InChI
1S/C8H10N2O3S.2Na.H2O4S/c1-7-3-5-8(6-4-7)14(12,13)10(2)9-11;;;1-5(2,3)4/h3-6H,1-2H3;;;(H2,1,2,3,4)/q;2*+1;/p-2
SMILES string
[Na+].[Na+].[O-]S([O-])(=O)=O.CN(N=O)S(=O)(=O)c1ccc(C)cc1
InChI key
QCKUXDQKDJXWCU-UHFFFAOYSA-L
concentration
20 wt. % in sodium sulfate (mixture)
storage temp.
2-8°C
Legal Information
Diazald is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
M Börzsönyi et al.
Neoplasma, 35(3), 257-262 (1988-01-01)
N-nitroso-N-methyl-p-toluenesulfonamide (NMTS, diazald, CAS 80-11-5) is a widely used compound for laboratory production of diazomethane. The present results showed that the noncarcinogenic NMTS reacts as a transnitrosating agent with amino nitrogen of secondary amines and amide both in vitro (human
Contact dermatitis from Diazald.
H S Young et al.
Contact dermatitis, 50(5), 315-316 (2004-06-24)
J V Uri et al.
Acta microbiologica Hungarica, 39(3-4), 317-322 (1992-01-01)
Diazald, a chemical intermediate for the synthesis of biologically active compounds, was found to be a potent in vitro antimicrobial agent against yeasts, yeast-like and filamentous fungi as well as Gram-positive and Gram-negative bacterial strains. Its activity is not inhibited
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