4628-08-4

Usage

Uses

Used in Herbicide Production:
2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine is used as an active ingredient in herbicides for its ability to control a broad spectrum of annual and perennial weeds. It is effective in both pre-emergent and post-emergent applications, providing farmers and gardeners with a versatile tool for weed management.
Used in Agriculture:
In the agricultural industry, 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine is used as a herbicide to protect various crops from unwanted plant growth. Its application helps to ensure the healthy growth of crops by reducing competition for nutrients, water, and sunlight.
Used in Non-Cropland Areas:
2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine is also used in non-cropland areas such as lawns, gardens, and industrial sites to maintain a clear and weed-free environment. Its effectiveness in controlling a wide range of weeds makes it a popular choice for these applications.
It is crucial to handle, store, and apply 2,4-dichloro-6-(dodecyloxy)-1,3,5-triazine with caution due to its potential environmental and health risks. Proper safety measures and guidelines should be followed to minimize any adverse effects.

Upstream product

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

Relevant academic research and scientific papers

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.

A reagent for analysis of blood and preparation method therof

The present invention relates to a compound for analysis of blood capable of replacing existing reagents for analysis of blood, and a preparation method thereof. A compound of the present invention can rapidly dissolve blood cells, thereby being applicable as a composition for dissolving blood cells. Also, the compound can be applied as a composition for analysis of blood, thereby being capable of replacing existing reagents (compositions) for analysis of blood and improving analysis efficiency. To this end, the compound is represented by chemical formula 1c or 1d.COPYRIGHT KIPO 2018