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D14204

Sigma-Aldrich

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

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

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
Dmitry V Klinov et al.
Colloids and surfaces. B, Biointerfaces, 196, 111321-111321 (2020-08-26)
High-resolution atomic force microscopy (AFM) of biomacromolecules is a valuable method for structural studies in biology. Traditionally, the surfaces used for AFM imaging of individual molecules are limited to mica, graphite, and glass. Because these substrates have certain shortcomings, new
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
Georges R Younes et al.
ACS omega, 5(47), 30657-30670 (2020-12-08)
A sol/gel curing method is used in this work to synthesize hybrid partially bio-based polyhydroxyurethanes (PHUs) from dicarbonates derived from glycerol and various diamines. The method consists of end-capping the PHU prepolymers with moisture-sensitive groups, so sealants and adhesives can
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