Interesting facts
Interesting Facts about N-(2-hydroxyethyl)octadecanamide
N-(2-hydroxyethyl)octadecanamide, often simply called HEODA, is a fascinating compound with unique characteristics that make it noteworthy in various fields, including materials science and medicinal chemistry. Here are some intriguing aspects of this compound:
- Amidation and Surfactant Properties: The presence of the amide functional group imparts distinct surfactant qualities, making HEODA useful in the formulation of various emulsions, creams, and lotions. This helps improve the stability and texture of products in the cosmetic industry.
- Biosafety: As a derivative of fatty acids, this compound is often regarded as having lower toxicity, making it preferable in formulations aiming for skin compatibility. Its natural origin may contribute to its reputation as a 'gentler' agent in comparison to synthetic alternatives.
- Biodegradability: One of the significant advantages of HEODA is its biodegradability, which is essential in today’s environmentally-conscious market. This feature aligns with ongoing efforts to reduce environmental impact from chemical products.
- Versatility: Beyond cosmetics, HEODA is also finding applications in pharmaceutical formulations. Its properties allow it to serve as an excipient, aiding in drug delivery systems, where controlling the interaction between the drug and delivery medium is crucial.
- Research and Innovation: Researchers are continuously exploring the potential uses of HEODA in innovative fields such as nanotechnology, where it may assist in the creation of new materials with enhanced performance characteristics.
In summary, N-(2-hydroxyethyl)octadecanamide is more than just a chemical compound; it plays a pivotal role in various industries, promoting safety, effectiveness, and ecological sustainability. As scientists and chemists continue to explore its potential, HEODA may pave the way for new advancements in both product development and environmental stewardship.
Synonyms
N-(2-Hydroxyethyl)octadecanamide
111-57-9
N-stearoylethanolamine
Stearic ethanolamide
N-(Hydroxyethyl)stearamide
OCTADECANAMIDE, N-(2-HYDROXYETHYL)-
Monoethanolamine stearic acid amide
03XV449Q24
DTXSID9042178
DTXCID7022178
Stearoyl ethanolamide
Stearoylethanolamide
N-(2-Hydroxyethyl)stearamide
Stearamide MEA
Stearic monoethanolamide
Stearic acid monoethanolamide
Stearamyl
Stearoyl-ethanolamine
Cycloamide SM
Comperlan HS
Stearoylmonoethanolamide
Stearoylethanolamine
Stearic ethylolamide
Marlamid M 18
Ceramid
Clindrol 200-MS
Loramine S 280
Stearic monoethanolamine
Stearoyl-EA
Stearoyl monoethanolamide
N-(octadecanoyl)ethanolamine
NSC 3377
N-(Octadecanoyl)-ethanolamine
CHEMBL171447
CHEBI:85299
NSC-3377
MFCD00045971
8038-89-9
Mackamide SMA
Monamid S
UNII-03XV449Q24
Amidex SME
Witcamide 70
EINECS 203-883-2
Alkamide S-280
N-Stearoylethanolamide
INCROMIDE SMEA
Rewomid S 280
1:1 Stearamide MEA
octadecanoyl ethanolamide
N-octadecanoylethanolamine
Stearic Acid Ethanolamide
N-octadecanoyl ethanolamine
Stearamide-MEA (1:1)
EC 203-883-2
N-(otadecanoyl)-ethanolamine
SCHEMBL50178
GTPL3621
orb1707816
N-(2-hydroxyethyl)stearoylamide
NSC3377
STEARAMIDE MONOETHANOLAMINE
Stearamide, N-(2-hydroxyethyl)-
HMS3649H17
N-(2-Hydroxyethyl)-octadecanamide
NAE 18:0
NSC52619
BDBM50074620
LMFA08040051
NAE(18:0)
NSC-52619
STL454871
AKOS002676465
FS171406
MS-24898
SEA
Octadecanoic acid (2-hydroxy-ethyl)-amide
DB-040991
HY-113015
Stearoyl ethanolamide, >=98%, crystalline
CS-0059359
NS00003181
G12117
EN300-18537220
SR-01000946662
SR-01000946662-1
Q15427850
Z3222444503
Solubility of N-(2-hydroxyethyl)octadecanamide
N-(2-hydroxyethyl)octadecanamide, a compound with the formula C18H37NO2, exhibits unique solubility properties that can be attributed to its molecular structure. Generally, the solubility of this compound can be categorized as follows:
In summary, the solubility of N-(2-hydroxyethyl)octadecanamide is largely influenced by its structure, and it can be expected to behave differently in varying solvent environments. This characteristic is vital for applications where solvent selection is critical. As one might say, "The solubility is a reflection of the compound's ability to interact with its surroundings, whether in a friendly embrace or a distant separation."