O3750
Oxamic acid
≥98%
Synonyme(s) :
Aminooxoacetic acid, Oxalic acid monoamide
Se connecter pour consulter les tarifs organisationnels et contractuels.
Sélectionner une taille de conditionnement
A propos de cet article
Formule linéaire :
NH2COCO2H
Numéro CAS:
Poids moléculaire :
89.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-443-0
Beilstein/REAXYS Number:
1743294
MDL number:
Assay:
≥98%
Form:
powder
Service technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderService technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderInChI key
SOWBFZRMHSNYGE-UHFFFAOYSA-N
InChI
1S/C2H3NO3/c3-1(4)2(5)6/h(H2,3,4)(H,5,6)
SMILES string
NC(=O)C(O)=O
assay
≥98%
form
powder
mp
207-210 °C (dec.) (lit.)
Quality Level
Catégories apparentées
Application
Oxamic acid (OA) can be used as a reactant to prepare 6-phenanthridinecarboxamide by direct C-H carbamoylation reaction using ammonium persulfate in DMSO. It can also be used as an organic ligand to prepare functionalized metal oxide nanoparticles for various biological applications. OA along with p-aminobenzoic acid is used to functionalize Au nanoparticles for the development of a sensor to detect Fe3+ ions by the calorimetric method.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
Xiao-Wen Li et al.
European journal of medicinal chemistry, 46(9), 3851-3857 (2011-06-15)
A novel dissymmetrical N,N'-bis(substituted)oxamide ligand, N-(2-aminopropyl)-N'-(2-oxido- phenyl)oxamide (H(3)apopoxd) (L), and its three bicopper(II) complexes, [Cu(2)(apopoxd)(bpy)]- (ClO(4))·H(2)O (1), [Cu(2)(apopoxd)(dabt)](ClO(4))·2H(2)O (2), and [Cu(2)(apopoxd)(phen)(2)](ClO(4)) (3) (bpy = 2,2'-bipyridine; dabt = 2,2'-diamino-4,4'-bithiazole; phen = 1,10-phenanthroline) have been synthesized and characterized. The crystal structures of
Jijie Kong et al.
Chemosphere, 253, 126708-126708 (2020-04-17)
The role of illumination and cathode is important to improve the efficiency of photoelectro-Fenton (PEF) system. In this study, cathodes with black carbon-poly tetra fluoro ethylene (BC-PTFE) for increase the concentration of hydrogen peroxide in PEF. A new PEF system
Oxamic acid and p-aminobenzoic acid functionalized gold nanoparticles as a probe for colorimetric detection of Fe3+ ion
Buduru P
Sensors and Actuators B, Chemical, 237(36), 935-943 (2016)
Sergi Garcia-Segura et al.
Water research, 45(9), 2975-2984 (2011-04-12)
Oxalic and oxamic acids are the ultimate and more persistent by-products of the degradation of N-aromatics by electrochemical advanced oxidation processes (EAOPs). In this paper, the kinetics and oxidative paths of these acids have been studied for several EAOPs using
Luigi Fiume et al.
Pharmacological research, 63(4), 328-334 (2010-12-21)
Protein kinase inhibitors are a relatively new class of promising anticancer drugs, most of which exert their action by binding to the ATP site on the targeted kinases. We hypothesized that a decrease in ATP levels in neoplastic cells could
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
Contacter notre Service technique