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等級
JIS special grade
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
expl. lim.
1-21 %, 100 °F
存貨情形
available only in Japan
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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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
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
P Adlercreutz
Biochimica et biophysica acta, 1163(2), 144-148 (1993-05-13)
Horse liver alcohol dehydrogenase and alpha-chymotrypsin were deposited on a porous support material, Celite. After equilibration at a well-defined water activity, the catalytic activity was measured with diisopropyl ether as reaction medium. The effects of the presence of polyols and
B E Cham et al.
Journal of virological methods, 137(1), 160-163 (2006-07-01)
Many viruses including HIV, hepatitis C and hepatitis B, have an outer lipid envelope which maintains inserted viral peptides in the "correct" functional conformation and orientation. Disruption of the lipid envelope by most solvents destroys infectivity and often results in
R Gonzalez-Olmos et al.
Chemosphere, 71(11), 2098-2105 (2008-02-27)
Methyl tert-butyl ether (MTBE) is the most widely used oxygenate in gasoline blending and has become one of the world's most widespread groundwater and surface water pollutants. Alternative oxygenates to MTBE, namely ethyl tert-butyl ether (ETBE), tert-amyl ether (TAME) and
R van Gijn et al.
Journal of chromatography. B, Biomedical applications, 667(2), 269-276 (1995-05-19)
The staurosporine derivative, N-benzoylstaurosporine (CGP 41 251; I), is a protein kinase C inhibitor that has been selected for phase I clinical evaluation in cancer patients. We have developed a selective and sensitive assay of the drug and three potential
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
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