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Benzylmethylcarbamimidoylmethylammonium sulfate

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Identification
Molecular formula
C11H19N3O4S
CAS number
93820-07-6
IUPAC name
(N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium;sulfate
State
State

At room temperature, the compound is typically in a solid state. It may dissolve in water, forming a clear or slightly opalescent solution due to the presence of its sulfate component. The compound may exhibit hygroscopic properties.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
256.34g/mol
Molar mass
256.3000g/mol
Density
1.2000g/cm3
Appearence

The compound usually appears as a white to off-white crystalline powder. It is often sold in its salt form with a sulfate anion, contributing to its stability and solubility in water. It may appear slightly opaque and becomes clumpy if exposed to moisture.

Comment on solubility

Solubility of (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium sulfate

The solubility of (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium sulfate can be quite intriguing due to its unique structural composition. This compound, which features an organic ammonium cation coupled with a sulfate anion, displays specific solubility characteristics influenced by several factors:

  • Polar Nature: The presence of the sulfate ion, which is highly polar, often leads to increased solubility in polar solvents such as water. Organic ammonium salts are generally soluble due to their ability to interact favorably with water molecules.
  • Hydrogen Bonding: The potential for hydrogen bonding between the compound and water can enhance solubility, as the functional groups in the ammonium part can donate and accept hydrogen bonds, promoting a favorable solvation environment.
  • Concentration Factors: As with many salts, the solubility can also be affected by concentration. In some cases, increased concentrations can lead to saturation and precipitation, making it essential to understand the equilibrium in solution.
  • Temperature Dependence: Typically, solubility is also a function of temperature; many salts become more soluble with increasing temperatures, although specific behavior can vary.

In summary, the solubility of (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium sulfate is largely dictated by its polar nature, potential for hydrogen bonding, and external conditions such as concentration and temperature. Therefore, one can expect this compound to show reasonable solubility in polar solvents like water, making it accessible for various applications.

Interesting facts

Interesting Facts about (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium; sulfate

The compound (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium; sulfate is a fascinating example of a synthetic chemical that plays a significant role in various fields, particularly in pharmaceuticals and research applications. Here are some noteworthy points to consider:

  • Structure and Functionality: This compound features a complex organic structure that allows for *multi-functionality*. The presence of the benzyl and methyl groups contributes to its unique properties.
  • Biological Relevance: Compounds structurally similar to this one are often explored for their potential in medications and therapeutic interventions. Researchers study its interactions in biological systems to devise new treatments.
  • Research Utility: Due to its diverse functional groups, it can be used as a building block in organic synthesis and chemical research, aiding scientists in the development of more complex compounds.
  • Industry Applications: This compound may find applications in the chemical industry, particularly in the production of agricultural chemicals or in catalysis due to its ammonium group.
  • Collaboration with Other Chemicals: The sulfate component often enhances the solubility and *stability* of the compound in various solvents, making it valuable in formulating products.

In summary, (N-benzyl-N'-methyl-carbamimidoyl)-methyl-ammonium; sulfate presents an intriguing subject for ongoing research and application in various fields. Its versatility and potential underscore the importance of studying compounds that, on the surface, may appear complicated but hold immense promise for innovation and development.

Synonyms
Bethanidine sulfate
Benzanidine
Bendogen
Bentanidol
Benzaidin
Benzanidin
Benzoxine
Betaling
Esbatal
Eusmanid
Hypersin
Tenathan
Batel
Bethanidine, hemisulfate
Bethanidine sulfate [USAN]
EINECS 204-056-9
UNII-J4THI5N7O2
BW 467 C-60
1-Benzyl-2,3-dimethylguanidinium sulfate
N-Benzyl-N',N''-dimethylguanidine sulfate
N-Benzyl-N',N''-dimethylguanidine sulphate
1-Benzyl-2,3-dimethylguanidine sulfate (1:(12))
N,N-Dimethyl''-(phenylmethyl)guanidine sulphate (2:1)
Guanidine, N,N'-dimethyl-N''-(phenylmethyl)-, sulfate (2:1)
1-Benzyl-2,3-dimethylguanidine sulfate (1:1/2)
114-85-2
GUANIDINE, 1-BENZYL-2,3-DIMETHYL-, SULFATE(2:1)
BW-467-C-60
NCGC00183050-01
Tenathan (TN)
1-Benzyl-2,3-dimethylguanidinium sulphate (2:1)
Bethanidine sulfate (JAN/USAN)
Guanidine, N,N'-dimethyl-N'-(phenylmethyl)-, sulfate (2:1)
D01603