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3886-90-6

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3886-90-6 Usage

General Description

N,N-Dimethyl-9-octadecenamide, also known as oleamide, is a fatty acid primary amide that is used as a lubricant, anti-static agent, and slip additive in various industries. It is a white, waxy solid that is insoluble in water but soluble in most organic solvents. Oleamide is known to have various physiological effects, including regulating sleep and having potential neuroprotective properties. It is also being studied for its potential use in the treatment of substance abuse and addiction. Additionally, oleamide has been investigated for its antioxidant and anti-inflammatory properties, making it a compound of interest in the field of pharmaceuticals and nutraceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 3886-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3886-90:
(6*3)+(5*8)+(4*8)+(3*6)+(2*9)+(1*0)=126
126 % 10 = 6
So 3886-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H41NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(22)21(2)3/h4-19H2,1-3H3

3886-90-6SDS

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 N,N-dimethyloctadecanamide

1.2 Other means of identification

Product number -
Other names Hallcomid M 18

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:3886-90-6 SDS

3886-90-6Relevant articles and documents

A METHOD OF TREATING PERIPHERAL INFLAMMATORY DISEASE

-

Paragraph 0078-0084; 0137-0128, (2016/12/01)

An active for use in the treatment or inhibition of an inflammatory disease associated with over-activation of Toll-like Receptor 4 (TLR4), Toll-like Receptor 2 (TLR2) and Myeloid differentiating protein 88 (Myd88) adaptor-like protein (Mal) while maintaining a subject's ability to respond normally to a pathogen, in which the active is an oleamide or a derivative thereof.

PROCESS FOR PRODUCING ALIPHATIC CARBOXYLIC ACID AMIDE

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Page/Page column 5, (2010/12/29)

The present invention relates to a process for producing an aliphatic carboxylic acid amide, including the step of reacting an aliphatic carboxylic acid or an alkyl ester thereof containing an alkyl group having 1 to 4 carbon atoms with a mono- or dialkylamine containing an alkyl group or groups having 1 to 4 carbon atoms in the presence of a solid acid catalyst containing titanium oxide as a main component and an oxide or oxides of at least one element selected from elements (except titanium) belonging to Groups 4, 5 and 14 of the long form of the periodic table, wherein the catalyst has an average particle diameter of 2 μm or more. The process for producing an aliphatic carboxylic acid amide according to the present invention has a high reaction efficiency of the reaction of the aliphatic carboxylic acid or alkyl ester thereof with the mono- or dialkylamine, and shows an excellent filtration efficiency in separation of the catalyst.

A CONVENIENT METHOD FOR THE SYNTHESIS OF CARBOXAMIDES AND PEPTIDES BY THE USE OF TETRABUTYLAMMONIUM SALTS

Watanabe, Yutaka,Mukaiyama, Teruaki

, p. 285 - 288 (2007/10/02)

Various carboxamides and peptides are prepared in good yields by treatment of free acids and amines in H2O-dichloromethane or aqueous THF with bis(o-nitrophenyl) phenylphosphonate in the presence of tetrabutylammonium hydrogen sulfate or bromide.Carboxylic esters are also successfully converted to amides via carboxylate salts in one-pot.

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