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D14204

1,10-Diaminodecane

Name: 1,10-Diaminodecane
Brand: ALDRICH

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

Assay:

97%

Form:

solid

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Properties

Quality Level

100

assay

97%

form

solid

bp

140 °C/12 mmHg (lit.)

mp

59-61 °C (lit.)

SMILES string

NCCCCCCCCCCN

InChI

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

InChI key

YQLZOAVZWJBZSY-UHFFFAOYSA-N

Description

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pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

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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Effect of aliphatic diamine spacer length on enzymatic performance of myrosinase immobilized on chitosan microsphere and its application for sulforaphene production.

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

Polymer-Supported Optically Active fac(S)-Tris(thiotato)rhodium(III) Complex for Sulfur-Bridging Reaction With Precious Metal Ions.

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

Dual functional dinuclear platinum complex with selective reactivity towards c-myc G-quadruplex.

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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Global Trade Item Number

SKU	GTIN
D14204-5G	04061832090283
D14204-25G	04061833559895