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D-glycero-D-galacto-Heptonic acid

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Identification
Molecular formula
C7H14O8
CAS number
2214-08-0
IUPAC name
(2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid
State
State

At room temperature, (2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid is typically found in a solid state, often as a crystalline powder. This characteristic allows it to be easily handled for laboratory uses.

Melting point (Celsius)
188.00
Melting point (Kelvin)
461.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
242.24g/mol
Molar mass
242.2380g/mol
Density
1.7280g/cm3
Appearence

This compound is typically a white crystalline solid. Its crystalline nature gives it a structured appearance, and it can appear translucent or opaque, exhibiting a fine, powdery consistency when in a pure form.

Comment on solubility

Solubility of (2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid

(2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid, with the chemical formula C7H14O8, is a compound that presents interesting solubility characteristics due to its multiple hydroxyl (-OH) groups. The presence of these functional groups greatly influences its interaction with polar solvents such as water.

Factors Influencing Solubility:

  • Hydrogen Bonding: The hydroxyl groups can form hydrogen bonds with water molecules, enhancing solubility.
  • Molecular Size: The relatively small size of the heptanoic acid structure allows for efficient packing with water.
  • Polarity: The polar nature of the hydroxyl groups contributes to a higher affinity for polar solvents.

As a result, it is probable that this compound is highly soluble in water, which is a common characteristic for many hydroxy acids. However, solubility can also be affected by temperature and pH, which should be considered in practical applications. In summary, (2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid is likely to demonstrate significant solubility in aqueous environments, primarily due to its configuration and the abundance of hydroxyl groups.

Interesting facts

Interesting Facts about (2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid

(2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid is an intriguing compound that belongs to the class of polyhydroxy acids. Its unique structure and configuration give it several interesting properties and potential applications.

Key Features:

  • Natural Origin: This compound is often found in various natural sources, particularly related to microbial metabolism.
  • Chirality: The designation R/S indicates that this compound has multiple chiral centers, making it important in stereochemistry for understanding its biological interactions.
  • Potential in Medicine: Due to its multiple hydroxyl (-OH) groups, it shows promise in pharmaceuticals, particularly in drug design and delivery systems that enhance solubility and bioavailability.
  • Interesting Chemical Behavior: The presence of multiple hydroxyl groups may engage in hydrogen bonding, significantly impacting its reactivity and interactions with other molecules.

One of the fascinating aspects of (2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid is its role as a potential building block for larger biomolecules. Scientists are keen on exploring how similar structures can lead to novel compounds beneficial for various applications in biochemistry and materials science.

In conclusion, this compound exemplifies the complexity and beauty of organic chemistry. As we unravel its properties and potential applications further, it serves as a reminder of how intricate molecular design can lead to advancements in science and technology.

Synonyms
Glucoheptonic acid
alpha-Glucoheptonic acid
D-glycero-D-gulo-Heptonic acid
87-74-1
(2R,3R,4S,5R,6R)-2,3,4,5,6,7-hexahydroxyheptanoic acid
GLUCO-HEPTONIC ACID
B1F50160Z2
GLUCOHEPTONIC ACID (D)
GLUCOHEPTONIC ACID [MI]
CHEBI:67270
GLUCOHEPTONIC ACID, .ALPHA.-
EINECS 245-601-0
copper glucoheptonate
GLUCOHEPTONIC ACID [INCI]
GLUCOHEPTONIC ACID, ALPHA-
201-769-7
Gluceptate
Gluceptate [INN]
UNII-B1F50160Z2
calcium-gluceptate
EINECS 201-769-7
GLUCEPTATE [VANDF]
SCHEMBL6406
GLUCEPTATE [WHO-DD]
DTXSID3048077
KWMLJOLKUYYJFJ-VFUOTHLCSA-N
AKOS016009919
PD062368
NS00002118
BRD-K35952844-236-01-6
BRD-K35952844-238-01-2
Q27135733