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95251

Supelco

Diisopropyl ether

analytical standard

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
Beilstein:
1731256
EC Number:
203-560-6
MDL number:
MFCD00008880
UNSPSC Code:
41116107
PubChem Substance ID:
329770429
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

3.5 (vs air)

vapor pressure

120 mmHg ( 20 °C)

Assay

≥99.7% (GC)

autoignition temp.

827 °F

shelf life

limited shelf life, expiry date on the label

contains

~0.006% 2,6-di-tert-butyl-4-methylphenol as stabilizer

expl. lim.

1-21 %, 100 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.367 (lit.)
n20/D 1.368

bp

68-69 °C (lit.)

mp

−85 °C (lit.)

density

0.725 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

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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General description

Diisopropyl ether is a secondary ether , which finds applications as an extractant and oxygenate gasoline additive.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Description
Pricing

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H336

Hazard Classifications

Flam. Liq. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

EUH019,EUH066

WGK

WGK 1

Flash Point(F)

-20.2 °F

Flash Point(C)

-29 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number

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Organic Chemistry: Chemistry, Organic chemistry (2016)
Introduction to Spectroscopy (2016)
Purification and analysis of gangliosides.
S Ladisch et al.
Methods in enzymology, 312, 135-145 (2000-11-09)
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
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
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