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Thiram

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Identification
Molecular formula
C6H12N2S4
CAS number
137-26-8
IUPAC name
dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate
State
State
Solid at room temperature.
Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
130.00
Boiling point (Kelvin)
403.15
General information
Molecular weight
240.44g/mol
Molar mass
240.4360g/mol
Density
1.2900g/cm3
Appearence
Thiram is a pale yellow or tan powder with a faint odor. It is usually found as a crystalline solid.
Comment on solubility

Solubility of Dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate

The solubility characteristics of dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate can provide valuable insights into its behavior in various environments. Generally, compounds like this one, which contain multiple alkyl groups and sulfur functionalities, may exhibit specific solubility traits:

  • Solvent compatibility: This compound is likely to be soluble in organic solvents due to its long alkyl chains.
  • Water solubility: It is expected to have limited solubility in water because of hydrophobic interactions from the dibutyl groups.
  • Temperature effects: Solubility might increase with temperature, potentially aiding in its application in various chemical processes.
  • pH influence: Alteration of pH can affect solubility; compounds with thiol or thiolate groups can show variations in solubility depending on acidity or basicity.

As with many organosulfur compounds, its solubility profile could also give us hints about its reactivity and interaction mechanisms in environmental or industrial contexts. Remember, solubility can vary widely based on factors such as purity, aggregation state, and the presence of other solutes. Understanding the solubility fundamentals of dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate is essential for utilizing it effectively in various applications.

Interesting facts

Dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate

Dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate is a fascinating compound that falls into the category of thiocarbonyl compounds. This unique class of compounds features sulfur within its functional groups, imparting characteristic properties and reactivity.

Key Features and Applications

  • Organosulfur Chemistry: The presence of sulfur in its structure makes this compound significant in organosulfur chemistry, a field that explores the diverse roles of sulfur-containing molecules.
  • Potential Agrochemical Use: Compounds similar to dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate have been studied for their applications in agriculture, particularly as pesticides or herbicides.
  • Lead Research Analogs: Scientists often use such dithiocarbamate derivatives as key analogs in research, investigating their biological activity and potential medicinal properties.

“The study of organosulfur compounds opens pathways to understanding new reaction mechanisms and developing innovative therapeutic agents.”

Chemical Properties

This compound's unique chemical structure allows for interesting interactions with various reagents, potentially leading to different synthetic pathways and applications. In particular, the dithiocarbamate moiety is known for its ability to engage in ligand formation with metal ions, expanding its utility in coordination chemistry.

Overall, dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate is more than just a compound; it's a gateway to exploring the rich area of sulfur chemistry and its significant implications in both industrial and biological contexts.

Synonyms
Tetrabutylthiuram disulfide
TETRA-N-BUTYLTHIURAM DISULFIDE
Tetrabutylthiuram disulphide
Thiuram disulfide tetrabutyl
DISULFIDE, BIS(DIBUTYLTHIOCARBAMOYL)
Thiuram, tetrabutyl-, disulfide
Tetrabutylthioperoxydicarbamic acid
Bis(dibutylthiocarbamoyl) disulfide
Thioperoxydicarbonic diamide ([(H2N)C(S)]2S2), N,N,N',N'-tetrabutyl-
NSC 677476
Butyl tuads
EINECS 216-652-6
UNII-D969886EAB
BRN 1715575
DTXSID6049226
D969886EAB
NSC-677476
Thioperoxydicarbonic diamide, tetrabutyl-
DTXCID2029082
Thioperoxydicarbonic diamide (((H2N)C(S))2S2), tetrabutyl-
4-04-00-00595 (Beilstein Handbook Reference)
Thioperoxydicarbonic diamide (((H2N)C(S))2S2), N,N,N',N'-tetrabutyl-
Tetrabutyl thioperoxydicarbonic diamide
Thioperoxydicarbonic diamide ([(H2N)c(S)]2S2), tetrabutyl-
Methanethioamide, 1,1'-dithiobis[N,N-dibutyl-
METHANETHIOAMIDE, 1,1'-DITHIOBIS(N,N-DIBUTYL-
Thiuram, tetrabutyl, disulfide
Thioperoxydicarbonic diamide (((H2N)C(S))2S2), tetrabutyl
Thioperoxydicarbonic diamide (((H2N)C(S))2S2), N,N,N',N'tetrabutyl
pgaxjqvahdtgbb-uhfffaoysa-n
1634-02-2
dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate
Zinc ionophore I
tetra-n-butylthiuramdisulfide
CHEMBL333177
NSC-67746
NSC677476
MFCD00027191
SCHEMBL24804
Bis-(dibutylthiocarbamoyl) disulfide
Tox21_202809
BDBM50570514
AKOS015839733
NCGC00260355-01
LS-14693
CAS-1634-02-2
NS00025335
T0635
E78822
Zinc ionophore I, Selectophore(TM), function tested
Q27276262
THIOPEROXYDICARBONIC DIAMIDE (((H2N)C(S))2S2), N,N,N',N'- TETRABUTYL-