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Sigma-Aldrich

2-Methyl-2-butene

≥95.0% (GC)

Sinonimo/i:

β-Isoamylene, Amylene

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About This Item

Formula condensata:
CH3CH=C(CH3)2
Numero CAS:
Peso molecolare:
70.13
Beilstein:
1361353
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Densità del vapore

2.4 (vs air)

Saggio

≥95.0% (GC)

Forma fisica

liquid

Limite di esplosione

8.7 %

Indice di rifrazione

n20/D 1.385 (lit.)
n20/D 1.388

P. eboll.

35-38 °C (lit.)

Punto di fusione

−134 °C (lit.)

Densità

0.662 g/mL at 25 °C (lit.)

Stringa SMILE

C\C=C(\C)C

InChI

1S/C5H10/c1-4-5(2)3/h4H,1-3H3
BKOOMYPCSUNDGP-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

2-Methyl-2-butene may be employed as precursor for peroxyacetyl nitrate for the calibration purposes.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - Muta. 2 - STOT SE 3

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

-4.0 °F

Punto d’infiammabilità (°C)

-20 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves


Certificati d'analisi (COA)

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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)
Mehdi Nabi et al.
Journal of AOAC International, 103(5), 1243-1249 (2020-11-27)
A simple, rapid, selective and sensitive sample preparation and derivatization method was performed for determination of bromate ions in water by means of dispersive liquid-liquid extraction (DLLE) by gas chromatography-electron capture detection (GC-ECD). This method is based on 2-methyl-2-butene derivatization
Gas-phase reaction of ozone with 2-methyl-2-butene: Dicarbonyl formation from Criegee biradicals.
Grosjean D.
Environmental Science & Technology, 24(9), 1428-1432 (1990)
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)

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