Weight | 102.097 g/mol |
---|---|
Formula | C2H6N4O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Guanylurea (141-83-3, 926-72-7)
guanidine carboxamide, monohydroiodide · guanidine carboxamide, monohydrobromide · guanidine carboxamide, monohydrochloride
Score:
#5299 in Biology
,
#6971 in Chemistry
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- Thermal conversion of guanylurea dicyanamide into graphitic carbon nitride via prototype CNx precursors (Chemistry of Materials, 2005)
- Occurrence and fate of the antidiabetic drug metformin and its metabolite guanylurea in the environment and during drinking water treatment (Water Research, 2012)
- Incomplete aerobic degradation of the antidiabetic drug Metformin and identification of the bacterial dead-end transformation product Guanylurea (Chemosphere, 2011)
- N-guanylurea-dinitramide: a new energetic material with low sensitivity for propellants and explosives applications (Thermochimica Acta, 2002)
- Occurrence of the antidiabetic drug Metformin and its ultimate transformation product Guanylurea in several compartments of the aquatic cycle. (Environment International, 2014)
- Effectively designed molecularly imprinted polymers for selective isolation of the antidiabetic drug metformin and its transformation product guanylurea from aqueous media (Analytica Chimica Acta, 2015)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - guanidine carboxamide, monohydroiodide
- guanidine carboxamide, monohydrobromide
- guanidine carboxamide, monohydrochloride
- guanidine carboxamide, sulfate (1:1)
- guanidine carboxamide, sulfate (2:1)
- guanidine carboxamide
- amidinourea
- guanidine carboxamide phosphate
-
SMILESC(=NC(=O)N)(N)N
-
InChIKeySQSPRWMERUQXNE-UHFFFAOYSA-N
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