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Sigma-Aldrich

Dodecylamine

puriss., ≥99.5% (GC)

Synonym(s):

1-Aminododecane, Laurylamine

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About This Item

Linear Formula:
CH3(CH2)11NH2
CAS Number:
Molecular Weight:
185.35
Beilstein:
1633576
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

64 mmHg ( 170 °C)

Quality Level

grade

puriss.

Assay

≥99.5% (GC)

form

solid

impurities

≤0.5% water

bp

247-249 °C (lit.)

mp

27-29 °C (lit.)

solubility

water: 3.5 g/L at 25 °C

density

0.806 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCN

InChI

1S/C12H27N/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-13H2,1H3

InChI key

JRBPAEWTRLWTQC-UHFFFAOYSA-N

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General description

Dodecylamine is a linear primary amine. It participates in the synthesis of kaolinite-dodecylamine complex, useful for the processing of polymer composites. It has been reported to inhibit the mild steel hydrochloric acid corrosion under certain conditions.

Application

Dodecylamine may be used in the following studies:
  • Preparation of novel surfactant copper(II) complexes.
  • As a template for the preparation of hexagonal mesoporous silicate (HMS) materials containing Ti, Zr and Al ions.
  • Synthesis of sponge mesoporous silica (SMS).

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Skin Corr. 1B - STOT RE 2 Oral - STOT SE 3

Target Organs

Gastrointestinal tract,Liver,Immune system, Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

239.0 °F - closed cup

Flash Point(C)

115 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Cong Yao et al.
Journal of chromatography. A, 1218(12), 1556-1566 (2011-02-18)
Functionalized ionic liquids containing the tris(pentafluoroethyl)trifluorophosphate (FAP) anion were used as extraction solvents in dispersive liquid-liquid microextraction (DLLME) for the extraction of 14 emerging contaminants from water samples. The extraction efficiencies and selectivities were compared to those of an in
Pingjing Li et al.
Journal of chromatography. A, 1218(52), 9414-9421 (2011-11-22)
In this paper, a novel sample pretreatment technique termed phase transfer based liquid-liquid-liquid microextraction (PT-LLLME) was proposed for the simultaneous extraction of inorganic and organic mercury species. In PT-LLLME, an intermediate solvent (acetonitrile) was added into the donor phase to
Immobilization of 12-molybdophosphoric and 12-tungstophosphoric acids on metal-substituted hexagonal mesoporous silica.
Damyanova S, et al.
Applied Catalysis A: General, 256(1), 183-193 (2003)
Synthesis of sponge mesoporous silicas from lecithin/dodecylamine mixed-micelles in ethanol/water media: a route towards efficient biocatalysts.
Galarneau A, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 104(1), 103-114 (2007)
Karuppiah Nagaraj et al.
Colloids and surfaces. B, Biointerfaces, 122, 151-157 (2014-07-18)
The novel surfactant copper(II) complexes, [Cu(ip)2DA](ClO4)21, [Cu(dpqc)2DA](ClO4)22, [Cu(dppn)2DA](ClO4)23, where ip=imidazo[4,5-f][1,10]phenanthroline, dpqc=dipyrido[3,2-a:2',4'-c](6,7,8,9-tetrahydro)phenazine, dppn=benzo[1]dipyrido[3,2-a':2',3'-c]phenazine and DA-dodecylamine, were synthesized and characterized by physico-chemical and spectroscopic methods. In these complexes 1-3, the geometry of copper metal ions was described as square pyramidal. The critical

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