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Thiram

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Identification
Molecular formula
C6H12N2S4
CAS number
137-26-8
IUPAC name
dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate
State
State

At room temperature, Thiram exists as a solid. It appears generally as a powder and is stable under normal conditions.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
143.00
Boiling point (Kelvin)
416.15
General information
Molecular weight
240.43g/mol
Molar mass
240.4260g/mol
Density
1.2930g/cm3
Appearence

Thiram is a yellow to orange-yellow powder with a slight sulfurous odor. It is typically observed as a crystalline solid.

Comment on solubility

Solubility of Dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate

The solubility of dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate can be characterized as follows:

  • Solvent Interaction: This compound demonstrates varying solubility depending on the type of solvent used. It is generally more soluble in polar solvents.
  • Molecular Structure: The presence of multiple functional groups, including carbamothioyl and dithioate moieties, influences its solubility profile.
  • Temperature Dependency: As with many chemical compounds, solubility may increase with temperature, making it essential to consider temperature when working with it.
  • pH Sensitivity: The solubility can also vary with changes in pH, as the ionization state of the compound will alter its interactions with water.

In summary, when dealing with dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate, it is crucial to consider these factors to achieve optimal solubility, especially when preparing solutions for laboratory purposes. To quote a common principle: "Like dissolves like," highlighting the importance of matching solute and solvent polarities.

Interesting facts

Discovering Dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate

Dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate is a fascinating compound with unique properties and applications in various fields such as agriculture and chemistry. Here are some intriguing facts about this compound:

1. Origin and Composition

This compound is part of a class known as thioates, containing sulfur atoms within its structure. The presence of both dimethylcarbamothioyl and dimethylcarbamodithioate groups highlights its potential reactivity and versatility in chemical synthesis.

2. Role in Agriculture

Dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate has garnered attention for its applications as a pesticide. It is frequently studied for its effectiveness against a range of pests, helping improve crop yields and preserve plant health.

3. Chemical Reactions

As a part of its chemical behavior, this compound can participate in various reactions, such as:

  • Nucleophilic substitutions: Engaging with electrophiles to form new bonds.
  • Hydrolysis: Breaking down in the presence of water, leading to potential biodegradation pathways.

4. Safety Considerations

While its utility in agriculture is notable, there are safety considerations to keep in mind. Protective measures are often recommended when handling this compound due to its chemical nature.

5. Future Potential

Researchers continue to explore the possibilities of dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate, particularly its applications in sustainable agriculture. There is hope that innovations in this area could pave the way for more environmentally friendly pest control solutions.

In summary, dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate is not just another chemical; it represents the intricate intersection of chemistry and agricultural science, with the potential to impact food security and sustainability positively.

Synonyms
22656-77-5
methylene bis(dimethylcarbamodithioate)
Methylenebis(N,N-dimethyldithiocarbamate)
dimethylcarbamothioylsulfanylmethyl N,N-dimethylcarbamodithioate
Carbamodithioic acid, dimethyl-, methylene ester
HHF0ZKY88A
CARBAMIC ACID, DIMETHYLDITHIO-, METHYLENE ESTER
Methylenebis(dimethyldithiocarbamate)
NSC-14971
3-04-00-00150 (Beilstein Handbook Reference)
Bis(dimethyldithiocarbamic acid)methylene ester
DTXSID50177195
F1019-0023
N,N-dimethyl({[(dimethylcarbamothioyl)sulfanyl]methyl}sulfanyl)carbothioamide
USAF SN-32
NSC 14971
BRN 1785205
Methylene-bis (dimethyl-dithiocarbamate)
C7H14N2S4
UNII-HHF0ZKY88A
RefChem:1089685
Carbamic acid, methylene ester
DTXCID7099686
SCHEMBL11222141
SVEFOVSCPCGMJS-UHFFFAOYSA-N
SMSSF-0062864
NSC14971
Carbamodithioic acid, methylene ester
methylenebis(dimethylcarbamodithioate)
AKOS003631027
methanediyl bis(dimethylcarbamodithioate)
BIS(DIMETHYLTHIOCARBAMOYLTHIO)METHANE
EN300-264818
carbamodithioic acid, N,N-dimethyl-, methylene ester
dimethylamino(dimethylaminothiocarbonylthio)methylcarbodithioate