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N-Acetylaspartic acid

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Identification
Molecular formula
C9H15NO5
CAS number
997-55-7
IUPAC name
3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid
State
State
At room temperature, N-Acetylaspartic acid is found in a solid state. It is a crystalline substance that is stable under standard conditions.
Melting point (Celsius)
242.00
Melting point (Kelvin)
515.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
189.19g/mol
Molar mass
189.1920g/mol
Density
1.3400g/cm3
Appearence

N-Acetylaspartic acid typically appears as a white crystalline solid. It has a powdery texture and is often used in research and chemical applications where precise measurements are required.

Comment on solubility

Solubility of 3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid (C9H15NO5)

The solubility of 3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid is an important characteristic that influences its behavior in various chemical environments. This compound has several functional groups that significantly affect its solubility:

  • Hydroxyl Groups: The presence of two hydroxyl (-OH) groups typically suggests an increased ability to form hydrogen bonds with water, enhancing solubility in polar solvents.
  • Amino Group: The amino (-NH2) group also contributes to solubility by engaging in hydrogen bonding, further promoting its interaction with water molecules.
  • Hydrophobic Segment: The 3,3-dimethyl-butanoyl moiety introduces a hydrophobic component, which may limit solubility in water, depending on its size relative to the polar functional groups.

Overall, the solubility behavior can be summarized as follows:

  1. It is expected to be soluble in polar solvents such as water due to its multiple polar functional groups.
  2. The extent of solubility may vary with concentration and temperature, as is common with many organic molecules.
  3. Interactions with other compounds in solution could also alter its effective solubility.

In conclusion, while the hydrophilic character appears to dominate due to the presence of multiple polar functional groups, the specific solubility characteristics should be experimentally verified for precise applications.

Interesting facts

Exploring 3-[(2,4-Dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic Acid

This fascinating compound, often encountered in the realm of biochemical studies, presents a unique array of features that draw the attention of chemists and biochemists alike.

Significance in Biochemistry

3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid plays an integral role in various biological processes. Its structure suggests potential interactions with enzyme mechanisms and metabolic pathways. Understanding such compounds can lead to greater insights into:

  • Metabolic Regulation: It can be involved in controlling certain metabolic processes.
  • Biomolecular Interactions: Its amino and hydroxyl groups can interact with other biomolecules, affecting cellular functions.
  • Pharmacological Applications: The compound may have therapeutic potential, making it a candidate for drug development.

Structural Characteristics

The structural complexity of this compound can be particularly intriguing. The presence of multiple functional groups, including:

  • Amino Group: Critical for the formation of peptides and proteins.
  • Hydroxy Groups: Contributing to the compound's polarity and potential solubility in biological systems.
  • Dimethyl Group: This modification can influence the compound's steric properties and its overall interaction with other molecules.

Potential Research Applications

Due to its unique chemical properties, 3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid is a subject of ongoing research. Some areas of focus include:

  • Drug Discovery: Researchers are investigating how this compound can influence pharmacokinetics and pharmacodynamics.
  • Biochemical Pathways: It may impact the synthesis of important biomolecules, giving insights into metabolic disorders.
  • Analytical Chemistry: Its various functional groups make it an interesting target for analytical studies to understand its reactivity and stability.

As scientists delve deeper into the properties and applications of 3-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]propanoic acid, they unlock the potential for new discoveries that may significantly contribute to both basic and applied sciences.

Synonyms
DL-Pantothenic acid
599-54-2
3-[(2,4-dihydroxy-3,3-dimethylbutanoyl)amino]propanoic acid
3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoic acid
CHEBI:7916
DTXSID7047229
66Y94D1203
( inverted exclamation markA)-Pantothenic acid
N-(2,4-dihydroxy-3,3-dimethylbutanoyl)-beta-alanine
beta-Alanine, N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-
.beta.-Alanine, N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-
(+/-)-pantothenate;(+/-)-vitamin B5
pantothensaure
MFCD00020513
UNII-66Y94D1203
EINECS 209-965-4
(+-)-Pantothenic acid
Pantothenic Acid, Racemic
(+/-)-Pantothenic acid
(A+/-)-Pantothenic acid
SCHEMBL5437
PANTOTHENIC ACID, DL-
(+)-(R)-3-(2,4-Dihydroxy-3,3-dimethylbutanamido)propanoic acid
CHEMBL2110806
DTXCID5027229
Rotenone;(R)-3-(2,4-Dihydroxy-3,3-dimethylbutanamido)propanoic acid
HY-B0430B
PANTOTHENIC ACID, (+/-)-
STL453482
AKOS015892833
1113-70-8
DA-48601
SY046441
DB-254578
CS-0103035
NS00013937
Q179894
(1)-N-(2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl)-beta-alanine
(R)-3-(2,4-Dihydroxy-3,3-dimethylbutanamido)propionic Acid
5482E43E-7047-44E0-A595-B7F3533CC058
(+/-)-N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-beta-alanine
3-[[(2S)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoic acid
(+/-)-3-(2,4-DIHYDROXY-3,3-DIMETHYLBUTYRAMIDO)PROPIONIC ACID
.BETA.-ALANINE, N-(2,4-DIHYDROXY-3,3-DIMETHYL-1-OXOBUTYL)-, (+/-)-