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Merck
CN

278351

Isobutyl vinyl ether

contains 0.1% potassium hydroxide as stabilizer, 99%

Synonym(s):

Vinyl isobutyl ether

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About This Item

Linear Formula:
(CH3)2CHCH2OCH=CH2
CAS Number:
109-53-5
Molecular Weight:
100.16
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24856809
EC Number:
203-678-8
Beilstein/REAXYS Number:
1560159
MDL number:
MFCD00008934

Key Documents

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InChI key

OZCMOJQQLBXBKI-UHFFFAOYSA-N

InChI

1S/C6H12O/c1-4-7-5-6(2)3/h4,6H,1,5H2,2-3H3

SMILES string

CC(C)COC=C

vapor density

3.45 (vs air)

vapor pressure

68 mmHg ( 20 °C)

assay

99%

form

liquid

contains

0.1% potassium hydroxide as stabilizer

refractive index

n20/D 1.395 (lit.)

bp

82-83 °C (lit.)

mp

−112 °C (lit.)

density

0.768 g/mL at 25 °C (lit.)

Quality Level

200

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General description

Isobutyl vinyl ether (IBVE) is a vinyl ether monomer that finds wide application in the polymer industry. It is utilized in various applications such as adhesives, coatings, sealants, ink production, elastomers, agricultural chemicals, and specialty polymer formulations due to its desirable properties, including high reactivity, oxygen permeability, good solvency, and crosslinking capability. It is also used in various Biomedical Applications which include, drug delivery systems, tissue engineering, and biocompatible coatings.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Flam. Liq. 2 - Skin Irrit. 2

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM9087
BCCB9884
BCBX0044
BCBT9650
BCBR7195V

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Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic

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