79162-70-2 Usage
Description
Methyl 30-hydroxytriacontanoate is a long-chain fatty acid ester derived from natural sources such as plant oils and waxes. It is known for its emollient and moisturizing properties, as well as its ability to soften and smooth the skin. With a high melting point and a thick, creamy texture, it is ideal for use in thick lotions and creams. Methyl 30-hydroxytriacontanoate also has skin-conditioning properties, helping to lock in moisture and create a protective barrier on the skin. Its non-greasy and non-comedogenic texture makes it suitable for all skin types.
Uses
Used in Cosmetic and Personal Care Products:
Methyl 30-hydroxytriacontanoate is used as an emollient and moisturizing agent for its ability to soften and smooth the skin. Its high melting point and thick, creamy texture make it ideal for use in thick lotions and creams.
Used in Skincare:
Methyl 30-hydroxytriacontanoate is used as a skin-conditioning agent to help lock in moisture and create a protective barrier on the skin. Its non-greasy and non-comedogenic texture makes it suitable for all skin types, providing hydration and improving skin texture without clogging pores or causing a greasy feel.
Check Digit Verification of cas no
The CAS Registry Mumber 79162-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79162-70:
(7*7)+(6*9)+(5*1)+(4*6)+(3*2)+(2*7)+(1*0)=152
152 % 10 = 2
So 79162-70-2 is a valid CAS Registry Number.
79162-70-2Relevant articles and documents
Synthesis of two Unique Compounds, a Ceramide and a Cerebroside, Occurring in Human Stratum Corneum
Mueller, Silvia,Schmidt, Richard R.
, p. 779 - 784 (2007/10/03)
The cerebroside 1a and the ceramide 1b, both playing important roles in epidermal barrier function, were synthesized by N-acylation of 1-O-glucosylated C18-sphingosine 2 and C18-sphingosine 8, respectively, with O-acyl fatty acid 3. The required compound 3 was obtained from ω-hydroxy fatty acid 6 and linoleic acid 7 by esterification. The ω-hydroxy C30-fatty acid 6 was prepared as follows: Copper-catalyzed coupling of ω-hydroxy alkyl halide 11 with the Grignard reagent derived from bromo compound 13 afforded after oxidation C17-aldehyde 15. Wittig reaction with phosphonium salt 10, derived from ω-bromo-tridecanoic acid 9, and subsequent hydrogenation and O-deprotection furnished 6 in high yield.
