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2-(2-Ethoxyethoxy)ethanol

From Wikipedia, the free encyclopedia
2-(2-Ethoxyethoxy)ethanol
Carbitol cellosolve molecule
Names
Preferred IUPAC name
2-(2-Ethoxyethoxy)ethan-1-ol
Other names
3,6-dioxa-1-octanol, DEGEE, diethylene glycol monoethyl ether, ethoxydiglycol, Carbitol, Carbitol Cellosolve, Transcutol, Dioxitol, Polysolv DE, Dowanal DE
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.563 Edit this at Wikidata
KEGG
RTECS number
  • KK8750000
UNII
  • InChI=1S/C6H14O3/c1-2-8-5-6-9-4-3-7/h7H,2-6H2,1H3 checkY
    Key: XXJWXESWEXIICW-UHFFFAOYSA-N checkY
  • InChI=1/C6H14O3/c1-2-8-5-6-9-4-3-7/h7H,2-6H2,1H3
    Key: XXJWXESWEXIICW-UHFFFAOYAC
  • CCOCCOCCO
  • OCCOCCOCC
Properties
C6H14O3
Molar mass 134.175 g·mol−1
Melting point −76 °C (−105 °F; 197 K)
Boiling point 196 to 202 °C (385 to 396 °F; 469 to 475 K)
Hazards
Flash point 96 °C (205 °F; 369 K)
204 °C (399 °F; 477 K)
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

2-(2-Ethoxyethoxy)ethanol, also known under many trade names, is the organic compound with the formula CH3CH2OCH2CH2OCH2CH2OH. It is a colorless liquid. It is a popular solvent for commercial applications.[1] It is produced by the ethoxylation of ethanol (CH3CH2OH).

Applications

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It is a solvent for dyes, nitrocellulose, paints, inks, and resins. It is a component of wood stains for wood, for setting the twist and conditioning yarns and cloth, in textile printing, textile soaps, lacquers, penetration enhancer in cosmetics, drying varnishes and enamels, and brake fluids.[2][3] It is used to determine the saponification values of oils and as a neutral solvent for mineral oil-soap and mineral oil-sulfated oil mixtures (giving fine dispersions in water).[citation needed]

It is also widely used as a solvent in a number of cosmetics and personal care products, including face cream, deodorant, makeup, hair dye, and sunless tanner.[4]

See also

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References

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  1. ^ Stoye, D. "Solvents". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a24_437. ISBN 978-3527306732.
  2. ^ "Diethylene Glycol Monoethyl Ether". PubChem. Retrieved 1 June 2024.
  3. ^ "2(2-Ethoxyethoxy)ethanol". ChemBK. Retrieved 1 June 2024.
  4. ^ Partridge, Joanna (5 November 2021). "UK supplies of fake tan threatened by shortage of key ingredient". The Guardian. Retrieved 2 June 2024.