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5392-36-9

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5392-36-9 Usage

Description

2-hydroxy-N,N-dioctylpropanamide is an organic compound that belongs to the family of amides. It is a derivative of propanamide, with two octyl groups attached to the nitrogen atom and a hydroxy group attached to the carbon atom.

Uses

Used in Inks, Coatings, and Adhesives Industry:
2-hydroxy-N,N-dioctylpropanamide is used as a surfactant and emulsifier for its ability to lower the surface tension of liquids, allowing them to mix more easily.
Used in Metalworking Fluids:
2-hydroxy-N,N-dioctylpropanamide is used as a corrosion inhibitor to protect metal surfaces from corrosion during the manufacturing process.
Used as a Lubricant Additive:
2-hydroxy-N,N-dioctylpropanamide is used to enhance the performance of lubricants by reducing friction and wear.
Used as a Dispersing Agent in Personal Care Products:
2-hydroxy-N,N-dioctylpropanamide is used to improve the stability and uniformity of formulations in personal care products.

Check Digit Verification of cas no

The CAS Registry Mumber 5392-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5392-36:
(6*5)+(5*3)+(4*9)+(3*2)+(2*3)+(1*6)=99
99 % 10 = 9
So 5392-36-9 is a valid CAS Registry Number.

5392-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dioctyl-DL-lactamide

1.2 Other means of identification

Product number -
Other names N-cyclohexyl-lactamide

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:5392-36-9 SDS

5392-36-9Downstream Products

5392-36-9Relevant articles and documents

Gamma-radiolytic stability of new methylated TODGA derivatives for minor actinide recycling

Galn, Hitos,Zarzana, Christopher A.,Wilden, Andreas,Nez, Ana,Schmidt, Holger,Egberink, Richard J. M.,Leoncini, Andrea,Cobos, Joaqun,Verboom, Willem,Modolo, Giuseppe,Groenewold, Gary S.,Mincher, Bruce J.

, p. 18049 - 18056 (2015/10/28)

The stability against gamma radiation of MeTODGA (methyl tetraoctyldiglycolamide) and Me2TODGA (dimethyl tetraoctyldiglycolamide), derivatives from the well-known extractant TODGA (N,N,N′,N′-tetraoctyldiglycolamide), were studied and compared. Solutions of MeTODGA and Me2TODGA in alkane diluents were subjected to 60Co γ-irradiation in the presence and absence of nitric acid and analyzed using LC-MS to determine their rates of radiolytic concentration decrease, as well as to identify radiolysis products. The results of product identification from three different laboratories are compared and found to be in good agreement. The diglycolamide (DGA) concentrations decreased exponentially with increasing absorbed dose. The MeTODGA degradation rate constants (dose constants) were uninfluenced by the presence of nitric acid, but the acid increased the rate of degradation for Me2TODGA. The degradation products formed by irradiation are also initially produced in greater amounts in acid-contacted solution, but products may also be degraded by continued radiolysis. The identified radiolysis products suggest that the weakest bonds are those in the diglycolamide center of these molecules.

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