InChI key
HORQAOAYAYGIBM-UHFFFAOYSA-N
InChI
1S/C6H6N4O4/c7-8-5-2-1-4(9(11)12)3-6(5)10(13)14/h1-3,8H,7H2
SMILES string
NNc1ccc(cc1[N+]([O-])=O)[N+]([O-])=O
grade
puriss. p.a.
assay
≥99.0% (HPLC)
quality
moistened with water
contains
~50% water as stabilizer
technique(s)
UV/Vis spectroscopy: suitable
mp
197-200 °C (lit.)
solubility
50% sulfuric acid: 10 mg/mL, clear (yellow to very dark yellow and green-yellow to very dark green-yellow and yellow-green)
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Other Notes
可能实行销售限制
用乙醛酸对蛋白的 α-氨基进行转氨作用后,用于 α-酮基的测定;用于通过比色法测定醛和酮以及酮类固醇的试剂;在液相色谱中用于进行羰基化合物的紫外-可见光吸收衍生化的试剂
This product has been replaced by D199303-ALDRICH | 2,4-Dinitrophenylhydrazine, reagent grade, 97% | (O2N)2C6H3NHNH2
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Sol. 1
supp_hazards
存储类别
4.1A - Other explosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Idem
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 51, 2157-2157 (1979)
[33] Specific modification of NH(2)-terminal residues by transamination.
H B Dixon et al.
Methods in enzymology, 25, 409-419 (1972-01-01)
T. Jupille
Journal of Chromatographic Science, 17, 160-160 (1979)
[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
J. Bartos et al.
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 51, 1803-1803 (1979)
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