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6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol

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Identification
Molecular formula
C6H12O6
CAS number
87-72-9
IUPAC name
6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol
State
State

At room temperature, the compound exists as a solid. It is stable under normal conditions but should be kept in a dry environment to prevent it from absorbing water.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
252.00
Boiling point (Kelvin)
525.15
General information
Molecular weight
182.17g/mol
Molar mass
182.1720g/mol
Density
1.5400g/cm3
Appearence

6-(Hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol typically appears as a white crystalline solid. The compound is usually powdery and may also present as granules. It is hygroscopic and readily absorbs moisture from the air.

Comment on solubility

Solubility of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol (C6H12O6)

The solubility of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol, a polyol compound, is generally characterized by its significant ability to dissolve in water. This characteristic is primarily due to the presence of multiple hydroxyl (–OH) groups, which can form hydrogen bonds with water molecules, enhancing its solubility. Here are some key points regarding its solubility:

  • Water Solubility: The multiple hydroxyl groups provide strong solvation, facilitating high solubility in polar solvents like water.
  • Non-Polar Solvents: The compound is expected to have limited solubility in non-polar solvents due to its polar character, which hinders interactions with less polar molecules.
  • Temperature Effects: As with many solutes, increased temperature generally improves solubility, allowing more of the compound to dissolve in a given volume of solvent.

In conclusion, 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol is highly soluble in water, making it useful in various applications where aqueous solutions are beneficial. As mentioned, the presence of numerous hydroxyl groups plays a critical role in this property.

Interesting facts

Interesting Facts About 6-(Hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol

6-(Hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol is a fascinating organic compound that plays a significant role in various fields, particularly in biochemistry and medicinal chemistry. Here are some intriguing aspects of this compound:

  • Biosynthesis: This compound is involved in the metabolism of carbohydrates, serving as an intermediate product. Understanding its role can shed light on metabolic pathways.
  • Structure and Function: The bicyclic structure of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol allows it to easily participate in both acid-base reactions and complexation with metal ions. This reactivity can be exploited in various synthetic processes.
  • Hydroxymethyl Groups: The presence of hydroxymethyl groups enhances its potential for biocompatibility, making it a candidate for applications in drug formulation and design.
  • Potential Applications: Researchers are investigating its application in the field of pharmaceuticals due to its unique properties and structural features, which could lead to novel therapeutic agents.
  • Natural Occurrence: This compound can be found in some natural products, signaling its importance in ecological and biological systems.

In conclusion, the study of 6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol not only uncovers the intricate details of carbohydrate metabolism but also opens avenues for innovation in medicinal chemistry. As scientific exploration continues, we may discover even more compelling characteristics of this intriguing compound!

Synonyms
Hexose
Hexopyranose
hexopyranoside
6-(hydroxymethyl)oxane-2,3,4,5-tetrol
D-[4,6-13C2]glucose
42752-07-8
D-Mannose-6-13C
D-(+)-Mannose
D-Mannose-2-13C
b-d-glucose
D-[1-18O]glucose
D-Mannose-1-C-d
D-[2,5-13C2]glucose
D-[4,5-13C2]glucose
D-[1-13C]gulose
D-[2-13C]gulose
D-[3-13C]galactose
D-[1-13c,1-2h]glucose
ALPHA-D-GLUCOSEANHYDROUS
D-[11-13C]TALOSE
L-[UL-13C6]galactose
DTXSID80858960
NSC8102
Glucose Oxidase from Aspergillus niger,
D-[2-2H]galactose
D-[4-2H]galactose
.beta.-D-Glucopyranose
B-D-ALLOPYRANOSE
D-[2-13C]talose
D-[3-13C]glucose
L-[2-13C]glucose
D-[5-13C]galactose
D-[6-13C,6,6'-2H2]GLUCOSE
(3R,4S,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
BETA-D-GLUCOSE (CONTAINS ALPHA-D-GLUCOSE)
D-[1,6-13C2,6,6'-2H2]GLUCOSE
L-(-)-ALLOSE
D-[3-2H]GALACTOSE
D-[1,2-13C2]galactose
D-[6,6'-2H2]galactose
D-hexose
Hexopyranose #
115973-81-4
39392-62-6
478529-30-5
D-[4,5-2H2]GLUCOSE
.alpha.-D-Glucose
D-[4,5,6,6'-2H4]glucose
Allose, D-
D(+)-Mannose
ZYMOSAN
478518-56-8
478518-63-7
478518-66-0
478518-71-7
70849-16-0
D-[4-2H]glucose
26655-34-5
.alpha.-D-Glucopyranose
.alpha.-d-Galactopyranose
(2S,3R,4S,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
D-[3-2H]GLUCOSE
157171-80-7
201136-45-0
288846-86-6
35669-34-2
39392-65-9
478518-62-6
54724-00-4
64429-86-3
70849-25-1
86595-19-9
D-[4,5,6-13C3]glucose
an aldopyranose
a pyranose
NSC-8102
Unknown Hexose
MFCD00064122
MFCD00066772
NSC-144657
?-D-Galactose
Allopyranose, D-
106032-60-4
287100-64-5
40825-89-6
478518-58-0
478518-70-6
478519-05-0
478529-33-8
478529-48-5
478529-49-6
83379-36-6
D-glucose anhydrous
Unknown Hexopyranose
.alpha.-d-Galactose
Unknown Hexopyranoside
alpha-d-(+)-glucose
GALACTOSE, (D)
MolMap_000072
SCHEMBL34307
SCHEMBL20094856
SCHEMBL21123450
SCHEMBL23758905
CHEBI:18133
DTXCID10196988
DTXCID40202844
CHEBI:167473
HMS3373C02
HMS3373E09
HMS3744K13
23403-54-5
478529-47-4
51517-59-0
579-36-2
DAA64673
DUA51863
DUA51871
DUA52930
JAA01072
PCA42986
QEA97381
VCA84916
BBL012219
NSC144657
NSC274237
NSC287045
STL163560
AKOS000119941
AKOS016038567
AKOS022061531
AKOS037503714
CCG-272298
NSC-287045
SB44851
SB45285
SB47940
Zymosan A from Saccharomyces cerevisiae
DA-19781
SY008815
SY012757
SY015251
SY057403
VS-03240
6-methyloltetrahydropyran-2,3,4,5-tetrol
DB-051616
DB-055683
DB-112935
NS00069768
NS00076953
EN300-33349
C00738
51DB4B86-692B-40EA-A7AD-4B20C8174CBE
WURCS=2.0/1,1,0/(axxxxh-1x_1-5_2*NCC/3=O)/1/
175348-09-1