m-Tolualdehyde
m-Tolualdehyde structure
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Common Name | m-Tolualdehyde | ||
|---|---|---|---|---|
| CAS Number | 620-23-5 | Molecular Weight | 120.148 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 199.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H8O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 78.3±0.0 °C | |
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Inhibition of rat respiratory-tract cytochrome P-450 isozymes following inhalation of m-Xylene: possible role of metabolites.
J. Toxicol. Environ. Health A 66(12) , 1133-43, (2003) Xylene is used as a solvent in paints, cleaning agents, and gasoline. Exposure occurs primarily by inhalation. The volatility and lipophilicity of the xylenes make the lung and nasal mucosa the primary target organs. m-Xylene (m-XYL) has been shown to alter c... |
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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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[Secondary metabolites of seaweed endophytic fungi ZJ27 in the South China Sea coast].
Zhong Yao Cai 34(4) , 544-6, (2011) To study the secondary metabolites of coastal seaweed endophytic fungi ZJ27.The compounds were isolated by chromatographic technique. The structures were identified by comprehensive physic-chemical properties and spectral methods.Five compounds were isolated ... |
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Triplet-state energies and substituent effects of excited aroyl compounds in the gas phase.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 56A(1) , 111-7, (2000) Triplet-state energy values obtained from the gas phase are still scarce. In this study, the triplet-state energies of 58 aroyl compounds, introduced as gas chromatographic peaks at atmospheric pressure and typically 473 K, have been determined from the 0-0 b... |