| Identification | Back Directory | [Name]
2-(N,N-diethylamino)-4-(-N-isopropylamino)-6-chloro-1,3,5-triazine | [CAS]
1912-25-0 | [Synonyms]
G-30031
Gesabal
2-Chloro-4-diethylamino-6-isopropylamino-1,3,5-triazine
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 | [Molecular Formula]
C10H18ClN5 | [MDL Number]
MFCD01679079 | [MOL File]
1912-25-0.mol | [Molecular Weight]
243.74 |
| Chemical Properties | Back Directory | [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) | [Uses]
Agricultural chemical. | [EPA Substance Registry System]
Ipazine (1912-25-0) |
| Hazard Information | Back Directory | [Hazard]
Moderately toxic by ingestion. | [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. | [Mechanism of action]
Blocks electron transport in photosystem II, preventing plants from converting light energy into chemical energy. | [Pesticide Type]
Herbicide |
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