Triacetin
1,3-diacetyloxypropan-2-yl acetate ; 2-acetyloxy-1-(acetyloxymethyl)ethyl acetate ; Captex 500 ; Enzactin ; Fungacetin ; Glycerin triacetate ; Glycerol triacetate ; Glyceryl triacetate ; 1,2,3-propane triol triacetate ; 1,2,3-propanetriol triacetate ; Triacetine ; Triacetylglycerol ; Vanay
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 102-76-1
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EINECS number : 203-051-9
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FEMA number : 2007
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Density : 1,16
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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 : 920
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 258°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C9H14O6
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Log P : 0,25
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Molecular Weight : 218,2 g/mol
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Fusion Point : 3°C
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Flash Point : 138°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Data not available.
Uses in perfumery :
Triacetin is a solvent sometimes found in some perfume concentrates.
For stability reasons, this solvent is suitable for use in shower gel base, cream base and dishwashing liquid base.
However, this solvent should not be used in candle base concentrates of any type.
Year of discovery :
Data not available.
Isomerism :
Triacetin does not have any isomer used in perfumery.
Synthesis precursor :
Triacetin does not intervene in the synthesis of a perfume compound.
Natural availability :
Triacetin is present in the fragrant principle of papaya, but is not extracted from this fruit and is only synthesized for its use in perfumery.
Synthesis route :
Triacetin can usually be made from glycerol and acetic acid. This esterification reaction is carried out in the presence of an acid catalyst such as concentrated sulfuric acid.
Regulations & IFRA
This ingredient is not restricted
