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Hexaethylene glycol, 96%, Thermo Scientific Chemicals
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Catalog number L02161.06
also known as L02161-06
Price (USD)/ Each
61.65
Online exclusive
68.30 Save 6.65 (10%)
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Quantity:
5 g
Price (USD)/ Each
61.65
Online exclusive
68.30 Save 6.65 (10%)
Hexaethylene glycol, 96%, Thermo Scientific Chemicals
Catalog numberL02161.06
Price (USD)/ Each
61.65
Online exclusive
68.30 Save 6.65 (10%)
-
Chemical Identifiers
CAS2615-15-8
IUPAC Name3,6,9,12,15-pentaoxaheptadecane-1,17-diol
Molecular FormulaC12H26O7
InChI KeyIIRDTKBZINWQAW-UHFFFAOYSA-N
SMILESOCCOCCOCCOCCOCCOCCO
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow
Refractive Index1.4610-1.4670 @ 20?C
Assay (Silylated GC)≥95.0%
FormLiquid
Hexaethylene glycol exhibits antioxidant, antimicrobial and anti-cancer properties. It also shows potential application as functional hydraulic fluids. It is used as a surfactant building block as well as used in biological sample preparation. Further, it is employed in the synthesis of binaphthol-based macrocyclic ethers using intramolecular oxidative coupling with CuCl(OH).
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Hexaethylene glycol exhibits antioxidant, antimicrobial and anti-cancer properties. It also shows potential application as functional hydraulic fluids. It is used as a surfactant building block as well as used in biological sample preparation. Further, it is employed in the synthesis of binaphthol-based macrocyclic ethers using intramolecular oxidative coupling with CuCl(OH).
Solubility
Miscible with chloroform and methanol.
Notes
Incompatible with strong oxidizing agents.
Hexaethylene glycol exhibits antioxidant, antimicrobial and anti-cancer properties. It also shows potential application as functional hydraulic fluids. It is used as a surfactant building block as well as used in biological sample preparation. Further, it is employed in the synthesis of binaphthol-based macrocyclic ethers using intramolecular oxidative coupling with CuCl(OH).
Solubility
Miscible with chloroform and methanol.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Complexing solvent analogous to the crown ethers (see Appendix 2). For a study of binding profiles as a function of chain length, see: J. Org. Chem., 48, 2837 (1983).
- Chizhov, A. O.; Sukhova, E. V.; Khatuntseva, E. A.; Tsvetkov, Y. E.; Gening, M. L.; Nifantiev, N. E. High-resolution electrospray mass spectra of hexaethylene glycol connected biotinylated HNK-1 antigenic trisaccharide molecular probe and its non-sulfated analogue. Carbohyd. Res. 2015, 417, 15-18.
- Watode, B. D.; Hudge, P. G.; Kumbharkhane, A. C. Comparative dielectric relaxation study of pentaethylene glycol (PEG) and hexaethylene glycol (HEG) in water mixture using time domain reflectometry. J. Mol. Liq. 2014, 198, 51-56.