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| | 3-Methoxysalicylaldehyde Basic information |
| | 3-Methoxysalicylaldehyde Chemical Properties |
| | 3-Methoxysalicylaldehyde Usage And Synthesis |
| Chemical Properties | Pale yellow to brown low melting solid | | Uses | o-Vanillin has been used to study the solvent-free reaction between o-vanillin and p-toluidine using NMR, DSC and XRD analysis. It was used in the synthesis of new ligand for Fe(III) and Al(lII). | | Uses | o-Vanillin has been used to study the solvent-free reaction between o-vanillin and p-toluidine using NMR, DSC and XRD analysis. It was used in the synthesis of new ligand for Fe(III) and Al(lII). It is also used in the study of mutagenesis and as a synthetic precursor for pharmaceuticals. | | Uses | A positional isomer of Vanillin. o-Vanillin is a more potent antioxidant than Vanillin. | | Definition | ChEBI: A member of the class of benzaldehydes that is salicylaldehyde substituted by a methoxy group at position 3. | | Hazard |
ortho-Vanillin is harmful if ingested, irritating to eyes, skin and respiratory system, but has an unmistakable high LD50 of 1330 mg/kg in mice.
| | Biochem/physiol Actions | o-Vanillin induces DNA damage as detected by comet assay. |
| | 3-Methoxysalicylaldehyde Preparation Products And Raw materials |
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