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443549

Diethyl ether

≥99.0%, anhydrous, ACS reagent, contains 1 ppm BHT as inhibitor

Synonym(s):

Et2O, Ethoxyethane, Ether, Ethyl ether

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About This Item

Linear Formula:
(CH3CH2)2O
CAS Number:
60-29-7
Molecular Weight:
74.12
UNSPSC Code:
12352112
PubChem Substance ID:
24868063
EC Number:
200-467-2
Beilstein/REAXYS Number:
1696894
MDL number:
MFCD00011646
eCl@ss:
39021002
Assay:
≥99.0%
Grade:
ACS reagent, anhydrous
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, anhydrous, ACS reagent, ≥99.0%, contains 1 ppm BHT as inhibitor

grade

ACS reagent, anhydrous

vapor density

2.6 (vs air)

vapor pressure

28.69 psi ( 55 °C), 8.59 psi ( 20 °C)

assay

≥99.0%

form

liquid

autoignition temp.

320 °F

contains

1 ppm BHT as inhibitor

expl. lim.

36.5 %

dilution

(for analytical testing)

impurities

Alcohol ( as CH3CH2OH ), passes test, ≤0.0002 meq/g Titr. acid, ≤0.001% Carbonyl ( as HCHO ), ≤0.03% water, ≤1 ppm Peroxide ( as H2O2 )

evapn. residue

≤0.001%

color

APHA: ≤10

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.)

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
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

EUH019,EUH066

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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Certificates of Analysis (COA)

Lot/Batch Number
07935DJ
02083AJ
01133PH
00550LH
00746KH

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Tatsuya Yoshino et al.
Organic letters, 14(16), 4290-4292 (2012-08-09)
A highly efficient total synthesis of the 11-membered cyclic aspercyclides A (1) and B (2) has been achieved by chemo- and regioselective intramolecular oxidative C-O bond formation from differently substituted diphenols.
Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst.
Gang Li et al.
Angewandte Chemie (International ed. in English), 52(4), 1245-1247 (2012-12-15)
Julia J Griese et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(43), 17189-17194 (2013-10-09)
Although metallocofactors are ubiquitous in enzyme catalysis, how metal binding specificity arises remains poorly understood, especially in the case of metals with similar primary ligand preferences such as manganese and iron. The biochemical selection of manganese over iron presents a
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