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[http://journal.scconline.org/pdf/cc1989/cc040n06/p00321-p00333.pdf Fulton, J. (1999) "Comedogenicty and irritancy of commonly used ingredients in skin care products". J''. Soc. Cosmet. Chem.'' '''40''': 321-33]</ref> |
[http://journal.scconline.org/pdf/cc1989/cc040n06/p00321-p00333.pdf Fulton, J. (1999) "Comedogenicty and irritancy of commonly used ingredients in skin care products". J''. Soc. Cosmet. Chem.'' '''40''': 321-33]</ref> |
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[http://www.imagenpersonal. |
[http://www.imagenpersonal.net/di_in_co_4ed_muestra.pdf Carrasco, F. (2009). ''Diccionario de ingredientes cosméticos'' (4 th ed.). Málaga: www.imagenpersonal.net . pp 26. ISBN 978-84-613-4979-1]</ref> so it is not recommended for skin with tendency to develop acne. |
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==References== |
==References== |
![]() | |
Names | |
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IUPAC name
Propan-2-yl tetradecanoate | |
Other names
Tetradecanoic acid, 1-methylethyl ester | |
Identifiers | |
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3D model (JSmol) |
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ECHA InfoCard | 100.003.412 ![]() |
EC Number |
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RTECS number |
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CompTox Dashboard (EPA) |
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Properties | |
C17H34O2 | |
Molar mass | 270.457 g·mol−1 |
Density | 0.85 g/cm³ |
Boiling point | 167 °C (333 °F; 440 K) |
Hazards | |
NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Isopropyl myristate is the esterofisopropanol and myristic acid.
Isopropyl myristate is used in cosmetic and topical medicinal preparations where good absorption through the skin is desired. It is also used as a pesticide-free treatment against head lice which works by dissolving the wax that covers the exoskeleton of head lice, killing them by dehydration.[2]
It is used as a solvent in perfume materials.
It is the non-aqueous component of the two-phase mouthwash, Dentyl pH, where it removes bacteria from the oral cavity.
It is also used in the removal process of prosthetic make-up.
It is also used in a flea and tick products for pets.
It is comedogenic [3] [4] so it is not recommended for skin with tendency to develop acne.