Acetyl-L-alanine
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Acetyl-L-alanine

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Category
L-Amino Acids
Catalog number
BAT-003862
CAS number
97-69-8
Molecular Formula
C5H9NO3
Molecular Weight
131.10
Acetyl-L-alanine
IUPAC Name
(2S)-2-acetamidopropanoic acid
Synonyms
Ac-L-Ala-OH
Appearance
White powder
Purity
≥ 98% (Assay by Titration)
Density
1.170±0.06 g/cm3(Predicted)
Melting Point
117.0-125.0 °C
Boiling Point
369.7°C at 760mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C5H9NO3/c1-3(5(8)9)6-4(2)7/h3H,1-2H3,(H,6,7)(H,8,9)/t3-/m0/s1
InChI Key
KTHDTJVBEPMMGL-VKHMYHEASA-N
Canonical SMILES
CC(C(=O)O)NC(=O)C

Acetyl-L-alanine, an acetylated derivative of the amino acid alanine, with diverse applications in scientific and industrial settings. Here are the key applications presented with high perplexity and burstiness:

Nutritional Supplement: Embraced in dietary supplements, Acetyl-L-alanine plays a pivotal role in supporting muscle function and overall well-being. It aids in protein metabolism and facilitates muscle recovery following strenuous physical activity. Athletes and fitness enthusiasts incorporate it into their regimens to elevate performance levels and endurance capacity.

Pharmaceutical Synthesis: Serving as a fundamental component in the synthesis of various pharmaceutical compounds, Acetyl-L-alanine serves as a cornerstone in the creation of drugs integrating amino acid derivatives into their molecular structures. Its significance lies in the development of novel pharmacological agents with heightened efficacy and diminished side effects, a breakthrough in the realm of pharmaceutical innovation.

Biochemical Research: Within laboratory settings, Acetyl-L-alanine assumes a crucial role in biochemical assays focused on the exploration of enzyme activities and protein functions. Operating as a substrate or inhibitor in enzymatic reactions, it aids researchers in unraveling intricate metabolic pathways. This knowledge is indispensable for shedding light on the biochemical functions of acetylated amino acids within biological systems, enriching our understanding of their physiological impact.

Cosmetic Formulations: In the domain of cosmetics, Acetyl-L-alanine is a coveted ingredient for its potential skin-conditioning attributes. Incorporated into cosmetic formulations, it is harnessed for enhancing skin texture and hydration levels. Cosmetic scientists leverage its benefits to optimize the appearance and vitality of the skin, contributing to the advancement of cosmetic science and skincare innovation.

1.The metabolism of n-butyl glycidyl ether in the rat and rabbit.
Eadsforth CV, Hutson DH, Logan CJ, Morrison BJ. Xenobiotica. 1985 Jul;15(7):579-89.
[1-14C]Butyl glycidyl ether administered orally to male rats and rabbits (20 mg/kg) is rapidly absorbed and metabolized. Most of the administered compound, 87% (rat) and 78% (rabbit), is eliminated in the 0-24 urine. Major metabolites in the rat include 3-butoxy-2-hydroxypropionic acid (9%), 3-butoxy-2-acetylaminopropionic acid (23%) and butoxyacetic acid (10%). 3-Butoxy-2-hydroxypropionic acid (35%) and butoxyacetic acid (5%) are also major metabolites in the rabbit. Biotransformations of the glycidyl ether and their likely biochemical mechanisms are discussed.
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