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2-Ethoxyethanol





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(Redirected from Ethyl cellosolve)
 


2-Ethoxyethanol, also known by the trademark Ethyl cellosolve, is a solvent used widely in commercial and industrial applications. It is a clear, colorless, nearly odorless liquid that is miscible with water, ethanol, diethyl ether, acetone, and ethyl acetate.[3]

2-Ethoxyethanol
2-Ethoxyethanol
Names
Preferred IUPAC name

2-Ethoxyethanol

Other names

Cellosolve
ethylene glycol ethyl ether
oxitol
Ethyl Cellosolve
EGEE

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

1098271
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.459 Edit this at Wikidata
EC Number
  • 203-804-1

Gmelin Reference

82142
KEGG

PubChem CID

RTECS number
  • KK8050000
UNII
UN number 1171

CompTox Dashboard (EPA)

  • InChI=1S/C4H10O2/c1-2-6-4-3-5/h5H,2-4H2,1H3

    Key: ZNQVEEAIQZEUHB-UHFFFAOYSA-N

  • InChI=1/C4H10O2/c1-2-6-4-3-5/h5H,2-4H2,1H3

    Key: ZNQVEEAIQZEUHB-UHFFFAOYAD

  • CCOCCO

Properties

Chemical formula

C4H10O2
Molar mass 90.122 g·mol−1
Appearance clear liquid
Odor sweet, ether-like
Density 0.930 g/cm3, liquid
Melting point −70 °C (−94 °F; 203 K)
Boiling point 135 °C (275 °F; 408 K)

Solubility in water

miscible
Vapor pressure 4 mmHg (20°C)[1]
Hazards
GHS labelling:

Pictograms

GHS02: FlammableGHS06: ToxicGHS07: Exclamation markGHS08: Health hazard

Signal word

Danger

Hazard statements

H226, H302, H331, H360

Precautionary statements

P201, P202, P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P281, P301+P312, P303+P361+P353, P304+P340, P308+P313, P311, P321, P330, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability (yellow): no hazard codeSpecial hazards (white): no code
2
2
Flash point 44 °C (111 °F; 317 K)
Explosive limits 1.7%-15.6%[1]
Lethal dose or concentration (LD, LC):

LD50 (median dose)

2451 mg/kg (mouse, oral)
2125 mg/kg (rat, oral)[2]

LC50 (median concentration)

2000 ppm (rat, 7 hr)
1820 ppm (mouse, 7 hr)[2]

LCLo (lowest published)

3000 ppm (guinea pig, 24 hr)[2]
NIOSH (US health exposure limits):

PEL (Permissible)

TWA 200 ppm (740 mg/m3) [skin][1]

REL (Recommended)

TWA 0.5 ppm (1.8 mg/m3) [skin][1]

IDLH (Immediate danger)

500 ppm[1]
Related compounds

Related ethers

2-Propoxyethanol
2-Butoxyethanol

Related compounds

Ethylene glycol

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 ?)

Infobox references

2-Ethoxyethanol is manufactured by the reaction of ethylene oxide with ethanol.

As with other glycol ethers, 2-ethoxyethanol has the useful property of being able to dissolve chemically diverse compounds. It will dissolve oils, resins, grease, waxes, nitrocellulose, and lacquers.[3] This is an ideal property as a multi-purpose cleaner, and, therefore, 2-ethoxyethanol is used in products such as varnish removers and degreasing solutions.

References

edit
  1. ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0258". National Institute for Occupational Safety and Health (NIOSH).
  • ^ a b c "2-Ethoxyethanol". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  • ^ a b National Research Council (U.S.). Subcommittee on Spacecraft Maximum Allowable Concentrations (1996). Spacecraft maximum allowable concentrations for selected airborne contaminants. National Academies Press. p. 189. ISBN 978-0-309-05478-2. Retrieved 19 February 2012.
  • edit

    Retrieved from "https://en.wikipedia.org/w/index.php?title=2-Ethoxyethanol&oldid=1206681394"
     



    Last edited on 12 February 2024, at 20:56  





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    This page was last edited on 12 February 2024, at 20:56 (UTC).

    Content is available under CC BY-SA 4.0 unless otherwise noted.



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