131296
Oxalyldihydrazide
98%
Synonyme(s) :
Oxalic dihydrazide, Oxalylhydrazide
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About This Item
Formule linéaire :
NH2NHCOCONHNH2
Numéro CAS:
Poids moléculaire :
118.09
Numéro Beilstein :
1072110
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
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Niveau de qualité
Pureté
98%
Pf
242-244 °C (dec.) (lit.)
Chaîne SMILES
NNC(=O)C(=O)NN
InChI
1S/C2H6N4O2/c3-5-1(7)2(8)6-4/h3-4H2,(H,5,7)(H,6,8)
Clé InChI
SWRGUMCEJHQWEE-UHFFFAOYSA-N
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Application
Oxalyldihydrazide was used as a crosslinker for enrichment of carbonylated proteins within a microfluid chip. It was also used to synthesize a new series of manganese and iron salt forming complexes by template condensation with glyoxal.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Les clients ont également consulté
Khlood Abou Melha
Journal of enzyme inhibition and medicinal chemistry, 23(2), 285-295 (2008-03-18)
The Schiff base ligand, oxalyl [( 2 - hydroxybenzylidene) hydrazone] [corrected].H(2)L, and its Cu(II), Ni(II), Co(II), UO(2)(VI) and Fe(III) complexes were prepared and tested as antibacterial agents. The Schiff base acts as a dibasic tetra- or hexadentate ligand with metal
Bryant C Hollins et al.
Lab on a chip, 12(14), 2526-2532 (2012-05-09)
We report a proof of principle study for the use of oxalyldihydrazide as a crosslinker for enrichment of carbonylated proteins within a microfluidic chip. Surface modification steps are characterized and analyzed using analytical techniques. We use oxidized cytochrome c as
D P Singh et al.
Journal of enzyme inhibition and medicinal chemistry, 24(3), 883-889 (2008-10-29)
A new series of complexes is synthesized by template condensation of oxalyldihydrazide and glyoxal in methanolic medium in the presence of trivalent chromium, manganese and iron salts forming complexes of the type: [M(C(8)H(8)N(8)O(4))X]X(2) where M = Cr(III), Mn(III), Fe(III) and
Zahid H Chohan et al.
Journal of enzyme inhibition and medicinal chemistry, 17(1), 1-7 (2002-10-09)
Schiff bases derived from oxaldiamide/oxalylhydrazine and pyrrol-2-carbaldehyde, or salicylaldehyde respectively, as well as their Zn(II) complexes have been prepared and tested as antibacterial agents. These Schiff bases function as tetradentate ligands, forming octahedral Zn(II) complexes. The ketonic form for the
M Rizk et al.
Acta pharmaceutica Hungarica, 62(4), 158-166 (1992-07-01)
A sensitive and selective colorimetric method has been devised for the micro-determination of copper (II) ions in pure form, some chemicals and multivitamin preparations. The method depends on the formation of stable blue complexes in ammonia medium peaking at 615
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