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N-Acetylglucosamine

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Identification
Molecular formula
C8H15NO6
CAS number
7512-17-6
IUPAC name
N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide
State
State

At room temperature, N-Acetylglucosamine is a solid and typically found in crystalline form.

Melting point (Celsius)
221.00
Melting point (Kelvin)
494.15
Boiling point (Celsius)
398.15
Boiling point (Kelvin)
671.30
General information
Molecular weight
221.21g/mol
Molar mass
221.2080g/mol
Density
1.8330g/cm3
Appearence

N-Acetylglucosamine appears as a white or off-white crystalline powder. It is soluble in water and has a slightly sweet taste.

Comment on solubility

Solubility of N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide

The solubility characteristics of N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide (C8H15NO6) can be quite fascinating due to its unique chemical structure. This compound possesses multiple hydroxyl groups, which generally enhances its affinity for water through hydrogen bonding.

Factors Influencing Solubility:

  • Hydroxyl Groups: The presence of three hydroxyl groups contributes to a higher degree of solubility in polar solvents, particularly water.
  • Polarity: As a polar molecule, it can interact favorably with other polar molecules, facilitating solvation.
  • Temperature: Solubility can increase with temperature, as higher temperatures often help overcome intermolecular forces.

In general, compounds with similar structural features often exhibit notable solubility in aqueous environments, thanks to their ability to form hydrogen bonds. Thus, one could surmise that N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide, due to its highly hydrophilic characteristics, would likely demonstrate good solubility in water. However, it may show varying solubility levels in organic solvents, which could depend on their polarity.

In summary, if you're investigating the solubility of this intriguing compound, consider its hydrophilic nature and the role it plays in determining its behavior in various solvent systems!

Interesting facts

Interesting Facts about N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide

N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide is a fascinating compound due to its unique structure and potential applications. This compound belongs to a class of molecules known as glycosides, which are derived from sugars and can offer a range of biological activities. Here are some noteworthy points about this compound:

  • Biological Significance: The presence of multiple hydroxyl groups in its structure often indicates that the compound may have significant biological interactions. This can include effects on enzyme activity or interactions with various biomolecules.
  • Potential Therapeutic Applications: Due to its structural resemblance to certain natural products, this compound could serve as a candidate for therapeutic agents designed to treat metabolic disorders or other health conditions.
  • Research Interest: Scientists are increasingly interested in compounds like this one, as they can provide insight into the modification of glycosidic linkages that can influence biological functions.
  • Natural Occurrence: Structures similar to this compound can be found in many natural sources, suggesting it may play a role in plant metabolism or defense mechanisms.
  • Versatile Synthesis: The complex chemical structure allows for diverse synthetic pathways, making it a valuable compound in organic chemistry education and research.

In summary, N-[2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide stands out as a compelling subject of study due to its biochemistry relevance. As you explore this compound further, remember the quote by Lavoisier: "Nothing is lost, nothing is created, everything is transformed." This encapsulates the essence of understanding compounds like this, showcasing the beautiful complexity of chemistry.

Synonyms
HexNAc
N-Acetyl-Hexosamine
2-Acetamido-2-Deoxy-Hexose
N-Acetylhexosamine
14215-68-0
Cyclic N-Acetyl-mannosamine
Croton Oil ,
N-acetylmannosamine
N-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
CHEBI:7203
2-ACETAMIDO-2-DEOXY-D-[1-13C]GALACTOSE
N-Acetylchondrosamine
2-acetamido-2-deoxy-D-[1-13C]glucose
2-[1,2-13C2,15N]ACETAMIDO-2-DEOXY-D-[1-13C]GLUCOSE
2-[15N]ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE
2-[1-13C]ACETAMIDO-2-DEOXY-D-GLUCOSE
2-ACETAMIDO-2-DEOXY-D-[2-13C]GLUCOSE
n-acetyl mannosamine
2-[1,2-13C2,15N]ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE
478518-87-5
6813-82-7
4773-29-9
SMR000857252
2-[2-13C]ACETAMIDO-2-DEOXY-D-GLUCOSE
N-Acetylmannosamine; ManNAc
2-ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE
478529-39-4
478529-43-0
2-[1,2-13C2]ACETAMIDO-2-DEOXY-D-GLUCOSE
2-[1,2-13C2]ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE
MFCD00065372
N-Acetyl-2-amino-2-deoxy-D-glucose
2-(Acetylamino)-2-deoxyhexopyranose #
1398-61-4
2-Deoxy-2-(acetylamino)-D-glucopyranose
72-87-7
6-Acetamido-6-deoxy-acpha-D-glucopyranose
N-acetyl-d-man-nosamine
MLS001333153
MLS001333154
CHEMBL83479
SCHEMBL256545
N-(2,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-acetamide
SCHEMBL19604061
SCHEMBL24105621
SCHEMBL24978032
DTXSID80859634
2-Acetamido-2-Deoxy-Hexopyranose
N-(2,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-acetamide,(N-Acetyl-D-
Chitin from shrimp and crab shells
HMS2233G11
HMS3373E07
N-ACETYL-?-D-GALACTOSAMINE
2-Acetamido-2-Deoxy-Hexopyranoside
CDA36911
DUA51887
HDA61901
PAA21568
AKOS030212680
MA15631
SB45257
SB46979
SB47153
N-Acetyl-D-[UL-13C6,15N]glucosamine
SY057410
DB-056247
6-Acetamido-6-deoxy-.alpha.-D-glucopyranose
NS00096435
C02711
EN300-270189
L001205
Q27107455
N-Acetylglucosamine; 2-Acetamido-2-deoxy-D-glucopyranose
Z1509532067