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ChemicalBook--->CAS DataBase List--->112-99-2

112-99-2

112-99-2 Structure

112-99-2 Structure
IdentificationBack 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 PropertiesBack 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)
[BRN ]

1801688
[EPA Substance Registry System]

1-Octadecanamine, N-octadecyl- (112-99-2)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[F ]

10-34
Hazard InformationBack 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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