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
grade
SAJ first grade
vapor density
3.5 (vs air)
vapor pressure
120 mmHg ( 20 °C)
assay
≥99.0%
form
liquid
autoignition temp.
827 °F
expl. lim.
1-21 %, 100 °F
availability
available only in Japan
bp
68-69 °C (lit.)
mp
−85 °C (lit.)
density
0.725 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-18.4 °F
flash_point_c
-28 °C
法规信息
新产品
此项目有
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 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
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
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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