4628-08-4

Basic information

• Product Name: 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine
• Synonyms: 2,4-DICHLORO-6-DODECYLOXY-S-TRIAZINE
• CAS NO: 4628-08-4
• Molecular Formula: C₁₅H₂₅Cl₂N₃O
• Molecular Weight: 334.2845
• Mol File: 4628-08-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 452.4°C at 760 mmHg
• Flash Point: 227.4°C
• Density: 1.119g/cm³
• Vapor Pressure: 6.05E-08mmHg at 25°C
• Refractive Index: 1.5
• CAS DataBase Reference: 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine(4628-08-4)
• EPA Substance Registry System: 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine(4628-08-4)

Safety Data

• Hazardous Substances Data: 4628-08-4(Hazardous Substances Data)

Usage

General Description

2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine is a chemical compound that is composed of a triazine ring with two chlorine atoms and a dodecyl chain attached. It is commonly used in the production of herbicides, specifically as a pre-emergent and post-emergent herbicide to control a broad spectrum of annual and perennial weeds in various crops and non-cropland areas. This chemical is effective in inhibiting the growth of unwanted plants by disrupting the photosynthetic electron transport system, ultimately leading to their death. It is important to handle, store, and use this chemical with care due to its potential for environmental and health hazards.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 112-53-8 1-dodecyl alcohol 

Relevant articles and documents

Triazine natural gas drag reducer as well as synthesis method and application thereof

The invention discloses a triazine natural gas drag reducer and a synthesis method thereof. The molecular structural formula of the drag reducer is shown in the description. The synthesis method of the drag reducer comprises the following steps: dissolving cyanuric chloride in a solvent, dropwise adding an alcohol and an inorganic alkali at -15-0 DEG C, carrying out a reaction at -15-0 DEG C for 2-6 h, adding morpholine and the inorganic alkali after the reaction ends, carrying out a reaction at 50-100 DEG C for 6-12 h, washing the obtained reaction product with water after the reaction ends,and drying the washed reaction product to obtain the product. The drag reducer has a multi-polar end and a non-polar end, and has a good adsorption performance and excellent drag reducing and transportation increasing effects. The synthesis method has the advantages of simplicity, mild conditions, short time, low device requirements, and easiness in realization of large-scale industrial production.