 General chemical structure of cocamide where n = 6, 8, 10, 12, 14, 16
| |
| Names | |
|---|---|
Other names
| |
| Identifiers | |
| EC Number |
|
| UNII | |
| Properties | |
| CH3(CH2)nCONH2 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Cocamide is a mixture of amides manufactured from the fatty acids obtained from coconut oil. As coconut oil contains about 50% of lauric acid, in formulas only the 12-carbon chains tend to be considered. [1] Therefore the formula of cocamide can be written as C H3(CH2)10C O NH2, though the number of carbon atoms in the chains varies (it is always even). [2]
Cocamide is the structural basis of many surfactants. Common are ethanolamines ( cocamide MEA, cocamide DEA), betaine compounds ( cocamidopropyl betaine), and hydroxysultaines ( cocamidopropyl hydroxysultaine). [3]
References
- ^ Groot, Anton (2021). Monographs in Contact Allergy, Volume 1,Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2). CRC Press. p. 4. ISBN 9781000421842.
- ^ Ash, Michael (1998). Handbook of Green Chemicals. Synapse Information Resources. p. 814. ISBN 9781890595791.
- ^ Flick, Ernest (1998). Industrial Surfactants An Industrial Guide. Elsevier Science. p. 122.
|
General chemical structure of cocamide where n = 6, 8, 10, 12, 14, 16
| |
| Names | |
|---|---|
Other names
| |
| Identifiers | |
| EC Number |
|
| UNII | |
| Properties | |
| CH3(CH2)nCONH2 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Cocamide is a mixture of amides manufactured from the fatty acids obtained from coconut oil. As coconut oil contains about 50% of lauric acid, in formulas only the 12-carbon chains tend to be considered. [1] Therefore the formula of cocamide can be written as C H3(CH2)10C O NH2, though the number of carbon atoms in the chains varies (it is always even). [2]
Cocamide is the structural basis of many surfactants. Common are ethanolamines ( cocamide MEA, cocamide DEA), betaine compounds ( cocamidopropyl betaine), and hydroxysultaines ( cocamidopropyl hydroxysultaine). [3]
References
- ^ Groot, Anton (2021). Monographs in Contact Allergy, Volume 1,Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2). CRC Press. p. 4. ISBN 9781000421842.
- ^ Ash, Michael (1998). Handbook of Green Chemicals. Synapse Information Resources. p. 814. ISBN 9781890595791.
- ^ Flick, Ernest (1998). Industrial Surfactants An Industrial Guide. Elsevier Science. p. 122.