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Merck

44172

Dodecylamine

puriss., ≥99.5% (GC)

Synonym(s):

1-Aminododecane, Laurylamine

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About This Item

Linear Formula:
CH3(CH2)11NH2
CAS Number:
124-22-1
Molecular Weight:
185.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329756460
EC Number:
204-690-6
Beilstein/REAXYS Number:
1633576
MDL number:
MFCD00008154

Product Name

Dodecylamine, puriss., ≥99.5% (GC)

InChI key

JRBPAEWTRLWTQC-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCCCN

vapor pressure

64 mmHg ( 170 °C)

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.)

functional group

amine

Quality Level

200

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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).

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.

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Danger

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

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

239.0 °F - closed cup

flash_point_c

115 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
0000463658
0000463658
0000458170
0000458170
0000352447

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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
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
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)
Tukayi Kudanga et al.
Journal of biotechnology, 149(1-2), 81-87 (2010-07-06)
Enzymatic processes provide new perspectives for modification of lignocellulose materials. In the current study, laccase catalyzed coupling of long chain alkylamines to lignin model molecules and lignocellulose was investigated. Up to two molecules of dodecylamine (DA) and dihexylamine (DHA) were
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