32889-45-5

Basic information

• Product Name: 2-N-Cyclopropylamino-4,6-DichloroTriazine
• Synonyms: 2-N-Cyclopropylamino-4,6-DichloroTriazine;4,6-Dichloro-N-cyclopropyl-1,3,5-triazin-2-aMine
• CAS NO: 32889-45-5
• Molecular Formula: C6H8Cl2N4
• Molecular Weight: 207.06052
• Mol File: 32889-45-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 401.8±28.0 °C(Predicted)
• Appearance: /
• Density: 1.684±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 0.96±0.10(Predicted)
• CAS DataBase Reference: 2-N-Cyclopropylamino-4,6-DichloroTriazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-N-Cyclopropylamino-4,6-DichloroTriazine(32889-45-5)
• EPA Substance Registry System: 2-N-Cyclopropylamino-4,6-DichloroTriazine(32889-45-5)

Safety Data

• Hazardous Substances Data: 32889-45-5(Hazardous Substances Data)

Usage

General Description

2-N-Cyclopropylamino-4,6-DichloroTriazine is a chemical compound most commonly known for its use in herbicides. This synthetic compound, often found in agricultural contexts, works by inhibiting photosynthesis in plants, causing them to wither and die. It's particularly effective against broadleaf plants and grasses. Due to its chlorine atoms, it's highly reactive and is not naturally occurring. As a herbicide, its use and disposal are governed by regulations to mitigate impact on the environment. Initial exposure may cause skin and eye irritation in humans and fauna. Despite these potential hazards, it is invaluable in maintaining crop health and increasing yield.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 765-30-0 Cyclopropylamine 

Downstream Products

• 66215-27-8 cyromazine 
• 35516-73-5 6-chloro-N-cyclopropyl-[1,3,5]triazine-2,4-diamine 

Relevant articles and documents

Synthesis method of cyromazine active compound with high yield

The invention relates to a synthesis method of a cyromazine active compound with high yield, cyanuric chloride, cyclopropylamine and ammonia gas are used as raw materials, single toluene is used as a solvent to synthesize the cyromazine active compound, the purity is more than 98%, and the yield is as high as 93%. The method has the characteristics of simplicity in operation, high solvent utilization rate, high product yield, less environmental pollution and the like. The labor load of workers is reduced, the production cost is reduced, and the environmental pollution is reduced.

Synthesis of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine hybrids as potential antimalarial agents

We report herein synthesis of a series of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine hybrids and evaluate their antimalarial activity against D6 and W2 strains of Plasmodium falciparum. To study the structure-activi

Influence of the hapten design on the development of a competitive ELISA for the determination of the antifouling agent Irgarol 1051 at trace levels

Enzyme-linked immunosorbent assays (ELISAs) with a high detectability have been developed for determination of the antifouling agent Irgarol 1051. The features of the resulting assays have been rationalized by using molecular mechanic calculations (MM2+) to correlate the chemical structure of different immunizing haptens and the corresponding avidities of the obtained antisera. The ability of Irgarol 1051 to compete for the antibody binding sites with 11 horseradish peroxidase enzyme tracers, differing in the chemical structures of the hapten, has been investigated. The present paper demonstrates that high-quality antibodies and, therefore, immunoassays reaching very low detection limits could be predicted by molecular modeling studies of the analyte conformations and of the immunizing haptens' geometries, hydrogen-bonding capabilities, and electronic distributions. Two of the ELISAs obtained have been optimized to obtain reproducible immunoassays. The dynamic ranges of both assays are between 30 and 200 ng/L, and the limits of detection are ~16 ng/L. The reported immunoassays have been evaluated and validated by analyzing spiked and real seawater samples. Irgarol 1051 has been found to be present in two of the geographical locations analyzed at concentration levels dependent on the time of year. The analytical results obtained with these immunoassays have been validated by chromatographic methods.