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Disodium Lauryl Sulfate

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Identification
Molecular formula
C12H26Na2O4S
CAS number
151-21-3
IUPAC name
disodium;(2-chlorophenyl)methyl-[9-[(2-chlorophenyl)methylammonio]nonyl]ammonium
State
State

At room temperature, Disodium Lauryl Sulfate is typically a solid state. It can be stored in its crystalline powder or fine granular form under standard conditions.

Melting point (Celsius)
206.00
Melting point (Kelvin)
479.00
Boiling point (Celsius)
373.00
Boiling point (Kelvin)
646.00
General information
Molecular weight
288.37g/mol
Molar mass
288.3720g/mol
Density
1.0400g/cm3
Appearence

Disodium Lauryl Sulfate (DLS) appears as a white or off-white powder. It is usually crystalline in nature and can also be found in the form of fine granules. The compound is known for its surfactant properties and is commonly used in several industrial applications including detergents.

Comment on solubility

Solubility of Disodium (2-chlorophenyl)methyl-[9-[(2-chlorophenyl)methylammonio]nonyl]ammonium

The solubility of the compound disodium (2-chlorophenyl)methyl-[9-[(2-chlorophenyl)methylammonio]nonyl]ammonium can be quite intriguing, particularly given its complex structure. Here's a deeper look into its solubility characteristics:

  • General Solubility: Compounds with ammonium groups, especially when they are quaternary amines or modified amines like this, tend to exhibit better solubility in polar solvents due to their ionic nature.
  • Influence of Substituents: The presence of chlorophenyl groups can also impact solubility. In general, chlorinated compounds can vary in solubility depending on the overall molecular framework.
  • Solvent Compatibility: This compound is likely to be soluble in aqueous solutions, particularly because the disodium nature contributes to ionic interactions in water.
  • Temperature Effects: As with many compounds, increased temperature may enhance solubility, allowing for more effective interactions with solvent molecules.

In essence, while the core attributes point towards favorable solubility in polar solvents, experimenting with different solvent systems and temperatures would provide valuable insights into its overall solubility behavior.

Interesting facts

Interesting Facts about Disodium (2-Chlorophenyl)methyl-[9-[(2-chlorophenyl)methylammonio]nonyl]ammonium

This compound, often referred to by its more simplified names in various contexts, presents an intriguing case study in the world of synthetic chemistry.

Here are some notable aspects of this compound:

  • Ammonium Compounds: As a quaternary ammonium compound, it exhibits unique surfactant properties, making it useful in various industrial applications, including detergents and disinfection.
  • Dual Chlorine Substituents: The presence of two chlorine atoms on the phenyl groups enhances its lipophilicity, potentially increasing its efficacy in penetrating biological membranes.
  • Pharmaceutical Relevance: Interestingly, compounds like this one are often explored in medicinal chemistry for their abilities to modulate cellular activities or serve as drug delivery systems.
  • Synthesis Challenges: The multi-step synthesis of this compound requires careful execution of reactions, and each step must be monitored closely to ensure purity and yield, which is a real challenge for synthetic chemists.
  • Binary Interactions: In biological contexts, this compound may interact with various cellular receptors, making it a valuable subject for understanding drug-receptor interactions.

As noted in an outreach program for budding chemists, "The beauty of chemistry lies not just in its principles but in the stories that compounds like these tell about innovation and discovery." This compound exemplifies how complex structures can lead to revolutionary advancements in chemistry.

Continued research on compounds similar to this one can further illuminate their potential applications, making them a significant focus in both academic research and practical applications.

Synonyms
2056-23-7
NONAMETHYLENEDIAMINE, N,N'-BIS(o-CHLOROBENZYL)-, DIHYDROCHLORIDE
N,N'-Nonamethylenebis(2-chlorobenzylamine) dihydrochloride
N,N'-Bis(o-chlorobenzyl)nonamethylenediamine dihydrochloride
1,9-Nonanediamine, N,N'-bis(o-chlorobenzyl)-, dihydrochloride
Benzylamine, N,N'-nonamethylenebis(2-chloro-, dihydrochloride
DTXSID30174561
DTXCID3097052