| 3-Methoxysalicylaldehyde Basic information |
| Product Name: | 3-Methoxysalicylaldehyde |
| Synonyms: | TIMTEC-BB SBB000109;O-VANILLIN (2-HYDROXY-3-METHOXYBENZALDEHYDE);2-Hydroxy-3-methoxybenzaldehyde, 2-Hydroxy-m-anisaldehyde, 3-Methoxysalicylaldehyde;2-HYDROXY-3-METHOXYBENZALDEHYDE / O-VANILLIN;Adjacent vanillin;3-Methoxysalicyladehyde;NC 005;NSC 2150 |
| CAS: | 148-53-8 |
| MF: | C8H8O3 |
| MW: | 152.15 |
| EINECS: | 205-715-3 |
| Product Categories: | Aromatics;Aldehydes;Building Blocks;C8;Carbonyl Compounds;Chemical Synthesis;Aromatic Aldehydes & Derivatives (substituted);Organic Building Blocks |
| Mol File: | 148-53-8.mol |
| 3-Methoxysalicylaldehyde Chemical Properties |
| Melting point | 40-42 °C (lit.) |
| Boiling point | 265-266 °C (lit.) |
| density | 1.2143 (rough estimate) |
| refractive index | 1.4945 (estimate) |
| Fp | >230 °F |
| storage temp. | Store below +30°C. |
| solubility | Chloroform (Sparingly), Methanol (Slightly) |
| form | Low Melting Solid |
| pka | pK1:7.912 (25°C) |
| color | Pale yellow to brown |
| Water Solubility | slightly soluble |
| Sensitive | Air Sensitive |
| BRN | 471913 |
| Stability: | Hygroscopic |
| CAS DataBase Reference | 148-53-8(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzaldehyde, 2-hydroxy-3-methoxy-(148-53-8) |
| EPA Substance Registry System | Benzaldehyde, 2-hydroxy-3-methoxy- (148-53-8) |
| Safety Information |
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38 |
| Safety Statements | 23-36-24/25-36/37/39-27-26 |
| WGK Germany | 3 |
| RTECS | CU6530000 |
| F | 10-23 |
| TSCA | Yes |
| HS Code | 29124900 |
| MSDS Information |
| Provider | Language |
|---|---|
| 3-Methoxysalicylaldehyde | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| 3-Methoxysalicylaldehyde Usage And Synthesis |
| Chemical Properties | Pale yellow to brown low melting solid |
| Uses | A positional isomer of Vanillin. o-Vanillin is a more potent antioxidant than Vanillin. |
| 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 | 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). |
| Definition | ChEBI: A member of the class of benzaldehydes that is salicylaldehyde substituted by a methoxy group at position 3. |
| Biochem/physiol Actions | o-Vanillin induces DNA damage as detected by comet assay. |
| 3-Methoxysalicylaldehyde Preparation Products And Raw materials |
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