26424-27-1

Basic information

• Product Name: 2,4-dichloro-6-(2-ethoxyethoxy)-1,3,5-triazine
• Synonyms: 2,4-dichloro-6-(2-ethoxyethoxy)-1,3,5-triazine
• CAS NO: 26424-27-1
• Molecular Formula: C₇H₉Cl₂N₃O₂
• Molecular Weight: 238.07126
• EINECS: 247-687-5
• Mol File: 26424-27-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 382.3°Cat760mmHg
• Flash Point: 185°C
• Appearance: /
• Density: 1.376g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.521
• PKA: -1.59±0.10(Predicted)
• CAS DataBase Reference: 2,4-dichloro-6-(2-ethoxyethoxy)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-6-(2-ethoxyethoxy)-1,3,5-triazine(26424-27-1)
• EPA Substance Registry System: 2,4-dichloro-6-(2-ethoxyethoxy)-1,3,5-triazine(26424-27-1)

Safety Data

• Hazardous Substances Data: 26424-27-1(Hazardous Substances Data)

Usage

Type of compound

chemical compound (herbicide and pesticide)

Usage

used in the agricultural industry for weed control in crops such as corn, wheat, and soybeans, as well as in non-crop settings like lawns and golf courses.

Known for

ability to control a wide range of broadleaf and grassy weeds.

Controversy

potential environmental and health impacts.

Safety

it is important to always follow safety guidelines when using or handling this compound.

InChI:InChI=1/C7H9Cl2N3O2/c1-2-13-3-4-14-7-11-5(8)10-6(9)12-7/h2-4H2,1H3

Upstream product

• 110-80-5 2-ethoxy-ethanol 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 

Relevant articles and documents

KINETICS OF FORMATION OF MONOALKOXY-s-TRIAZINES FROM CYANURIC CHLORIDE.

2-R-alkoxy-4,6-dichloro-s-triazines (I) are used as intermediates for synthesis of herbicides, and are obtained by reactions of 2,4, 6-trichloro-s-triazine (II) (cyanuric chloride) with various alcohols in aqueous-organic mixtures in presence of hydrogen chloride acceptors. The purpose of this work was to study the quantitive relationships of the main reaction of cyanuric chloride alkoxylation and of the competing reactions of hydrolysis and alkoxylation of compound (I), for optimization of production of monoalkoxy-s-triazines. It is found that the reaction temperature has a significant influence on the yield of 2-(2-R-ethoxy)-4, 6-dichloro-s-triazine; decrease of temperature raises the yield of (I) owing to decrease of the contributions of hydrolysis of compounds (I) and (II) and alkoxylation of (I). The asolute values of the rate constants of hydrolysis (k//3, k//4) and alkoxylation (k//2) decrease more rapidly than k//1 with decrease of temperature. This makes it possible to raise the selectivity of the process by raising the alkali concentration and lowering the reaction temperature.