25114-70-9

Usage

Uses

Used in Pharmaceutical Industry:
Triethanolamine hydrobromide is used as a buffering agent, emulsifier, and stabilizer in the manufacturing of pharmaceuticals. Its properties help improve the solubility, stability, and efficacy of various medications.
Used in Cosmetic and Personal Care Industry:
In cosmetics and personal care products, triethanolamine hydrobromide serves as a buffering agent, emulsifier, and stabilizer. It helps maintain the pH balance, consistency, and shelf life of products such as creams, lotions, and shampoos.
Used in Metalworking Industry:
Triethanolamine hydrobromide is used as a corrosion inhibitor in metalworking fluids. It helps prevent the corrosion of metal surfaces during manufacturing processes, thereby extending the life of machinery and equipment.
Used in Organic Synthesis:
As an intermediate in organic synthesis, triethanolamine hydrobromide is utilized in the production of various chemical compounds and pharmaceuticals. Its reactivity and versatility make it a valuable component in the synthesis of new molecules.
Safety Precautions:
It is important to handle triethanolamine hydrobromide with caution, as it can be harmful if ingested or inhaled and can cause irritation to the skin and eyes. Proper safety measures, such as wearing protective gear and following handling guidelines, should be taken to minimize potential risks.

Upstream product

• 102-71-6 triethanolamine 

Downstream Products

• 3890-99-1 bis(2-bromoethyl)amine 
• 4328-04-5 tetrakis(2-hydroxyethyl)ammonium bromide 
• 89583-07-3 N-(2-bromoethyl)morpholine 

Relevant academic research and scientific papers

Tris(2-hydroxyethyl)ammonium salts: 2,8,9-Trihydroprotatranes

New method of synthesis of tris(2-hydroxyethyl)ammonium salts, 2,8,9-trihydroprotatranes X-[HN(CH2CH2OH) 3]+, based on the reaction of tris(2-hydroxyethyl)amine (triethanolamine) with ammonium salts NH4X (X = F, Cl, Br, I, NO 3, ClO4) was developed. 1H, 13C, 15N NMR and IR spectra of these protatranes were investigated, as well as those of their analogs with X = RCH2COO (R = H; 2-MeC 6H4O; 2-Me-4ClC6H3O; 2-MeC 6H4S; 4-ClC6H4S; 4-ClC 6H4SO2; 3-IndS; 3-(PhCH2-IndS) prepared from the corresponding acids RCH2COOH and triethanolamine. The parameters of IR and NMR spectra of the studied protatranes were governed by the nature of substituent X, which also determined the character of the intra and intermolecular hydrogen bonds NH...O and OH...O in the protatrane framework.

S-(trimethoxysilylmethyl)- and S-(silatranylmethyl)isothiuronium halides and their N-substituted derivatives

Previously unknown S-(trimethoxysilylmethyl)- and S-(silatranylmethyl) isothiuronium halides and their N-substituted derivatives were prepared. According to the IR and UV spectra, these compounds exist in the solid state and in methanol and acetonitrile solutions in the form of two equilibrium salt structures: those with the positively charged nitrogen and carbon atoms, or predominantly in one of these. In solutions of the iodides in highly polar acetonitrile, the first salt structure can occur in an equilibrium with its dissociation products, S-organylisothiourea (or its N-substituted derivative) and hydrogen iodide.