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91238

Supelco

Diethyl ether

analytical standard

Synonym(s):
Ethyl ether, Ether
Linear Formula:
(CH3CH2)2O
CAS Number:
Molecular Weight:
74.12
Beilstein:
1696894
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

Quality Level

grade

analytical standard

vapor density

2.6 (vs air)

vapor pressure

2311 hPa ( 60 °C)

assay

≥99.9% (GC)

form

neat

autoignition temp.

320 °F

shelf life

limited shelf life, expiry date on the label

contains

~0.0005% 2,6-di-tert.-butyl-4-methylphenol as stabilizer

expl. lim.

36.5 %

application(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.1% water
water

refractive index

n20/D 1.3530 (lit.)
n20/D 1.353

bp

34.6 °C (lit.)

mp

−116 °C (lit.)

density

0.706 g/mL at 25 °C (lit.)

Featured Industry

Environmental

format

neat

SMILES string

CCOCC

InChI

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

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

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General description

Diethyl ether is a colorless and highly volatile organic compound, which commonly finds applications as an extraction solvent.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

1, 10 mL in glass bottle

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Central nervous system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK Germany

WGK 1

Flash Point(F)

-40.0 °F - closed cup

Flash Point(C)

-40 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Macroscale and Microscale Organic Experiments (2016)
Diethyl Ether: Organic Compound, Flammable Liquid, Boiling Point, Solvent, Ether, General Anaesthetic, Ramon Llull, Alcohol Dehydrogenase, Cellular Respiration, Cellulose Acetate, Carbureted Compression Ignition Model Engines (2010)
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)
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...

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