N17351
Nitroguanidine
Sinonimo/i:
NSC 41036
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About This Item
Prodotti consigliati
contiene
20-25% water
Livello qualitativo
Punto di fusione
239 °C (dec.) (lit.)
Stringa SMILE
NC(=N)N[N+]([O-])=O
InChI
1S/CH4N4O2/c2-1(3)4-5(6)7/h(H4,2,3,4)
IDCPFAYURAQKDZ-UHFFFAOYSA-N
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Applicazioni
Reactant involved in the synthesis of:
Reactant involved in:
- 1,5-Disubstituted-1,3,5-hexahydrotriazine-2-(N-nitro)imines with insecticidal activity
- Hexahydrotriazine-N-nitroimine analogs with insecticidal activity via Mannich reactions
Reactant involved in:
- The study of the effects of vessel materials on exothermic decomposition energy
- Nitration of arenes
- Nitration of (nitrimino)tetrahyrdooxadiazine and (nitrimino)hexahydrotriazine
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Desen. Expl. 4
Codice della classe di stoccaggio
4.1B - Flammable solid hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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I clienti hanno visto anche
Toxicity and uptake of nitroguanidine in plants.
Bulletin of environmental contamination and toxicology, 44(5), 751-758 (1990-05-01)
Journal of agricultural and food chemistry, 57(14), 6369-6374 (2009-06-19)
The metabolism of thiamethoxam [(EZ)-3-(2-chloro-1,3-thiazol-5-yl-methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene (nitro) amine] was investigated in whole plant, callus, and heterotrophic cell suspension culture of aseptically and field grown tomato (Lycopersicon esculentum Mill.) plants. The structure of the metabolites was elucidated by chromatographic (HPLC) and spectroscopic
[Research and determination of occupational exposure limits of nitroguanidine in air of working places].
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 28(5), 380-382 (2010-09-22)
Chemical research in toxicology, 19(1), 38-43 (2006-01-18)
The nitroguanidine or nitromethylene moiety of the newest major class of insecticides, the neonicotinoids, is important for potency at insect nicotinic receptors and selectivity relative to mammalian receptors. Aldehyde oxidase (AOX) was recently identified as the imidacloprid nitroreductase of mammalian
Environmental science & technology, 46(11), 6035-6040 (2012-05-09)
Nitroguanidine (NQ) is an energetic material that is used as a key ingredient of triple-base propellants and is currently being considered as a TNT replacement in explosive formulations. NQ was efficiently degraded in aerobic microcosms when a carbon source was
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