Palmityl acetate
Palmityl acetate Basic information
- Product Name:
- Palmityl acetate
- Synonyms:
-
- CETYL ACETATE
- HEXADECYL ACETATE
- 1-Acetoxyhexadecane
- 1-Hexadecanol,acetate
- 1-HEXADECYL ACETATE
- PALMITYL ACETATE
- Acelan A
- Palmityl AcetatePalmityl Acetate
- CAS:
- 629-70-9
- MF:
- C18H36O2
- MW:
- 284.48
- EINECS:
- 211-103-7
- Product Categories:
-
- Alcohol Acetates
- Esters
- Saturated fatty acids and derivatives
- Mol File:
- 629-70-9.mol
Palmityl acetate Chemical Properties
- Melting point:
- 24.2°C
- Boiling point:
- 326.96°C (estimate)
- Density
- 0.8672 (estimate)
- vapor pressure
- 0.005Pa at 25℃
- refractive index
- 1.4439 (estimate)
- storage temp.
- −20°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- solid
- color
- Colourless
- InChI
- InChI=1S/C18H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-18(2)19/h3-17H2,1-2H3
- InChIKey
- LSTDYDRCKUBPDI-UHFFFAOYSA-N
- SMILES
- C(OC(=O)C)CCCCCCCCCCCCCCC
- LogP
- 8.66 at 40℃
- EPA Substance Registry System
- Cetyl acetate (629-70-9)
MSDS
- Language:English Provider:SigmaAldrich
Palmityl acetate Usage And Synthesis
Description
Palmityl acetate is an ester compound with a waxy odour. Palmityl acetate, an acetate ester derived from hexadecan-1-ol (palmityl alcohol), is used as an emollient, masking agent and skin conditioner. It can also be used as a plasticizer or stabilizer in producing plastics and resins. It is a pheromone constituent present in various species of mouse, arachnid and insect. It has a cosmetic role, as well as a pheromone and an epitope.
Uses
Hexadecyl Acetate is a plant sex pheromone.
Definition
ChEBI: Palmityl acetate is an acetate ester derived from hexadecan-1-ol (palmityl alcohol); used as an emollient, masking agent and skin conditioner; pheromone constituent present in various species of mouse, arachnid and insect. It has a role as a cosmetic, a pheromone and an epitope. It is functionally related to a hexadecan-1-ol.
Flammability and Explosibility
Non flammable
Purification Methods
Distil the ester in a vacuum twice, then recrystallise it several times from diethyl ether/MeOH. [Beilstein 2 H 136, 2 II 146, 2 III 265, 2 IV 171.]
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