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| | TRIFENMORPH Basic information |
| Product Name: | TRIFENMORPH | | Synonyms: | 4-(TRIPHENYLMETHYL)-MOROPHOLINE;Triphenomorph;TRIFENMORPH;4-(triphenylmethyl)-morpholin;4-(triphenylmethyl)morpholine;4-trityl-morpholin;frescon;n-(triphenyl-methyl)morpholine | | CAS: | 1420-06-0 | | MF: | C23H23NO | | MW: | 329.43 | | EINECS: | 215-812-2 | | Product Categories: | | | Mol File: | 1420-06-0.mol |  |
| | TRIFENMORPH Chemical Properties |
| Melting point | 174-176°, resolidifies and melts again at 185-187° | | Boiling point | 467.03°C (rough estimate) | | density | 1.0859 (rough estimate) | | refractive index | 1.5614 (estimate) | | pka | 4.58±0.10(Predicted) | | Water Solubility | 20ug/L(20 ºC) | | Henry's Law Constant | 7.6×104 mol/(m3Pa) at 25℃, HSDB (2015) | | EPA Substance Registry System | Trifenmorph (1420-06-0) |
| | TRIFENMORPH Usage And Synthesis |
| Uses | As molluscicide (against snails carrying bilharzia flukes). | | Definition | ChEBI: Trifenmorph is a member of morpholines. | | Production Methods | Trifenmorph is commercially produced by reacting morpholine with trityl chloride to form N-tritylmorpholine. The synthesis involves the alkylation of morpholine, a cyclic amine, with trityl chloride (triphenylmethyl chloride) under controlled conditions, typically in the presence of a base such as triethylamine or sodium carbonate. | | Mechanism of action | A highly selective neurotoxin to aquatic and semi-aquatic snails, acts by increasing the intracellular chloride levels | | Pesticide Type | Insecticide; Molluscicide |
| | TRIFENMORPH Preparation Products And Raw materials |
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