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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-489-6
Beilstein/REAXYS Number:
1742765
MDL number:
Assay:
98%
Form:
flakes
InChI key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
InChI
1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
SMILES string
NCCCCCCCCCCCCN
assay
98%
form
flakes
Quality Level
Related Categories
Application
Feedstock for polymer synthesis. Source of twelve carbon chain for medicinal drugs.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
311.0 °F - closed cup
flash_point_c
155 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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
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
R Hochreiter et al.
Naunyn-Schmiedeberg's archives of pharmacology, 361(3), 235-246 (2000-03-24)
A series of diamines with the general structure NH2(CH2)xNH2, x=2-12, was tested for their potential effects on cell proliferation of cultured rat C6 glioma cells in comparison to natural polyamines. Long chain diamines reduced cell number after 48 h in
Michelle J Pisani et al.
Dalton transactions (Cambridge, England : 2003), 39(8), 2078-2086 (2010-02-12)
A simpler method for the purification of cucurbit[10]uril (Q[10]) from the Q[10].Q[5] inclusion complex is reported. 1,12-Diaminododecane was used to displace Q[5], as opposed to the synthetic melamine derivative currently used. The binding of trans-[{PtCl(NH(3))(2)}(2)(micro-NH(2)(CH(2))(8)NH(2))](2+) (CT008) and [{Ru(phen)(2)}(2)(micro-bb(5))](4+) {phen =
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
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