4397-81-3 Usage
Chemical structure
Hydroxyl groups at each end The molecule has a hydroxyl (-OH) group at both the first and thirteenth carbon atoms, making it a diol.
Type of compound
Fatty alcohol 1,13-Docosanediol belongs to the class of fatty alcohols, which are long-chain alcohols derived from fatty acids.
Industrial applications
Surfactants, lubricants, and plasticizers This chemical is used in various industries, including the production of surfactants (substances that reduce surface tension), lubricants (substances that reduce friction between surfaces), and plasticizers (additives that increase the flexibility of materials).
Potential applications
Pharmaceutical and cosmetic industries Due to its emollient and moisturizing properties, 1,13-Docosanediol has potential uses in the development of pharmaceutical and cosmetic products.
Safety profile
Relatively safe and non-toxic The compound is considered to be relatively safe and non-toxic, with a low potential for skin irritation.
Emollient properties
Enhances skin softness As an emollient, 1,13-Docosanediol helps to soften and smooth the skin, making it a valuable ingredient in cosmetic products.
Moisturizing properties
Retains skin moisture This diol has the ability to help the skin retain moisture, which can be beneficial in the development of moisturizing products.
Low skin irritation potential
Suitable for sensitive skin Due to its low potential for skin irritation, 1,13-Docosanediol may be suitable for use in products designed for sensitive skin.
Check Digit Verification of cas no
The CAS Registry Mumber 4397-81-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4397-81:
(6*4)+(5*3)+(4*9)+(3*7)+(2*8)+(1*1)=113
113 % 10 = 3
So 4397-81-3 is a valid CAS Registry Number.
4397-81-3Relevant academic research and scientific papers
Improved method for the selective conversion of aliphatic esters to alcohols by zinc borohydride in tetrahydrofuran
Narasimhan, S,Palmer, Prem
, p. 701 - 702 (2007/10/02)
Selective conversion of aliphatic esters to the corresponding alcohols has been achieved in excellent yields by zinc borohydride in tetrahydrofuran under mild conditions (67 deg C, 6 hr).Unsaturated esters produce the corresponding diols.
