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MX0760
2-Methylbutane
2-Methylbutane
Practical
Sinonimo/i:
2-Methylbutane, Isopentane
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About This Item
Formula condensata:
(CH3)2CHCH2CH3
Numero CAS:
Numero MDL:
Codice UNSPSC:
12191502
Numero indice EU:
201-142-8
Prezzi e disponibilità al momento non sono disponibili
Prodotti consigliati
Tensione di vapore
800 hPa ( 20 °C)
Livello qualitativo
Saggio
≥95% (GC)
Stato
liquid
Colore
APHA: ≤30
P. ebollizione
28 °C/1013 hPa
Punto di fusione
-160 °C
Temp. transizione
flash point -57 °C
Solubilità
0.048 g/L
Densità
0.62 g/cm3 at 20 °C
Condizioni di spedizione
ambient
Temperatura di conservazione
room temp
Stringa SMILE
C(CC)(C)C
InChI
1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3
QWTDNUCVQCZILF-UHFFFAOYSA-N
Categorie correlate
Applicazioni
2-Methylbutane can be used as a reactant to synthesize:
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.[3]
- Isoprene by two-stage dehydrogenation process using chromia-alumina catalyst.[1]
- Alkyl aromatic compounds via silver-catalyzed selective C(sp3)–H benzylation reaction in the presence of N-triftosylhydrazones as carbene precursor.[2]
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.[3]
Confezionamento
M-Bottle for Solvents
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Risultati analitici
Assay (GC): 95% min
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - STOT SE 3
Organi bersaglio
Central nervous system
Rischi supp
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
-59.8 °F - closed cup
Punto d’infiammabilità (°C)
-51 °C - closed cup
Certificati d'analisi (COA)
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
Power-efficient synthesis of isoprene via two-stage dehydrogenation of isopentane
Karimov OK, et al.
World Applied Sciences Journal , 24(3) (2013)
Synthesis, characterization and photophysical properties of a new class of pyrene substituted 1, 3, 4-oxadiazole derivatives
Najare Mahesh S, et al.
Optical Materials, 88 (2019)
Site-selective C-H benzylation of alkanes with N-triftosylhydrazones leading to alkyl aromatics
Liu Zhaohong, et al.
Chem, 6(8) (2020)
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