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| | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine Basic information |
| Product Name: | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine | | Synonyms: | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine;6-chloro-2-N,2-N-diethyl-4-N-propan-2-yl-1,3,5-triazine-2,4-diamine;2-Chloro-4-diethylamino-6-isopropylamino-1,3,5-triazine;G-30031;Gesabal;1,3,5-Triazine-2,4-diamine, 6-chloro-N2,N2-diethyl-N4-(1-methylethyl)-;Heptazine | | CAS: | 1912-25-0 | | MF: | C10H18ClN5 | | MW: | 243.74 | | EINECS: | | | Product Categories: | | | Mol File: | 1912-25-0.mol |  |
| | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine Chemical Properties |
| Melting point | 73-75 °C | | Boiling point | 387.03°C (rough estimate) | | density | 1.1767 (rough estimate) | | refractive index | 1.6110 (estimate) | | pka | 2.57±0.10(Predicted) | | Water Solubility | 40mg/L(21 ºC) | | EPA Substance Registry System | Ipazine (1912-25-0) |
| | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine Usage And Synthesis |
| Uses | Agricultural chemical. | | Uses | Ipazine is often used in the composition of herbicides for weed control has also recently been used in a method for promoting ozone to rapidly produce hydroxyl free radical by using thiosulfate. | | Definition | ChEBI: Ipazine is a member of 1,3,5-triazines. | | Production Methods | Ipazine was produced through the standard triazine condensation route used for many early s-triazine herbicides. Manufacturers began with cyanuric chloride, then carried out stepwise nucleophilic substitution: first introducing a diethylamino group, followed by substitution with isopropylamine, and finally installing the chlorine bearing substituent under controlled temperature to avoid over substitution. Each substitution step required careful temperature staging because cyanuric chloride reacts sequentially at low, moderate, and higher temperatures. The resulting technical-grade ipazine was then purified by crystallisation or solvent washing to remove unreacted amines and partially substituted triazines. | | Hazard | Moderately toxic by ingestion. | | Mechanism of action | Blocks electron transport in photosystem II, preventing plants from converting light energy into chemical energy. | | Pesticide Type | Herbicide |
| | 2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine Preparation Products And Raw materials |
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