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ChemicalBook--->CAS DataBase List--->3731-59-7

3731-59-7

3731-59-7 Structure

3731-59-7 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Melting point ]

211-214 °C(lit.)
[Boiling point ]

274.0±50.0 °C(Predicted)
[density ]

1.51±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

13.01±0.10(Predicted)
[Merck ]

13,6295
[CAS DataBase Reference]

3731-59-7(CAS DataBase Reference)
Safety DataBack 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
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Hydrochloric acid-->Activated carbon-->Dicyandiamide-->Morpholine
[Preparation Products]

Cyclic AMP
Hazard InformationBack 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
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

3731-59-7(sigmaaldrich)
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