French "palmitique", the pith of the palm tree. Butter, cheese, milk and meat also contain this fatty acid.

Palmitate is a term for the salts or esters of palmitic acid. The palmitate anion is the observed form of palmitic acid at physiological pH.

Palmitic acid is the first fatty acid produced during lipogenesis (fatty acid synthesis) and from which longer fatty acids can be produced. Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC) which is responsible for converting acetyl-ACP to malonyl-ACP on the growing acyl chain, thus preventing further palmitate generation.

Palmitate is an antioxidant and a vitamin A compound added to low fat milk to replace the vitamin content lost through the removal of milk fat. Palmitate is attached to the alcohol form of vitamin A, retinol, in order to make vitamin A stable in milk.

Derivatives of palmitic acid were used in World War II to produce napalm.

Reduction of palmitic acid yields cetyl alcohol.