| Identification | Back Directory | [Name]
SIMETON | [CAS]
673-04-1 | [Synonyms]
G-30004
G-30044
Pimeton
SIMETON
Simetone
Gesadural
NSC 163050
geigy30,044
Geigy 30,044
methoxysimazine
Methoxy simazine
Simeton @100 μg/mL in MeOH
Simeton Solution in Methanol, 100μg/mL
2,4-bis(ethylamino)-6-methoxy-s-triazin
2-Methoxy-4,6-bis(ethylamino)-s-triazine
4,6-Bis(ethylamino)-2-methoxy-s-triazine
2，4-Bis(ethylamino)-6-methoxy-s-triazine
s-Triazine, 2,4-bis(ethylamino)-6-methoxy-
2-Methoxy-4,6-bis(ethylamino)-1,3,5-triazine
N,N'-diethyl-6-methoxy-1,3,5-triazine-2,4-diamine
N2,N4-diethyl-6-methoxy-1,3,5-triazine-2,4-diamine
1,3,5-Triazine-2,4-diamine,N2,N4-diethyl-6-methoxy-
1,3,5-Triazine-2,4-diamine, N,N'-diethyl-6-methoxy-
2-N,4-N-diethyl-6-methoxy-1,3,5-triazine-2,4-diamine
ethyl-[4-(ethylamino)-6-methoxy-s-triazin-2-yl]amine | [EINECS(EC#)]
211-601-4 | [Molecular Formula]
C8H15N5O | [MDL Number]
MFCD01311011 | [MOL File]
673-04-1.mol | [Molecular Weight]
197.24 |
| Chemical Properties | Back Directory | [Melting point ]
119°C | [Boiling point ]
334.34°C (rough estimate) | [density ]
1.1685 (rough estimate) | [refractive index ]
1.8000 (estimate) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
neat | [pka]
4.60±0.10(Predicted) | [Appearance]
White to off-white Solid | [Water Solubility ]
3.2g/L(21 ºC) | [BRN ]
11608 | [Henry's Law Constant]
1.5×104 mol/(m3Pa) at 25℃, Hilal et al. (2008) | [EPA Substance Registry System]
Simetone (673-04-1) |
| Hazard Information | Back Directory | [Uses]
Simeton-d3 (N2,N4-Diethyl-6-(methoxy-d3)-1,3,5-triazine-2,4-diamine) is deuterium labeled Simeton[1]. | [Definition]
ChEBI: A methoxy-1,3,5-triazine that is 6-methoxy-1,3,5-triazine-2,4-diamine in which one of the hydrogens of each amino group has been replaced by an ethyl group. | [Production Methods]
Information is currently sparse but, based on the chemistry of methoxy substituted triazines, simeton is made by first forming a chloro substituted triazine core, then sequentially replacing the chlorine atoms with ethylamine nucleophiles, and finally introducing the methoxy group via substitution or methoxylation of the remaining reactive position. The resulting mixture is purified to yield the solid herbicide. | [Mechanism of action]
Selective, systemic, absorbed through roots and folage. Inhibits photosynthesis | [References]
[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110 | [Pesticide Type]
Herbicide |
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