1-Dekanol

1-Dekanol
	Dekan-1-ol
Drugi nazivi	decil alkohol; n-decil alkohol; kaprinski alkohol; epal 10; antak; agens 504
Identifikacija
CAS registarski broj	112-30-1
PubChem	8174
ChemSpider	7882
UNII	89V4LX791F
KEGG	C01633
ChEBI	28903
ChEMBL	CHEMBL25363
Jmol-3D slike	Slika 1
SMILES
	OCCCCCCCCCC
InChI
	InChI=1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3 ; Kod: MWKFXSUHUHTGQN-UHFFFAOYSA-N InChI=1/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3; Kod: MWKFXSUHUHTGQN-UHFFFAOYAN
Svojstva
Molekulska formula	C10H22O
Molarna masa	158,28 g/mol
Agregatno stanje	Viskozna tečnost
Gustina	0,8297 g/cm3
Tačka topljenja	6.4 °C, 280 K, 44 °F
Tačka ključanja	232.9 °C, 506 K, 451 °F
Rastvorljivost u vodi	Nije rastvoran
Opasnost
Podaci o bezbednosti prilikom rukovanja (MSDS)	Oxford MSDS
Tačka paljenja	108 °C
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1-Dekanol je masni alkohol pravo lanca sa deset atoma ugljenika i molekulskom formulom C₁₀H₂₁OH. On je bezbojna viskozna tečnost, koja je nerastvorna u i ima jak miris.^[7]

Upotreba uredi

Dekanol se koristi u proizvodnji plastifikatora, maziva, surfikanata i rastvarača.

Toksičnost uredi

Dekanol uzrokuje iritaciju kože i očiju. Ako prsne na oči može da uzrokuje permanentno oštećenje. Inhalacija i gutanje mogu da budu štetni. On takođe može da deluje kao narkotik. On je štetan za životnu sredinu.^[8]

Reference uredi

↑ Susan Budavari, ur. (2001). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th izd.). Merck Publishing. ISBN 0-911910-13-1.
↑ 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
↑ 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.
↑ 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
↑ ICSC [1]
↑ MSDS Safety Sheet [2] Arhivirano 2007-10-11 na Wayback Machine-u

Literatura uredi

[Merck13th-1] Susan Budavari, ur. (2001). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th izd.). Merck Publishing. ISBN 0-911910-13-1.

[2] 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

[3] 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.

[4] 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

[5] 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.

[6] 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

[7] ICSC [1]

[8] MSDS Safety Sheet [2] Arhivirano 2007-10-11 na Wayback Machine-u

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