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Merck
CN

D14204

1,10-Diaminodecane

97%

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24277977
EC Number:
211-471-9
Beilstein/REAXYS Number:
1738591
MDL number:
MFCD00008151

Key Documents

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Product Name

1,10-Diaminodecane, 97%

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

assay

97%

form

solid

bp

140 °C/12 mmHg (lit.)

mp

59-61 °C (lit.)

Quality Level

100

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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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS9729
SHBS9296
SHBS8741
SHBS7714
SHBS2927

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Sen-Ichi Aizawa et al.
Chirality, 28(1), 85-91 (2015-10-30)
The optically active mixed-ligand fac(S)-tris(thiolato)rhodium(III) complexes, ΔL -fac(S)-[Rh(aet)2 (L-cys-N,S)](-) (aet = 2-aminoethanethiolate, L-cys = L-cysteinate) () and ΔLL -fac(S)-[Rh(aet)(L-cys-N,S)2 ](2-) were newly prepared by the equatorial preference of the carboxyl group in the coordinated L-cys ligand. The amide formation reaction
Jie Zhang et al.
Journal of biotechnology, 299, 79-85 (2019-05-03)
Glucosinolates can be hydrolyzed by the enzyme commonly known as myrosinase (E.C. 3.2.1.147) to a variety of biological compounds. Myrosinase (MYR) has been immobilized through the flexible spacers of different length on cross-linked chitosan resin (CCR). Ethylene diamine, hexamethylenediamine and
Gabriela E Davey et al.
Nature communications, 8(1), 1575-1575 (2017-11-18)
The 'acidic patch' is a highly electronegative cleft on the histone H2A-H2B dimer in the nucleosome. It is a fundamental motif for protein binding and chromatin dynamics, but the cellular impact of targeting this potentially therapeutic site with exogenous molecules
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Lei He et al.
Scientific reports, 8(1), 767-767 (2018-01-18)
G-quadruplexes (GQ) folded by the oncogenic G-rich sequences are the promising targets for developing anticancer therapeutic molecules. However, the current drug development mainly focused on non-covalent dynamic binders to stabilize GQ structures, while the covalent targeting from inorganic complexes via
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