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Sucrose

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Identification
Molecular formula
C12H22O11
CAS number
57-50-1
IUPAC name
(3R,4S,5R,6R)-2-[[(2R,3S,4S,5R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl]oxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]methoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol
State
State
Sucrose is a solid at room temperature. It is typically found in a crystalline form and is often packaged as granules for ease of use in culinary applications.
Melting point (Celsius)
186.00
Melting point (Kelvin)
459.00
Boiling point (Celsius)
459.00
Boiling point (Kelvin)
732.00
General information
Molecular weight
342.30g/mol
Molar mass
342.2960g/mol
Density
1.5870g/cm3
Appearence

Sucrose is a white, crystalline solid with a sweet taste. It is commonly known as table sugar or cane sugar and is widely used as a sweetener in foods and beverages. The crystals are moderately hard and characterized by their transparent or translucent appearance.

Comment on solubility

Solubility of (3R,4S,5R,6R)-2-[[[2R,3S,4S,5R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl]oxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]methoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

The solubility of this compound, a complex polyol, can be intriguing due to its multiple hydroxyl groups which generally enhance solubility in polar solvents. Here are some considerations regarding its solubility:

  • Highly soluble in water: The presence of multiple hydroxyl (-OH) groups suggests that this compound is likely to form strong hydrogen bonds with water, leading to high solubility.
  • Solvent effects: Solubility can vary significantly depending on the nature of the solvent used. The compound may show lower solubility in non-polar solvents due to its hydrophilic character.
  • Concentration dependencies: The solubility might increase or decrease with temperature changes, which is a typical behavior for many organic compounds.
  • Impact of molecular structure: The stereochemical configuration (R and S designations) and the overall three-dimensional shape can influence how well the compound interacts with the solvent molecules.

In summary, the extensive presence of hydroxyl groups is a strong indicator that this compound will exhibit significant solubility in aqueous environments, making it potentially useful in various applications where solubility is a critical factor.

Interesting facts

Interesting Facts about (3R,4S,5R,6R)-2-[[(2R,3S,4S,5R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl]oxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]methoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

This complex compound is part of a class of chemical structures known for their biological significance and medicinal properties. Here are some intriguing aspects of this compound:

  • Stereochemistry: The compound has multiple stereocenters, contributing to a diverse array of isomers, which can have significantly different biological activities.
  • Biological Role: Compounds with similar structures are often found to exhibit activity in various biological pathways, such as antidiabetic effects, highlighting their importance in medicinal chemistry.
  • Natural Occurrence: Many complex glycosides and polyols similar to this compound are naturally occurring in plants, showcasing nature's incredible ability to synthesize intricate compounds with essential functions.
  • Therapeutic Potential: The hydroxymethyl and hydroxy groups in the structure suggest potential interactions with enzymes and receptors in the human body, which can lead to the development of new therapeutic agents.

As a fascinating example of the interplay between structure and function in chemistry, this compound serves as a reminder of how tiny structural differences can lead to vast differences in biological activity. As one chemistry student aptly noted, “Understanding complex molecules like this one is crucial to unlocking the secrets of nature’s pharmacopoeia.” This demonstrates the essential role of structural chemistry in developing new drugs and understanding biochemical processes.

Synonyms
CHEMBL1203920
SCHEMBL33744
CHEMBL175500
CHEBI:181444
MUPFEKGTMRGPLJ-BQCSWRFHSA-N
6227-50-5
BDBM50377970
MFCD00006630
AKOS016009348
(3R,4S,5R,6R)-2-[[(2R,3S,4S,5R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol