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Merck
CN

32880

1,10-Diaminodecane

purum, ≥98.0% (GC)

Synonym(s):

1,10-Decanediamine, Decamethylenediamine

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About This Item

Linear Formula:
NH2(CH2)10NH2
CAS Number:
646-25-3
Molecular Weight:
172.31
EC Number:
211-471-9
UNSPSC Code:
12352100
PubChem Substance ID:
24859749
Beilstein/REAXYS Number:
1738591
MDL number:
MFCD00008151

Key Documents

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InChI key

YQLZOAVZWJBZSY-UHFFFAOYSA-N

InChI

1S/C10H24N2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-12H2

SMILES string

NCCCCCCCCCCN

grade

purum

assay

≥98.0% (GC), ≥98.0% (NT)

bp

140 °C/12 mmHg (lit.)

mp

59-61 °C (lit.), 59-63 °C

solubility

dioxane: soluble, clear, colorless (hot)

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General description

The interactions of 1,10-diaminodecane with α-cyclodextrin was studied in aqueous solutions by NMR diffusion measurements.

Application

1,10-Diaminodecane was used in preparation of electrostatically self-assembled multilayer film based on a Keggin-type phosphomolybdate.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

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Li-Hua Gao et al.
Journal of nanoscience and nanotechnology, 11(11), 9861-9864 (2012-03-15)
An electrostatically self-assembled multilayer film has successfully been prepared on quartz or indium-tin-oxide substrates by alternating adsorption of a Keggin-type phosphomolybdate H3PMo12O40 (PMo12) and 1,10-diaminodecane (1,10-DAD). The formation of (PMo12/1,10-DAD), film was investigated by ultraviolet (UV) spectroscopy. The UV spectra
Liat Avram et al.
The Journal of organic chemistry, 67(8), 2639-2644 (2002-04-13)
The interactions of 1,4-diaminobutane (1), 1,6-diaminohexane (2), 1,8-diaminooctane (3), 1,10-diaminodecane (4), and 1,12-diaminododecane (5) with alpha-cyclodextrin (alpha-CD) were studied in aqueous solutions by NMR diffusion measurements before and after protonation. The correlation between the association constant and the length of
Fátima M F Vergara et al.
Bioorganic & medicinal chemistry letters, 19(17), 4937-4938 (2009-08-04)
A series of 11 alpha,omega-diaminoalkanes, (H(2)N(CH(2))(n)NH(2), n=2-12) have been evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis H37Rv. Compounds, (H(2)N(CH(2))(n)NH(2), n=9-12), exhibited a very good activities in the range 2.50-3.12 microg/mL, which can be compared with that of
Jing Yuan et al.
Nature chemical biology, 5(10), 765-771 (2009-09-08)
Studies of gene function and molecular mechanisms in Plasmodium falciparum are hampered by difficulties in characterizing and measuring phenotypic differences between individual parasites. We screened seven parasite lines for differences in responses to 1,279 bioactive chemicals. Hundreds of compounds were
Phedias Diamandis et al.
Nature chemical biology, 3(5), 268-273 (2007-04-10)
The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain cancer. However, the complete repertoire of signaling pathways that governs the

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