Sulfuric acid, monoester with α-D-glucopyranose

Identification

Molecular formula

C₆H₁₃NO₈S

CAS number

56038-13-2

IUPAC name

[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid

State

The compound is a solid at room temperature. It is stable under normal conditions but decomposes upon heating.

Melting point (Celsius)

122.00

Melting point (Kelvin)

395.00

Boiling point (Celsius)

0.00

Boiling point (Kelvin)

0.00

General information

Molecular weight

221.22g/mol

Molar mass

221.2180g/mol

Density

1.6500g/cm³

Appearence

The compound typically appears as a white crystalline solid. It is a colorless and odorless powder that is soluble in water. It has a sweet taste and is commonly used as an artificial sweetener in a variety of food and beverage products.

Comment on solubility

Solubility of [2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid

The solubility of [2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid (C₆H₁₃NO₈S) can be characterized as follows:

General solubility trend: This compound is likely to exhibit decent solubility in polar solvents due to the presence of multiple hydroxyl groups (-OH) that can form hydrogen bonds with water molecules.
Hydrophilicity: The structure contains several hydroxyl functional groups, which significantly increases its hydrophilicity.
Aqueous solubility: It is expected to be soluble in water, allowing it to participate in reactions in an aqueous environment.
Influence of pH: The solubility might also vary with pH changes, as sulfonic acid groups are known to be more soluble under acidic conditions.

Overall, the solubility characteristics of this compound suggest that it can be effectively utilized in various aqueous systems, enhancing its applicability in different chemical processes.

Interesting facts

Interesting Facts about [2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid

[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid, often encountered in biochemical studies, is a fascinating compound for various reasons:

Biological Relevance: This compound acts as a sulfamic acid derivative, which is essential in modifying biological molecules. Its structure suggests potential roles in carbohydrate chemistry and enzyme interactions.
Functional Groups: The presence of multiple hydroxyl groups contributes to its hydrophilicity, allowing it to participate effectively in hydrogen bonding, which may enhance its interactions in aqueous environments.
Potential Applications: Due to its unique structural features, this compound may be investigated for its use as a pharmaceutical intermediate or in synthetic organic chemistry, particularly in creating more complex molecules.
Research Opportunities: Scientists may explore its effects on biological systems, especially in regard to glycosylation processes where similar compounds exhibit significant biological activity.
Historical Context: Sulfamic acids have been studied since the early 19th century. Their derivatives continue to intrigue chemists, paving the way for innovative applications in industry and medicine.

In summary, the multifaceted aspects of [2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]sulfamic acid make it an intriguing subject for further exploration within the realms of organic and medicinal chemistry. As we continue to delve deeper into its properties and potential uses, this compound stands as a testament to the complexity and elegance of chemical science.

Synonyms

2-deoxy-2-sulfoaminohexose

ZINC03869699