73340
5-Nitro-2-furaldehyde semicarbazone
≥97.0% (HPLC)
Synonym(s):
5-Nitro-2-furfural semicarbazone, Furacin, NFZ, Nitrofurazone
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About This Item
Empirical Formula (Hill Notation):
C6H6N4O4
CAS Number:
Molecular Weight:
198.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-443-1
Beilstein/REAXYS Number:
86403
MDL number:
Assay:
≥97.0% (HPLC)
Form:
powder
Quality Level
assay
≥97.0% (HPLC)
form
powder
mp
242-244 °C (lit.)
functional group
amine, nitro
SMILES string
NC(=O)N\N=C\c1ccc(o1)[N+]([O-])=O
InChI
1S/C6H6N4O4/c7-6(11)9-8-3-4-1-2-5(14-4)10(12)13/h1-3H,(H3,7,9,11)/b8-3+
InChI key
IAIWVQXQOWNYOU-FPYGCLRLSA-N
General description
Molecules of 5-nitro-2-furaldehyde semicarbazone are linked via bifurcated hydrogen bonds. Its crystal structure has been studied. It is reported to induce mammary fibroadenomas in Holtzman female rats and can be subcutaneously transplanted into male and female newborn Holtzman rats. Chemotheraupetic potential of 5-nitro-2-furaldehyde semicarbazone has been evaluated. 5-Nitro-2-furaldehyde semicarbazone is a synthetic nitrofuran derivative, having good bacteriostatic and bactericidal properties, with an antibacterial action against a number of gram-negative and gram-positive microorganisms. In Vitro toxicity of 5-nitro-2-furaldehyde semicarbazone has been investigated in hamster cells.
Disclaimer
The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.
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Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Muta. 2 - Repr. 2 - Skin Sens. 1 - STOT RE 2
target_organs
male reproductive organs
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Nitrofurans as radiosensitizers of hypoxic mammalian cells.
J D Chapman et al.
Cancer research, 32(12), 2616-2624 (1972-12-01)
Sonoelectrodeposition of gold nanorods at a gold surface-Application for electrocatalytic reduction and determination of nitrofurazone.
Rahi A, et al.
Sensors and Actuators B, Chemical (2014)
5-Nitro-2-furaldehyde semicarbazone.
Olszak TA, et al.
Acta Crystallographica Section C, Structural Chemistry, 50(6), 948-950 (1994)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 73340-100G | 04061832867359 |
| 73340-500G | 04061832867373 |