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13998-76-0

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13998-76-0 Usage

General Description

(Methylimino)diethane-1,2-diyl distearate, also known as MDDS, is a chemical compound commonly used as an emollient and skin conditioning agent in cosmetic and personal care products. It is typically derived from the reaction between stearic acid and diethanolamine, and is known for its ability to moisturize and protect the skin. MDDS is often included in lotions, creams, and lipsticks due to its smooth and creamy texture, as well as its ability to enhance the spreadability and feel of the products. However, it is important to note that MDDS can be a potential allergen for some individuals and may cause skin irritation in high concentrations. Therefore, it is recommended to use products containing MDDS with caution and to discontinue use if any adverse reactions occur.

Check Digit Verification of cas no

The CAS Registry Mumber 13998-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13998-76:
(7*1)+(6*3)+(5*9)+(4*9)+(3*8)+(2*7)+(1*6)=150
150 % 10 = 0
So 13998-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C41H81NO4/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-40(43)45-38-36-42(3)37-39-46-41(44)35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-5-2/h4-39H2,1-3H3

13998-76-0SDS

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 2-[methyl(2-octadecanoyloxyethyl)amino]ethyl octadecanoate

1.2 Other means of identification

Product number -
Other names (Methylimino)diethane-1,2-diyl distearate

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:13998-76-0 SDS

13998-76-0Downstream Products

13998-76-0Relevant articles and documents

Synthesis, Surface Properties, and Antibacterial Activity of Novel Ester-Containing Cationic Silicone Surfactants and Their Utilization as Fabric-Finishing Agents

Wei, Yuan,Zheng, Cheng,Zhang, Zhenqiang,Zeng, Zhaowen,Mao, Taoyan,Long, Shikang,Ling, Hui

, p. 285 - 299 (2018/10/24)

In this study, a series of cationic silicone surfactants SiQCnCl containing ester groups and double long-chain alkyls (n = 9, 11, 13, 15, and 17) were synthesized by microwave irradiation and characterized using infrared Fourier transform (FTIR), 1H nuclear magnetic resonance (1H NMR), and thermogravimetric analysis (TGA). Surface activity and adsorption of these surfactants were investigated by measuring the equilibrium surface tension. The critical micelle concentration (CMC) decreased with increasing alkyl length of SiQCnCl at 25 °C and so did the corresponding surface tension at the CMC (γCMC). The aggregation behavior in aqueous solutions was also investigated systemically through transmission electron microscopy (TEM) and dynamic light scattering (DLS). Spherical or ellipsoidal-like aggregates with diameters ranging from 300 to 900 nm were observed. It is also shown that the cationic silicone surfactants exhibit certain antibacterial properties against Staphylococcus aureus but slightly poor to Escherichia coli. The morphological structure of SiQC15Cl-treated cotton fabrics was observed using scanning electron microscopy (SEM), which showed that the surface became neat and smooth. What is more, the finished cotton fabrics maintained some antibacterial properties with improved softness, which may provide a more comfortable and healthy lifestyle. This work may also be helpful to the design and application of functional cationic silicone surfactants.

SATURATED AND POLYMERIZABLE AMPHIPHILES WITH FLUOROCARBON CHAINS. INVESTIGATION IN MONOLAYERS AND LIPOSOMES.

Elbert,Folda,Ringsdorf

, p. 7687 - 7692 (2007/10/02)

The synthesis and characterization of several saturated and polymerizable amphiphiles with fluorocarbon chains are described. Monolayers of lipids containing fluorocarbon chains are more stable than those formed from their hydrocarbon counterparts. The creation of phase-separated monolayers and liposomes is possible when the membrane is composed of a mixture of lipids containing hydrocarbon chains and lipids containing fluorocarbon chains. Phase separation even occurs when the two lipids bear the same head group. Complete phase separation of a natural lipid (DMPC) and a lipid with fluorocarbon chains, 1, could be demonstrated in liposomes by using freeze-fracture electron microscopy. Phase separation was even confirmed when the percentage of the fluorocarbon amphiphile was as low as 5 mol%. The polymerization behavior of unsaturated amphiphiles with fluorocarbon chains was investigated in monolayers and liposomes.

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