暫時無法取得訂價和供貨情況
推薦產品
等級
reagent
品質等級
蒸汽密度
3.5 (vs air)
蒸汽壓力
120 mmHg ( 20 °C)
產品線
ReagentPlus®
化驗
99%
形狀
liquid
自燃溫度
827 °F
expl. lim.
1-21 %, 100 °F
dilution
(for general lab use)
折射率
n20/D 1.367 (lit.)
bp
68-69 °C (lit.)
mp
−85 °C (lit.)
密度
0.725 g/mL at 25 °C (lit.)
SMILES 字串
CC(C)OC(C)C
InChI
1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3
InChI 密鑰
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N
尋找類似的產品? 前往 產品比較指南
一般說明
Diisopropyl ether is a colorless liquid. It is widely used as a solvent for the isolation of fats and oils. It can be synthesized from isopropyl alcohol. Its mixture with isooctane has been added to the gasoline fuel as an antiknocking agent.[1] Its synthesis from propylene and water in a single-pass trickle-bed reactor in the presence of an ion-exchange resin catalyst Amberlyst 15 has been proposed.[2] Its efficacy as a fuel additive has been reported. When released in the atmosphere, it undergoes photodecomposition by reacting with OH radicals. Kinetics and mechanism of its reaction in atmosphere have been reported.[3]
應用
Diisopropyl ether may be employed as a solvent for the preparation of aliphatic and aromatic cyanohydrins.[4]
法律資訊
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險聲明
危險分類
Flam. Liq. 2 - STOT SE 3
標靶器官
Central nervous 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)
-20.2 °F - closed cup
閃點(°C)
-29 °C - closed cup
客戶也查看了
Atmospheric chemistry of automotive fuel additives: diisopropyl ether.
Wallington TJ, et al.
Environmental Science & Technology, 27(1), 98-104 (1993)
Single stage synthesis of diisopropyl ether-an alternative octane enhancer for lead-free petrol.
Heese FP, et al.
Catalysis Today, 49(1), 327-335 (1999)
Novel (R)-oxynitrilase sources for the synthesis of (R)-cyanohydrins in diisopropyl ether.
Kiljunen E and Kanerva LT.
Tetrahedron Asymmetry, 8(8), 1225-1234 (1997)
Eagleson M.
Concise Encyclopedia Chemistry, 325-325 (1994)
I Linhart et al.
Toxicology and applied pharmacology, 136(1), 155-160 (1996-01-01)
Biotransformation of acrolein (ACR) was studied in vivo in the rat following inhalation and ip administration. The major and minor urinary metabolites were 3-hydroxypropylmercapturic acid (HPMA) and 2-carboxyethylmercapturic acid (CEMA), respectively. Male Wistar rats were exposed to ACR, 23, 42
Active Filters
我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.
聯絡技術服務