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279633

Sigma-Aldrich

p-Xylylenediamine

99%

Synonym(s):

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

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About This Item

Linear Formula:
C6H4(CH2NH2)2
CAS Number:
539-48-0
Molecular Weight:
136.19
Beilstein:
2206190
EC Number:
208-719-3
MDL number:
MFCD00009821
UNSPSC Code:
12162002
PubChem Substance ID:
24856898
NACRES:
NA.23

Quality Level

200

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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Related Categories

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Shuai Yuan et al.
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Compared to efficient green and near-infrared light-emitting diodes (LEDs), less progress has been made on deep-blue perovskite LEDs. They suffer from inefficient domain [various number of PbX6- layers (n)] control, resulting in a series of unfavorable issues such as unstable
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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