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5465-96-3

N-Nitroiminoimidazolidine

CAS: 5465-96-3

Molecular Formula: C3H6N4O2

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5465-96-3 - Names and Identifiers

Name N-Nitroiminoimidazolidine
Synonyms NNI

Alkylimidazole
2-Nitroaminoimidazoline
N-Nitroiminoimidazolidine
2-Nitroiminoimidazolidine
2-Nitroimino Imidazolidine
N-NITROIMINO IMIDAZOLIDINE
2-(Nitroimino)imidazolidine
2-(NITROIMINO)IMIDAZOLIDINE
2-NITRO-1-IMINOIMIDAZOLIDINE
4,5-dihydro-n-nitro-1h-imidazol-2-amine
4,5-Dihydro-N-nitro-1H-imidazol-2-amine
N-nitro-4,5-dihydro-1H-imidazol-2-amine
4,5-DIHYDRO-N-NITRO-1H-IMIDAZOL-2-AMINES
2-NITROAMINOIMIDAZOLINE[FOR IMIDACLOPRID]
2-(nitroamino)-4,5-dihydro-1H-imidazol-3-ium
2-(4,5-dihydro-1H-imidazol-2-yl)-1-hydroxy-1-oxohydrazinium
CAS 5465-96-3
InChI InChI=1/C3H6N4O2/c8-7(9)6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)/p+1

5465-96-3 - Physico-chemical Properties

Molecular FormulaC3H6N4O2
Molar Mass130.11
Density1.81±0.1 g/cm3(Predicted)
Melting Point220 °C
Boling Point255.1±23.0 °C(Predicted)
Flash Point108.1°C
Solubility DMSO (Slightly), Methanol (Slightly)
Vapor Presure0.0167mmHg at 25°C
AppearanceWhite crystal
ColorPale Yellow
pKa8.55±0.20(Predicted)
Storage ConditionAmber Vial, Refrigerator
MDLMFCD00047040
Physical and Chemical PropertiesImidazolidine pure white crystals, m.p.213 ~ 215 ℃ (decomposition), industrial products for white or light yellow powder, content is greater than or equal to 98.0%, slightly soluble in cold water, soluble in hot water.
UseUsed as a high efficiency and low toxicity pesticide imidacloprid intermediates; Used as pesticide intermediates, mainly for the synthesis of a net pesticide

5465-96-3 - Reference Information

Uses N-nitroimidazolidine is abbreviated as imidazolidine, which is an intermediate of the insecticide imidacloprid.
Used as an intermediate for high-efficiency and low-toxicity pesticide imidacloprid
Production method The preparation method is to cyclize nitroguanidine and ethylenediamine to obtain N-nitroimidazolidine. Nitroguanidine and lye are added to the reaction kettle, ethylenediamine and 30% industrial hydrochloric acid are added at 0 ℃ to form a salt suspension, slowly raise the temperature to 60 ℃, react for 0.5h, and immediately transfer to the precooling kettle. Imidazolidine is obtained by crystallization, centrifugal filtration and drying.
Last Update:2024-04-09 21:04:16
5465-96-3
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5465-96-3
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