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
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
A Azim et al.
Bioorganic & medicinal chemistry, 9(5), 1345-1348 (2001-05-30)
An efficient lipase catalysed synthesis of optically enriched alpha-halogenated amides with concomitant optical enrichment of the starting alpha-haloesters is described. Candida antarctica lipase (CAL) was found to be a better catalyst over porcine pancreatic lipase (PPL) and Candida cylindracea lipase
W Dalbey et al.
Journal of toxicology and environmental health, 49(1), 29-43 (1996-09-01)
Two inhalation studies were performed with a vaporized sample of commercial-grade diisopropyl ether (DIPE). In the subchronic study, Sprague-Dawley rats (14/sex) were exposed to 0 (both untreated and sham-exposed controls), 480, 3300, or 7100 ppm DIPE for 6 h/d, 5
A Hickel et al.
Biotechnology and bioengineering, 65(4), 425-436 (1999-10-03)
A novel recycle reactor has been designed to determine the interfacial activity of hydroxynitrile lyase in a diisopropyl ether (DIPE)/water two-phase system. The reactor provides a known interfacial area. Enzyme activity toward mandelonitrile cleavage is continuously measured in the reactor
Ali N Saleemi et al.
International journal of pharmaceutics, 430(1-2), 56-64 (2012-03-28)
Pharmaceutical regulatory bodies require minimal presence of solvent in an active pharmaceutical ingredient (API) after crystallization. From a processing point of view bigger crystals with minimal agglomeration and uniform size distribution are preferred to avoid solvent inclusion and for improved
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