531537
1,2-Epoxy-2-methylpropane
97%
Synonyme(s) :
1,2-Epoxy-isobutane, 2,2-Dimethyloxirane, Isobutylene oxide
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About This Item
Formule empirique (notation de Hill):
C4H8O
Numéro CAS:
Poids moléculaire :
72.11
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Niveau de qualité
Pureté
97%
Indice de réfraction
n20/D 1.374 (lit.)
Point d'ébullition
50-51 °C (lit.)
Densité
0.812 g/mL at 25 °C (lit.)
Chaîne SMILES
CC1(C)CO1
InChI
1S/C4H8O/c1-4(2)3-5-4/h3H2,1-2H3
Clé InChI
GELKGHVAFRCJNA-UHFFFAOYSA-N
Catégories apparentées
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Carc. 2 - Flam. Liq. 2 - Muta. 2 - Skin Corr. 1C
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
-26.5 °F
Point d'éclair (°C)
-32.5 °C
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves
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M Cornet et al.
Archives of toxicology, 65(4), 263-267 (1991-01-01)
Until now, no data are available concerning the biotransformation and toxicity of 2-methylpropene (or isobutene), a gaseous alkene widely used in industry (rubber, fuel additives, plastic polymers, adhesives, antioxidants). In this work, the biotransformation of 2-methylpropene (MP) has been studied
U Jorritsma et al.
Mutagenesis, 10(2), 101-104 (1995-03-01)
2-Methylpropene (isobutene), a gaseous compound widely used in chemical industries, is metabolized to the epoxide 2-methyl-1,2-epoxypropane. The parent compound has previously been shown to be non-mutagenic in a modified Ames test, whereas the epoxide metabolite gave a positive result. In
M Cornet et al.
Chemical research in toxicology, 8(7), 987-992 (1995-10-01)
The biotransformation of 2-methylpropene, a gaseous alkene widely used in industry, was investigated in vitro in liver tissue of rats, mice, and humans. Interspecies comparison revealed that the lowest levels of the primary epoxide metabolite were detected in incubations of
Paul R Carlier et al.
The Journal of organic chemistry, 71(4), 1592-1597 (2006-02-14)
Protonated epoxides feature prominently in organic chemistry as reactive intermediates. Herein, we describe 10 protonated epoxides using B3LYP, MP2, and CCSD/6-311++G calculations. Relative to CCSD, B3LYP consistently overestimates the C2-O bond length. Protonated 2-methyl-1,2-epoxypropane is the most problematic species studied
M Cornet et al.
Mutation research, 271(3), 213-221 (1992-06-01)
The mutagenic properties of 2-methylpropene (MP) and 2-methyl-1,2- epoxypropane (MEP) were investigated in the Salmonella assay. A simple exposure system, consisting of gastight tissue culture flasks, was used. This method has the advantage that the volatile test chemical is present
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