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Thiram

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Identification
Molecular formula
C6H12N2S4
CAS number
97-74-5
IUPAC name
(dimethylamino)methyl N,N-dimethylcarbamodithioate
State
State

At room temperature, Thiram is typically a solid. It is commonly encountered as a powder or in crystalline form.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.00
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.00
General information
Molecular weight
240.43g/mol
Molar mass
240.4360g/mol
Density
1.2900g/cm3
Appearence

Thiram is a compound that usually appears as a bright yellow to orange-yellow crystalline solid. It may also be found as a colorless or yellowish powder when in a pure state. It has a characteristic unpleasant odor that can be identified easily.

Comment on solubility

Solubility of (dimethylamino)methyl N,N-dimethylcarbamodithioate

The compound (dimethylamino)methyl N,N-dimethylcarbamodithioate, with the chemical formula C6H12N2S4, exhibits intriguing solubility characteristics that can significantly influence its applications.

Key Points on Solubility:

  • Polarity: The presence of multiple sulfur atoms and nitrogen groups suggests that this compound may have polar characteristics, potentially enhancing solubility in polar solvents.
  • Solvent Compatibility: It is likely soluble in organic solvents and may have limited solubility in water due to hydrophobic interactions from the carbon chain.
  • Temperature Dependence: Solubility could vary with temperature; increasing temperature typically increases solubility for many compounds.

In summary, the solubility of (dimethylamino)methyl N,N-dimethylcarbamodithioate depends on the nature of the solvent and external conditions. Understanding these solubility properties is essential for effectively utilizing this compound in various scientific fields.

Interesting facts

Interesting Facts about (Dimethylamino)methyl N,N-Dimethylcarbamodithioate

(Dimethylamino)methyl N,N-dimethylcarbamodithioate, often referred to as a compound used in agricultural applications, embodies a unique blend of functional groups that contribute to its chemical behavior.

Key Characteristics

  • Thioamide Structure: The presence of dithioate functional groups enhances its reactivity, making it a pivotal component in various chemical reactions.
  • Biological Relevance: Similar compounds have been studied for their potential in herbicidal and insecticidal properties, underlining their importance in agricultural chemistry.
  • Complexity in Design: The integration of two dimethylamino groups endows the molecule with unique steric and electronic properties, which can influence how it interacts with biological systems.

Applications

This compound has garnered attention for its possible applicability in the following areas:

  • Pest Control: Explored as a candidate for developing new agrochemicals to combat pests effectively.
  • Synthesis Partner: Utilized in various synthetic pathways in organic chemistry due to its reactive nature.

Significance in Research

Researchers are continually investigating the properties and applications of (dimethylamino)methyl N,N-dimethylcarbamodithioate. The ongoing studies focus on:

  • Mechanism of Action: Understanding how the functional groups engage with enzymes or other biological targets.
  • Environmental Impact: Assessing its stability and breakdown in environmental settings to ensure minimal ecological disruption.

As the scientific community delves deeper into this compound’s potential, it repackages the age-old adage of chemistry: "The journey of discovery is often more significant than the destination." The exploration of such compounds is crucial for driving innovation in both chemistry and environmental science.

Synonyms
51-82-1
Carbamodithioic acid, dimethyl-, (dimethylamino)methyl ester
Dimethylaminomethyl dimethyldithiocarbamate
HSDB 5193
DIMETHYLAMINOMETHYL N,N-DIMETHYLDITHIOCARBAMATE
EINECS 200-126-8
NSC 25049
BRN 1757112
N,N-Dimethyldithiocarbamic acid dimethylaminomethyl ester
N,N-Dimethyl-dithiocarbaminsaeure-dimethylaminomethyl-ester
Carbamic acid, dimethyldithio-, (dimethylamino)methyl ester
DTXSID6058762
N,N-Dimethyl-dithiocarbaminsaeure-dimethylaminomethyl-ester [German]
(dimethylamino)methyl N,N-dimethylcarbamodithioate
Carbamic acid, dithio-, N,N-dimethyl-, dimethylaminomethyl ester
Carbamodithioic acid, N,N-dimethyl-, (dimethylamino)methyl ester
N,N-DIMETHYL-DITHIOCARBAMINSAEURE-DIMETHYLAMINOMETHYL-ESTER (GERMAN)
DTXCID1040950
WGPLCRLRYUGWKC-UHFFFAOYSA-N
NSC25049
WLN: 1N1&YUS&S1N1&1
NSC-25049
Carbamic acid, (dimethylamino)methyl ester
NS00032352
Carbamodithioic acid, (dimethylamino)methyl ester
Carbamic acid, N,N-dimethyl-, (dimethylamino)methyl ester
N,N-(Dimethyldithio)carbamic acid (dimethylamino)methyl ester
Carbamic acid, dimethyldithio-, (dimethylamino)methyl ester (8CI)