Izopropil palmitat
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| Nazivi | |
|---|---|
| IUPAC naziv
izopropil estar heksadekanoinske kiseline
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| Drugi nazivi
Heksadekanoinska kiselina, 1-metiletilestar
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| Identifikacija | |
3D model (Jmol)
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| ChemSpider | |
| ECHA InfoCard | 100.005.065 |
| KEGG[2] | |
| UNII | |
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| Svojstva | |
| C19H38O2 | |
| Molarna masa | 298,50 |
| Gustina | 0,8525 g/cm3 |
| Tačka topljenja | 135 °C (275 °F; 408 K) |
| Nije rastvoran | |
| Opasnosti | |
| NFPA 704 | |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
 verifikuj (šta je   ?)
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| Reference infokutije | |
Izopropil palmitat je na palminom ulju baziran ovlaživač, zgušnjavajući agenss, i anti-statik.[5] Njegova hemijska formula je CH3(CH2)14COOCH(CH3)2.
Reference[uredi | uredi izvor]
- ^ MSDS
- ^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
- ^ US 1993, JE Ramirez, M Vishnupad, "Anhydrous foaming composition containing low concentrations of detergents and high levels of glycerin amd emollients such as oils and esters"
