2174-16-5 Usage
Description
Triethanolamine Salicylate, also known as TEA-salicylate, is a pale yellow to amber crystalline solid that serves as an intermediate in the manufacturing process of various products. It is a water-soluble chemical with limited UV absorption capability and is recognized as a pharmaceutical aid and alkalizer.
Uses
Used in Surface Active Agents:
Triethanolamine Salicylate is used as an intermediate for the production of surface active agents, which are essential in the creation of textile specialties, waxes, polishes, herbicides, petroleum demulsifiers, toilet goods, cement additives, and cutting oils.
Used in Emulsions:
It is utilized in making emulsions with mineral and vegetable oils, paraffin, and waxes, which are crucial in various industries for different applications.
Used as a Solvent:
Triethanolamine Salicylate serves as a solvent for casein, shellac, and dyes, playing a vital role in the manufacturing process of these substances.
Used in Synthetic Resins:
It is employed in the production of synthetic resins, which are widely used in the plastics and coatings industries.
Used in Wood and Paper Treatment:
The compound is used to increase the penetration of organic liquids into wood and paper, enhancing their properties and performance.
Used in the Textile Industry:
Triethanolamine Salicylate is used in the production of lubricants for the textile industry, improving the quality and efficiency of textile manufacturing processes.
Used as a Pharmaceutical Aid:
It functions as an alkalizer and is recognized as a pharmaceutic aid, contributing to the development and formulation of various medications.
Used in Sunscreen Products:
TEA-salicylate is a chemical UVB absorber, one of the 21 FDA-approved sunscreen chemicals with an approved usage level of 5 to 12 percent. It is used as a preservative in the formulation of sunscreen products, providing protection against harmful UV radiation.
Used in the Cosmetics Industry:
Formulators may also use Triethanolamine Salicylate as a preservative in the cosmetics industry, ensuring the stability and longevity of various cosmetic products.
Check Digit Verification of cas no
The CAS Registry Mumber 2174-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2174-16:
(6*2)+(5*1)+(4*7)+(3*4)+(2*1)+(1*6)=65
65 % 10 = 5
So 2174-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O3.C6H15NO3/c8-6-4-2-1-3-5(6)7(9)10;8-4-1-7(2-5-9)3-6-10/h1-4,8H,(H,9,10);8-10H,1-6H2
2174-16-5Relevant articles and documents
Triethanolammonium salts of biologically active carboxylic acids
Kondratenko, Yu. A.,Kochina,Fundamensky,Vlasov, Yu. G.
, p. 2710 - 2714 (2015)
Triethanolammonium salts (protatranes) of biologically active carboxylic acids (nicotinic, cinnamic, benzoic, salicylic, oxalic, malonic, succinic, malic, citric) were synthesized in yields exceeding 90%. The structure of the synthesized compounds was studied by IR spectroscopy and X-ray diffraction analysis.
Biological Activity of Protic Ionic Liquids Based on Tris(2-hydroxyethyl)ammonium Salts and the Crystal Structure of Tris(2-hydroxyethyl)ammonium Malate
Anikina, L. M.,Gurzhii, V. V.,Kochina, T. A.,Kondratenko, Yu. A.,Krutikov, V. I.,Panova, G. G.,Udalova, O. R.,Ugolkov, V. L.
, p. 1407 - 1415 (2020/10/02)
Abstract: The antimicrobial and growth-stimulating activities of nine protic ionic liquids (PILs)—tris(2-hydroxyethyl)ammonium salts (protatranes) of cinnamic, benzoic, salicylic, oxalic, malonic, succinic, malic and citric acids—were investigated for the first time. It was found that tris(2-hydroxyethyl)ammonium salts of cinnamic, benzoic and malonic acids have a positive impact on seeds germination and growth characteristics of garden cress (Lepidium sativum L.) sprouts. All the investigated PILs exhibited selective activity against Staphylococcus aureus bacteria. PILs based on tris(2-hydroxyethyl)ammonium malate with the melting point of 41°C were isolated as crystals to perform a comparative study of the crystal structure by single-crystal X-ray diffraction. In contrast to cations in tris(2-hydroxyethyl)ammonium succinate, cations in malate have a tricyclic endo conformation that is most typical of tris(2-hydroxyethyl)ammonium salts.
Biologically active protic (2-hydroxyethyl)ammonium ionic liquids. Liquid aspirin
Adamovich,Mirskov,Mirskova,Voronkov
, p. 1260 - 1261 (2013/07/26)
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