Quality Level
assay
97%
form
powder
mp
183-185 °C (lit.)
SMILES string
NC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C7H5N3O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H,(H2,8,11)
InChI key
UUKWKUSGGZNXGA-UHFFFAOYSA-N
N W Shappell et al.
Chemosphere, 38(8), 1757-1762 (1999-04-02)
Colostomized chickens given oral doses of 3,5-dinitrobenzamide (nitromide) cleared nitromide predominantly through the urine (58% of dose) and feces (21% of dose). Rats cleared 52% of nitromide via urinary excretion and 44% via feces. Major urinary metabolites for both chickens
V Facchini et al.
Xenobiotica; the fate of foreign compounds in biological systems, 10(4), 299-305 (1980-04-01)
1. Nitromide (3,5-dinitrobenzamide) is reduced to monoamino- and diamino-metabolites in vitro on anaerobic incubation with rat intestinal microflora. This conversion is suppressed by the antibiotics neomycin, tetracycline and bacitracin. 2. Nitromide is also in part reduced to monoamino but not
V Facchini et al.
Xenobiotica; the fate of foreign compounds in biological systems, 10(4), 289-297 (1980-04-01)
1. Following oral administration of nitromide (3,5-dinitrobenzamide) to rats, 67.9% of the dose was excreted in urine and 32.6% in the faeces in 96 h. Significant biliary excretion of nitromide metabolites also occurred, although no evidence of enterohepatic cycling was
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| D193801-100G | 04061831835724 |
