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Identification
Molecular formula
C11H25ClN2
CAS number
4637-24-5
IUPAC name
2-(1,1,3,3-tetramethylbutyl)guanidine;hydrochloride
State
State

The compound is a solid at room temperature.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.00
Boiling point (Celsius)
264.60
Boiling point (Kelvin)
537.80
General information
Molecular weight
221.79g/mol
Molar mass
221.7700g/mol
Density
1.0430g/cm3
Appearence

2-(1,1,3,3-Tetramethylbutyl)guanidine hydrochloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(1,1,3,3-tetramethylbutyl)guanidine;hydrochloride

The solubility of 2-(1,1,3,3-tetramethylbutyl)guanidine;hydrochloride can be characterized by several key points:

  • Solvent Interaction: This compound tends to be more soluble in polar solvents such as water due to the presence of the guanidine group, which can form hydrogen bonds.
  • Temperature Dependency: Like many salts, its solubility can increase with temperature. An increase in temperature generally enhances the dissolution process.
  • Concentration Effects: When dissolved, there is a limit to its solubility. Beyond this point, the solution may become supersaturated, leading to precipitation.
  • Ionic Considerations: The hydrochloride form indicates the presence of chloride ions, which can also influence solubility and stability in solution.

In conclusion, the solubility behavior of 2-(1,1,3,3-tetramethylbutyl)guanidine;hydrochloride is predominantly influenced by its ionic nature, solvent interactions, and environmental conditions. Understanding these factors can provide deeper insights into its application in various scientific settings.

Interesting facts

Interesting Facts about 2-(1,1,3,3-Tetramethylbutyl)guanidine Hydrochloride

2-(1,1,3,3-Tetramethylbutyl)guanidine hydrochloride is a fascinating compound, particularly noted for its unique structure and applications in various fields. This compound is categorized as a guanidine derivative, which positions it within a class of compounds known for their biological activity and potential medicinal properties.

Key Features

  • Biological Activity: Guanidine derivatives are often explored for their roles in biological systems, including the regulation of insulin and other metabolic processes.
  • Structure-Activity Relationship: The incorporation of bulky groups, such as the tetramethylbutyl moiety, enhances the compound's activity by affecting its interaction with biological targets.
  • Industrial Applications: This compound may serve as an intermediate in the synthesis of various agrochemicals and pharmaceuticals due to the functional versatility of guanidine chemistry.

Fun Facts

  • The guanidine group is known for its strong basicity, which can be both a blessing and a curse in synthesis.
  • Compounds like this one are actively being researched for their potential as new therapeutic agents, particularly in managing diabetes and obesity.

Researchers often say that "understanding the structure of a compound is key to unlocking its potential." In the case of 2-(1,1,3,3-tetramethylbutyl)guanidine hydrochloride, its sophisticated structure provides insights into its functionality in various chemical processes.

As scientists continue to explore the vast realm of guanidine derivatives, this compound stands out as a promising candidate for further investigation, balancing intricate chemistry with practical applications.

Synonyms
GUANOCTINE HYDROCHLORIDE
1070-95-7
Guanoctine HCl
A-7283
BP-1184
Guanoctine hydrochloride [USAN]
Guanidine, (1,1,3,3-tetramethylbutyl)-, monohydrochloride
UNII-Z1B7625421
(1,1,3,3-Tetramethylbutyl)guanidine monohydrochloride
Guanoctine hydrochloride (USAN)
Z1B7625421
DTXSID90147872
DTXCID5070363
1-(2,4,4-Trimethylpentan-2-yl)guanidine hydrochloride
2-(2,4,4-trimethylpentan-2-yl)guanidine;hydrochloride
BP 1184
starbld0001534
A 7283
SCHEMBL121121
CHEMBL2107664
AKOS040748498
D04387
Q27294868