CAS 111-57-9
:N-(2-hydroxyethyl)stearamide
Description:
N-(2-hydroxyethyl)stearamide, with the CAS number 111-57-9, is an amide derived from stearic acid and 2-hydroxyethylamine. This compound typically appears as a white to off-white solid or waxy substance. It is characterized by its long hydrophobic hydrocarbon chain, which contributes to its surfactant properties, and the presence of a hydroxyl group, which enhances its solubility in polar solvents. N-(2-hydroxyethyl)stearamide is known for its emulsifying, thickening, and stabilizing properties, making it useful in various applications, including cosmetics, personal care products, and industrial formulations. It exhibits good thermal stability and can function effectively in a range of pH environments. Additionally, this compound is generally considered to have low toxicity, but safety data should always be consulted for specific handling and usage guidelines. Its unique structure allows it to interact with both hydrophilic and hydrophobic substances, making it a versatile ingredient in formulation chemistry.
Formula:C20H41NO2
InChI:InChI=1/C20H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h22H,2-19H2,1H3,(H,21,23)
InChI key:InChIKey=OTGQIQQTPXJQRG-UHFFFAOYSA-N
SMILES:C(CCCCCCCCCCCCCCC)CC(NCCO)=O
Synonyms:- Abriflo 65
- Alkamide S 280
- Am 1105
- Aminon SM
- Amisol SME
- Ceramid
- Clindrol 200-MS
- Clindrol 200MS
- Comperlan HS
- Cycloamide SM
- Emcol 70
- Loramine S 280
- Lubsize K 12
- Mackamide SMA
- Marlamid M 18
- Monamid 972
- Monamid S
- Monoethanolamine stearic acid amide
- Monoethanolstearamide
- N-(2-Hydroxyethyl)octadecanamide
- N-(Hydroxyethyl)stearamide
- N-Octadecanoylethanolamine
- N-Stearoylethanolamine
- NSC 52619
- Nsc 3377
- Octadecanamide, N-(2-hydroxyethyl)-
- Onyx Wax EL
- Profan SME
- Rewomid S 280
- S 280
- Stearamide MEA
- Stearamide monoethanolamine
- Stearamyl
- Stearic acid ethanolamide
- Stearic acid monoethanolamide
- Stearic ethanolamide
- Stearic ethylolamide
- Stearic monoethanolamide
- Stearic monoethanolamine
- Stearoyl monoethanolamide
- Stearoylethanolamide
- Stearoylethanolamine
- Stearoylmonoethanolamide
- Witcamide 70
- N-(2-Hydroxyethyl)stearic acid amide
- N-(2-hydroxyethyl)stearamide
- Stearinsuremonoethanolamid
- Stearic acid-ethanolamine condensate
- N-Stearoylethanolamide
- SEA
- STEAROYL ETHANOLAMIDE
- N-(octadecanoyl)ethanolamine
- Stearic acid monoethanolamide Tech. Grade
- n-(2-hydroxyethyl)-octadecanamid
- Stearoylethanolamide(SEA)
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Found 8 products.
Stearoyl Ethanolamide
CAS:Controlled Product<p>Applications Stearoyl Ethanolamide is a prolific fatty acid ethanolamide produced by PLD hydrolysis of membrane phospholipids. Stearoyl Ethanolamide is also used for studying the effect on endocannabinoid signalling and BBB integrity in systemic inflammation.<br>References Kasatkina, L. A., et al.: Biochem. Pharmacol. 174, 113783 (2020)<br></p>Formula:C20H41NO2Color and Shape:NeatMolecular weight:327.55Stearoylethanolamide
CAS:<p>Stearoylethanolamide(N-(2-Hydroxyethyl)octadecanamide) is a cannabinoid compound present in the brains of humans, rats, and mice with pro-apoptotic activity.</p>Formula:C20H41NO2Purity:98.68%Color and Shape:Drypowder Pelletslargecrystals Liquid Othersolid PelletslargecrystalsMolecular weight:327.55Stearoyl Ethanolamide-d4
CAS:Controlled Product<p>Applications Stearoyl Ethanolamide-d4 is the labelled analogue of Stearoyl Ethanolamide (S686608), which is a prolific fatty acid ethanolamide produced by PLD hydrolysis of membrane phospholipids.<br>References Kasatkina, L. A., et al.: Biochem. Pharmacol. 174, 113783 (2020)<br></p>Formula:C20D4H37NO2Color and Shape:NeatMolecular weight:331.57Stearoyl ethanolamide
CAS:<p>Stearoyl ethanolamide is a glycol ester that has been shown to inhibit the growth of bacteria by binding to their receptor site. Stearoyl ethanolamide has also been shown to have an effect on the locomotor activity of experimental animals and may reduce energy metabolism. This compound has been used as an antimicrobial agent in a number of applications, including treatment of infectious diseases, anti-inflammatory cytokine IL-10, and pharmacological treatment for obesity. The receptor activity of stearoyl ethanolamide was studied using an experimental model involving α7 nicotinic acetylcholine receptors in Chinese hamster ovary (CHO) cells.</p>Formula:C20H41NO2Purity:Min. 95%Molecular weight:327.55 g/mol






