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product name
二乙醚, ACS reagent, ≥98.0%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
等級
ACS reagent
品質等級
蒸汽密度
2.6 (vs air)
蒸汽壓力
28.5 psi ( 55 °C)
8.38 psi ( 20 °C)
化驗
≥98.0%
形狀
liquid
自燃溫度
320 °F
包含
≤2% ethanol and ≤10ppm BHT as inhibitor
expl. lim.
36.5 %
雜質
≤0.0002 meq/g Titr. acid
≤0.001% Carbonyl (as HCHO)
≤0.5% (water)
≤1 ppm Peroxide (as H2O2)
蒸發殘留物
≤0.001%
顏色
APHA: ≤10
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 字串
CCOCC
InChI
1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3
InChI 密鑰
RTZKZFJDLAIYFH-UHFFFAOYSA-N
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一般說明
Diethyl ether (also known as ethyl ether or ether) is a laboratory solvent. It is a desirable solvent for oils, fats, waxes, perfumes, dyes, resins, hydrocarbons, and gums. It is also used as fuel and to synthesize other chemical compounds. DEE is widely employed as a solvent for Grignard synthesis.
應用
Diethyl ether is used as a solvent in the 3D-printed reaction ware device for chemical synthesis.
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3
標靶器官
Respiratory system
安全危害
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
-40.0 °F - closed cup
閃點（°C）
-40 °C - closed cup
其他客户在看
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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
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)
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.
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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