| Identification | Back Directory | [Name]
DIOCTADECYLAMINE | [CAS]
112-99-2 | [Synonyms]
DODA
DISTEARYLAMINE
AURORA KA-7662
FENTAMINE SA18
DIOCTADECYLAMINE
n-octadecyl-1-octadecanamin
N-octadecyl-1-Octadecanamine
N-octadecyloctadecan-1-amine
DioctadecylaMine >=99.0% (NT)
1-Octadecanamine, N-octadecyl- | [EINECS(EC#)]
204-020-2 | [Molecular Formula]
C36H75N | [MDL Number]
MFCD00048494 | [MOL File]
112-99-2.mol | [Molecular Weight]
521.99 |
| Chemical Properties | Back Directory | [Melting point ]
71-73 °C | [Boiling point ]
524.75°C (estimate) | [density ]
0.9086 (estimate) | [refractive index ]
1.4841 (estimate) | [solubility ]
water: soluble(lit.) | [pka]
10.84±0.19(Predicted) | [Water Solubility ]
water: soluble(lit.) | [BRN ]
1801688 | [InChI]
1S/C36H75N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h37H,3-36H2,1-2H3 | [InChIKey]
HKUFIYBZNQSHQS-UHFFFAOYSA-N | [SMILES]
CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC | [EPA Substance Registry System]
1-Octadecanamine, N-octadecyl- (112-99-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26-36 | [WGK Germany ]
3 | [F ]
10-34 | [TSCA ]
TSCA listed | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
Dioctadecylamine (DODA) is suitable reagent used in the synthesis of the following:
- Dioctadecylamine-BCN (bicyclo[6.1.0]nonyne) conjugate.
- Lipid derivatives of bisethylnorspermine (BSP).
- Functional VP (N-vinylpyrrolidone ) polymers.
It may be used in the following studies:
- As a reactant in the synthesis of 4,4′-azobis(4-cyano-N,N-dioctadecyl)pentanamide (DODA-501) by reacting with disuccinimidyl 4,4′-azobis(4-cyanovalerate).
- As a reagent in the synthesis of dioctadecyl heptapeptides.
- As a phase transfer and stabilizer agent for gold nanoparticles (AuNPs) in non-polar solvent.
| [General Description]
Dioctadecylamine (DODA), a secondary amine, is a fatty amine derivative. Its biodegradation potential has been assessed. It has been observed that in aqueous medium DODA self organizes into plate like structures. Its partial charge distribution as a function of its conformation has been analyzed. The phase diagram of dioctadecylamine Langmuir monolayers has been determined and investigations show it does not form a monolayer above pH 3.9. DODA has been utilized in forming liposomes, cationic lipids or lipid chelating agents. |
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