- DESMETRYN
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2025-12-24
- CAS:1014-69-3
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 1000KG
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| | DESMETRYN Basic information |
| Product Name: | DESMETRYN | | Synonyms: | 2-Isopropylamino-4-methylamino-6-methylthio-1,3,5-triazine;2-isopropylamino-4-methyl-amino-6-methylthio-s-triazine;2-Methylamino-4-methylthio-6-isopropylamino-1,3,5-triazine;2-methylmercapto-4-methylamino-6-isopropylamino-s-triazine;2-methylthio-3-methylamino-6-isopropylamino-1,3,5-triazine;2-Methylthio-4-isopropylamino-6-methylamino-s-triazine;5-triazine-2,4-diamine,n-methyl-n’-(1-methylethyl)-6-(methylthio)-3;semeron250 | | CAS: | 1014-69-3 | | MF: | C8H15N5S | | MW: | 213.3 | | EINECS: | 213-800-1 | | Product Categories: | Alpha sort;D;DA - DHPesticides&Metabolites;DAlphabetic;Herbicides;Pesticides&Metabolites;Triazines | | Mol File: | 1014-69-3.mol |  |
| | DESMETRYN Chemical Properties |
| Melting point | 85°C | | Boiling point | 345°C (rough estimate) | | density | 1.1553 (rough estimate) | | refractive index | 1.5500 (estimate) | | Fp | 11 °C | | storage temp. | APPROX 4°C | | pka | 3.66±0.41(Predicted) | | Water Solubility | 0.6g/L(20 ºC) | | BRN | 612017 | | Henry's Law Constant | 2.1×104 mol/(m3Pa) at 25℃, HSDB (2015) | | EPA Substance Registry System | Desmetryn (1014-69-3) |
| | DESMETRYN Usage And Synthesis |
| Description | Desmetryn is a selective herbicide. It has a moderate aqueous solubility and is volatile. Based on its chemical properties it is not expected to leach to groundwater. It is not usually persistent in soils but may persist in water under some conditions. Desmetryn is moderately toxic to mammals. It is moderately toxic to birds, most aquatic organisms and earthworms. It is relatively non-toxic to honeybees. | | Uses | Desmetryn is used as an herbicide in the treatment of crops and vegetables. It is used to control specifically white goosefoot, as well as other weeds and grasses. | | Definition | ChEBI: Desmetryn is a member of 1,3,5-triazines. | | Production Methods | Desmetryn is commercially synthesised through a multi-step process involving the formation of its core triazine ring. The production typically begins with the reaction of cyanuric chloride with appropriate alkylamines, such as dimethylamine and isopropylamine, under controlled conditions to form the substituted triazine structure. This process is carried out in organic solvents with temperature regulation to ensure high yield and purity. | | Mechanism of action | Selective, absorbed by leaves and roots, photosynthetic electron transport inhibitor | | Pesticide Type | Herbicide |
| | DESMETRYN Preparation Products And Raw materials |
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