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Sucrose

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Identification
Molecular formula
C12H22O11
CAS number
57-50-1
IUPAC name
2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol
State
State

At room temperature, sucrose is a solid, crystalline compound.

Melting point (Celsius)
186.00
Melting point (Kelvin)
459.15
Boiling point (Celsius)
186.00
Boiling point (Kelvin)
459.15
General information
Molecular weight
342.30g/mol
Molar mass
342.2970g/mol
Density
1.5870g/cm3
Appearence

Sucrose appears as a white, odorless, crystalline powder with a sweet taste. It is highly soluble in water.

Comment on solubility

Solubility Analysis of 2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol

The compound 2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol, with the chemical formula C12H22O11, exhibits notable solubility characteristics primarily due to its extensive hydroxyl (-OH) groups.

Key Highlights of Solubility:

  • Hydrophilic Nature: The presence of multiple hydroxyl groups significantly enhances the compound's affinity for water, promoting solubility in aqueous environments.
  • Polarity: With a substantial number of polar functional groups, the compound interacts favorably with water molecules, forming hydrogen bonds.
  • Dissolution Dynamics: This compound tends to dissolve readily at ambient temperatures, making it a suitable candidate for applications in various solutions or formulations.
  • Concentration Influences: While soluble, the solubility may vary depending on concentration; lower concentrations typically result in better solubility.

In summary, the solubility of 2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol can be considered significant due to its molecular structure, characterized by a balance of hydrophilic interactions. This makes it particularly relevant in fields such as pharmaceuticals or biochemistry where solubility plays a crucial role in functionality and efficacy.

Interesting facts

2-(Hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol: An Exploration

2-(Hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol, often referred to as a complex carbohydrate, is a fascinating compound with a variety of interesting properties. This compound possesses a unique structural architecture that allows it to play significant roles in both biological systems and potential applications.

Key Features:

  • Complexity: The compound consists of multiple hydroxymethyl groups and tetrahydropyran rings, making it structurally intricate. This complexity contributes to its biological activity and interaction with other molecules.
  • Biological Relevance: Compounds that resemble sugar structures often exhibit interactions with various biological systems. This compound may function in signaling pathways, cellular recognition, and metabolism.
  • Potential Applications: Investigating such compounds can lead to advancements in pharmacology, particularly in drug design that targets specific biological pathways or receptors.
  • Research Interest: The presence of multiple hydroxyl groups suggests strong potential for hydrogen bonding, which is a focal point in studies related to molecular interactions and thermodynamics.

As a scientist or chemistry student, delving into the properties of this compound emphasizes the importance of sugar-like molecules. The intricate interactions at play not only advance our understanding of biochemical processes but also inspire future innovations in synthetic chemistry.

In summary, the exploration of 2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-3,4,5-triol invites intrigue and excitement in the field of chemistry, demonstrating how complex structures lead to a deeper understanding of nature and technology.

Synonyms
1174299-27-4
2-(hydroxymethyl)-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxane-3,4,5-triol
.alpha.-D-Glucopyranoside, .alpha.-D-glucopyranosyl
2-(hydroxymethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol
NSC2093
a,b-Trehalose
alpha-D-Glucopyranoside, alpha-D-glucopyranosyl
.alpha.-Trehalose
.alpha.-D-Trehalose
Hexopyranosyl hexopyranoside
Trehalose, alpha,alpha'-
.alpha.,.alpha.-Trehalose
2-(Hydroxymethyl)-6-((3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy)oxane-3,4,5-triol
2-(hydroxymethyl)-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyoxane-3,4,5-triol
D(+)-Trehalose anhydrous
SCHEMBL137621
DTXSID40859175
HDTRYLNUVZCQOY-UHFFFAOYSA-N
BCP07695
ZWB29927
SB19117
|A-D-Glucopyranosyl-|A-D-glucopyranoside
SY009512
DB-053233
EN300-19821
Z104475610
87F82840-8E16-44B0-BF95-F1CBF910BF92
2-(Hydroxymethyl)-6-([3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl]oxy)tetrahydro-2h-pyran-3,4,5-triol
963-334-4