673-04-1

Basic information

• Product Name: SIMETON
• Synonyms: 2,4-bis(ethylamino)-6-methoxy-s-triazin;2-Methoxy-4,6-bis(ethylamino)-1,3,5-triazine;2-Methoxy-4,6-bis(ethylamino)-s-triazine;4,6-Bis(ethylamino)-2-methoxy-s-triazine;G-30044;Geigy 30,044;geigy30,044;Gesadural
• CAS NO: 673-04-1
• Molecular Formula: C₈H₁₅N₅O
• Molecular Weight: 197.24
• EINECS: 211-601-4
• Mol File: 673-04-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 119°C
• Boiling Point: 334.34°C (rough estimate)
• Appearance: /
• Density: 1.1685 (rough estimate)
• Refractive Index: 1.8000 (estimate)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.60±0.10(Predicted)
• Water Solubility: 3.2g/L(21 oC)
• BRN: 11608
• CAS DataBase Reference: SIMETON(CAS DataBase Reference)
• NIST Chemistry Reference: SIMETON(673-04-1)
• EPA Substance Registry System: SIMETON(673-04-1)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 673-04-1(Hazardous Substances Data)

Usage

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that is 6-methoxy-1,3,5-triazine-2,4-diamine in which one of the hydrogens of each amino group has been replaced by an ethyl group.

Upstream product

• 122-34-9 Simazine 
• 124-41-4 sodium methylate 
• 67-56-1 methanol 

Relevant articles and documents

Atrazine transformation using synthetic enzymes prepared by molecular imprinting.

Atrazine imprinted synthetic polymers were prepared using a combination of methacrylic acid and 2-sulfoethyl methacrylate that bound and converted atrazine and other 6-chlorotriazine herbicides to less toxic compounds. A chloride at the 6-position of the triazines was converted to a methoxy group by the polymer in a methanol-containing solvent, where the imprinting effects enhanced the catalytic activity. Competitive inhibition of the atrazine methanolysis was observed in the presence of a structurally related binder, ametryn, suggesting that the catalytic reaction proceeded in the binding sites generated by the molecular imprinting process.

4,5-Dichloroimidazole-2-carboxylic acid derivatives

4,5-Dichloroimidazole-2-carboxylic acid derivatives of the formula STR1 in which the group STR2 represents a carbon atom which has three bonds to hetero-atoms, and their salts with bases, possess insecticidal, acaricidal, fungicidal, nematicidal and herbicidal properties.