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2174-16-5

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2174-16-5 Usage

Chemical Properties

pale yellow to amber crystalline solid

Uses

Different sources of media describe the Uses of 2174-16-5 differently. You can refer to the following data:
1. TriethanolaMine salicylate can be used as intermediate in the manufacture of surface active agents, textile specialties, waxes, polishes, herbicides, petroleum demulsifiers, toilet goods, cement additives, cutting oils. In making emulsions with mineral and vegetable oils, paraffin and waxes. Solvent for casein, shellac, dyes; manufacture of synthetic resins; increasing the penetration of organic liquids into wood and paper. In the production of lubricants for the textile industry. Pharmaceutic aid (alkalizer).
2. TEA-salicylate is a chemical uVB absorber. This is one of the 21 FDAapproved sunscreen chemicals with an approved usage level of 5 to 12 percent. TeA-salicylate is a water-soluble chemical with limited uV absorption capability. Formulators may also use it as a preservative.

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

2174-16-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (74412)  Trolamine salicylate  analytical standard

  • 2174-16-5

  • 74412-100MG

  • 1,100.97CNY

  • Detail

2174-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIETHANOLAMINE SALICYLATE

1.2 Other means of identification

Product number -
Other names Salicylic acid

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:2174-16-5 SDS

2174-16-5Synthetic route

triethanolamine
102-71-6

triethanolamine

aspirin
50-78-2

aspirin

triethanolamine salicylate
2174-16-5

triethanolamine salicylate

Conditions
ConditionsYield
With methanol for 1h; Reflux;99%
triethanolamine
102-71-6

triethanolamine

salicylic acid
69-72-7

salicylic acid

triethanolamine salicylate
2174-16-5

triethanolamine salicylate

Conditions
ConditionsYield
In methanol for 1h; Reflux;99%
In methanol at 60 - 65℃;99%
In ethanol

2174-16-5Downstream Products

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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