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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:
556-88-7
Molecular Weight:
104.07
Beilstein:
1756640
MDL number:
MFCD00007039
UNSPSC Code:
12352100
PubChem Substance ID:
24897518
NACRES:
NA.22

contains

20-25% water

Quality Level

100

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
GHS02

Signal Word

Warning

Hazard Statements

H208

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 5: Self-reactive substances
Nitro compounds
Hazardous rank I
1st self-reactive materials

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

N17351-250G:
N17351-VAR:
N17351-1KG:
N17351-BULK:
N17351-100G:
N17351-25KG:
N17351-5G:
N17351-500G:
N17351-5KG:

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Certificates of Analysis (COA)

Lot/Batch Number
STBL1413
STBK5387
STBJ4833
STBG4169V
STBD4703V

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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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