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1-Heptanol
	Heptan-1-ol
Drugi nazivi	Heptil alkohol; n-Heptil alkohol; Enantinski alkohol
Identifikacija
CAS registarski broj	111-70-6
PubChem	8129
ChemSpider	7837
UNII	8JQ5607IO5
ChEMBL	CHEMBL273459
Jmol-3D slike	Slika 1
SMILES
	OCCCCCCC
InChI
	InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3 ; Kod: BBMCTIGTTCKYKF-UHFFFAOYSA-N InChI=1/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3; Kod: BBMCTIGTTCKYKF-UHFFFAOYAV
Svojstva
Molekulska formula	C7H16O
Molarna masa	116.2 g mol−1
Gustina	0,8187 g/cm3
Tačka topljenja	-34.6 °C, 239 K, -30 °F
Tačka ključanja	175.8 °C, 449 K, 348 °F
Indeks prelamanja (nD)	1,423
Termohemija
Std entalpija; sagorevanja ΔcHo298	-4637,9 kJ/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1-Heptanol je alkohol sa sedam ugljenika dugim lancom i strukturnom formulom CH₃(CH₂)₆OH.^[5] On je bezbojna tečnost koja je neznatno rastvorna u vodi, ali se meša sa etrom i etanolom.

Pregled

Postoje tri druga izomera heptanola koji imaju prav lanac, 2-heptanol, 3-heptanol, i 4-heptanol. Oni se razlikuju po lokaciji alkoholne funkcionalne grupe.

Heptanol se koristi u eksperimentima srčane elektrofiziologije.

1-Heptanol ima prijatan miris, te se koristi se u kozmetici.

Povezano

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

[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

[2] 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.

[3] 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

[4] 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-5] 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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