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Terbuthylazine

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Identification
Molecular formula
C9H16ClN5
CAS number
5915-41-3
IUPAC name
N2-tert-butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine;N2-tert-butyl-N4-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine
State
State

At room temperature, terbuthylazine is in a solid state, commonly used in a granulated or powdered form for agricultural applications.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
229.71g/mol
Molar mass
229.7000g/mol
Density
1.2150g/cm3
Appearence

Terbuthylazine is typically a colorless or white crystalline solid. It is odorless and has a particulate form that resembles small granules or powder.

Comment on solubility

Solubility of N2-tert-butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine and N2-tert-butyl-N4-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine

The solubility of the triazine derivatives N2-tert-butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine and N2-tert-butyl-N4-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine is influenced by their structural characteristics, specifically the presence of bulky tert-butyl and ethyl groups as well as the chloro and methylthio substituents.

Key Factors Affecting Solubility:

  • Polarity: These compounds exhibit moderate polarity due to their functional groups, which can significantly impact their interaction with solvents.
  • Hydrophobicity: The bulky tert-butyl group may lead to increased hydrophobicity, making these compounds less soluble in polar solvents like water, while enhancing solubility in non-polar organic solvents.
  • Temperature: As with many organic compounds, solubility can vary with temperature, often increasing at elevated temperatures.
  • Presence of other solvents: Mixtures of solvents may facilitate solubility through synergetic effects between polar and non-polar components.

In conclusion, the solubility of these triazine compounds is a complex interplay of various factors including polarity and structural attributes. As stated, "the solubility of a compound is a key determinant of its utility in various applications," underscoring the importance of thorough solubility assessments in chemical research and development.

Interesting facts

Compound Overview: N2-tert-butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine

This fascinating compound belongs to the triazine family, which is known for its applications in the fields of agriculture and pharmaceuticals. The presence of the triazine ring is notable for its chemical stability and versatility in creating various derivatives.

Key Features:

  • Triazine Framework: The triazine structure offers a robust platform for the attachment of multiple functional groups, increasing the potential for biological activity.
  • Chlorine Substitution: The chloro group at position 6 contributes to its reactivity, opening up possibilities for further chemical modifications.
  • Tert-butyl and Ethyl Groups: These bulky substituents enhance lipophilicity, which may improve the compound's ability to permeate biological membranes.

Applications:

Due to its unique structure, this compound is often researched for:

  • Pesticide Development: Its functionality can be tailored to develop herbicides or fungicides.
  • Pharmaceutical Research: Investigations into its potential therapeutic effects against various diseases are ongoing.

Compound Overview: N2-tert-butyl-N4-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine

This compound, which also belongs to the triazine family, introduces a sulfur-containing methylene group that significantly alters its chemical properties. The incorporation of a methylsulfanyl group is interesting because it can enhance the compound's potential reactivity.

Key Features:

  • Methylsulfanyl Group: This group can participate in nucleophilic substitutions, potentially leading to novel compounds.
  • Functional Diversity: The combination of nitrogen, sulfur, and carbon groups presents opportunities for exciting chemistry.
  • Stability of Triazine: Maintains the stability inherent in triazine derivatives while introducing new functional properties.

Applications:

This compound is particularly notable in:

  • Agricultural Chemistry: Its unique structure may lead to new agrochemicals with improved efficacy or selectivity.
  • Organic Synthesis: The reactivity of the methylsulfanyl group makes it a target for synthetic chemists aiming to forge new bonds and structures.

In summary, both compounds highlight the richness of chemistry in the triazine family, revealing their potential in various fields of research and application. As scientists continue to explore these compounds, they open the door to innovative solutions in agriculture and medicine.

Synonyms
TOPOGARD
8066-11-3
2-N-tert-butyl-6-chloro-4-N-ethyl-1,3,5-triazine-2,4-diamine;2-N-tert-butyl-4-N-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine
8072-81-9
1,3,5-Triazine-2,4-diamine, 6-chloro-N-(1,1-dimethylethyl)-N'-ethyl-, mixt. with N-(1,1-dimethylethyl)-N'-ethyl-6-(methylthio)-1,3,5-triazine-2,4-diamine
1,3,5-Triazine-2,4-diamine, 6-chloro-N-(1,1-dimethylethyl)-N'-ethyl-, mixt. with N-(1,1-dimethylethyl)-N'-ethyl-6-methoxy-1,3,5-triazine-2,4-diamine
Opogard
Solanex
Camparol 3303
Topogard 3623
A 3620 (pesticide)
VUAgT 179
Terbutryne-terbuthylazine mixt.
SCHEMBL16594385
Terbuthylazine - terbutryn mixt.
A 3620