50731-08-3 Usage
16-carbon hydrocarbon chain
A straight chain of 16 carbon atoms that forms the backbone of the compound.
Amine group (-NH2)
A nitrogen atom bonded to two hydrogen atoms, which is attached to the second carbon atom of the hydrocarbon chain.
Two hydroxyl groups (-OH)
A group consisting of one oxygen atom bonded to a hydrogen atom, which are attached to the first and third carbon atoms of the hydrocarbon chain.
Surfactant properties
The presence of the amine and hydroxyl groups gives 2-aminohexadecane-1,3-diol the ability to lower the surface tension between two liquids or a liquid and a solid.
Industrial and commercial applications
2-aminohexadecane-1,3-diol is used in the production of detergents, emulsifiers, and foaming agents.
Cosmetic and personal care uses
The compound is also used in skincare and haircare formulations as a moisturizing and conditioning agent.
Long hydrocarbon chain
The 16-carbon chain gives the compound a good balance of hydrophilic (water-loving) and lipophilic (fat-loving) properties, which enhances its surfactant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 50731-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,3 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50731-08:
(7*5)+(6*0)+(5*7)+(4*3)+(3*1)+(2*0)+(1*8)=93
93 % 10 = 3
So 50731-08-3 is a valid CAS Registry Number.
50731-08-3Relevant articles and documents
Synthesis of sphinganine analogues modified in the head group
Kolter, Thomas,Van Echten-Deckert, Gerhild,Sandhoff, Konrad
, p. 13425 - 13432 (1994)
The synthesis of sphinganine analogues modified in the head group is reported. The target compounds are efficiently prepared by means of the Henry reaction. Synthesis and results of preliminary investigations of the derivatives as potential inhibitors of sphingolipid biosynthesis are presented.
