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Merck
CN

24004

Sigma-Aldrich

二乙醚

≥99.5% (GC), puriss, contains ~5 mg/L 2, 6-di-tert.-butyl-4-methylphenol as stabilizer, meets analytical specification of Ph. Eur., BP

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别名:
乙醚, 醚
线性分子式:
(CH3CH2)2O
CAS号:
分子量:
74.12
Beilstein:
1696894
EC 号:
MDL编号:
UNSPSC代码:
12352112
PubChem化学物质编号:
NACRES:
NA.07

蒸汽密度

2.6 (vs air)

质量水平

等级

puriss.

检测方案

≥99.5% (GC)

形式

liquid

自燃温度

320 °F

包含

~5 mg/L 2,6-di-tert.-butyl-4-methylphenol as stabilizer

expl. lim.

36.5 %

杂质

acidic reac. Impurities, in accordance
aldehydes, in accordance
residual solvents, in accordance
≤0.0002% peroxides (as H2O2)
≤0.002% free acid (as CH3COOH)
≤0.002% non-volatile matter
≤0.2% water (Karl Fischer)

折射率

n20/D 1.3530 (lit.)

bp

34.6 °C (lit.)

mp

−116 °C (lit.)

密度

0.706 g/mL at 25 °C (lit.)

SMILES字符串

CCOCC

InChI

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

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

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应用

Diethyl ether may be employed as a solvent for the conversion of secondary alcohols into ketones.

其他说明

The article number 24004-4X2.5L-R will be discontinued. Please order the single bottle 24004-2.5L-R which is physically identical with the same exact specifications.

象形图

FlameExclamation mark

警示用语:

Danger

危险声明

危险分类

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

靶器官

Respiratory system

补充剂危害

WGK

WGK 1

闪点(°F)

closed cup

闪点(°C)

closed cup

法规信息

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Diels-Alder reactions in ionic liquids. A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures.
Earle MJ, et al.
Green Chemistry, 1(1), 23-25 (1999)
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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