Interesting facts
Interesting Facts about S-ethyl N,N-diisobutylcarbamothioate
S-ethyl N,N-diisobutylcarbamothioate is a fascinating compound with various applications and properties that intrigue chemists and scientists alike. Here are some notable aspects of this compound:
- Pesticidal Properties: This compound is primarily used in the agricultural sector as a pesticide. Its effectiveness against a wide range of pests makes it a valuable resource for farmers looking to protect their crops.
- Mechanism of Action: As a carbamate, S-ethyl N,N-diisobutylcarbamothioate works by interfering with the normal function of the enzyme acetylcholinesterase, leading to an accumulation of acetylcholine in the nervous systems of pests. This mechanism results in paralysis and ultimately death of the pest.
- Environmental Considerations: Research on the environmental impact of carbamate pesticides, including S-ethyl N,N-diisobutylcarbamothioate, is crucial for sustainable agriculture. Scientists are continually studying its degradation products and long-term effects on non-target species.
- Structure-Activity Relationship (SAR): Chemists often explore the SAR of this compound to understand how modifications to its structure can improve its efficacy or reduce toxicity to non-target organisms. This research can lead to the development of safer and more effective pesticides.
- Regulatory Status: Understanding the regulatory landscape around compounds like S-ethyl N,N-diisobutylcarbamothioate is vital. Scientists must stay informed about safety regulations, usage restrictions, and required testing for new pesticides entering the market.
In conclusion, S-ethyl N,N-diisobutylcarbamothioate is more than just a chemical compound; it is a crucial player in modern agriculture, posing both potential benefits and challenges. Scientists continue to investigate its many facets to harness its advantages while minimizing risks.
Synonyms
Butylate
2008-41-5
Anelda
Diisocarb
S-Ethyl N,N-diisobutylthiocarbamate
SUTAN
Aneldazine
Tomahawk
Genate
Suazin
Genate plus
Stauffer R-1910
Sutan 6E
Butylate [BSI:ISO]
Caswell No. 434A
Butilate [ISO-French]
Sutar' 85 E
Butylate [ISO]
Ethyl N,N-diisobutylthiocarbamate
Ethyl N,N-diisobutylthiolcarbamate
Diisobutylthiocarbamic acid S-ethyl ester
Ethyl-N,N-diisobutyl thiolcarbamate
S-Ethyldiisobutylthiocarbamate
S-Ethyl N,N-diisobutyl thiocarbamate
S-Ethyldiisobutyl thiocarbamate
S-Ethyl N,N-diisobutyl thiolcarbamate
Carbamic acid, diisobutylthio-, S-ethyl ester
S-Ethyl di-isobutylthiocarbamate
Ethyl-N,N-diisobutylthiocarbamate
HSDB 1714
S-Ethyl bis(2-methylpropyl)carbamothioate
Bis(2-methylpropyl)carbamothioic acid S-ethyl ester
EINECS 217-916-3
Carbamothioic acid, bis(2-methylpropyl)-, S-ethyl ester
S-ethyl N,N-bis(2-methylpropyl)carbamothioate
R 1910
R-1910
EPA Pesticide Chemical Code 041405
BRN 1770420
CCRIS 9244
DTXSID7023936
SUTAN PLUS
AI3-52053
S-Ethyl bis(2-methylpropyl) carbamothioate
3U78PG73G7
BUTYLATE [HSDB]
R1910
BUTYLATE [MI]
Carbamothioic acid, N,N-bis(2-methylpropyl)-, S-ethyl ester
Bis(2-methylpropyl)carbamothioic acid, S-ethyl ester
DTXCID403936
4-04-00-00651 (Beilstein Handbook Reference)
N,N-Bis(2-methylpropyl)carbamothioic acid S-ethyl ester
S-ETHYL DIISOBUTYL(THIOCARBAMATE)
Butilate (ISO-French)
butylic acid
Stauffer R1910
SEthyldiisobutylthiocarbamate
SEthyl diisobutylthiocarbamate
SEthyldiisobutyl thiocarbamate
EthylN,Ndiisobutylthiocarbamate
Ethyl N,Ndiisobutylthiocarbamate
Ethyl N,Ndiisobutylthiolcarbamate
EthylN,Ndiisobutyl thiolcarbamate
SEthyl N,Ndiisobutylthiocarbamate
SEthyl N,Ndiisobutyl thiocarbamate
SEthyl N,Ndiisobutyl thiolcarbamate
SEthyl bis(2methylpropyl)carbamothioate
Diisobutylthiocarbamic acid Sethyl ester
SEthyl bis(2methylpropyl) carbamothioate
Carbamic acid, diisobutylthio, Sethyl ester
Bis(2methylpropyl)carbamothioic acid Sethyl ester
N,N-bis(2-methylpropyl)(ethylsulfanyl)formamide
Carbamothioic acid, bis(2methylpropyl), Sethyl ester
217-916-3
Butilate
Butylat
S-ethyl diisobutylcarbamothioate
CHEBI:34594
Butylate 100 microg/mL in Acetonitrile
S-Ethyl diisobutylthiocarbamate
UNII-3U78PG73G7
N-BUTYLATE
starbld0016555
Stauffer R-1,910
SCHEMBL66484
s-ethyl diisobutyl thiocarbamate
CHEMBL1873329
S-Ethyl diisobutylthiocarbamate #
Tox21_300762
MFCD00055338
S-ethyl N,N-diisobutyl-thiocarbamate
AKOS015898728
NCGC00163807-01
NCGC00163807-02
NCGC00163807-03
NCGC00254666-01
CAS-2008-41-5
Butylat, PESTANAL(R), analytical standard
DB-045080
NS00006903
Q16724472
Solubility of S-ethyl N,N-diisobutylcarbamothioate
S-ethyl N,N-diisobutylcarbamothioate, also known as a carbamate compound, exhibits unique solubility characteristics. Understanding these properties is essential for various applications in chemistry and agriculture. Here are some notable points regarding its solubility:
In summary, the solubility of S-ethyl N,N-diisobutylcarbamothioate highlights the balance between its polar and non-polar characteristics, providing a fascinating glimpse into its behavior in different environments. As with many chemical compounds, deeper insights into solubility can lead to better utilization in scientific advancements.