Is triethylamine hydrochloride soluble?

Soluble in water at 20°C 1440 g/L. Soluble in ethanol, chloroform, and alcohol. Insoluble in ether. Hygroscopic.

What are the products of the reaction between triethylamine and HCL?

Such reactions lead to the production of hydrogen chloride which combines with triethylamine to form the salt triethylamine hydrochloride, commonly called triethylammonium chloride.

Is triethylamine soluble in water?

Triethylamine is a polar organic compound with intermolecular forces not compatible with water. Therefore triethylamine is slightly soluble in water.

Is triethylamine hydrochloride soluble in THF?

Triethylamine hydrochloride is a by-product. My product (polyamide) is soluble in most organic solvents (water, ethanol, methanol, dichlorometane) and insoluble in acetone, DMSO, hexane, THF, dioxane, ethyl acetate… Can you suggest any method to separate my product?

How do you remove triethylamine from a compound?

If it deprotonated, you can use vaccuum (bp is about 90 degrees) or rinse with a non-polar solvent like ether. If it is protonated, you can wash with water, methanol, ethanol, etc.

How do you remove triethylamine from a sample?

– Distillation may work if the product or mixture of products are stable in the distillation conditions. If so, vacuum distillation may work fine. The use of co-solvents cal also help and depending on the desired final level of triethylamine you can apply stripping with nitrogen of vapour.

Is triethylamine a tertiary amine?

A tertiary amine that is ammonia in which each hydrogen atom is substituted by an ethyl group.

What is the density of triethylamine?

726 kg/m³Triethylamine / Density

Is triethylamine a strong or weak base?

The highest pKaH value here is 10.8 for triethylamine. That makes triethylamine the strongest base out of all of those listed.

Which of the following amines is most soluble in water?

primary amine
The highest soluble amine would be primary amine, because it can form more H-bonds with water since 1o amine have −NH2 (2 Hydrogen) for H-bonding which decreases as we move on to secondary or tertiary amine.

Is triethylamine a strong base?

How do you remove triethylamine from a solution?