MYRISTIC ACID N-BUTYL ESTER
- CAS NO.：110-36-1
- Empirical Formula: C18H36O2
- Molecular Weight: 284.48
- MDL number: MFCD00015077
- EINECS: 203-759-8
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-08-05 20:55:42
What is MYRISTIC ACID N-BUTYL ESTER?
The Uses of MYRISTIC ACID N-BUTYL ESTER
MYRISTIC ACID N-BUTYL ESTER is occasionally used in perfumery to introduce fatty, Orris-like notes or flower-wax notes in floral bases, artificial flower absolutes, etc. Occasionally used in flavor compositions for imitation Cognac and Nutmeg, again mainly for its peculiar fatty notes.
Production Methods
MYRISTIC ACID N-BUTYL ESTER can be produced from n-Butanol and Myristic acid by direct esterification under azeorropic conditions.
Properties of MYRISTIC ACID N-BUTYL ESTER
| Melting point: | 6.8°C |
| Boiling point: | 195 °C / 18mmHg |
| Density | 0,86 g/cm3 |
| refractive index | 1.4380 to 1.4410 |
| Flash point: | 166°C |
| form | clear liquid |
| color | Colorless to Almost colorless |
| Odor | at 100.00 %. mild oily fatty |
| CAS DataBase Reference | 110-36-1(CAS DataBase Reference) |
| EPA Substance Registry System | Butyl myristate (110-36-1) |
Safety information for MYRISTIC ACID N-BUTYL ESTER
Computed Descriptors for MYRISTIC ACID N-BUTYL ESTER
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium THOMAIND PAPER PH 2.0 TO 4.5 1 BOX BUFFER CAPSULE PH 9.2 - 10 CAP SODIUM CHLORIDE 0.1N CVS ALLOXAN MONOHYDRATE 98% PLATINUM 0.5% ON 3 MM ALUMINA PELLETS (TYPE 73) LITHIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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