2-Methylbenzaldehyde
2-Methylbenzaldehyde structure
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Common Name | 2-Methylbenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 529-20-4 | Molecular Weight | 120.148 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 201.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H8O | Melting Point | -35 °C | |
| MSDS | Chinese USA | Flash Point | 79.5±4.9 °C | |
| Symbol |
GHS05, GHS07 |
Signal Word | Danger | |
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Oxidation of tolualdehydes to toluic acids catalyzed by cytochrome P450-dependent aldehyde oxygenase in the mouse liver.
Drug Metab. Dispos. 23(2) , 261-5, (1995) Mouse hepatic microsomal enzymes catalyzed the oxidation of o-, m-, and p-tolualdehydes, intermediate metabolites of xylene, to the corresponding toluic acids. Cofactor requirement for the catalytic activity indicates that the microsomes contain NAD- and NADP... |
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The atmospheric photolysis of o-tolualdehyde.
Environ. Sci. Technol. 45(22) , 9649-57, (2011) The photolysis of o-tolualdehyde by natural sunlight has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. The photolysis rate coefficient was measured directly under different solar flux levels, with values in the ran... |
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Long-term performance of passive materials for removal of ozone from indoor air.
Indoor Air 22(1) , 43-53, (2012) The health effects associated with exposure to ozone range from respiratory irritation to increased mortality. In this paper, we explore the use of three green building materials and an activated carbon (AC) mat that remove ozone from indoor air. We studied t... |
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Inhibitory effects on mushroom tyrosinase by some alkylbenzaldehydes.
J. Enzyme Inhib. Med. Chem. 18(6) , 491-6, (2003) The inhibition kinetics on the diphenolase activity of mushroom tyrosinase by some alkylbenzaldehydes has been investigated. The results show that the alkylbenzaldehydes assayed can lead to reversible inhibition to the enzyme; o-tolualdehyde and m-tolualdehyd... |
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Measurement of acid-catalyzed isomerization of unsaturated aldehyde-2, 4-dinitrophenylhydrazone derivatives by high-performance liquid chromatography analysis. Uchiyama S, et al.
Anal. Chim. Acta 523(2) , 157-163, (2004)
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