Pentaethylene glycol monododecyl ether

Pentaethylene glycol monododecyl ether^[1]
Names
	Preferred IUPAC name 3,6,9,12,15-Tetraoxaheptacosan-1-ol
	Other names Dodecylpentaglycol; Laureth-5
Identifiers
CAS Number	3055-95-6 ;
3D model (JSmol)	Interactive image;
Abbreviations	C12E5
ChEBI	CHEBI:91323 ;
ChemSpider	17268 ;
PubChem CID	18281;
UNII	Q9F4A7XYE8 ;
	InChI InChI=1S/C22H46O6/c1-2-3-4-5-6-7-8-9-10-11-13-24-15-17-26-19-21-28-22-20-27-18-16-25-14-12-23/h23H,2-22H2,1H3 Key: LAPRIVJANDLWOK-UHFFFAOYSA-N ; InChI=1/C22H46O6/c1-2-3-4-5-6-7-8-9-10-11-13-24-15-17-26-19-21-28-22-20-27-18-16-25-14-12-23/h23H,2-22H2,1H3 Key: LAPRIVJANDLWOK-UHFFFAOYAV;
	SMILES O(CCO)CCOCCOCCOCCOCCCCCCCCCCCC;
Properties
Chemical formula	C22H46O6
Molar mass	406.59704
Density	0.963 g/mL at 20 °C
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Within chemical compound surfactants, Pentaethylene glycol monododecyl ether (C12E5) is a nonionic surfactant. It is formed by the ethoxylation chemical reaction of dodecanol (lauryl alcohol) to give a material with 5 repeat units of ethylene glycol.

Multilamellar vesicle formation

Within the study of biological membranes and cell biology, for vesicle formation, the lamellar phase at 40wt% solution of C12E5 (Pentaethylene glycol monododecyl ether) dissolved in D₂O form multilamellar vesicles under shear rate.^[3]

↑ Pentaethylene glycol monododecyl ether at Sigma-Aldrich
↑ Kyoko Shinzawa-ltoh; Hidefumi Ueda; Shinya Yoshikawa; Hiroshi Aoyama; Eiki Yamashita; Tomitake Tsukihara (1995). "Effects of Ethyleneglycol Chain Length of Dodecyl Polyethyleneglycol Monoether on the Crystallization of Bovine Heart Cytochrome c Oxidase". J. Mol. Biol. 246 (5): 572–575. doi:10.1016/S0022-2836(05)80106-8. PMID 7877177.
↑ Gentile, Luigi; Rossi, Cesare Oliviero; Olsson, Ulf; Ranieri, Giuseppe Antonio (2011). "Effect of Shear Rates on the MLV Formation and MLV Stability Region in the C12E5/D2O System: Rheology and Rheo-NMR and Rheo-SANS Experiments". Langmuir 27 (6): 2088. doi:10.1021/la1046047. PMID 21261313.

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Names

Preferred IUPAC name 3,6,9,12,15-Tetraoxaheptacosan-1-ol
Other names Dodecylpentaglycol Laureth-5
Identifiers
CAS Number	3055-95-6^Y
3D model (JSmol)	Interactive image
Abbreviations	C12E5
ChEBI	CHEBI:91323^N
ChemSpider	17268^Y
PubChem CID	18281
UNII	Q9F4A7XYE8^Y
InChI InChI=1S/C22H46O6/c1-2-3-4-5-6-7-8-9-10-11-13-24-15-17-26-19-21-28-22-20-27-18-16-25-14-12-23/h23H,2-22H2,1H3^Y Key: LAPRIVJANDLWOK-UHFFFAOYSA-N^Y InChI=1/C22H46O6/c1-2-3-4-5-6-7-8-9-10-11-13-24-15-17-26-19-21-28-22-20-27-18-16-25-14-12-23/h23H,2-22H2,1H3 Key: LAPRIVJANDLWOK-UHFFFAOYAV
SMILES O(CCO)CCOCCOCCOCCOCCCCCCCCCCCC
Properties
Chemical formula	C₂₂H₄₆O₆
Molar mass	406.59704
Density	0.963 g/mL at 20 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references