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Merck

32203

Diethyl ether

≥99.8% (GC), ACS reagent, puriss. p.a., contains BHT as inhibitor, reag. Ph. Eur., reag. ISO, USP/NF

Synonym(s):

Et2O, Ethoxyethane, Ether, Ethyl ether

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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
assay:
≥99.8% (GC)
technique(s):
GC/GC: suitable
bp:
34.6 °C (lit.)

Product Name

Diethyl ether, contains BHT as inhibitor, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8% (GC)

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

InChI

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

SMILES string

CCOCC

grade

ACS reagent
puriss. p.a.

agency

USP/NF
reag. ISO
reag. Ph. Eur.

vapor density

2.6 (vs air)

assay

≥99.8% (GC)

form

liquid

autoignition temp.

320 °F

contains

BHT as inhibitor

expl. lim.

36.5 %

technique(s)

GC/GC: suitable

impurities

≤0.00003% peroxides (as H2O2)
≤0.00007% adehydes (as HCHO)
≤0.0002% free acid (as CH3COOH)
≤0.001% carbonyl compounds (as CO)
≤0.001% non-volatile matter
≤0.005% acetone (GC)
≤0.02% ethanol (GC)
0.03% water (Karl Fischer)
5-8 ppm BHT (GC)

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.)

cation traces

Al: ≤0.5 mg/kg
B: ≤0.02 mg/kg
Ba: ≤0.1 mg/kg
Ca: ≤0.5 mg/kg
Cd: ≤0.05 mg/kg
Co: ≤0.02 mg/kg
Cr: ≤0.02 mg/kg
Cu: ≤0.02 mg/kg
Fe: ≤0.05 mg/kg
Mg: ≤0.1 mg/kg
Mn: ≤0.02 mg/kg
Ni: ≤0.02 mg/kg
Pb: ≤0.05 mg/kg
Sn: ≤0.1 mg/kg
Zn: ≤0.05 mg/kg

suitability

passes test for reaction against H2SO4

Quality Level

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Application

Diethyl ether may be employed as solvent for the oxidation of secondary alcohols into ketones. It may be employed as solvent in the preparation of triblock copolymer of PCL-PEG-PCL, acrylated PCL-PEG-PCL and the pentablock copolymer PAE-PCL-PEG-PCL-PAE [PAE = poly(β-amino ester), PEG = poly(ethylene glycol), PCL = poly(ε-caprolactone)].

General description

Diethyl ether (DEE) is widely employed as solvent for Grignard synthesis. Its efficacy as solvent for formalin-ether (F-E) sedimentation technique has been studied. It has been reported as a hydroboration solvent. DEE is a promising compression-ignition fuel and its energy density is much higher than ethanol. It is also one of the components in a blend used in diesel fuel. It can also be used as alternative of diesel fuel.

Other Notes

The article number 32203-4X2.5L will be discontinued. Please order the single bottle 32203-2.5L which is physically identical with the same exact specifications.
The article number 32203-4X2.5L-M will be discontinued. Please order the single bottle 32203-2.5L-M which is physically identical with the same exact specifications.
The article number 32203-6X1L will be discontinued. Please order the single bottle 32203-1L which is physically identical with the same exact specifications.
The article number 32203-6X1L-M will be discontinued. Please order the single bottle 32203-1L-M which is physically identical with the same exact specifications.

pictograms

FlameExclamation mark

signalword

Danger

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

flash_point_c

-40 °C


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Dai P Huynh et al.
Biomaterials, 29(16), 2527-2534 (2008-03-11)
The concept of this research is using poly(beta-amino ester) (PAE) as a duo-functional group for synthesis of the novel sensitive injectable hydrogel for controlled drug/protein delivery. Firstly, PAE made of 1,4-butanediol diacrylate and 4,4'-trimethylene dipiperidine is used as a pH-sensitive
Diethyl ether (DEE) as a renewable diesel fuel.
Bailey B, et al.
No. 972978. SAE technical paper (1997)
K H Young et al.
Journal of clinical microbiology, 10(6), 852-853 (1979-12-01)
Ethyl acetate appears to be a satisfactory subsitute solvent for diethyl ether in the Formalin-ether sedimentation technique. In comparative studies, concentration of organisms with ethyl acetate was equal to or greater than that with diethyl ether. No distortion or alteration
Eagleson M.
Concise Encyclopedia Chemistry, 471-471 (1994)
Oxidation of secondary alcohols in diethyl ether with aqueous chromic acid. Convenient procedure for the preparation of ketones in high epimeric purity.
Brown HC, et al.
The Journal of Organic Chemistry, 36(3), 387-390 (1971)

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