N-HYDROXYPROPIONAMIDINE
N-HYDROXYPROPIONAMIDINE Basic information
- Product Name:
- N-HYDROXYPROPIONAMIDINE
- Synonyms:
-
- AKOS B030359
- N-HYDROXYPROPIONAMIDINE
- Propionamidoxime
- (1Z)-N'-hydroxypropanimidamide hydrochloride
- propanimidamide, N'-hydroxy-, (1Z)-
- N'-hydroxypropaniMidaMide
- PropaniMidaMide, N-hydroxy-
- N-HydroxypropioniMidaMide
- CAS:
- 29335-36-2
- MF:
- C3H8N2O
- MW:
- 88.11
- Product Categories:
-
- pharmacetical
- Mol File:
- 29335-36-2.mol
N-HYDROXYPROPIONAMIDINE Chemical Properties
- Boiling point:
- 132.8±23.0 °C(Predicted)
- Density
- 1.12±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 7.48±0.69(Predicted)
- Appearance
- Colorless to off-white Viscous Liquid
- Water Solubility
- Slightly soluble in water.
- Sensitive
- Hygroscopic
- CAS DataBase Reference
- 29335-36-2
Safety Information
- Hazard Codes
- T
- Risk Statements
- 36/37/38-25
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN3267
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 2925290090
MSDS
- Language:English Provider:ALFA
N-HYDROXYPROPIONAMIDINE Usage And Synthesis
Uses
Propionamidoxime is used as pharmaceutical intermediate.
Synthesis
107-12-0
29335-36-2
The general procedure for the synthesis of N-hydroxypropionic acid amidine from propionitrile was as follows: hydroxylamine hydrochloride (18.9 g, 272.7 mmol) and anhydrous potassium carbonate (37.6 g, 272.7 mmol) were suspended in a mixed solvent of ethanol/water (200 mL/50 mL), and stirred for 1 h at room temperature. Subsequently, propionitrile (10.0 g, 181.8 mmol) was added to the reaction system. The reaction mixture was heated to reflux and stirred continuously for 20 h. The reaction process was monitored by thin layer chromatography (unfolding agent: dichloromethane/methanol, 50/1 volume ratio). Upon completion of the reaction, the inorganic salts were removed by filtration and the filtrate was concentrated under reduced pressure to afford N-hydroxypropionic acid amidine (13.5 g, 81% yield) as a light yellow solid.
References
[1] Patent: CN104513235, 2017, B. Location in patent: Paragraph 1308; 1309
[2] Chemische Berichte, 1884, vol. 17, p. 2753
[3] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1957, vol. 245, p. 419,420
[4] Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1966, vol. 262, p. 592 - 595
[5] Monatshefte fuer Chemie, 1982, vol. 113, p. 781 - 792
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