32203

Sigma-Aldrich

Diethyl ether

contains BHT as inhibitor, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8%

Synonym(s):
Ethyl ether, Ether
Linear Formula:
(CH3CH2)2O
CAS Number:
Molecular Weight:
74.12
Beilstein/REAXYS Number:
1696894
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.07

Quality Level

grade

ACS reagent
puriss. p.a.

Agency/Method

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

vapor density

2.6 (vs air)

assay

≥99.8% (GC)
≥99.8%

form

liquid

autoignition temp.

320 °F

contains

BHT as inhibitor

expl. lim.

36.5 %

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

SMILES string

CCOCC

suitability

passes test for reaction against H2SO4

InChI

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

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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.

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)].

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

Signal Word

Danger

Hazard Statements

Target Organs

Central nervous system

Supp Hazards

EUH019 - EUH066

RIDADR

UN1155 - class 3 - PG 1 - Diethyl ether

WGK Germany

WGK 1

Flash Point(F)

-40.0 °F

Flash Point(C)

-40 °C

Certificate of Analysis

Certificate of Origin

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service

Social Media

LinkedIn icon
Twitter icon
Facebook Icon
Instagram Icon

MilliporeSigma

Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

© 2021 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.

Reproduction of any materials from the site is strictly forbidden without permission.