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4636-83-3

4636-83-3 Structure

4636-83-3 Structure
IdentificationBack Directory
[Name]

Morfamquat(dichloride((content>65%)
[CAS]

4636-83-3
[Synonyms]

Ceroxone
morfamquat
Einecs 225-062-8
morfamquat dichloride
Morfamquat(dichloride((content>65%)
Morfamquat aqueous solution(content>15%)
Morfamquat dichloride@100 μg/mL in Methanol
1,1-bis(3,5-dimethylmorpholinocarbonylmethyl)-4,4-bipyridinium dichloride
1,1'-BIS(3,5-DIMETHYLMORPHOLINOCARBONYLMETHYL)-4,4'-BIPYRIDYNIUMDICHLORIDE
1,1'-Bis(3,5-dimethylmorpholinocarbonylmethyl)-4,4'-bipyridinium-dichlorid
1,1'-Bis(3,5-dimethylmorpholinocarbamylmethyl)-4,4'-bipyridilium dichloride
1,1'-Bis(3,5-dimethylmorpholinocarbonylmethyl)-4,4'-bipyridylium dichloride
1,1'-Bis(2-(3,5-dimethyl-4-morpholinyl)-2-oxoethyl)-4,4'-bipyridinium dichloride
4,4'-Bipyridinium, 1,1'-bis(((3,5-dimethylmorpholino)carbonyl)methyl)-, dichloride
1,1'-Bis(3,5-dimethylmorpholinocarbonylmethyl)-4,4'-bipyridinium-dichlorid [german]
[EINECS(EC#)]

225-062-8
[Molecular Formula]

C26H37Cl2N4O4
[MOL File]

4636-83-3.mol
[Molecular Weight]

540.502
Chemical PropertiesBack Directory
[Melting point ]

>300 °C
Safety DataBack Directory
[RIDADR ]

2781
[HazardClass ]

6.1(b)
[PackingGroup ]

III
Hazard InformationBack Directory
[Description]

Morfamquat is a selective herbicide in that dicots but not monocots are affected at the normal field rates (19). The mechanism of this difference is not clearly understood but probably relates to the ability of morfamquat to be enzymatically converted to paraquat by esterases that cleave the bulky side groups on the molecule. Once in the cell, morfamquat then behaves identically to paraquat.
[Definition]

ChEBI: Morfamquat is an organic molecular entity.
[Production Methods]

Morfamquat dichloride is synthesised through a multi-step process involving the quaternization of bipyridinium compounds with morpholine derivatives. The production begins with the preparation of 4,4'-bipyridine, which undergoes alkylation using chloromethyl morpholinederivatives to form the bis-substituted intermediate. This intermediate is then reacted with hydrochloric acid to yield the dichloride salt, enhancing its solubility and stability for herbicidal applications.
[Mechanism of action]

Broad-spectrum, non-residual activity with contact and some desiccant action. Photosystem I (electron transport) inhibitor.
[Pesticide Type]

Herbicide
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