Ethyl vanillin
3-ethoxy-4-hydroxybenzaldehyde ; Bourbonal ; Ethavan ; Ethovan ; 3-ethoxy protocatechualdehyde ; 2-ethoxy-4-formyl phenol ; 3-ethoxy-4-hydroxybenzaldehyde ; 3-ethoxy-4-oxidanylbenzaldehyde ; Ethyl protal ; Ethyl protocatechualdehyde-3-ethyl ether ; Ethyl protocatechuic aldehyde ; Ethylprotal ; Ethylprotocatechuic aldehyde ; Ethylvanillin ; 4-hydroxy-3-ethoxybenzaldehyde ; Quantrovanil ; Rhodiarome ; Rhodiascent ; Vanirome
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Ethyl Vanilline - 30 Gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 121-32-4
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EINECS number : 204-464-7
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FEMA number : 2464
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Density : 1,186
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Base
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Price Range : €€
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Appearance : White solid
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FLAVIS number : 05.019
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JECFA number : 893
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 295°C
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Detection Threshold : 0,1 ppm (0,00001%)
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Molecular formula : C9H10O3
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Log P : Donnée indisponible.
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Molecular Weight : 166,17 g/mol
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Fusion Point : 76°C
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Flash Point : 145°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Ethyl Vanillin has a more artificial and foody aspect than Vanillin. It is however very used in perfumery.
Stability :
Becomes red under the effect of light. This raw material is not convenient in every functional base : can't be used in a candle or shower gel base.
Uses in perfumery :
Ethyl Vanillin is used in vanillic and fruity notes, often in association with Vanillin, in smaller proportions, as it is a more powerful product.
Year of discovery :
1894
Isomerism :
Ethyl Vanillin does not have any isomer used in perfumery.
Synthesis precursor :
Ethyl Vanillin may undergo acetalization reactions in the presence of various alcohols or diols. It can also undergo esterification reactions in the presence of carboxylic acids.
Natural availability :
Ethyl Vanillin is not available in its natural state.
Synthesis route :
Ethyl Vanillin synthesis can follow a similar pathway to Vanillin synthesis, starting from Guaethol rather than Guaiacol. A first step consists in reacting Guaethol with glyoxylic acid, at room temperature, in a basic medium and with a slight excess of Guaethol. A catalytic air oxidation of the intermediate product, followed by a decarboxylation in an acidic medium, releasing CO2, allows to obtain Ethyl Vanillin.
Regulations & IFRA
This ingredient is not restricted
