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5-(Aminomethyl)isothiazol-3-one

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Identification
Molecular formula
C4H6N2OS
CAS number
N/A
IUPAC name
5-(aminomethyl)isothiazol-3-one
State
State
Solid at room temperature.
Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
114.15g/mol
Molar mass
114.1530g/mol
Density
1.3950g/cm3
Appearence

5-(Aminomethyl)isothiazol-3-one typically appears as a crystalline solid, white to off-white in color. It is a chemical compound used in various industrial and chemical applications.

Comment on solubility

Solubility of 5-(Aminomethyl)isothiazol-3-one

5-(Aminomethyl)isothiazol-3-one, with the chemical formula C4H6N2OS, exhibits unique solubility characteristics that are important for its applications in various fields. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is generally soluble in both polar and non-polar solvents, which makes it versatile for various chemical reactions and formulations.
  • Water Solubility: It is moderately soluble in water, allowing for ease of use in aqueous processes while retaining some hydrophobic properties due to its structure.
  • Organic Solvents: 5-(Aminomethyl)isothiazol-3-one readily dissolves in common organic solvents such as methanol, ethanol, and acetone, enhancing its applicability in organic chemistry.

As with many chemical compounds, the solubility can be influenced by factors such as temperature, pH, and the presence of other solutes. Therefore, it is vital to consider these factors when formulating solutions or conducting experiments. Overall, the solubility of 5-(Aminomethyl)isothiazol-3-one plays a critical role in determining its functionality and effectiveness in various applications.

Interesting facts

Interesting Facts About 5-(Aminomethyl)isothiazol-3-one

5-(Aminomethyl)isothiazol-3-one, often abbreviated as AMIT, is a noteworthy compound that belongs to the isothiazolone family. This compound is particularly significant in the field of chemistry and various industrial applications due to its unique properties and functionalities. Here are some engaging facts about this fascinating chemical:

  • Biocidal Activity: AMIT is primarily recognized for its biocidal properties, making it an effective agent in controlling the growth of bacteria, fungi, and algae. This characteristic makes it particularly useful in the formulation of preservatives for paints, coatings, and personal care products.
  • Structure and Reactivity: The distinctive structure of AMIT, featuring a five-membered ring containing sulfur and nitrogen, contributes to its reactivity. This scaffolding provides sites for further chemical transformations, enabling it to participate in various organic synthesis reactions.
  • Environmental Impact: As a synthetic compound, the environmental implications of AMIT’s use are a significant concern. As part of ongoing studies in green chemistry, scientists are exploring safer alternatives while ensuring effective antimicrobial properties.
  • Application Spectrum: Beyond its role in preserving materials, AMIT has garnered attention in the formulation of agricultural products, particularly as a component in pesticides due to its efficacy in combating microbial threats to crops.
  • Safety Considerations: It is vital to handle AMIT with care. The compound can be irritating to skin and eyes, emphasizing the importance of using appropriate personal protective equipment when working with it.

In conclusion, 5-(Aminomethyl)isothiazol-3-one stands out not only for its chemical properties but also for its broad applications across various fields. As research continues, the understanding of AMIT’s behavior and interactions will lead to innovative uses and improved formulations in chemistry.

Synonyms
Thiomuscimol
62020-54-6
5-(aminomethyl)-1,2-thiazol-3-one
5-(Aminomethyl)isothiazol-3(2H)-one
5-Aminomethyl-3-isothiazolol
5-(Aminomethyl)-3(2H)-isothiazolone
DTXSID00211078
5-(aminomethyl)-2,3-dihydro-1,2-thiazol-3-one
Thiomuscimol hydrobromide
CHEMBL133628
SCHEMBL7778711
SCHEMBL25042518
BDBM85196
DTXCID00133569
CAS_5448
NSC_5448
AKOS006338836
AKOS030538857
5-(Aminomethyl)- 3(2H)-isothiazolone
HY-129927
CS-0108507
EN300-7298563
Q15634088