| Identification | More | [Name]
Moroxydine | [CAS]
3731-59-7 | [Synonyms]
moroxydine
MOROXYDINUM
n-(aminoiminomethyl)-4-morpholinecarboximidamide
TIMTEC-BB SBB003847
1-(1-morpholinoformimidoyl)guanidine
Moroxydine (base and/or unspecified salts)
N-[amino(imino)methyl]morpholine-4-carboximidamide hydrochloride
ABOB
Vironil
4-morpholinecarboximidamide, N-(aminoiminomethyl)- | [EINECS(EC#)]
223-093-1 | [Molecular Formula]
C6H13N5O | [MDL Number]
MFCD00460678 | [Molecular Weight]
171.2 | [MOL File]
3731-59-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT |
| Hazard Information | Back Directory | [Originator]
Grippe,Nissin | [Uses]
antiviral | [Definition]
ChEBI: N-(diaminomethylidene)-4-morpholinecarboximidamide is a member of biguanides. | [Manufacturing Process]
43.5 g morpholine, 41.7 ml concentrated hydrochloric acid, 40 ml of water,
and 42 g dicyandiamide are refluxed for 48 hours, whereupon the reaction
mixture is cooled to +5°C and filtered. The filtrate is evaporated to dryness
and extracted and extracted with boiling ethanol. Yield: 50 g. The formed 4-
morpholinecarboximidoylguanidine hydrochloride is purified by recrystallization
from methanol. The salt may be converted into the base by adding equivalent
of any basic compound (triethylamine, sodium bicarbonate and so on).
In practice it is usually used as hydrochloride. | [Therapeutic Function]
Antiviral |
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