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10 Gram |
Negotiable |
3,4-Dimethoxybenzaldehyde purity 98% Veratraldehyde high quality cas 120-14-9
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Basic information
Product Name: |
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Synonyms: |
3,4-dimethoxybenzaldehhyde;3,4-dimethoxy-benzaldehyd;4-O-Methylvanillin;Benzaldehyde, 3,4-dimethoxy-veratraldehyde;Protocatechuecaldehyde dimethyl ether;protocatechuecaldehydedimethylether;p-Veratric aldehyde;p-veratricaldehyde |
CAS: |
|
MF: |
C9H10O3 |
MW: |
166.17 |
Product Categories: |
Pharmaceutical Raw Materials;FINE Chemical & INTERMEDIATES;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Veratraldehyde;aldehyde Flavor;Aromatics;Miscellaneous Reagents;Pharmaceutical intermediate;API Intermediate |
Mol File: |
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Chemical Properties |
melting point |
40-43 °C(lit.) |
boiling point |
281 °C(lit.) |
density |
1.114 g/cm3 |
Fp |
>230 °F |
vapour pressure |
0.00366 mmHg at 25°C |
Water Solubility |
<0.1 g/100 mL at 22 ºC |
Sensitive |
Air Sensitive |
Stability |
Stable. Incompatible with strong bases, strong oxidizing agents. |
Usage And Synthesis |
General Description |
Needles or chunky light peach powder. Has an odor of vanilla beans. |
Air & Water Reactions |
Insoluble in water. |
Reactivity Profile |
Veratraldehyde is incompatible with strong oxidizing agents and strong bases. . Veratraldehyde is an aldehyde. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). |
Fire Hazard |
Veratraldehyde is probably combustible. |
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