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74750

Sigma-Aldrich

Octadecylamine

≥99.0% (GC)

Synonym(s):

ODA, 1-Aminooctadecane, Stearylamine

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About This Item

Linear Formula:
CH3(CH2)17NH2
CAS Number:
Molecular Weight:
269.51
Beilstein:
636111
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

10 mmHg ( 72 °C)

Quality Level

Assay

≥99.0% (GC)

form

powder

bp

232 °C/32 mmHg (lit.)

mp

50-52 °C (lit.)
52-55 °C

SMILES string

CCCCCCCCCCCCCCCCCCN

InChI

1S/C18H39N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-19H2,1H3

InChI key

REYJJPSVUYRZGE-UHFFFAOYSA-N

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Application

Octadecylamine (ODA) is used:
  • To induce hydrophobicity in nanodiamond (ND) powders.
  • In the surface modification of graphite and fullerenes.
  • As a dual source of carbon and nitrogen in the synthesis of N-doped carbon nanotubes (CNTs).
  • To synthesize a single-chain cationic surfactant, bis(amidoethylcarbamoylethyl) octadecylamine.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2

Target Organs

Liver,Gastrointestinal tract,Immune system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

298.4 °F - closed cup

Flash Point(C)

148 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Direct solvent-free amination of closed-cap carbon nanotubes: a link to fullerene chemistry.
Basiuk EV, et al.
Nano Letters, 4(5), 863-866 (2004)
Micro-structural, electron-spectroscopic and field-emission studies of carbon nitride nanotubes grown from cage-like and linear carbon sources.
Ghosh K, et al.
Carbon, 47(6), 1565-1575 (2009)
Wet chemistry route to hydrophobic blue fluorescent nanodiamond.
Mochalin VN and Gogotsi Y
Journal of the American Chemical Society, 131(13), 4594-4595 (2009)
Graphite oxide: chemical reduction to graphite and surface modification with primary aliphatic amines and amino acids.
Bourlinos AB, et al.
Langmuir, 19(15), 6050-6055 (2003)
Influence of pH on the aggregation morphology of a novel surfactant with single hydrocarbon chain and multi-amine headgroups.
Wang W, et al.
The Journal of Physical Chemistry B, 112(5), 1409-1413 (2008)

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