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Moroxydine

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Moroxydine Basic information

Product Name:
Moroxydine
Synonyms:
  • TIMTEC-BB SBB003847
  • n-(aminoiminomethyl)-4-morpholinecarboximidamide
  • MOROXYDINUM
  • moroxydine
  • N-(morpholine-4-carboximidoyl)guanidine
  • N-(diaminomethylidene)-4-morpholinecarboximidamide hydrochloride
  • 1-(1-morpholinoformimidoyl)guanidine
  • Moroxydine (base and/or unspecified salts)
CAS:
3731-59-7
MF:
C6H13N5O
MW:
171.2
EINECS:
223-093-1
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Guanidines
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
3731-59-7.mol
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Moroxydine Chemical Properties

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)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36
WGK Germany 
3
HazardClass 
IRRITANT
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Moroxydine Usage And Synthesis

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

Moroxydine Preparation Products And Raw materials

Raw materials

Preparation Products

MoroxydineSupplier

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