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Merck
CN

07-3890

Diisopropyl ether

SAJ first grade, ≥99.0%

Synonym(s):

Isopropyl ether

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About This Item

Linear Formula:
(CH3)2CHOCH(CH3)2
CAS Number:
108-20-3
Molecular Weight:
102.17
PubChem Substance ID:
329748427
UNSPSC Code:
12352112
Beilstein/REAXYS Number:
1731256
MDL number:
MFCD00008880

Key Documents

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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

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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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H336

Hazard Classifications

Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

supp_hazards

EUH019,EUH066

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

-18.4 °F

flash_point_c

-28 °C

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
F2644
F9566
F5548
A1535
F0465

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Fiorella Belpoggi et al.
Annals of the New York Academy of Sciences, 982, 70-86 (2003-02-04)
Tert-amyl-methyl ether (TAME) was administered by gavage in extra virgin olive oil solution at concentrations of 750, 250, or 0 mg/kg bw to groups of 100 male and 100 female Sprague-Dawley rats 8 weeks old at the start of the
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
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
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
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
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