| Identification | Back Directory | [Name]
Imidazolidine | [CAS]
504-74-5 | [Synonyms]
mizuolin
imidazoline
Imidazolidine
1,3-Diazacyclopentane
Oil soluble imidazoline
Imidazolidine ISO 9001：2015 REACH | [Molecular Formula]
C3H8N2 | [MDL Number]
MFCD19216513 | [MOL File]
504-74-5.mol | [Molecular Weight]
72.11 |
| Chemical Properties | Back Directory | [Melting point ]
68.2-68.8 °C | [Boiling point ]
92.8±8.0 °C(Predicted) | [density ]
0.892±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [pka]
10.33±0.20(Predicted) | [EPA Substance Registry System]
Imidazolidine (504-74-5) |
| Hazard Information | Back Directory | [Uses]
The imidazolines, was
discovered at American Cyanamid in the early 1980s.
Extensive research has led to the development of
four commercial compounds: imazapyr, imazamethabenzmethyl,
imazethapyr, and imazaquin. Like
the sulfonylureas, the imidazolines are extremely active
at low rates. | [Definition]
ChEBI: Imidazolidine is a saturated organic heteromonocyclic parent, a member of imidazolidines and an azacycloalkane. | [Structure and conformation]
Dihydroimidazole is a five-membered, nonplanar, and nonaromatic heterocycle, derived by the partial reduction of one of the two double bonds of the imidazole ring. The dihydroimidazoles are also referred to as imidazolines and there are three possible regioisomeric forms: 4,5-dihydroimidazole (2-imidazoline), 2,5-dihydroimidazole
(3-imidazoline), and 2,3- dihydroimidazole (4-imidazoline). The 2- and 3-imidazolines contain an imine center, while
4-imidazoline contains an alkene substructure. Among these three isomeric forms, the chemistry of 2-imidazoline is
more developed than 3- and 4-imidazolines.
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