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Dazomet

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Identification
Molecular formula
C5H10N2OS
CAS number
533-74-4
IUPAC name
1,3-bis(hydroxymethyl)imidazolidine-2-thione
State
State

At room temperature, Dazomet is present in a solid state. It is usually handled as granules or powder in its technical-grade form.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
120.00
Boiling point (Kelvin)
393.15
General information
Molecular weight
162.23g/mol
Molar mass
162.2330g/mol
Density
1.3300g/cm3
Appearence

Dazomet is typically a white, crystalline solid. It may also appear as an off-white powder depending on the purity and granulation.

Comment on solubility

Solubility of 1,3-bis(hydroxymethyl)imidazolidine-2-thione

1,3-bis(hydroxymethyl)imidazolidine-2-thione is an intriguing compound with specific solubility characteristics that bear interesting implications for its applications. Its solubility can be summarized as follows:

  • Solvent Compatibility: This compound is primarily soluble in polar solvents such as water and alcohols due to the presence of hydroxymethyl groups.
  • pH Dependence: The solubility may vary with pH; it tends to be higher in acidic conditions, enhancing its interactions with surrounding molecules.
  • Temperature Influence: Like many organic compounds, its solubility can increase with temperature, making it easier to dissolve at elevated temperatures.
  • Hydrogen Bonding: The hydroxyl groups can form hydrogen bonds, further assisting in solubility by stabilizing interactions with solvent molecules.

In conclusion, the solubility of 1,3-bis(hydroxymethyl)imidazolidine-2-thione is characterized by its compatibility with polar solvents and its responsiveness to environmental conditions such as pH and temperature. Understanding these properties is essential for effectively utilizing this compound in chemical applications.

Interesting facts

Interesting Facts about 1,3-bis(hydroxymethyl)imidazolidine-2-thione

1,3-bis(hydroxymethyl)imidazolidine-2-thione is a fascinating chemical compound that plays a significant role in various fields of chemistry and materials science. Here are some interesting aspects of this compound:

  • Versatile Applications: This compound is often used in the synthesis of various complex molecules, showcasing its versatility in organic chemistry.
  • Regenerative Properties: It has been highlighted for its potential regenerative properties, making it a candidate for research in pharmaceuticals and biocompatible materials.
  • Structural Significance: The imidazolidine ring structure provides a stable framework, allowing for modifications that can lead to a diverse array of derivatives and applications.
  • Energy Transfer: It has been reported to participate in energy transfer processes, which is crucial in developing new materials for energy applications.
  • Research Frontier: Ongoing research is being conducted to explore novel uses in medicinal chemistry, particularly due to its thione functional group, which can exhibit unique reactivity.

Researchers have remarked, “The ability to manipulate the functionalities of 1,3-bis(hydroxymethyl)imidazolidine-2-thione can lead to exciting innovations in sustainable chemistry.” This emphasizes the compound’s potential to contribute to sustainable practices in the chemical industry.

In summary, 1,3-bis(hydroxymethyl)imidazolidine-2-thione stands at the confluence of innovative chemistry and practical applications, making it a compound of significant interest for future discoveries.

Synonyms
15534-95-9
Dimethylol ethylene thiourea
Dimethylolethylenethiourea
1,3-Bis(hydroxymethyl)-2-imidazolidinethione
2-IMIDAZOLIDINETHIONE, 1,3-BIS(HYDROXYMETHYL)-
1,3-Bis(hydroxymethyl)imidazolidin-2-thione
BRN 0638446
EINECS 239-579-1
UNII-H09EK3X952
AI3-51415
H09EK3X952
DTXSID3065908
BIS(HYDROXYMETHYL)IMIDAZOLIDIN-2-THIONE, 1,3-
DTXCID3035000
DIMETHYLOL ETHYLENE THIOUREA [INCI]
239-579-1
1,3-Bis(hydroxymethyl)imidazolidine-2-thione
SCHEMBL1068943
QXYJLKUVMPXXKA-UHFFFAOYSA-N
NS00013599
E83755
Q27279399