Skip to main content

N-Nitroso-N-methyl-D-glucamine

ADVERTISEMENT
Identification
Molecular formula
C8H16N2O8
CAS number
null
IUPAC name
1-methyl-1-nitroso-3-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]urea
State
State

At room temperature, N-Nitroso-N-methyl-D-glucamine is a solid. It is generally encountered as a dry powder, bearing the typical characteristics of organic solid compounds, such as crystalline structure.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
236.20g/mol
Molar mass
236.1990g/mol
Density
1.6850g/cm3
Appearence

N-Nitroso-N-methyl-D-glucamine typically appears as a crystalline solid, often presenting as a white to off-white powder. Its form can be influenced by its degree of purity and any related substances it might be crystallized with.

Comment on solubility

Solubility of 1-methyl-1-nitroso-3-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]urea

The compound 1-methyl-1-nitroso-3-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]urea, with the chemical formula C8H16N2O8, displays interesting solubility characteristics due to its unique structural components. This compound contains multiple hydroxyl (-OH) groups, which are known to enhance solubility in polar solvents.

Key aspects of its solubility include:

  • High polar character: The presence of several hydroxyl groups suggests that the compound is likely to be soluble in water and other polar solvents.
  • Hydrogen bonding: The hydroxyl groups can engage in hydrogen bonding with solvent molecules, which greatly increases solubility.
  • Potential for variable solubility: Depending on the specific solvent and conditions (such as temperature), the degree of solubility may vary significantly.
  • Moderate stability: The compound's solubility may also be influenced by its ability to remain intact in solution without undergoing degradation.

In conclusion, while specific data on the solubility of this compound may be limited, we can infer its likely solubility trends based on its functional groups and molecular structure. As always, empirical testing is needed to confirm these hypotheses in practical applications.

Interesting facts

Interesting Facts About 1-methyl-1-nitroso-3-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]urea

This compound, known for its complex structure and fascinating properties, belongs to a unique class of organic chemicals. It serves as an excellent topic of study within medicinal and organic chemistry. Here are some noteworthy aspects of this intriguing compound:

  • Role in Research: The compound has been investigated for its potential applications in drug development, particularly due to its ability to interact with biological systems in novel ways.
  • Hydroxymethyl Groups: The presence of multiple hydroxymethyl groups in its structure is significant. These functional groups can enhance the compound's solubility and reactivity, making it a versatile candidate for various synthetic reactions.
  • Tetrahydropyran Ring: The inclusion of a tetrahydropyran moiety contributes to the compound's cyclic structure, which can impact its conformational properties. This cyclic nature may affect how it interacts with enzymes or receptors in biological systems.
  • Biological Activity: Preliminary studies suggest that this compound might exhibit interesting biological activities. Its nitroso group can potentially donate nitric oxide, a signaling molecule that plays crucial roles in numerous physiological processes.
  • Potential in Agriculture: Some derivatives of compounds similar to this may have applications in agriculture, particularly as plant growth regulators or in pest control.

In summary, 1-methyl-1-nitroso-3-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]urea presents numerous avenues for exploration in both medicinal chemistry and related fields. As the journey into its study continues, many exciting discoveries are likely to emerge, showcasing the compound's functional diversity.

Synonyms
streptozocin
STREPTOZOTOCIN
18883-66-4
Streptozotocin;U 9889
CHEMBL163484
SCHEMBL18402588
DTXSID50860232
HMS3268I11
HMS3654F15
HMS3871H13
NSC236997
NSC-236997
LS-13492
SY066622
2-deoxy-2-{[methyl(nitroso)carbamoyl]amino}hexopyranose