| Identification | Back Directory | [Name]
MYRISTYL MYRISTATE | [CAS]
3234-85-3 | [Synonyms]
Cetiol MM
Crodamol MM
ceraphyl424
cyclochemmm
Kemester MM
Liponate MM
Waxenol 810
Ceraphyl 424
Cyclochem MM
Alkamuls MM/M
Schercemol MM
Goodway MME-01
Tetradecylmyristat
MYRISTYL MYRISTATE
tetradecylmyristate
Tetradecyl myristate
etradecyltetradecanoate
Myristyl tetradecanoate
tetradecyltetradecanoate
Tetradecyl tetradecanoate
MYRISTIC ACID MYRISTYL ESTER
myristicacid,tetradecylester
Myristic acid, tetradecyl ester
MYRISTIC ACID MYRISTYL ESTER 99%
Tetradecanoicacid,tetradecylester
MYRISTYL MYRISTATE ISO 9001：2015 REACH | [EINECS(EC#)]
221-787-9 | [Molecular Formula]
C28H56O2 | [MDL Number]
MFCD00056201 | [MOL File]
3234-85-3.mol | [Molecular Weight]
424.74 |
| Chemical Properties | Back Directory | [Melting point ]
37.4 °C | [Boiling point ]
462.2±13.0 °C(Predicted) | [density ]
0.859±0.06 g/cm3(Predicted) | [vapor pressure ]
0Pa at 20℃ | [storage temp. ]
-20°C | [Odor]
at 100.00?%. bland | [InChI]
InChI=1S/C28H56O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-30-28(29)26-24-22-20-18-16-14-12-10-8-6-4-2/h3-27H2,1-2H3 | [InChIKey]
DZKXJUASMGQEMA-UHFFFAOYSA-N | [SMILES]
C(OCCCCCCCCCCCCCC)(=O)CCCCCCCCCCCCC | [LogP]
13.013 (est) | [Uses]
myristyl myristate is an occlusive skin-conditioning agent that enhances product spreadability and can reduce a product’s transparency. It is particularly useful in emulsions that have to “melt” once they come in contact with the skin. This is an ester formed by the combination of the myristyl alcohol and myristic acid fractions of coconut oil. | [CAS DataBase Reference]
3234-85-3 | [EPA Substance Registry System]
Myristyl myristate (3234-85-3) |
| Hazard Information | Back Directory | [Description]
Myristyl Myristate is the ester of myristyl alcohol and myristic acid. It is a white-to-yellow waxy solid with a typical waxy odor. It is soluble in mineral oils, but insoluble in water, isopropanol, ethanol, glycerol, and propylene glycol. It is produced by esterification of myristic acid and myristic alcohol in the presence of an acid catalyst. The product is stripped to remove excess s myristyl alcohol, neutralized the catalyst with alkali, and then purified to separate Myristyl Myristate[1-2]. | [Definition]
ChEBI: Tetradecyl tetradecanoate is a tetradecanoate ester (myristate ester) resulting from the formal condensation of the carboxy group of tetradecanoic acid (myristic acid) with the hydroxy group of tetradecan-1-ol (myristyl alcohol). Used as an emollient. It has a role as an algal metabolite. It is a wax ester and a tetradecanoate ester. It is functionally related to a tetradecan-1-ol. | [Flammability and Explosibility]
Nonflammable | [References]
[1] Mitsutake H, et al. Evaluation of miscibility and polymorphism of synthetic and natural lipids for nanostructured lipid carrier (NLC) formulations by Raman mapping and multivariate curve resolution (MCR). European Journal of Pharmaceutical Sciences, 2019; 135: 51-59.
[2] Schlipk?ter K, et al. Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation. Organic Biomolecular Chemistry, 2020; 18: 7862-7867. |
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