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Merck
CN

309958

Diethyl ether

≥99.9%, spectrophotometric grade, inhibitor-free

Synonym(s):

Et2O, Ethoxyethane, Ether, Ethyl ether

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About This Item

Linear Formula:
(CH3CH2)2O
CAS Number:
Molecular Weight:
74.12
UNSPSC Code:
12352112
PubChem Substance ID:
EC Number:
200-467-2
Beilstein/REAXYS Number:
1696894
MDL number:
Assay:
≥99.9%
Grade:
spectrophotometric grade
Bp:
34.6 °C (lit.)
Vapor pressure:
28.69 psi ( 55 °C), 8.59 psi ( 20 °C)
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Product Name

Diethyl ether, spectrophotometric grade, ≥99.9%, inhibitor-free

grade

spectrophotometric grade

vapor density

2.6 (vs air)

vapor pressure

28.69 psi ( 55 °C), 8.59 psi ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

320 °F

expl. lim.

36.5 %

impurities

≤0.03% water, ≤1 ppm peroxides (as H2O2)

evapn. residue

<0.0003%

refractive index

n20/D 1.3530 (lit.)

bp

34.6 °C (lit.)

mp

−116 °C (lit.)

density

0.706 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 218 nm Amax: 1.0, λ: 250 nm Amax: 0.20, λ: 275 nm Amax: 0.04, λ: 300-400 nm Amax: 0.01

SMILES string

CCOCC

InChI

1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

Other Notes

A -D suffix exists for administrative purposes only.
All -D packages are 100% the same product, same quality, same specification as the package sizes previously sold without a -D.


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pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3

target_organs

Central nervous system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

-40.0 °F - closed cup

flash_point_c

-40 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Daniel L Villeneuve et al.
Ecotoxicology and environmental safety, 68(1), 20-32 (2007-04-24)
An in vitro steroidogenesis assay using H295R human adenocarcinoma cells has been suggested as a possible alternative to gonad explant assays for use as a Tier I screening assay to detect endocrine active chemicals capable of modulating steroid hormone synthesis.
Daniel L Villeneuve et al.
Toxicological sciences : an official journal of the Society of Toxicology, 104(1), 113-123 (2008-04-10)
A number of environmental contaminants and plant flavonoid compounds have been shown to inhibit the activity of 3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase (3beta-HSD). Because 3beta-HSD plays a critical role in steroid hormone synthesis, inhibition of 3beta-HSD represents a potentially important mode of
Diethyl ether (DEE) as a renewable diesel fuel.
Bailey B, et al.
No. 972978. SAE technical paper (1997)