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Sigma-Aldrich

Dodecylamine

≥99%

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
Beilstein:
1633576
EC Number:
204-690-6
MDL number:
MFCD00008154
UNSPSC Code:
12352100
PubChem Substance ID:
24859488
NACRES:
NA.22

vapor pressure

64 mmHg ( 170 °C)

Assay

≥99%

form

solid

bp

247-249 °C (lit.)

mp

27-29 °C (lit.)

solubility

water: soluble 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

Intercalation of dodecylamine into the layer space of kaolinite was investigated. Dodecylamine was investigated as inhibitor of mild steel hydrochloric acid corrosion.

Application

Dodecylamine was used in preparation of novel surfactant copper(II) complexes.

Signal Word

Danger

Hazard Statements

H304,H314,H335,H373,H410

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

Certificates of Analysis (COA)

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Journal of hazardous materials, 198, 103-112 (2011-10-26)
The extraction of Red 3BS reactive dye from aqueous solution was studied using emulsion liquid membrane (ELM). ELM is one of the processes that have very high potential in treating industrial wastewater consisting of dyes. In this research, Red 3BS
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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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