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N17351

Sigma-Aldrich

Nitroguanidine

Sinonimo/i:

NSC 41036

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About This Item

Formula condensata:
NO2NHC(=NH)NH2
Numero CAS:
Peso molecolare:
104.07
Beilstein:
1756640
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

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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Categorie correlate

Applicazioni

Reactant involved in the synthesis of:
  • 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

Pittogrammi

Flame

Avvertenze

Warning

Indicazioni di pericolo

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


Certificati d'analisi (COA)

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I clienti hanno visto anche

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R K Gupta et al.
Journal of applied toxicology : JAT, 13(4), 231-234 (1993-07-01)
Nitroguanidine (NG) and its degradation product nitrosoguanidine (NSG) were evaluated for their mutagenic potential by using Drosophila melanogaster sex-linked recessive lethal (SLRL) assay. Following 72 h of feeding exposure, NG and NSG at concentrations of 4-8 micrograms ml-1 and 15-20
Toxicity and uptake of nitroguanidine in plants.
J J Heitholt et al.
Bulletin of environmental contamination and toxicology, 44(5), 751-758 (1990-05-01)
Rajib Karmakar et al.
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
N Gupta et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1453-1456 (2000-07-25)
A spectrometer based on acousto-optic tunable filters is developed for use in measuring Raman spectra as part of a detection system that is low-cost, reliable, and field-portable. The system is coupled with a fiber optic bundle to carry the excitation
A Wiater et al.
Acta biologica Hungarica, 57(1), 123-132 (2006-05-02)
Conidia of Trichoderma harzianum F-340, an active producer of fungal mutanase, were mutagenized with physical and chemical mutagens used separately or in combination. After mutagenesis, the drop in conidia viability ranged from 0.004% to 71%. Among the applied mutagens, nitrosoguanidine

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