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EPTC

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Identification
Molecular formula
C9H19NOS
CAS number
759-94-4
IUPAC name
S-ethyl N,N-dipropylcarbamothioate
State
State

At room temperature, EPTC exists as a liquid. It is generally stable when stored properly, but can degrade over time if exposed to excessive heat or light.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
180.00
Boiling point (Kelvin)
453.15
General information
Molecular weight
189.33g/mol
Molar mass
189.3500g/mol
Density
0.9684g/cm3
Appearence

EPTC is typically a colorless to pale yellow liquid. It may possess a faint, characteristic odor, which can vary in intensity depending on its concentration and the presence of impurities.

Comment on solubility

Solubility of S-ethyl N,N-dipropylcarbamothioate

S-ethyl N,N-dipropylcarbamothioate, a member of the carbamate family, exhibits unique solubility characteristics that merit consideration in various applications. The solubility of this compound is influenced by several factors, such as polarity, molecular structure, and the presence of functional groups.

Key Points on Solubility:

  • Polar vs. Nonpolar: The presence of the carbamothioate group contributes to its polar nature, which can enhance solubility in polar solvents.
  • Solvent Choices: Common solvents like water and alcohol may interact favorably with the compound, increasing its solubility.
  • Temperature Effects: Solubility can be temperature-dependent, often increasing with rising temperature for such organic compounds.

Quotes from experts in the field suggest that "the degree of solubility is not only critical for the compound's effectiveness but also for its environmental impact." This emphasizes the need to consider solubility when assessing the practical usage of S-ethyl N,N-dipropylcarbamothioate in various chemical processes.

Overall, understanding the solubility of S-ethyl N,N-dipropylcarbamothioate is essential for its effective application in agricultural and industrial contexts, where solubility can affect bioavailability and interaction with other substances.

Interesting facts

Interesting Facts about S-ethyl N,N-dipropylcarbamothioate

S-ethyl N,N-dipropylcarbamothioate, commonly known as a type of carbamate, holds significant importance in various fields, particularly in agriculture and chemical research. Here are some intriguing aspects of this compound:

  • Origin and Discovery: The carbamate class, to which S-ethyl N,N-dipropylcarbamothioate belongs, was first developed in the mid-20th century. They were appreciated for their effectiveness as insecticides and herbicides.
  • Mechanism of Action: This compound acts on the nervous system of pests. It primarily inhibits the enzyme acetylcholinesterase, which is crucial for nerve signal transmission, making it a potent agent against certain agricultural pests.
  • Applications: Used predominantly in agricultural settings, this compound serves as an effective pesticide. Its purpose includes:
    • Controlling insects
    • Managing weeds
    • Promoting higher crop yields
  • Environmental Impact: While useful in agriculture, the use of carbamates, including S-ethyl N,N-dipropylcarbamothioate, raises concerns about environmental safety. Proper application techniques and adherence to regulatory guidelines are crucial to mitigate negative impacts.
  • Safety Precautions: Handling this compound necessitates careful precautionary measures. It’s essential to use personal protective equipment (PPE) to avoid exposure, as it can be harmful if ingested or absorbed through the skin.
  • Research & Development: Ongoing studies aim to enhance the efficacy of S-ethyl N,N-dipropylcarbamothioate and explore its potential in new applications, including its use in pest-resistant crops.

In summary, S-ethyl N,N-dipropylcarbamothioate exemplifies the dual nature of chemical compounds, offering both agricultural benefits and environmental challenges. Understanding its properties and applications is essential for maximizing its advantages while ensuring ecological safety.

Synonyms
S-Ethyl dipropylthiocarbamate
EPTAM
Ethyl dipropylthiocarbamate
Carbamothioic acid, dipropyl-, S-ethyl ester
DTXSID1024091
R7PI3287F4
NSC-40486
DTXCID504091
Ethyl N,N-di-n-propylthiocarbamate
Carbamothioic acid, N,N-dipropyl-, S-ethyl ester
FDA-1541
ETHYL DIPROPYLTHIOCARBAMATE, S-
S-ETHYL DIPROPYL(THIOCARBAMATE)
DIPROPYLTHIOCARBAMIC ACID, S-ETHYL ESTER
N,N-DIPROPYLTHIOCARBAMIC ACID S ETHYL ESTER
EPTC
759-94-4
Torbin
Alirox
Niptan
Eptam 6E
S-Ethyl-N,N-dipropylthiocarbamate
Witox
Stauffer R 1608
ERADICANE
S-ethyl N,N-dipropylcarbamothioate
Genep EPTC
S-Ethyl N,N-di-n-propylthiocarbamate
S-Ethyl N,N-dipropylthiocarbamate
FDA 1541
S-Aethyl-N,N-dipropylthiolcarbamat
N,N-Dipropylthiocarbamic acid S-ethyl ester
Carbamic acid, dipropylthio-, S-ethyl ester
NSC 40486
R 1608
Dipropylcarbamothioic acid S-ethyl ester
R-1608
Ethyl di-n-propylthiolcarbamate
CHEBI:4738
Ethyl N,N-dipropylthiolcarbamate
EPTC 10 microg/mL in Cyclohexane
EPTC (herbicide)
Caswell No. 435
EPTC [BSI:ISO]
CAS-759-94-4
CCRIS 6035
HSDB 394
EINECS 212-073-8
EPA Pesticide Chemical Code 041401
Dipropylthiocarbamic acid S-ethyl ester
BRN 1762751
UNII-R7PI3287F4
S-Aethyl-N,N-dipropylthiolcarbamat [German]
EPTC (pesticide)
Genep (Salt/Mix)
Knoxweed (Salt/Mix)
Eradicane (Salt/Mix)
EPTC [HSDB]
EPTC [ISO]
EPTC [MI]
EC 212-073-8
s-ethyl-dipropylthiocarbamate
SCHEMBL66482
Carbamic acid, S-ethyl ester
MLS002415729
S-Ethyl dipropylcarbamothioate
WLN: 3N3&VS2
CHEMBL1371350
Carbamothioic acid, S-ethyl ester
NSC40486
Ethyl N,N-di-n-propylthiolcarbamate
N,N-dipropyl(ethylsulfanyl)formamide
S-ethyl N,N-di-propyl-thiocarbamate
Tox21_201962
Tox21_300727
AC-398
MFCD00053780
AKOS006228453
S-Ethyl N,N-di-n-propylthiolcarbamate
NCGC00091900-01
NCGC00091900-02
NCGC00091900-03
NCGC00091900-04
NCGC00091900-05
NCGC00091900-06
NCGC00254633-01
NCGC00259511-01
EPTC, PESTANAL(R), analytical standard
SMR000777891
Eptam (S-Ethyl-N,N-dipropylthiocarbamate)
DB-056011
CS-0031607
NS00005221
(dipropyl-amino)-methanethioic acid S-ethyl ester
Q424784