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16260-26-7

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16260-26-7 Usage

Description

Octyl myristate, also known as Octyl Tetradecanoate, is an ester derived from myristic acid and octanol. It is a colorless to pale yellow liquid with a slight characteristic odor. Octyl myristate is a non-ionic, non-irritating, and non-toxic compound, making it suitable for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
Octyl myristate is used as an excipient for the formulation of pharmaceutical products, such as creams, lotions, and ointments, due to its emollient, solubilizing, and stabilizing properties.
Used in Cosmetic Industry:
In the cosmetic industry, octyl myristate is used as an emollient, solvent, and consistency agent in products like makeup, skincare, and hair care formulations. Its ability to provide a smooth and soft texture without greasiness makes it a popular choice.
Used in Food Industry:
Octyl myristate is used as an additive in the food industry, particularly in the production of flavors and fragrances, due to its ability to dissolve and stabilize these compounds.
Used in Antimicrobial Applications:
Octyl myristate exhibits antibacterial activity against both Gram-positive and Gram-negative bacteria in vitro, making it a potential candidate for use in antimicrobial products and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16260-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16260-26:
(7*1)+(6*6)+(5*2)+(4*6)+(3*0)+(2*2)+(1*6)=87
87 % 10 = 7
So 16260-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H44O2/c1-3-5-7-9-11-12-13-14-15-16-18-20-22(23)24-21-19-17-10-8-6-4-2/h3-21H2,1-2H3

16260-26-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name octyl tetradecanoate

1.2 Other means of identification

Product number -
Other names n-Tetradecansaeure-n-octylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16260-26-7 SDS

16260-26-7Downstream Products

16260-26-7Relevant articles and documents

Esterification of Tertiary Amides by Alcohols Through C?N Bond Cleavage over CeO2

Toyao, Takashi,Nurnobi Rashed, Md.,Morita, Yoshitsugu,Kamachi, Takashi,Hakim Siddiki,Ali, Md. A.,Touchy,Kon, Kenichi,Maeno, Zen,Yoshizawa, Kazunari,Shimizu, Ken-ichi

, p. 449 - 456 (2018/09/11)

CeO2 has been found to promote ester forming alcoholysis reactions of tertiary amides. The present catalytic system is operationally simple, recyclable, and it does not require additives. The esterification process displays a wide substrate scope (>45 examples; up to 93 % isolated yield). Results of a density functional theory (DFT) study combined with in situ FT-IR observations indicate that the process proceeds through rate limiting addition of a CeO2 lattice oxygen to the carbonyl group of the adsorbed acetamide species with energy barrier of 17.0 kcal/mol. This value matches well with experimental value (17.9 kcal/mol) obtained from analysis of the Arrhenius plot. Further studies by in situ FT-IR and temperature programmed desorption using probe molecules demonstrate that both acidic and basic properties are important, and consequently, CeO2 showed the best performance for the C?N bond cleavage reaction.

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