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Merck

346136

Éther diéthylique

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

Synonyme(s) :

Éther, Éther éthylique

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A propos de cet article

Formule linéaire :
(CH3CH2)2O
Numéro CAS:
60-29-7
Poids moléculaire :
74.12
NACRES:
NA.07
PubChem Substance ID:
329755042
UNSPSC Code:
12352112
EC Number:
200-467-2
MDL number:
MFCD00011646
Beilstein/REAXYS Number:
1696894
Assay:
≥99.0%
Grade:
ACS reagent, anhydrous
Vapor pressure:
28.66 psi ( 55 °C), 8.56 psi ( 20 °C)

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Nom du produit

Éther diéthylique, ACS reagent, anhydrous, ≥99.0%, contains BHT as inhibitor

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

InChI

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

SMILES string

CCOCC

grade

ACS reagent, anhydrous

vapor density

2.6 (vs air)

vapor pressure

28.66 psi ( 55 °C), 8.56 psi ( 20 °C)

assay

≥99.0%

form

liquid

autoignition temp.

320 °F

contains

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.)

Quality Level

200

mp

−116 °C (lit.)

density

0.706 g/mL at 25 °C (lit.)

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Catégories apparentées

General description

Diethyl ether is a versatile organic solvent used in the fields of diesel engines, agriculture, food, chemical, biological, pharmaceutical, and medical industries.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

Application

Diethyl ether can be used as a solvent in the:
  • Ring-opening polymerization of ε-caprolactone to synthesize polycaprolactone.
  • Rh-catalyzed C-H allylation of amides with allyl halides to synthesize allylated amides.
  • Photochemical α-bromination of aromatic and aliphatic carbonyl compounds with N-bromosuccinimide to synthesize α-brominated ketones.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

EUH019,EUH066

Classe de stockage

3 - Flammable liquids

wgk

WGK 1

flash_point_f

-40.0 °F

flash_point_c

-40 °C

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Certificats d'analyse (COA)

Lot/Batch Number
SHBT1505
SHBS7327
SHBS6695
SHBS3597
SHBR9332

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Consulter la Bibliothèque de documents

Nema Hafezi et al.
Journal of the American Chemical Society, 134(30), 12861-12868 (2012-07-13)
A dynamic covalent library of interconverting imine constituents, dissolved in an acetonitrile/water mixture, undergoes constitutional reorganization upon phase separation induced by a physical stimulus (heat) or a chemical effector (inorganic salt, carbohydrate, organic solvent). The process has been made reversible
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
Alessandra Forni et al.
Journal of molecular graphics & modelling, 38, 31-39 (2012-10-23)
The solvent effect on the I⋯O halogen bonding in complexes of iodobenzene derivatives with formaldehyde has been investigated by systematically varying the substituents on the iodobenzene ring. Calculations have been performed at MP2 and DFT levels of theory, using the
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