Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(O2N)2C6H3NHNH2
CAS Number:
Molecular Weight:
198.14
PubChem Substance ID:
UNSPSC Code:
41116105
Beilstein/REAXYS Number:
615586
MDL number:
grade
JIS special grade
contains
50% water (minimum)
availability
available only in Japan
mp
197-200 °C (lit.)
SMILES string
NNc1ccc(cc1[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C6H6N4O4/c7-8-5-2-1-4(9(11)12)3-6(5)10(13)14/h1-3,8H,7H2
InChI key
HORQAOAYAYGIBM-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under 2,4-Dinitrophenylhydrazine
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Desen. Expl. 1
supp_hazards
Storage Class
4.1A - Other explosive hazardous materials
wgk
WGK 3
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Zhihui Ai et al.
Journal of hazardous materials, 179(1-3), 141-150 (2010-03-30)
Nanocrystalline Zn(2)SnO(4) microcubes were hydrothermally synthesized and systematically characterized by XRD, SEM, TEM, XPS, N(2) adsorption-desorption, and UV-vis DRS analysis. The resulting Zn(2)SnO(4) microcubes with the edge size ranging from 0.8 to 1.2 microm were composed of numerous nanoparticles with
Ravi Ch Bollineni et al.
Journal of proteomics, 74(11), 2351-2359 (2011-06-15)
Reactive oxygen species (ROS) can oxidize proteins at almost any amino acid residue. Whereas some modifications are reversible within the cells, the higher oxidation states are especially irreversible. These irreversible post translational modifications are widely used as biomarkers of oxidative
[13C2]-Acetaldehyde promotes unequivocal formation of 1,N2-propano-2'-deoxyguanosine in human cells.
Camila Carrião M Garcia et al.
Journal of the American Chemical Society, 133(24), 9140-9143 (2011-05-25)
Acetaldehyde is an environmentally widespread genotoxic aldehyde present in tobacco smoke, vehicle exhaust and several food products. Endogenously, acetaldehyde is produced by the metabolic oxidation of ethanol by hepatic NAD-dependent alcohol dehydrogenase and during threonine catabolism. The formation of DNA

