1-Pentanol

1-Pentanol
	Pentan-1-ol
Identifikacija
CAS registarski broj	71-41-0
PubChem	6276
ChemSpider	6040
UNII	M9L931X26Y
EINECS broj	200-752-1
UN broj	1105
KEGG	C16834
MeSH	n-Pentanol
ChEBI	44884
ChEMBL	CHEMBL14568
RTECS registarski broj toksičnosti	SB9800000
Bajlštajn	1730975
Gmelin Referenca	25922
Jmol-3D slike	Slika 1
SMILES
	CCCCCO
InChI
	InChI=1S/C5H12O/c1-2-3-4-5-6/h6H,2-5H2,1H3 ; Kod: AMQJEAYHLZJPGS-UHFFFAOYSA-N
Svojstva
Molekulska formula	C5H12O
Molarna masa	88.15 g mol−1
Gustina	814,4 mg cm−3
Tačka topljenja	-78 °C, 195 K, -109 °F
Tačka ključanja	137-139 °C, 410-412 K, 278-282 °F
Rastvorljivost u vodi	22 g dm-3
log P	1.348
Napon pare	200 Pa (na 20 °C)
Indeks prelamanja (nD)	1,409
Termohemija
Standardna entalpija stvaranja jedinjenja ΔfHo298	−351,90–−351,34 kJ mol−1
Std entalpija; sagorevanja ΔcHo298	−3331,19–−3330,63 kJ mol−1
Standardna molarna entropija So298	258,9 J K−1 mol−1
Specifični toplotni kapacitet, C	207,45 J K−1 mol−1
Opasnost
EU-klasifikacija	Xn
EU-indeks	603-200-00-1
NFPA 704	2 1 0
R-oznake	R10, R20, R37, R66
S-oznake	(S1/2), S46
Tačka paljenja	49 °C
Tačka spontanog paljenja	300 °C
Srodna jedinjenja
Srodna jedinjenja	Heksani; Pentilamin
	(šta je ovo?) (verifikuj); Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1-Pentanol (n-pentanol, pentan-1-ol) je alkohol sa pet atoma ugljenika i molekulskom formulom C₅H₁₂O.^[7] 1-Pentanol je bezbojna tečnost neprijatnog mirisa. Postoji 8 alkohola sa tom molekulskom formulom (amil alkohol). Estar formiran iz buterne kiseline i 1-pentanola, pentil butirat, miriše poput kajsija. Estar sirćetne kiseline i 1-pentanola, amil acetat (pentil acetat), miriše poput banaja.

Reference uredi

↑ „n-pentanol - Compound Summary”. PubChem Compound. USA: National Center for Biotechnology Information. 26. 3. 2005.. Identification and Related Records. Pristupljeno 10. 10. 2011.
↑ 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
↑ Lide David R., ur. (2006). CRC Handbook of Chemistry and Physics (87th izd.). Boca Raton, FL: CRC Press. 0-8493-0487-3.

Literatura uredi

-

[1] „n-pentanol - Compound Summary”. PubChem Compound. USA: National Center for Biotechnology Information. 26. 3. 2005.. Identification and Related Records. Pristupljeno 10. 10. 2011.

[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

[crc-7] Lide David R., ur. (2006). CRC Handbook of Chemistry and Physics (87th izd.). Boca Raton, FL: CRC Press. 0-8493-0487-3.

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