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Methyl 2,3,4,5,6-pentahydroxyhexylcarbamodithioic acid

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Identification
Molecular formula
C8H15NO6S2
CAS number
12221-49-5
IUPAC name
methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic acid
State
State

The compound is typically a solid at room temperature. It can be crystallized from solutions as necessary for analytical or synthetic purposes.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
240.29g/mol
Molar mass
240.2900g/mol
Density
1.8000g/cm3
Appearence

The compound typically appears as a solid at room temperature. It may be colorless or have a slight yellowish tint, depending on the purity and specific preparation method.

Comment on solubility

Solubility of Methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic Acid

The solubility characteristics of methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic acid (C8H15NO6S2) are notable due to its unique molecular structure, which features multiple hydroxy (-OH) groups. These hydroxyl groups significantly influence the compound's interactions with solvents.

Key Points on Solubility:

  • Hydrophilicity: The presence of five hydroxyl groups suggests a strong potential for hydrophilic behavior, making the compound likely soluble in water.
  • Polarity: The overall polarity, attributed to the -OH groups and the carbamodithioic acid moiety, enhances solubility in polar solvents.
  • Solvent Interaction: According to common solubility rules, molecules with multiple polar functional groups tend to have better solubility in polar solvents like water, while being less soluble in non-polar solvents.
  • Table of Solubility:
    • Highly soluble in: Water, Ethanol
    • Poorly soluble in: Hexane, Benzene

In summary, methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic acid is expected to be primarily soluble in water and other polar solvents due to its extensive hydroxyl functionalization. Understanding these solubility properties can aid in various applications and reactions involving this compound.

Interesting facts

Interesting Facts about Methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic Acid

Methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic acid is a fascinating compound with several unique characteristics and applications in the field of chemistry. Here are some intriguing facts that highlight its significance:

  • Structure Complexity: This compound contains a hexyl chain with multiple hydroxyl groups, specifically five, which significantly enhances its reactivity and solubility in various environments.
  • Functional Groups: The presence of both dithiocarbamate and hydroxyl functionalities makes it versatile for various chemical transformations, making it a subject of interest for organic synthesis.
  • Biological Relevance: Compounds with similar structures have demonstrated biological activity, potentially functioning in detoxification or as agents for heavy metal ion chelation in biological systems.
  • Potential Applications: Given its structural attributes, this compound may find use in fields such as pharmaceuticals, agricultural chemicals, and materials science. Researchers are exploring its properties for possible uses in drug delivery systems and as anti-cancer agents.
  • Research Opportunities: Its complex nature provides a rich area for study, particularly in understanding the behavior of multi-functionalized compounds in chemical reactions and their interactions within biological systems.

In the words of chemist Robert H. Grubbs, "Innovation is the key to progress in chemistry," and compounds like methyl(2,3,4,5,6-pentahydroxyhexyl)carbamodithioic acid exemplify this spirit by pushing the boundaries of traditional chemistry.

Overall, this compound opens up a myriad of possibilities for research and application, prompting scientists to uncover the depth of its properties and potential uses.

Synonyms
MDCG
SCHEMBL12359360