Pendimethalin

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Identification

Molecular formula
C13H19Cl2N3O4
CAS Number
40487-42-1
IUPAC Name
N,N-bis(2-chloroethyl)-4-methyl-2,6-dinitro-aniline
Molecular Weight
281.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1690g/cm3
Synonyms
CHLORNIDINE
Interesting facts

Interesting Facts about N,N-bis(2-chloroethyl)-4-methyl-2,6-dinitro-aniline

N,N-bis(2-chloroethyl)-4-methyl-2,6-dinitro-aniline, often referred to by its less formal name or shorthand, is a compound with unique characteristics and applications. Here are some fascinating insights:

  • Chemical Structure: This compound features two distinct parts – the dinitroaniline base and ethyl groups that are chlorinated. Such a structure often indicates a high level of reactivity and utility in various chemical reactions.
  • Application in Agriculture: Due to its chemical properties, this compound has been explored for use as a herbicide. It’s particularly valued for its ability to control the growth of specific weeds, thus aiding agricultural productivity.
  • Synthetic Potential: The presence of chlorine and nitro groups in its structure makes this compound an interesting candidate for further chemical modifications. Chemists can potentially create derivatives that may exhibit different properties, leading to new applications.
  • Toxicology Considerations: Scientists study the toxicological implications of compounds like this, as the chloroethyl and nitro groups can pose environmental and health risks. Understanding these aspects is crucial for developing safety protocols in any industrial usage.
  • Historical Significance: Certain analogs of dinitroaniline compounds have historical relevance in the development of explosives. Although N,N-bis(2-chloroethyl)-4-methyl-2,6-dinitro-aniline itself may not be an explosive, its structural relatives have contributed to advancements in this field.

In conclusion, the study of N,N-bis(2-chloroethyl)-4-methyl-2,6-dinitro-aniline highlights the intricate balance between its applications in agriculture and the required safety measures due to its reactive nature. As with many chemical compounds, it serves as a prime example of the dual-use nature of chemicals in both industry and academic research.

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