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CAS

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10287-60-2

2-aminoethyl stearate is a chemical compound that consists of a stearic acid molecule bound to an aminoethyl group. It possesses surfactant properties, allowing it to interact with both water and oil, and is known for its conditioning and moisturizing effects on the skin and hair.

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  • 10287-60-2 Structure

  • Basic information

    1. Product Name: 2-aminoethyl stearate
    2. Synonyms: 2-aminoethyl stearate;Ethanolamine octadecanoate;Octadecanoic acid 2-aminoethyl ester;Stearic acid 2-aminoethyl ester;Einecs 233-636-4
    3. CAS NO:10287-60-2
    4. Molecular Formula: C20H41NO2
    5. Molecular Weight: 327.54504
    6. EINECS: 233-636-4
    7. Product Categories: N/A
    8. Mol File: 10287-60-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 421.3°Cat760mmHg
    3. Flash Point: 249.1°C
    4. Appearance: /
    5. Density: 0.895g/cm3
    6. Vapor Pressure: 2.63E-07mmHg at 25°C
    7. Refractive Index: 1.459
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-aminoethyl stearate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-aminoethyl stearate(10287-60-2)
    12. EPA Substance Registry System: 2-aminoethyl stearate(10287-60-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10287-60-2(Hazardous Substances Data)

10287-60-2 Usage

Uses

Used in Cosmetic and Personal Care Industry:
2-aminoethyl stearate is used as an emulsifier and thickening agent for its ability to create stable emulsions, which helps in maintaining the texture and consistency of various cosmetic and personal care products.
Used in Industrial Applications:
2-aminoethyl stearate is used as a corrosion inhibitor in metalworking fluids, providing protection against metal corrosion and extending the life of machinery and equipment.
Used as a Lubricant Additive:
2-aminoethyl stearate is used in lubricant formulations to enhance their performance, reduce friction, and improve the overall efficiency of mechanical systems.

Check Digit Verification of cas no

The CAS Registry Mumber 10287-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,8 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10287-60:
(7*1)+(6*0)+(5*2)+(4*8)+(3*7)+(2*6)+(1*0)=82
82 % 10 = 2
So 10287-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(22)23-19-18-21/h2-19,21H2,1H3

10287-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoethyl octadecanoate

1.2 Other means of identification

Product number -
Other names Octadecanoic acid,2-aminoethyl ester

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:10287-60-2 SDS

10287-60-2Relevant articles and documents

An Improved method for synthesis of N-stearoyl and N-palmitoylethanolamine

Wang, Xiaosan,Wang, Tong,Wang, Xingguo

, p. 1305 - 1313 (2012)

Certain N-acylethanolamines interact with cannabinoid receptors and have anorexic and neuroprotective effects. Traditional methods for the synthesis of N-acylethanolamines use fatty acid chlorides, fatty acid methyl esters, free fatty acids and triacylgly

METHOD OF MAKING FATTY ACID N-ACYLALKANOLAMINES

-

Paragraph 0069-0074; 0076-0082; 0089; 0090, (2013/11/19)

The present invention relates to methods for making a fatty acid N-acylalkanolamine having the formula: One of the methods comprises the steps of providing a vinyl ester of a fatty acid having the formula: providing a primary or secondary alkanolamine having the formula: NHR1R2; and reacting the vinyl ester of the fatty acid with the alkanolamine under conditions effective to form the fatty acid N-acylalkanolamine. The other method comprises the steps of providing a fatty acid; purifying the fatty acid; providing a primary or secondary alkanolamine having the formula: NHR1R2; reacting the fatty acid with the alkanolamine under conditions effective to form the fatty acid N-acylalkanolamine; and purifying the formed fatty acid N-acylalkanolamine.

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