346144
二乙醚
≥98%, reagent grade, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
别名:
乙醚, 醚
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线性分子式:
(CH3CH2)2O
化学文摘社编号:
分子量:
74.12
NACRES:
NA.07
PubChem Substance ID:
UNSPSC Code:
12352112
EC Number:
200-467-2
MDL number:
Beilstein/REAXYS Number:
1696894
Assay:
≥98%
Grade:
reagent grade
Vapor pressure:
28.5 psi ( 55 °C), 8.38 psi ( 20 °C)
产品名称
二乙醚, reagent grade, ≥98%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
InChI key
RTZKZFJDLAIYFH-UHFFFAOYSA-N
InChI
1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3
SMILES string
CCOCC
grade
reagent grade
vapor density
2.6 (vs air)
vapor pressure
28.5 psi ( 55 °C), 8.38 psi ( 20 °C)
assay
≥98%
form
liquid
autoignition temp.
320 °F, 356 °F
contains
≤2% ethanol and ≤10ppm BHT as inhibitor
expl. lim.
36.5 %
dilution
(for analytical testing)
impurities
≤0.5% (water)
refractive index
n20/D 1.3530 (lit.)
Quality Level
mp
−116 °C (lit.)
density
0.706 g/mL at 25 °C (lit.)
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General description
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-40.0 °F - closed cup
flash_point_c
-40 °C - closed cup
法规信息
新产品
此项目有
A review on the advancement of ether synthesis from organic solvent to water
Mandal S, et al.
Royal Society of Chemistry Advances, 6(73), 69605-69614 (2016)
Oxidation mechanism of diethyl ether: a complex process for a simple molecule
Di Tommaso S, et al.
Physical Chemistry Chemical Physics, 13(32), 14636-14645 (2011)
The potency of hydrothermally prepared sulfated silica (SO4/SiO2) as a heterogeneous acid catalyst for ethanol dehydration into diethyl ether
Pratika RA, et al.
Chemosphere, 341, 139822-139822 (2023)
The grignard reagents
Seyferth D
Organometallics, 28(6), 1598-1605 (2009)
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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