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Merck

398276

Sigma-Aldrich

二异丙基醚

contains either BHT or hydroquinone as stabilizer, ACS reagent, ≥99.0%

别名:

异丙醚

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About This Item

线性分子式:
(CH3)2CHOCH(CH3)2
CAS号:
分子量:
102.17
Beilstein:
1731256
EC號碼:
MDL號碼:
分類程式碼代碼:
12191502
PubChem物質ID:
NACRES:
NA.07

等級

ACS reagent

品質等級

蒸汽密度

3.5 (vs air)

蒸汽壓力

120 mmHg ( 20 °C)

化驗

≥99.0%

形狀

liquid

自燃溫度

827 °F

包含

either BHT or hydroquinone as stabilizer

expl. lim.

1-21 %, 100 °F

雜質

≤0.0007 meq/g Titr. acid
≤0.05% Peroxide (as C6H14O2)

蒸發殘留物

≤0.01%

顏色

APHA: ≤25

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

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一般說明

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.

應用

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.

象形圖

FlameExclamation mark

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


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Cross-linked enzyme aggregates (CLEAs): stable and recyclable biocatalysts.
Sheldon RA.
Biochemical Society Transactions, 35(6) (2007)
Molecular structure and conformation of diisopropyl ether: a gas electron diffraction investigation.
Takeuchi H, et al.
The Journal of Physical Chemistry, 91(5), 1015-1019 (1987)
The influence of reaction conditions on the photooxidation of diisopropyl ether.
Collins EM, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 176(1), 86-97 (2005)
Diisopropyl ether one-step generation from acetone-rich feedstocks.
Taylor RJ, et al.
Catalysis Letters, 68(1-2), 1-5 (2000)
Diisopropyl ether syntheses from crude acetone.
Knifton JF and D PSE.
Catalysis Letters, 57(4), 193-197 (1999)

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