62732-70-1 Usage
Molecular structure
1-Pentadecanol, methanesulfonate consists of a 15-carbon alcohol (1-pentadecanol) linked to a methanesulfonate group.
Water solubility
The compound is water-soluble due to the presence of the methanesulfonate group, which increases its solubility in aqueous solutions.
Non-reactivity
1-Pentadecanol, methanesulfonate is a non-reactive compound, making it stable and less likely to undergo chemical changes under various conditions.
Surfactant properties
The compound acts as a surfactant, reducing the surface tension between liquids and solids, which helps mix substances that would otherwise be immiscible.
Emulsifying capabilities
1-Pentadecanol, methanesulfonate can emulsify oil and water, allowing them to mix and form stable emulsions.
Solubilizing ability
The compound can solubilize various substances, improving their solubility and stability in different mediums.
Source of 1-pentadecanol
1-pentadecanol is typically derived from natural sources such as palm oil or coconut oil.
Chemical nature of methanesulfonate
Methanesulfonate is an organic sulfonate compound.
Industrial and cosmetic applications
1-Pentadecanol, methanesulfonate is commonly used in various industrial and cosmetic products, including personal care items, cleaning formulations, and pharmaceuticals.
Role in products
The compound is often utilized as an ingredient to improve the solubility and stability of other substances in the products it is added to.
Check Digit Verification of cas no
The CAS Registry Mumber 62732-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62732-70:
(7*6)+(6*2)+(5*7)+(4*3)+(3*2)+(2*7)+(1*0)=121
121 % 10 = 1
So 62732-70-1 is a valid CAS Registry Number.
62732-70-1Relevant articles and documents
Esters, retroesters, and a retroamide of palmitic acid: Pool for the first selective inhibitors of N-palmitoylethanolamine-selective acid amidase
Vandevoorde, Séverine,Tsuboi, Kazuhito,Ueda, Natsuo,Jonsson, Kent-Olov,Fowler, Christopher J.,Lambert, Didier M.
, p. 4373 - 4376 (2007/10/03)
Cyclohexyl hexadecanoate, hexadecyl propionate, and N-(3-hydroxypropionyl)pentadecanamide, respectively ester, retroester, and retroamide derivatives of N-palmitoylethanolamine, represent the first selective inhibitors of "N-palmitoylethanolamine hydrolase" described so far. These compounds are devoid of affinity for CB1 and CB 2 receptors and characterized by high percentages of inhibition of N-palmitoylethanolamine-selective acid amidase (84.0, 70.5, and 76.7% inhibition at 100 μM, respectively) with much lower inhibitory effect on either fatty acid amide hydrolase or the uptake of anandamide.
