N17351
硝基胍
别名:
NSC 41036
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线性分子式:
NO2NHC(=NH)NH2
化学文摘社编号:
分子量:
104.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1756640
InChI
1S/CH4N4O2/c2-1(3)4-5(6)7/h(H4,2,3,4)
SMILES string
NC(=N)N[N+]([O-])=O
InChI key
IDCPFAYURAQKDZ-UHFFFAOYSA-N
contains
20-25% water
mp
239 °C (dec.) (lit.)
Quality Level
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Application
参与合成的反应物：
反应物参与到：
- 具有杀虫活性的 1,5-二取代-1,3,5-六氢三嗪-2-（ N -硝基）亚胺
- 通过 Mannich 反应具有杀虫活性的六氢三嗪- N -硝基亚胺类似物
反应物参与到：
- 容器材料对放热分解能影响的研究
- 芳烃硝化
- （腈基）四氢恶二嗪和（腈基）六氢三嗪的硝化
signalword
Warning
hcodes
Hazard Classifications
Desen. Expl. 4
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
监管及禁止进口产品
此项目有
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
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
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