86262
2-Methyl-2-butene
≥95.0% (GC)
Synonym(s):
β-Isoamylene, Amylene
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About This Item
Linear Formula:
CH3CH=C(CH3)2
CAS Number:
Molecular Weight:
70.13
Beilstein:
1361353
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor density
2.4 (vs air)
Quality Level
Assay
≥95.0% (GC)
form
liquid
expl. lim.
8.7 %
refractive index
n20/D 1.385 (lit.)
n20/D 1.388
bp
35-38 °C (lit.)
mp
−134 °C (lit.)
density
0.662 g/mL at 25 °C (lit.)
SMILES string
C\C=C(\C)C
InChI
1S/C5H10/c1-4-5(2)3/h4H,1-3H3
InChI key
BKOOMYPCSUNDGP-UHFFFAOYSA-N
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General description
2-Methyl-2-butene is a trisubstituted olefin. It acts as guest and forms stable solid host-guest complexes with self-assembled benzophenone bis-urea macrocycles. The impact of active chlorine on photo-oxidation of 2-methyl-2-butene was studied. Photosensitized oxidation of 2-methyl-2-butene adsorbed on internal framework of Na-ZSM-5 zeolite was studied. Gas-phase reaction of 2-methyl-2-butene with ozone has been investigated. Kinetics of liquid-phase alkylation of 3-methylthiophene with 2-methyl-2-butene on supported phosphoric acid has been reported.
2-methyl-2-butene undergoes ultraviolet irradiation, leading to the formation of trimethylene oxides.
2-methyl-2-butene undergoes ultraviolet irradiation, leading to the formation of trimethylene oxides.
Application
2-Methyl-2-butene may be employed as precursor for peroxyacetyl nitrate for the calibration purposes.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - Muta. 2 - STOT SE 3
Target Organs
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-4.0 °F
Flash Point(C)
-20 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Light-catalyzed organic reactions. I. The reaction of carbonyl compounds with 2-methyl-2-butene in the presence of ultraviolet light
Buchi G, et al.
Journal of the American Chemical Society, 76, 4327-4331 (1954)
Kinetics and mechanism of liquid-phase alkylation of 3-methylthiophene with 2-methyl-2-butene over a solid phosphoric acid.
Belliere V, et al.
Applied Catalysis. B, Environmental, 64(3), 254-261 (2006)
Light-catalyzed organic reactions. I. The reaction of carbonyl compounds with 2-methyl-2-butene in the presence of ultraviolet light
Buchi G, et al.
Journal of the American Chemical Society, 76, 4327-4331 (1954)
Michael F Geer et al.
The Journal of organic chemistry, 78(11), 5568-5578 (2013-05-16)
This manuscript investigates how incorporation of benzophenone, a well-known triplet sensitizer, within a bis-urea macrocycle, which self-assembles into a columnar host, influences its photophysical properties and affects the reactivity of bound guest molecules. We further report the generation of a
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