| Identification | Back Directory | [Name]
Glyceryl tri(2-ethylhexanoate) | [CAS]
7360-38-5 | [Synonyms]
TRIETHYLHEXANOIN
Schercemol Esters
glyceryltriisocaprylate
Tricaprylin?(Trioctanoin)?
Glyceryl tri(2-ethylhexanoate)
GLYCEROL TRIS(2-ETHYLHEXANOATE)
Glycerin tris(2-ethylhexanoate)
Glycerol Tri(2-ethylhexanoate)
2-ethylcaproic acid triglyceride
Propan-1,2,3-triyl-2-ethylhexanoat
propane-1,2,3-triyl 2-ethylhexanoate
Octanoicacid,1,2,3,-Propanetriolester
1,2,3-Propanetriol tris(2-ethylhexanoate)
1-O,2-O,3-O-Tris(2-ethylhexanoyl)glycerol
trioctanoin,glyceryltri(2-ethylhexanoate)
2-Ethylhexanoic acid 1,2,3-propanetriyl ester
Hexanoic acid, 2-ethyl-, 1,2,3-propanetriyl ester
Tris(2-ethylhexanoic acid)1,2,3-propanetriyl ester
Tris(2-ethylhexanoic acid)propane-1,2,3-triyl ester
Hexanoic acid, 2-ethyl-, 1,1',1''-(1,2,3-propanetriyl) ester | [EINECS(EC#)]
230-896-0 | [Molecular Formula]
C27H50O6 | [MDL Number]
MFCD04038092 | [MOL File]
7360-38-5.mol | [Molecular Weight]
470.68 |
| Hazard Information | Back Directory | [Uses]
Triisocaprylic acid glyceride is an organic ester, and its chemical structure is basically the same as that of natural oils, and it has good affinity with the skin. On the other hand, the carbon chain part of the compound molecule is shorter than that of natural oil, and it is a light oil. When used on the skin, it does not feel greasy and has good spreadability. It is an ideal cosmetic oil. | [Flammability and Explosibility]
Nonflammable | [Synthesis]
2-ethylhexanoic acid, glycerol, cyclohexane (or xylene), p-toluenesulfonic acid were added to the reactor. Heating, stirring, then refluxing, adding the organic layer under reduced pressure distillation to obtain triisocaprylic acid glyceride. |
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