Interesting facts
Interesting Facts about 2-[dodecanoyl(methyl)amino]acetic acid
2-[dodecanoyl(methyl)amino]acetic acid is a fascinating compound that showcases the intricate relationship between structure and function in chemistry. Here are some notable aspects of this compound:
- Biological Importance: This compound is a member of a class of molecules known as fatty acid amides, which are integral to various biological processes, including cell signaling and membrane formation. It plays a role in the modulation of biochemical pathways.
- Amphiphilicity: The presence of both hydrophilic (water-attracting) and hydrophobic (water-repelling) regions in its structure allows the compound to interact with both the aqueous environment and lipid membranes, making it a potential candidate for drug delivery systems.
- Versatile Applications: Due to its unique properties, 2-[dodecanoyl(methyl)amino]acetic acid is explored for applications in drug design, particularly for developing medications that target specific diseases at a cellular level.
- Synthesis: The synthesis of this compound can involve various chemical reactions, including amidation and acylation techniques, highlighting the creativity and precision required in synthetic organic chemistry.
- Research Potential: Ongoing research is uncovering further applications and effects of this compound, particularly in pharmacology and biochemistry, paving the way for innovations in therapeutic interventions.
In essence, 2-[dodecanoyl(methyl)amino]acetic acid is not just an ordinary chemical compound; it represents a bridge between organic chemistry and biological functions. Its exploration could yield advancements in health sciences, underscoring the interconnection of chemistry with life.
Synonyms
N-LAUROYLSARCOSINE
97-78-9
Lauroyl sarcosine
Glycine, N-methyl-N-(1-oxododecyl)-
Lauroylsarcosine
N-Dodecanoylsarcosine
Hamposyl L
N-Laurylsarcosine
N-Dodecanoyl-N-methylglycine
N-Lauroyl sarcosinate
Maprosyl L
Sarcosyl L
Sarkosyl L
2-[dodecanoyl(methyl)amino]acetic acid
Sarkosyl
N-Lauroyl-N-methylaminoacetic acid
Sarcosine, N-lauroyl-
Crodasinic L
Nikkol sarcosinate LH
2-(N-methyldodecanamido)acetic acid
MFCD00021749
NSC 96994
LIJ19P3L6F
DTXSID7042011
NSC-96994
Lauroylsarcosine (sodium salt)
UNII-LIJ19P3L6F
Vanseal LS
EINECS 202-608-3
Glycine,N-methyl-N-(1-oxododecyl)-
LOWENOL L ACID
EC 202-608-3
SCHEMBL61098
LAUROYL SARCOSINE [II]
CHEMBL1907464
DTXCID5022011
CHEBI:183705
N-Methyl-N-(1-oxododecyl)glycine
N-Lauroylsarcosine, neat, >=95%
NSC96994
N-Methyl-N-(1-oxododecyl) glycine
Tox21_301352
STL452997
AKOS009158126
[Dodecanoyl(methyl)amino]acetic acid #
HY-W141881
CAS-97-78-9
NCGC00255839-01
DA-66121
LS-14453
CS-0201675
L0151
NS00011477
D78483
N-Lauroylsarcosine, purum p.a., >=98.0% (GC)
Q27283002
Solubility of 2-[dodecanoyl(methyl)amino]acetic acid
The solubility of 2-[dodecanoyl(methyl)amino]acetic acid, a complex molecule, can be quite intriguing due to its unique structure and functional groups. Understanding its solubility characteristics involves considering several factors:
In summary, while the compound may exhibit a degree of solubility in organic solvents due to its hydrophobic characteristics, it may show reduced solubility in aqueous solutions. It's essential to observe and test its behavior in various solvents to fully understand its solubility potential.