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Diethylcarbamodithioic acid

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Identification
Molecular formula
C3H7NS2
CAS number
105-55-5
IUPAC name
diethylcarbamodithioic acid
State
State

In its typical form, diethylcarbamodithioic acid is a liquid at room temperature. It may occasionally present as a viscous or oily substance, contingent on the given environmental conditions.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.20
Boiling point (Celsius)
158.90
Boiling point (Kelvin)
432.10
General information
Molecular weight
149.27g/mol
Molar mass
149.2730g/mol
Density
1.0186g/cm3
Appearence

Diethylcarbamodithioic acid is typically a yellow to brown liquid. It may have a viscous texture and is often oily in nature. The color and consistency can vary depending on the purity and specific sample.

Comment on solubility

Solubility of Diethylcarbamodithioic Acid

Diethylcarbamodithioic acid, represented by the chemical formula C5H11N2S2O2, offers interesting insights into its solubility characteristics. It is known for being a polar compound, which significantly influences its solubility in various solvents.

In general, the solubility of diethylcarbamodithioic acid can be summarized as follows:

  • Water Solubility: The presence of polar functional groups in the molecule allows for decent solubility in water, making it suitable for applications in aqueous environments.
  • Organic Solvents: It is also soluble in many organic solvents such as alcohols and ethers, further expanding its usability in chemical reactions.
  • Temperature Dependency: As with many chemicals, the solubility can vary with temperature; typically, increased temperature results in increased solubility.

According to solubility principles, "like dissolves like", which explains why diethylcarbamodithioic acid finds solubility in polar solvents. However, it may exhibit limited solubility in non-polar solvents due to its polar nature.

Overall, the solubility of diethylcarbamodithioic acid is influenced by its molecular structure, imparting it with versatile characteristics for both laboratory and industrial applications.

Interesting facts

Interesting Facts about Diethylcarbamodithioic Acid

Diethylcarbamodithioic acid, often known for its role as a ligand in coordination chemistry, presents a fascinating area of study. This compound is particularly noteworthy for its ability to form stable complexes with various metals, making it an essential player in different catalytic processes and agricultural applications.

Key Features

  • Ligand Properties: The unique structure of diethylcarbamodithioic acid allows it to act effectively as a bidentate ligand, meaning it can bond to a metal ion through two sites, enhancing the stability of metal complexes.
  • Stability and Reactivity: The reactivity profile of this compound provides insights into its potential applications in organic synthesis and its role in environmental chemistry.
  • Biological Significance: Studies have indicated that compounds like diethylcarbamodithioic acid can exhibit biological activity, including possible effects on plant growth and development.
  • Analytical Applications: It is also employed in certain analytical techniques, illustrating its versatility beyond mere chemical reactions.

As a chemistry student, examining diethylcarbamodithioic acid can lead to a deeper understanding of complexation, ligand theory, and the significance of sulfur-containing compounds in both industrial and environmental contexts. Its dual role in enhancing catalytic efficiency while providing insightful chemical interactions exemplifies the intricate dance of atoms that defines this fascinating field.

Thought to Ponder

As you explore this compound, consider the quote: "The beauty of chemistry lies in its ability to bring together seemingly unrelated elements to form something uniquely powerful." This encapsulates the essence of diethylcarbamodithioic acid's contributions to modern science.

Synonyms
Diethyldithiocarbamic acid
Ditiocarb
Diethylcarbamodithioic acid
147-84-2
Diethyl dithiocarbamate
Carbamodithioic acid, diethyl-
Diethyldithiocarbamate
Diethyldithione
Carbamic acid, diethyldithio-
Dithiocarb
Imuthiol
CCRIS 7364
EINECS 205-701-7
n,n-diethyldithiocarbamic acid
BRN 1747741
DIETHANOL-DITHIOCARBAMATE
diethyl-dithiocarbamate
Carbamodithioic acid, N,N-diethyl-
diethyl[sulfanyl(carbonothioyl)]amine
UNII-99Z2744345
DITIOCARB [WHO-DD]
N,N-diethylcarbamodithioic acid
DTXSID3045017
N,N-diethyldithiocarbamate
CHEBI:144353
4-04-00-00389 (Beilstein Handbook Reference)
Diethyldithiocarbamate, sodium
Cupral
Dieca
99Z2744345
DETC
Ditiocarb, Zinc Salt
diethyl(sulfanyl(carbonothioyl))amine
NSC4857
CHEBI:144359
NSC38583
Sodium Salt Ditiocarb
NCGC00166328-01
Diethyldione
4olc
ditiocarb-sodium-trihydrate
CHEMBL961
Diethyldithiocarbaminic acid
NCIMech_000185
SCHEMBL48382
Diethylcarbamodithioic acid #
DTXCID1025017
Diethyldithiocarbamic acid (DDC)
BDBM50428474
CCG-35356
AKOS006230661
DB02520
NCGC00166328-02
NCI60_004156
HY-126363
CS-0103019
NS00007744
C19150
EN300-7125024
SR-01000944438
SR-01000944438-1
BRD-K40654626-236-01-5
Q27093504