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15566-80-0

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15566-80-0 Usage

General Description

"(Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide" is a long-chain fatty acid derivative that is classified as an amide compound. It is also known as oleylamine, and its chemical formula is C20H40N2O. Oleylamine plays a role in various applications, including as a surfactant, emulsifier, and corrosion inhibitor. It is commonly used in the production of pharmaceuticals, personal care products, and industrial coatings. Oleylamine is also utilized in the synthesis of nanoparticles and as a stabilizing agent in the production of colloidal metal particles. Additionally, it has been studied for its potential antimicrobial and antifungal properties. Due to its diverse range of applications, oleylamine is an important chemical compound in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15566-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15566-80:
(7*1)+(6*5)+(5*5)+(4*6)+(3*6)+(2*8)+(1*0)=120
120 % 10 = 0
So 15566-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H45N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22(26)25-21-20-24-19-18-23/h9-10,24H,2-8,11-21,23H2,1H3,(H,25,26)/b10-9-

15566-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-N-[2-(2-aminoethylamino)ethyl]octadec-9-enamide

1.2 Other means of identification

Product number -
Other names (Z)-N-(2-((2-Aminoethyl)amino)ethyl)-9-octadecenamide

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:15566-80-0 SDS

15566-80-0Downstream Products

15566-80-0Relevant articles and documents

Combination of antimicrobial and endotoxin-neutralizing activities of novel oleoylamines

Zorko, Mateja,Majerle, Andreja,Sarlah, David,Keber, Mateja Mancek,Mohar, Barbara,Jerala, Roman

, p. 2307 - 2313 (2005)

A combination of antimicrobial and endotoxin-neutralizing activities is desired in order to prevent progression from infection to sepsis due to the release of lipopolysaccharide from dying gram-negative bacteria. Lipopolyamines have emerged as a new type of endotoxin-neutralizing compound, but their antimicrobial activity has not been investigated. We synthesized a series of 10 oleoylamines differing in the polyamino head group, particularly in the number and separation between nitrogen atoms and the position of the oleoyl moiety. Compounds showed activity against both gram-negative and gram-positive bacteria in the micromolar range. Compounds were able to provide penetration of ethidium bromide into bacteria, indicating effects on the bacterial membrane. Oleoylamines neutralized endotoxin in Limulus amoebocyte lysate assays and by neutralization of tumor necrosis factor alpha release in human blood. Comparison of biological activities of compounds identified structural properties responsible for antimicrobial activity, and quantitative structure-property relationship analysis provided a quantitative model for prediction of activity of oleoylamines. Copyright

Imidazoline Mannich base corrosion inhibitor and preparation method thereof

-

Paragraph 0033; 0045; 0054; 0063; 0072, (2019/10/01)

The invention relates to the technical field of corrosion inhibitors, and in particular relates to an imidazoline mannich base corrosion inhibitor and a preparation method thereof. The imidazoline mannich base corrosion inhibitor is of the structure shown in the formula I. The imidazoline mannich base corrosion inhibitor is prepared from, by mass, 10-20% of benzaldehyde, 5-15% of butanone, 40-60%of oleic acid imidazoline, 10-30% of ethanol, 1-5% of concentrated hydrochloric acid and 0.1-0.5% of a catalyst. According to the imidazoline mannich base corrosion inhibitor, a benzene ring, an imidazole ring and an ultra-long hydrophobic alkyl chain on imidazoline are introduced, the benzene ring in benzaldehyde and N atoms in the imidazoline ring have relatively high electron cloud density andcan form a firm coordination bond with an empty d track of metal, and the super-long hydrophobic alkyl chain forms a hydrophobic membrane layer away from the surface of the metal and has a peripheralshielding effect on the surface of the metal, so that the corrosion inhibitor has excellent corrosion inhibition performance in a high-temperature acidification environment.

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