Photo credits: ScenTree SAS
Isopropyl myristate
IPM ; Propan-2-yl tetradecanoate ; Bisomel ; Crodamol IPM ; Deltyl extra ; Dermol IPM ; Edenor IEM 17 ; Emcol-IM ; Emerest 2314 ; Estergel ; Exceparl IPM ; Hallstar IPM ; Kessco IPM ; Kesscomir ; Liponate IPM ; 1-methylethyl tetradecanoate ; Isomyst ; Nikkol IPM-100 ; Promyr ; Propan-2-yl tetradecanoate ; Sinnoester MIP ; Starfol IPM ; Tegester ; Unimate IPM ; Isopropyl tetradecanoate ; 1-methylethyl tetradecanoate ; Wickenol 101
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Myristate d'isopropyle - 500 mL | - |
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|
- | - | - | - | - | - |
Myristate d'isopropyle - 500 mL
Certifications :
General Presentation
-
CAS N° :
110-27-0 -
EINECS number :
203-751-4 -
FEMA number :
3556 -
FLAVIS number :
09.105
-
JECFA number :
311 -
Volatility :
NON TROUVE_N/A -
Price Range :
€
Physico chemical properties
-
Appearance :
Colorless liquid -
Density :
0,85 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
Data not available. -
Flash Point :
152°C
-
Molecular formula :
C17H34O2 -
Molecular Weight :
270,45 g/mol -
Log P :
7,71 -
Fusion Point :
3°C -
Boiling Point :
193°C (à 20 mmHg) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Year of discovery :
Data not available.
Natural availability :
Isopropyl Myristate is found in some fruits, but is not extracted in its natural state for its use in perfumery.
Isomerism :
Isopropyl Myristate does not have any isomer used in perfumery.
Synthesis precursor :
Isopropyl Myristate does not interfere with the synthesis of another perfume compound.
Synthesis route :
Originally, Isopropyl Myristate is synthesized by an esterification reaction between myristic acid and isopropanol. This reaction requires a very large excess of isopropanol (15 times greater than the acid amount) and an acid catalysis in the presence of sulfuric acid, for example. Today, many synthetic routes are being developed to make this synthesis greener. These methods are always esterification reactions, but they use a cleaner biocatalysis, multiple reactors including enzymes and dehydrating substances, to shift the equilibrium of the reaction and obtain a purer MIP, while recycling the remaining reagents.
Stability :
Data not available.
Other comments :
Data not available.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
