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Merck
CN

D193801

3,5-二硝基苯甲酰胺

97%

别名:

硝米特

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关于此项目

线性分子式:
(O2N)2C6H3CONH2
化学文摘社编号:
分子量:
211.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-499-8
Beilstein/REAXYS Number:
7096825
MDL number:
Assay:
97%
Form:
powder
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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



pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
D193801-100G04061831835724