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279633

Sigma-Aldrich

p-Xylylenediamine

99%

Sinónimos:

1,4-Bis(aminomethyl)benzene, α,α′-Diamino-p-xylene

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About This Item

Fórmula lineal:
C6H4(CH2NH2)2
Número de CAS:
539-48-0
Peso molecular:
136.19
Beilstein/REAXYS Number:
2206190
EC Number:
208-719-3
MDL number:
MFCD00009821
UNSPSC Code:
12162002
PubChem Substance ID:
24856898
NACRES:
NA.23

assay

99%

form

solid

bp

230 °C/10 mmHg (lit.)

mp

60-63 °C (lit.)

SMILES string

NCc1ccc(CN)cc1

InChI

1S/C8H12N2/c9-5-7-1-2-8(6-10)4-3-7/h1-4H,5-6,9-10H2

InChI key

ISKQADXMHQSTHK-UHFFFAOYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Solvent properties such as surface tension, dielectric constant, and viscosity have been extensively studied over more than 150 years to understand their influence on the growth kinetics of nanostructures. Interestingly, these nanoparticles-based studies have missed the influence of solvent molecular geometry.
Weiqiang Zhan et al.
Journal of medicinal chemistry, 50(23), 5655-5664 (2007-10-26)
In light of a proposed molecular mechanism for the C-X-C chemokine receptor type 4 (CXCR4) antagonist 1 (AMD3100), a template with the general structure 2 was designed, and 15 was identified as a lead by means of an affinity binding
Choon Young Lee et al.
Bioorganic & medicinal chemistry letters, 19(22), 6326-6330 (2009-10-14)
Three dendritic polyphenols (generation 1) were synthesized: a syringaldehyde-based dendrimer (1), a vanillin-based dendrimer (2), and an iodinated vanillin-based dendrimer (3). They all showed strong antioxidant activity according to the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical assay. The syringaldehyde dendrimer was twice and
Francesc Yraola et al.
Journal of medicinal chemistry, 49(21), 6197-6208 (2006-10-13)
Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contributing to the discovery of more efficient SSAO substrates. Experimental data were contrasted with computational docking studies, thereby

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