D16401
1,12-Diaminododecane
98%
Synonym(s):
1,12-Dodecanediamine, Dodecamethylenediamine
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About This Item
Linear Formula:
NH2(CH2)12NH2
CAS Number:
Molecular Weight:
200.36
Beilstein:
1742765
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
flakes
mp
67-69 °C (lit.)
SMILES string
NCCCCCCCCCCCCN
InChI
1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
InChI key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
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Related Categories
Application
Feedstock for polymer synthesis. Source of twelve carbon chain for medicinal drugs.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
311.0 °F - closed cup
Flash Point(C)
155 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A Sintov et al.
Biomaterials, 16(6), 473-478 (1995-04-01)
Chondroitin sulphate was cross-linked with 1,12-diaminododecane to give a series of cross-linked products with reduced water solubility. Since the water solubility of the modified polymers is low, their chemical characterization is complicated. A new method based on the adsorption of
Beibei Xue et al.
Journal of integrative plant biology, 51(3), 225-234 (2009-03-06)
Using pharmacological and biochemical approaches, the role of maize polyamine oxidase (MPAO) in abscisic acid (ABA)-induced antioxidant defense in leaves of maize (Zea mays L.) plants was investigated. Exogenous ABA treatment enhanced the expression of the MPAO gene and the
J Lee et al.
Journal of nanoscience and nanotechnology, 1(1), 59-64 (2003-08-14)
The partial exchange of surface-passivating trioctylphosphine oxide (TOPO) on CdSe and ZnS-clad CdSe (CdSe/ZnS) nanocrystals with primary amines was utilized to grow ultra-thin films of these nanocrystals under nonaqueous conditions. This growth was achieved using 1,12-diaminododecane in a layer-by-layer assembly
Andrew R Hirst et al.
Langmuir : the ACS journal of surfaces and colloids, 20(25), 10851-10857 (2004-12-01)
The self-assembly of diaminododecane with dendritic l-lysine-based peptides to form gel-phase materials was investigated in a range of different solvents. The degree of structuring was modulated by the solvent employed, an effect which induced subtle changes in the mesoscale aggregate
Zhong-Xiu Chen et al.
The journal of physical chemistry. B, 115(8), 1798-1806 (2010-12-31)
Molecular recognition by means of multiple hydrogen bonds is of great importance in biological functions. In this paper, an orotic acid derived bolaamphiphile 1,12-diaminododecane diorotate (DDO) with molecular recognition function moieties was designed. Both self-aggregation behavior and molecular recognition with
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