Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

View All Documentation

131296

Sigma-Aldrich

Oxalyldihydrazide

98%

Sinónimos:

Oxalic dihydrazide, Oxalylhydrazide

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula lineal:
NH2NHCOCONHNH2
Número de CAS:
996-98-5
Peso molecular:
118.09
Beilstein/REAXYS Number:
1072110
EC Number:
213-640-2
MDL number:
MFCD00007608
UNSPSC Code:
12352100
PubChem Substance ID:
24848005
NACRES:
NA.22

assay

98%

mp

242-244 °C (dec.) (lit.)

SMILES string

NNC(=O)C(=O)NN

InChI

1S/C2H6N4O2/c3-5-1(7)2(8)6-4/h3-4H2,(H,5,7)(H,6,8)

InChI key

SWRGUMCEJHQWEE-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

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
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
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
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
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico