13048-89-0

Usage

Explanation

The compound's full name, indicating its structure and composition.

Explanation

The compound is made up of two specific organic molecules and one inorganic molecule.

Explanation

The compound is utilized in the process of chemical synthesis, acting as a reagent to facilitate reactions.

Explanation

It is employed in industrial settings to prevent or slow down the corrosion of materials, particularly metals.

Explanation

The compound has the potential to be used in the creation of various drugs and pharmaceuticals, serving as a foundational component in their synthesis.

Explanation

The compound may have hazardous properties or effects, which is why safety precautions are necessary when handling and using it.

Composition

Two molecules of 1,4-Butanediaminium,N1,N1,N4,N4-tetramethyl-N1,N4-bis(phenylmethyl)and one molecule of bromide

Chemical Synthesis

Used as a reagent

Industrial Application

Corrosion inhibitor

Pharmaceutical Industry

Potential use as a building block for drug synthesis

Safety Precautions

Handle with care and follow safety guidelines

Potential Hazards

Not explicitly mentioned, but implied due to the need for safety precautions

Upstream product

• 111-51-3 N,N,N',N'-tetramethyl-1,4-butanediamine 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

Dependence of amine-accelerated silicate condensation on amine structure

Diatoms are known to grow elaborate nano- and microstructured silica shells by depositing material from precursor-containing vesicles at mild temperature and pH. Oligo(1-methylazetane) and related moieties, in some cases attached to proteins, are believed

Two-Phase Reaction of 1-Bromooctane with Sodium Acetate and Potassium Acetate Catalyzed by Diquaternary Ammonium Salts

New unsaturated diquaternary ammonium salts (diquats) were prepared in two ways from ditertiary amines 3 and 1-bromoalkanes or from 1,4-dibromobut-2t-ene and tertiary monoamines.A comparison of their catalytic ability with that of saturated diquats and with that of corresponding monoquats was made.The reaction of n-C8H17Br with NaOAc or KOAc in the two phase system liquid-liquid without an additional solvent is catalyzed more effectively by the unsaturated diquats than by the saturated diquats and the monoquats.Most of the used quats catalyze the ester formation from NaOAc more effectively in the system liquid-liquid, however, the ester formation from KOAc more effectively in the system solid-liquid; KOAc is generally superior to NaOAc in both systems.Consequently, in the phase-transfer catalyzed ester formation from alkali acetate and alkyl halides not only the structure of the quat but also the inorganic cation of the acetate have influence on the rate of conversion.