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D-Glucuronic acid

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Identification
Molecular formula
C6H10O7
CAS number
6556-12-7
IUPAC name
2,3,4,5,6-pentahydroxycyclohexanone
State
State
Solid at room temperature.
Melting point (Celsius)
164.00
Melting point (Kelvin)
437.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
194.14g/mol
Molar mass
194.1390g/mol
Density
1.8355g/cm3
Appearence

The compound is a crystalline solid. It is typically white in appearance when pure and may appear as a powder or in granule form. It is soluble in water, resulting in a clear solution.

Comment on solubility

Solubility of 2,3,4,5,6-Pentahydroxycyclohexanone

The solubility of 2,3,4,5,6-pentahydroxycyclohexanone (C6H10O7) is notably influenced by its polar hydroxyl (-OH) groups. These functional groups enhance interactions with water molecules, leading to its favorable solubility in aqueous environments. Here are key points about its solubility:

  • Highly Soluble in Water: The presence of five hydroxyl groups promotes hydrogen bonding with water, making it highly soluble.
  • Influence of Structure: The cyclic structure of the compound contributes to its stability in solution but does not hinder its solubility due to the numerous hydroxyls available for interaction.
  • Comparison with Similar Compounds: Compared to other sugars or polyols, 2,3,4,5,6-pentahydroxycyclohexanone exhibits a solubility profile that aligns closely with carbohydrates where multiple hydroxyls facilitate dissolution.

In summary, due to its significant number of hydroxyl groups, 2,3,4,5,6-pentahydroxycyclohexanone is expected to have a high solubility in polar solvents like water, making it a versatile compound in various chemical applications.

Interesting facts

Interesting Facts about 2,3,4,5,6-Pentahydroxycyclohexanone

2,3,4,5,6-pentahydroxycyclohexanone, often referred to as a sugar alcohol, is a fascinating compound with several intriguing characteristics:

  • Polyol Structure: This compound is notable for its unique arrangement of hydroxyl (-OH) groups, which are found at five different positions on the cyclohexanone ring. This configuration significantly impacts its chemical properties and reactivity.
  • Natural Occurrence: Pentahydroxycyclohexanone can be derived from various natural sources, including certain types of algae and plant materials. This link to nature has piqued the interest of researchers in both organic chemistry and biochemistry.
  • Health Implications: As a polyol, pentahydroxycyclohexanone has been studied for its potential applications as a sweetener. Its lower caloric content compared to traditional sugars makes it a candidate for sugar substitutes in the food industry.
  • Research and Applications: The compound is under investigation for use in pharmaceuticals and cosmetics. Its multiple hydroxyl groups can help improve the solubility and stability of various formulations.
  • Importance in Synthesis: Scientists often utilize this compound as an intermediate in synthesizing more complex organic molecules, showcasing its importance in chemical manufacturing.

In summary, 2,3,4,5,6-pentahydroxycyclohexanone is not just a simple molecule but a compound filled with **possibilities** and **potential** in various scientific fields. Its interplay between chemistry, health, and natural processes exemplifies the interconnectedness of science.

Synonyms
2,3,4,5,6-Pentahydroxycyclohexanone
2,3,4,5,6-pentahydroxycyclohexan-1-one
NSC55548
EPIINOSOSE-2
6623-68-3
NSC55553
488-66-4
myo-Inonosose
epi-Inosose-2
2,3,4,5,6-Pentahydroxy-cyclohexanone
MYOINOSOSE-2
MYOINOSOSE (D)
MYOINOSOSE (L)
CHEMBL341959
SCHEMBL1681832
SCHEMBL12834922
DTXSID60964119
NSC55547
NSC55559
NSC-55547
NSC-55548
NSC-55553
NSC-55559
DS-003483