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Ziram

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Identification
Molecular formula
C6H12N2S4Zn
CAS number
137-30-4
IUPAC name
1,1-dimethyl-3-[(3-methylisothiazol-5-yl)methyleneamino]isothiourea
State
State

Solid at room temperature.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
305.51g/mol
Molar mass
305.5140g/mol
Density
1.6600g/cm3
Appearence

Ziram appears as a white to yellowish powder or crystals. It is often found in its commercial form as wettable powder.

Comment on solubility

Solubility of 1,1-dimethyl-3-[(3-methylisothiazol-5-yl)methyleneamino]isothiourea

The solubility of 1,1-dimethyl-3-[(3-methylisothiazol-5-yl)methyleneamino]isothiourea can be quite intricate, given its complex structure. Key aspects to consider include:

  • Polarity: The presence of polar functional groups suggests potential solubility in polar solvents such as water.
  • Hydrogen Bonding: The amino and thiourea groups may facilitate hydrogen bonding, enhancing solubility characteristics.
  • Solvent Interaction: Its solubility is likely to be greater in organic solvents compared to nonpolar environments.
  • Temperature Dependence: The solubility may increase with temperature, which is common for many organic compounds.

Fundamentally, the solubility can be summarized with the phrase, "like dissolves like," which is pivotal when considering suitable solvents for this compound. Experimental confirmation through solubility testing in various solvents would provide the most accurate data for applications and practical use.

Interesting facts

Interesting Facts about 1,1-Dimethyl-3-[(3-Methylisothiazol-5-yl)methyleneamino]isothiourea

This fascinating compound belongs to a class of chemicals known for their diverse applications in both industry and research. Here are several intriguing aspects to consider:

  • Biological Activity: 1,1-Dimethyl-3-[(3-methylisothiazol-5-yl)methyleneamino]isothiourea exhibits notable biological properties, making it a subject of interest in the fields of pharmaceuticals and agricultural science.
  • Mechanism of Action: This compound functions as an inhibitor of various enzymes, which can impact metabolic pathways. Its ability to modulate biological processes makes it an important tool in biochemical research.
  • Isothiourea Derivatives: Compounds like this one, with isothiourea functionality, are often explored for their roles in medicinal chemistry. They can act as precursors to more complex molecules or serve as scaffolds for drug development.
  • Environmental Toxicology: The presence of heterocyclic structures, such as the isothiazole moiety, raises questions regarding the toxicity and environmental impact of this compound. Studying its behavior in ecological systems is crucial.
  • Historical Context: The synthesis and application of similar isothiourea derivatives can be traced back to early chemical research, illustrating the ongoing evolution of this field. Researchers continue to uncover the profound potential of these compounds.

In conclusion, 1,1-dimethyl-3-[(3-methylisothiazol-5-yl)methyleneamino]isothiourea is not just a simple compound; its unique structure and biological significance hold promise for innovative applications across various domains. As research progresses, it may uncover new horizons in science, emphasizing the importance of further exploration into compounds of this nature.