Nonadekanska kiselina
Nonadecilinska kiselina | |||
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IUPAC ime |
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Identifikacija | |||
CAS registarski broj | 646-30-0 Y | ||
PubChem[1][2] | 12591 | ||
ChemSpider[3] | 12071 Y | ||
EC-broj | 211-472-4 | ||
ChEBI | 39246 | ||
ChEMBL[4] | CHEMBL1169674 Y | ||
Jmol-3D slike | Slika 1 | ||
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Svojstva | |||
Molekulska formula | C19H38O2 | ||
Molarna masa | 298,50382 g/mol | ||
Agregatno stanje | Bele pahulje ili prah | ||
Tačka topljenja | 68-70 °C | ||
Tačka ključanja | 236 °C (10 mmHg) | ||
Rastvorljivost u vodi | Insoluble | ||
Opasnost | |||
Opasnost u toku rada | Iritant (Xi) | ||
R-oznake | R36/37/38 | ||
S-oznake | S26 | ||
Y (šta je ovo?) (verifikuj) Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |||
Infobox references |
Nonadekanska kiselina (nonadeciklinska kiselina, nonadekanoinska kiselina) je zasićena masna kiselina sa 19-ugljenika dugim lancom. Njena hemijska formula je CH3(CH2)18COOH. Ona formira soli zvane nonadecilati.[5][6]
Nonadekanska kiselina je prisutna u mastima i biljnim uljima. Insekti je koriste kao feromon.
Reference
- ↑ 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. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
- ↑ 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.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
- ↑ Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
- ↑ Morrison Robert Thornton, Boyd Robert Neilson (2006). Organic chemistry. Engelwood Cliffs, New Jersey: Prentice Hall. ISBN 8120307658.
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