Diethyl phtalate
PE ; Anozol ; DEP ; Diethylbenzene-1,2-dicarboxylate ; Di ethyl phtalate ; Diethyl 1,2-benzene dicarboxylate ; Diethyl ortho-phtalate ; Diethylphtalate ; Dpx-f5384 ; Ethyl 2-(ethoxycarbonyl)benzoate ; Neantine ; Palatinol A ; Phthalol ; Placidol E ; Solvanol ; Unimoll DA ; Uniplex 105
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 84-66-2
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EINECS number : 201-550-6
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FEMA number : Donnée indisponible.
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Density : 1,12
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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 : NON TROUVE_N/A
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 299°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H14O4
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Log P : 2,20 (à 41°C)
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Molecular Weight : 222,24 g/mol
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Fusion Point : 3°C
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Flash Point : 156°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Tends to form its monoacid or diacid after maceration in alcohol.
Uses in perfumery :
Diethyl Phtalate is an organic denaturant present in the alcohol of several perfumes, to make them unsuitable for oral consumption. It can also be used as a solvent in certain fragrance concentrates.
For stability reasons, it is one of the most suitable solvents for 100% natural candle base and for body and hair oils. It can also be used in shower gel (it can still affect viscosity), shampoo, cream, candle, fabric softener and household cleaner bases.
On the other hand, Diethyl Phtalate should not be placed in a dishwashing liquid base, still for stability reasons.
Year of discovery :
Data not available.
Isomerism :
Diethyl Phtalate does not have any isomer used in perfumery.
Synthesis precursor :
Diethyl phtalate is not used to synthesize another perfume compound.
Natural availability :
Diethyl Phtalate is not available in its natural state.
Synthesis route :
The synthesis of Diethyl Phtalate is an esterification reaction, carried out from phtalic anhydride, by a reaction with ethanol, in the presence of a small acid catalyst such as concentrated sulfuric acid. Phtalic anhydride is preferred to phtalic acid to improve the reaction yield.
Regulations & IFRA
This ingredient is not restricted
