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About This Item
Linear Formula:
(CH3CH2)2O
CAS Number:
Molecular Weight:
74.12
NACRES:
NA.07
PubChem Substance ID:
UNSPSC Code:
12352112
EC Number:
200-467-2
MDL number:
Beilstein/REAXYS Number:
1696894
eCl@ss:
39021002
Assay:
≥98%
Grade:
reagent grade
Bp:
34.6 °C (lit.)
Vapor pressure:
28.5 psi ( 55 °C), 8.38 psi ( 20 °C)
Product Name
Diethyl ether, reagent grade, ≥98%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
grade
reagent grade
Quality Level
vapor density
2.6 (vs air)
vapor pressure
28.5 psi ( 55 °C), 8.38 psi ( 20 °C)
assay
≥98%
form
liquid
autoignition temp.
320 °F, 356 °F
contains
≤2% ethanol and ≤10ppm BHT as inhibitor
expl. lim.
36.5 %
dilution
(for analytical testing)
impurities
≤0.5% (water)
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
General description
Diethylether, also known as ethyl ether or ether, is frequently used as a laboratory solvent. It is highly volatile, non-flammable, has limited solubility in water, and has high solubility in oil. Ethers are favored solvents for oils, fats, waxes, perfumes, dyes, resins, gums, and hydrocarbons. Additionally, it can be used as a fuel and to synthesize other chemical compounds. It is also employed as a solvent for Grignard synthesis.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3
target_organs
Respiratory 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
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Faysal Benaskar et al.
ChemSusChem, 6(2), 353-366 (2012-11-30)
A μ(2)-process in the Ullmann-type C-O coupling of potassium phenolate and 4-chloropyridine was successfully performed in a combined microwave (MW) and microflow process. Selective MW absorption in a micro-fixed-bed reactor (μ-FBR) by using a supported Cu nanocatalyst resulted in an
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)
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.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 346144-1L | 04061826760970 |

