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| 3-Methoxybenzaldehyde Basic information |
| 3-Methoxybenzaldehyde Chemical Properties |
Melting point | 187 °C | Boiling point | 143 °C50 mm Hg(lit.) | density | 1.117 g/mL at 20 °C(lit.) | vapor pressure | 1.3 hPa (73 °C) | refractive index | n20/D 1.553(lit.) | Fp | >230 °F | storage temp. | Store below +30°C. | solubility | Chloroform, Methanol (Slightly) | form | Liquid | Specific Gravity | 1.118 | color | Clear pale yellow to yellow | Odor | at 100.00?%. anisic | Water Solubility | insoluble | Sensitive | Air Sensitive | BRN | 606013 | LogP | 1.710 | CAS DataBase Reference | 591-31-1(CAS DataBase Reference) | NIST Chemistry Reference | Benzaldehyde, 3-methoxy-(591-31-1) | EPA Substance Registry System | Benzaldehyde, 3-methoxy- (591-31-1) |
Hazard Codes | Xi | Risk Statements | 36/37/38-36/38 | Safety Statements | 26-36-37/39 | WGK Germany | 3 | RTECS | BZ2605000 | F | 9-23 | Autoignition Temperature | 225 °C | TSCA | Yes | HazardClass | IRRITANT | HS Code | 29124900 | Toxicity | sce-hmn:lyms 1 mmol/L MUREAV 206,17,88 |
| 3-Methoxybenzaldehyde Usage And Synthesis |
Chemical Properties | clear pale yellow to yellow liquid | Uses | 3-Methoxybenzaldehyde is used to prepare 3-(3-methoxy-phenyl)-1-phenyl-propenone by reaction with benzldehyde. It is used as an eluent for mono-13C isotopomers of vanillin in normal phase silica gel chromatography. It acts as an inhibitor of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metabolism. | Definition | ChEBI: 3-methoxybenzaldehyde is a member of the class of benzaldehydes in which the hydrogen at position 3 of benzaldehyde has been replaced by a methoxy group. It has a role as a Brassica napus metabolite. It is a member of benzaldehydes and a monomethoxybenzene. | Synthesis Reference(s) | Synthetic Communications, 24, p. 2011, 1994 DOI: 10.1080/00397919408010209 | General Description | m-Anisaldehyde has significant antifungal activity against Candida sp., including the azole-resistant strains. | Safety Profile | Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. | Purification Methods | Wash it with saturated aqueous NaHCO3, then H2O, dry it with anhydrous MgSO4 and distil it under reduced pressure under N2. Store it under N2 in sealed glass ampoules. [Beilstein 8 IV 241.] |
| 3-Methoxybenzaldehyde Preparation Products And Raw materials |
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