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N17351

Sigma-Aldrich

Nitroguanidine

Synonym(s):

NSC 41036

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About This Item

Linear Formula:
NO2NHC(=NH)NH2
CAS Number:
Molecular Weight:
104.07
Beilstein:
1756640
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

contains

20-25% water

Quality Level

mp

239 °C (dec.) (lit.)

SMILES string

NC(=N)N[N+]([O-])=O

InChI

1S/CH4N4O2/c2-1(3)4-5(6)7/h(H4,2,3,4)

InChI key

IDCPFAYURAQKDZ-UHFFFAOYSA-N

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Application

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

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Desen. Expl. 4

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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)

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