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Key Documents

346144

Sigma-Aldrich

Éter dietílico

≥98%, reagent grade, contains ≤2% ethanol and ≤10ppm BHT as inhibitor

Sinônimo(s):

Éter, Éter etílico

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About This Item

Fórmula linear:
(CH3CH2)2O
Número CAS:
Peso molecular:
74.12
Beilstein:
1696894
Número CE:
Número MDL:
Código UNSPSC:
12352112
ID de substância PubChem:
NACRES:
NA.07

product name

Éter dietílico, reagent grade, ≥98%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor

grau

reagent grade

densidade de vapor

2.6 (vs air)

pressão de vapor

28.5 psi ( 55 °C)
8.38 psi ( 20 °C)

Ensaio

≥98%

forma

liquid

temperatura de autoignição

320 °F
356 °F

contém

≤2% ethanol and ≤10ppm BHT as inhibitor

Lim. expl.

36.5 %

Impurezas

≤0.5% (water)

índice de refração

n20/D 1.3530 (lit.)

pb

34.6 °C (lit.)

pf

−116 °C (lit.)

densidade

0.706 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCOCC

InChI

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

chave InChI

RTZKZFJDLAIYFH-UHFFFAOYSA-N

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Descrição geral

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.

Pictogramas

FlameExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Perigos de suplementos

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

-40.0 °F - closed cup

Ponto de fulgor (°C)

-40 °C - closed cup


Certificados de análise (COA)

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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.
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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
Julia J Griese et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(43), 17189-17194 (2013-10-09)
Although metallocofactors are ubiquitous in enzyme catalysis, how metal binding specificity arises remains poorly understood, especially in the case of metals with similar primary ligand preferences such as manganese and iron. The biochemical selection of manganese over iron presents a

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