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74918-57-3

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74918-57-3 Usage

Description

Isopalmitic chloride, with the chemical formula C16H33Cl, is a fatty acid chloride derived from palmitic acid. It is commonly found in natural sources such as palm oil and animal fats. This versatile compound is utilized in various chemical processes, particularly in the synthesis of esters, amides, and other organic compounds. Known for its ability to enhance the stability and functionality of formulations, Isopalmitic chloride plays a crucial role in the manufacturing of a wide range of products in the cosmetic, pharmaceutical, and personal care industries.

Uses

Used in Surfactant and Emulsifier Production:
Isopalmitic chloride is used as a key component in the production of surfactants and emulsifiers, which are essential for creating stable mixtures of oil and water in various applications.
Used in Cosmetics Industry:
In the cosmetics industry, Isopalmitic chloride is used as a stabilizer and functional agent for enhancing the performance and quality of cosmetic products.
Used in Pharmaceutical Industry:
Isopalmitic chloride is used as an ingredient in the synthesis of pharmaceutical compounds, contributing to the development of effective medications.
Used in Personal Care Industry:
Isopalmitic chloride is used in the personal care industry as a component in the formulation of products such as soaps, shampoos, and lotions, improving their overall quality and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 74918-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,1 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74918-57:
(7*7)+(6*4)+(5*9)+(4*1)+(3*8)+(2*5)+(1*7)=163
163 % 10 = 3
So 74918-57-3 is a valid CAS Registry Number.

74918-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hexyldecanoic acid chloride

1.2 Other means of identification

Product number -
Other names 2-hexyl-decanoyl chloride

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:74918-57-3 SDS

74918-57-3Upstream product

74918-57-3Relevant articles and documents

LIPIDS FOR LIPID NANOPARTICLE DELIVERY OF ACTIVE AGENTS

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Page/Page column 54, (2020/05/21)

Compounds are provided having the following structure: (I) or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein G1, R1, R2, L, and n are as defined herein. Use of the compounds as a component of lipid nanoparticle formulations for delivery of a therapeutic agent, compositions comprising the compounds and methods for their use and preparation are also provided.

LIPID DELIVERY OF THERAPEUTIC AGENTS TO ADIPOSE TISSUE

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Page/Page column 147-148, (2018/11/10)

A method of treating a disease mediated by protein expression in adipose tissue by intraperitoneally administering a composition comprising a lipid nanoparticle encapsulating or associated with a therapeutic agent (e.g., a nucleic acid), thereby delivering the therapeutic agent to adipose tissue of the subject and altering protein expression in the adipose tissue is provided herein. A method for delivering a therapeutic agent to adipose tissue of a subject in need thereof is also provided.

Method for cleaving alpha carbon-carbon single bonds in ketone under condition of metal-free catalysis

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Paragraph 0017; 0020, (2017/10/07)

The invention discloses a method for selectively activating and cleaving alpha carbon-carbon single bonds in ketone under the condition of metal-free catalysis. The method is characterized in that the alpha carbon-carbon single bonds in the ketone are activated and cleaved by solvent induction and driving of intermediate structure factors formed by the ketone and hydrazine without metal catalysts. Transition metal for catalysis is omitted, the method is environmentally friendly, reaction cost is reduced to a certain degree, methodology of selective cleavage of the carbon-carbon single bonds is enriched, and a new idea is provided for activation of inertial chemical bonds under mild conditions.

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