추천 제품
Grade
ACS reagent
Quality Level
vapor density
3.5 (vs air)
vapor pressure
120 mmHg ( 20 °C)
분석
≥99.0%
양식
liquid
autoignition temp.
827 °F
포함
either BHT or hydroquinone as stabilizer
expl. lim.
1-21 %, 100 °F
불순물
≤0.0007 meq/g Titr. acid
≤0.05% Peroxide (as C6H14O2)
증발 잔류물
≤0.01%
색상
APHA: ≤25
refractive index
n20/D 1.367 (lit.)
bp
68-69 °C (lit.)
mp
−85 °C (lit.)
density
0.725 g/mL at 25 °C (lit.)
SMILES string
CC(C)OC(C)C
InChI
1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3
InChI key
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N
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일반 설명
Diisopropyl ether (DIPE) is branched ether. It is a peroxide forming solvent. This process is catalyzed by heat, light and oxygen. For such solvents small amount of stabilizers like BHT (butylated hydroxytoluene) or hydroquinone is added which removes the free radicals that form peroxides. DIPE has been proposed as a potential alternative oxygenated fuel additive. Several methods have been proposed for its synthesis using acetone as starting material. The molecular structure and conformation has been studied using gas-phase electron diffusion. Its potential carcinogenicity has been studied in Sprague-Dawley rats.
애플리케이션
Diisopropyl ether may be used as a solvent in the following processes:
- Resolution of secondary alcohols.
- Enantioselective acylation of 1-phenethylamine.
- Synthesis of aliphatic and aromatic cyanohydrins.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 2 - STOT SE 3
표적 기관
Central nervous system
보충제 위험성
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
-20.2 °F - closed cup
Flash Point (°C)
-29 °C - closed cup
이미 열람한 고객
Cross-linked enzyme aggregates (CLEAs): stable and recyclable biocatalysts.
Biochemical Society Transactions, 35(6) (2007)
Molecular structure and conformation of diisopropyl ether: a gas electron diffraction investigation.
The Journal of Physical Chemistry, 91(5), 1015-1019 (1987)
The influence of reaction conditions on the photooxidation of diisopropyl ether.
Journal of Photochemistry and Photobiology A: Chemistry, 176(1), 86-97 (2005)
Diisopropyl ether one-step generation from acetone-rich feedstocks.
Catalysis Letters, 68(1-2), 1-5 (2000)
Diisopropyl ether syntheses from crude acetone.
Catalysis Letters, 57(4), 193-197 (1999)
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