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69943-69-7

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69943-69-7 Usage

General Description

N-octyldodecanamide, also known as octyldodecyl amide, is a chemical compound used in various applications including as a lubricant, an emollient in cosmetics, and as a surfactant in personal care products. It is a long-chain fatty acid amide with a molecular formula of C20H41NO. N-octyldodecanamide is derived from renewable sources and is considered to be safe for use in personal care products. It acts as a barrier agent, helping to maintain the skin's natural moisture balance and providing a soft, smooth feel. In addition, it has lubrication properties that make it suitable for use in industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69943-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69943-69:
(7*6)+(6*9)+(5*9)+(4*4)+(3*3)+(2*6)+(1*9)=187
187 % 10 = 7
So 69943-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H41NO/c1-3-5-7-9-11-12-13-14-16-18-20(22)21-19-17-15-10-8-6-4-2/h3-19H2,1-2H3,(H,21,22)

69943-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-octyldodecanamide

1.2 Other means of identification

Product number -
Other names Dodecanamide,N-octyl

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:69943-69-7 SDS

69943-69-7Downstream Products

69943-69-7Relevant articles and documents

Substrate-selective dehydrocondensation at the interface of micelles and emulsions of common surfactants

Kunishima, Munetaka,Kikuchi, Kanako,Kawai, Yukio,Hioki, Kazuhito

supporting information; experimental part, p. 2080 - 2083 (2012/05/20)

Scratch the surface: Dehydrocondensations between carboxylates and amines by using an amphiphilic 1,3,5-triazinylammonium-based coupling agent were accelerated by the interfacial effect of micelles and emulsions of common surfactants (see figure). The reaction of carboxylates was promoted by both anionic and nonionic surfactants, and that of amines was promoted by only a nonionic surfactant. High selectivities for more lipophilic substrates were observed in micelles or emulsions. Copyright

Catalytic properties of supramolecular systems based on polyoxyethylated calixarenes and amines

Mirgorodskaya,Yatskevich,Kudryashova,Solov'Eva,Antipin,Zakharova,Konovalov

scheme or table, p. 529 - 535 (2011/10/31)

The rate of carboxylic ester cleavage by amphiphilic low-molecular-weight and polymeric amines in the presence of polyoxyethylated calix[4]arenes with different degrees of oxyethylation is determined by the formation of mixed aggregates, by the shift of pK a of the amine, and the character of the distribution of the reactants in functional micelles. All of the systems show a high substrate specificity. In the case of octyl- and decylamines, the reaction of p-nitrophenyl acetate is catalyzed and the reaction of more hydrophobic p-nitrophenyl laurate is inhibited. An opposite situation is observed in the systems based on branched polyethyleneimine: the reaction of p-nitrophenyl acetate is inhibited and the process involving p-nitrophenyl laurate is accelerated.

Effect of micellar surfactant solutions on the reactivity of long-chain amines

Mirgorodskaya,Kudryavtseva,Zuev,Vylegzhanina

, p. 1849 - 1852 (2007/10/03)

The kinetics of the interaction of long-chain alkylamines with p-nitrophenyl laurate in aqueous micellar solutions of cetylpyridinium bromide was studied. It was found that the reactivity of the amines changes when mixed aggregates are formed and that it depends on the ratio between components of the system. A nonlinear increase in the molecular packing density of the mixed micelles with the amine concentration was recorded by spin probe EPR.

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