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Cosmetics Grade Vinyl isopropyl ether 926-65-8 For Sale with Good Price
- Molecular Formula: C5H10O
- Molecular Weight: 86.1338
- Appearance/Colour: colorless and transparent liquid
- Vapor Pressure: 230mmHg at 25°C
- Melting Point: -140oC
- Refractive Index: 1.388
- Boiling Point: 57.5 °C at 760 mmHg
- Flash Point: °C
- PSA： 9.23000
- Density: 0.762 g/cm3
- LogP: 1.55490
Vinyl isopropyl ether(Cas 926-65-8) Usage
|
General Description |
Vinyl isopropyl ether is a chemical compound with the molecular formula C5H10O. It is a colorless liquid with a mild, sweet odor, and is highly flammable. Vinyl isopropyl ether is commonly used as a solvent in the manufacturing of paints, varnishes, and other coatings. It is also used as an intermediate in the synthesis of various organic compounds and as a reagent in organic chemistry reactions. Additionally, it can be used as a monomer in the production of polymers and copolymers. However, vinyl isopropyl ether presents some health hazards, as it can cause irritation to the eyes, skin, and respiratory system, and may have harmful effects if ingested or inhaled. Therefore, proper safety precautions should be taken when handling and using this chemical. |
InChI:InChI=1/C5H10O/c1-4-6-5(2)3/h4-5H,1H2,2-3H3
926-65-8 Relevant articles
NATURE AND CONCENTRATION OF ACTIVE SPECIES IN CATIONIC POLYMERIZATION OF VINYL ETHERS: A KINETIC INVESTIGATION
Cramail, Henri,Deffieux, Alain
, p. 293 - 300 (1995)
The Kinetics of the polymerization of is...
Nucleophilic addition to acetylenes in superbasic catalytic systems: XIII. Fluoride cesium containing systems, efficient catalysts for alkanols vinylation
Oparina,Shaikhudinova,Parshina,Vysotskaya,Preiss,Henkelmann,Trofimov
, p. 656 - 660 (2007/10/03)
New catalytic systems CsF-MOH (M = Li, N...
Nucleophilic Addition to Acetylenes in Superbasic Catalytic Systems. VII. Vinylation of Lower Alcohols
Trofimov, B. A.,Oparina, L. A.,Lavrov, V. I.,Parshina, L. N.
, p. 597 - 600 (2007/10/03)
Superbasic systems KOH-DMSO and KOH-HMPA...
Dissociation of Positively Charged Aliphatic Epoxides. II. +. Epoxides and α,β Unsaturated Ethers
Bouchoux, Guy,Djazi, Feycal,Hoppilliard, Yannik,Jaudon, Pascale,Nouts, Nathalie
, p. 33 - 41 (2007/10/02)
The unimolecular dissociations of C5 epo...
926-65-8 Process route
-
-
67-63-0,8013-70-5
isopropyl alcohol
-
-
74-86-2,25067-58-7
acetylene
-
-
926-65-8
vinyl isopropyl ether
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide; cesium fluoride;
In
dimethyl sulfoxide;
at 100 ℃;
for 5.5h;
atmospheric pressure;
|
86%
|
|
With
potassium hydroxide;
In
dimethyl sulfoxide;
at 120 ℃;
for 2h;
|
53%
|
|
With
potassium hydroxide;
at 150 - 155 ℃;
|
-
-
54149-16-5
2-isopropyloxyethyl bromide
-
-
926-65-8
vinyl isopropyl ether
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
at 130 ℃;
|
|
|
With
potassium tert-butylate;
In
dimethyl sulfoxide;
at 90 ℃;
|
926-65-8 Upstream products
-
4285-59-0
1,1-diisopropoxy-ethane
-
84607-80-7
1-chloro-1-(1-methyletoxy)ethane
-
54149-16-5
2-isopropyloxyethyl bromide
-
111-34-2
-butyl vinyl ether
926-65-8 Downstream products
-
1123-27-9
1-(1-hydroxycyclohexyl)ethan-1-one
-
17902-91-9
diethyl-(1-isopropoxy-ethoxy)-phenyl-silane
-
75-07-0
acetaldehyde
-
104741-77-7
1-benzoyloxy-1-isopropoxy-ethane
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