| Identification | Back Directory | [Name]
ISOSTEARYL ALCOHOL | [CAS]
27458-93-1 | [Synonyms]
Aldo 66
isostearyl
Pro-xylane
Fine oxocol
JARCOL 1-18T
JARCOL I-18T
JARCOL I-18EX
OCTYL DECANOL
JARCOL 1-18CG
Jarcol I-18CG
ISOOCTADECANOL
ISOSTEARYL ALCOHO
Isotearyl Alcohol
isooctadecan-1-ol
ISOSTEARYL ALCOHOL
ISOOCTADECYL ALCOHOL
IsostearylalcoholJarcolI-18EX
Isostearylalcohol, 97% Sum of C16 C18 C20
Isostearyl alcohol Isooctadecanol 1-Heptadecanol
2-hexyldecan-1-ol and 2-hexyldodecan-1-ol and 2-octyldecan-
1-ol and 2-octyldodecan-1-ol | [EINECS(EC#)]
248-470-8 | [Molecular Formula]
C18H38O | [MDL Number]
MFCD00044081 | [MOL File]
27458-93-1.mol | [Molecular Weight]
270.49 |
| Chemical Properties | Back Directory | [Boiling point ]
343℃[at 101 325 Pa] | [refractive index ]
n20/D 1.451
| [pka]
15.8[at 20 ℃] | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - EMOLLIENT
SKIN CONDITIONING
VISCOSITY CONTROLLING | [InChI]
InChI=1S/C18H38O/c1-18(2)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19/h18-19H,3-17H2,1-2H3 | [InChIKey]
WNWHHMBRJJOGFJ-UHFFFAOYSA-N | [SMILES]
C(CCCCC(C)C)CCCCCCCCCCO | [LogP]
7.815 (est) | [Uses]
isostearyl alcohol is an emollient and viscosity builder derived from isostearic acid. It gives the skin a silky feel after product application. | [EPA Substance Registry System]
Isooctadecanol(27458-93-1) |
| Hazard Information | Back Directory | [Chemical Properties]
Isostearyl alcohol is colorless, odorless, does not oxidize, and is nontoxic and nonirritating. It is an ideal replacement for castor oil and oleyl alcohol for the oil phase. It is a branched-chain aliphatic alcohol[1].
| [Definition]
ChEBI: 16-methylheptadecan-1-ol is a long-chain primary fatty alcohol that is heptadecan-1-ol substituted by a hydroxy group at position 1 and a methyl group at position 16. It is functionally related to a heptadecan-1-ol. It derives from a hydride of a heptadecane. | [Flammability and Explosibility]
Nonflammable | [References]
[1] R. R. Egan, B. J. Hoffman. “Fatty glycols and isostearyl alcohol as lipstick components.” Journal of the American Oil Chemists Society 1 1 (1968): 726–728.
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