42231-99-2 Usage
Description
Hexyl myristate is a chemical compound derived from the esterification of hexyl alcohol and myristic acid. It is a versatile ingredient commonly used in personal care products for its emollient and conditioning properties, as well as its ability to act as a fragrance ingredient and solvent.
Uses
Used in Personal Care Industry:
Hexyl myristate is used as an emollient and conditioning agent for its ability to soften and smooth the skin, providing a protective barrier to prevent moisture loss. It is incorporated into lotions, creams, and hair care products to enhance their moisturizing and conditioning effects.
Used in Cosmetic Formulations:
Hexyl myristate is used as a fragrance ingredient and solvent in cosmetic formulations, contributing to the product's texture, stability, and performance. Its use in cosmetics is deemed safe by the Cosmetic Ingredient Review Expert Panel, ensuring the safety and efficacy of products containing this ingredient.
Check Digit Verification of cas no
The CAS Registry Mumber 42231-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,3 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42231-99:
(7*4)+(6*2)+(5*2)+(4*3)+(3*1)+(2*9)+(1*9)=92
92 % 10 = 2
So 42231-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O2/c1-3-5-7-9-10-11-12-13-14-15-16-18-20(21)22-19-17-8-6-4-2/h3-19H2,1-2H3
42231-99-2Relevant articles and documents
Design, synthesis, antibacterial, and QSAR studies of myristic acid derivatives
Narasimhan, Balasubramanian,Mourya, Vishnukant,Dhake, Avinash
, p. 3023 - 3029 (2008/09/20)
A series of esters and amides of myristic acid was synthesized and tested in vitro for antibacterial activity against Gram-positive and Gram-negative bacteria. All the compounds showed activity comparable to that of the standard drug, ciprofloxacin. The structural characteristics governing antibacterial activity of myristic acid derivatives was studied using QSAR methodology. The results showed that the antibacterial activity could be modeled using the topological descriptor, valence molecular connectivity index. The predictive ability of the models was cross-validated by construction of a test set. The low residual activity and high cross-validated r2 values ( rcv2 ) observed indicated the predictive ability of the developed QSAR models.
