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Pirimicarb

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Identification
Molecular formula
C11H18N2O2S
CAS number
23103-98-2
IUPAC name
S-ethyl N-[3-(dimethylamino)propyl]carbamothioate
State
State

At room temperature, Pirimicarb is typically found in a solid state. It is characterized by a crystalline structure and is stable under normal ambient conditions. The compound can be handled safely as a powder or crystal in its solid form.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
346.40
Boiling point (Kelvin)
619.55
General information
Molecular weight
238.34g/mol
Molar mass
238.3600g/mol
Density
0.9700g/cm3
Appearence

Pirimicarb appears as a white crystalline solid. The compound is often found in a solid state at room temperature, forming fine crystals or a crystalline powder. It is usually odorless and is known for its stability under normal atmospheric conditions.

Comment on solubility

Solubility of S-ethyl N-[3-(dimethylamino)propyl]carbamothioate

S-ethyl N-[3-(dimethylamino)propyl]carbamothioate is a compound that exhibits interesting solubility properties. Its solubility can largely depend on factors such as polarity, temperature, and the medium in which it is placed. Here are some key points to consider:

  • Polarity: The presence of the carbamothioate functional group gives the compound a degree of polarity, which typically enhances its solubility in polar solvents like water.
  • Solvent Interaction: In addition to water, S-ethyl N-[3-(dimethylamino)propyl]carbamothioate may also have good solubility in a variety of organic solvents, such as methanol and ethanol, due to its structural compatibility with hydrocarbon chains.
  • Temperature Effects: As with many compounds, an increase in temperature generally enhances solubility, allowing for greater molecular interactions and more favorable dissolution dynamics.
  • pH Sensitivity: Being an amine-containing compound, it may exhibit pH-dependent solubility; thus, the pH of the solution can significantly affect its dissolution behavior.

In summary, the solubility of S-ethyl N-[3-(dimethylamino)propyl]carbamothioate is influenced by its polar characteristics and solvent interactions. It is essential to consider these aspects when preparing solutions or formulating products containing this compound.
Understanding these variables will lead to better applications and effectiveness in chemical processes.

Interesting facts

Interesting Facts about S-ethyl N-[3-(dimethylamino)propyl]carbamothioate

S-ethyl N-[3-(dimethylamino)propyl]carbamothioate, commonly known for its role in organic synthesis, is an intriguing compound that showcases the versatility of carbamothioate derivatives. This compound possesses unique properties that make it a subject of interest for both chemists and pharmacologists alike.

Key Features:

  • Structural Significance: The presence of the dimethylamino group enhances the compound's ability to act as a nucleophile, making it valuable in various chemical reactions, including alkylation and acylation.
  • Applications in Agriculture: S-ethyl N-[3-(dimethylamino)propyl]carbamothioate is often explored in the context of agrochemicals, where it may serve as a pesticide or herbicide, contributing to improved crop protection.
  • Biomedical Potential: Research indicates that compounds in the carbamothioate family may exhibit biological activities, including antimicrobial properties, which could be beneficial in developing new pharmaceutical agents.
  • Synthesis Versatility: This compound can be synthesized through various pathways, allowing for the modification of its functional groups and enhancing its chemical properties for specific applications.

According to one review article, "The structural variations in carbamothioate derivatives are paramount in influencing their biological activities and synthetic utility." This highlights the importance of understanding the structure-activity relationship within this class of compounds.

In summary, S-ethyl N-[3-(dimethylamino)propyl]carbamothioate exemplifies the intricate relationship between chemical structure and function, paving the way for further research and application in both industrial and pharmaceutical fields.

Synonyms
PROTHIOCARB
19622-08-3
9FS76HFF04
S-ethyl N-[3-(dimethylamino)propyl]carbamothioate
S-ethyl (3-dimethylaminopropyl)thiocarbamate
DTXSID5058012
CHEBI:82084
N-(3-Dimethylaminopropyl)thiocarbamic acid S-ethyl ester hydrochloride
S-ETHYL N-(3-(DIMETHYLAMINO)PROPYL)CARBAMOTHIOATE
DTXCID8031780
N-(gamma-Dimethylaminopropyl)thiocarbamic acid S-ethyl ester
RefChem:870034
Prothiocarb [ISO]
UNII-9FS76HFF04
SN 41 703
SCHEMBL21052
YRRBXJLFCBCKNW-UHFFFAOYSA-N
NS00004817
C18943
S-ethyl [3-(dimethylamino)propyl]carbamothioate
Q18629965
N-(3-dimethylaminopropyl)thiocarbamic acid S-ethyl ester
N-(3-dimethylaminopropyl)-thiocarbamic acid-S-ethyl ester
Carbamothioic acid, (3-(dimethylamino)propyl)-, S-ethyl ester