Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	56590
Common Name:	Tetraethylene glycol
Systematic Name:	2,2'-[oxybis(ethane-2,1-diyloxy)]diethanol
RefMet Name:	Tetraethylene glycol
Synonyms:	2,2'-[oxybis(2,1-ethanediyloxy)]bisethanol; 2,2'-[oxybis(ethane-2,1-diyloxy)]diethanol; 2-(2-[2-(2-hydroxyethoxy)ethoxy]ethoxy)ethanol; 3,6,9-trioxaundecan-1,11-diol; 3,6,9-trioxaundecane-1,11-diol; PEG-4; TETRAETHYLENE GLYCOL [PubChem Synonyms]
Exact Mass:	194.1154 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C8H18O5
InChIKey:	UWHCKJMYHZGTIT-UHFFFAOYSA-N
ClassyFire superclass:	Organic oxygen compounds [C0004603]
ClassyFire class:	Organooxygen compounds [C0000323]
ClassyFire subclass:	Ethers [C0000254]
ClassyFire direct parent:	Polyethylene glycols [C0003338]
MoNA MS spectra:	View MS spectra
SMILES:	C(COCCOCCOCCO)O
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

Calculated physicochemical properties (?):

Heavy Atoms:	13
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	10
van der Waals Molecular volume:	190.91 Å3 molecule-1
Toplogical Polar Sufrace Area:	68.15 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	5
logP:	1.30
Molar Refractivity:	50.55
Fraction sp3 Carbons:	1.00
sp3 Carbons:	8

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y