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The pK a of protonated triethylamine is 10.75, [4] and it can be used to prepare buffer solutions at that pH. The hydrochloride salt, triethylamine hydrochloride (triethylammonium chloride), is a colorless, odorless, and hygroscopic powder, which decomposes when heated to 261 °C. Triethylamine is soluble in water to the extent of 112.4 g/L at ...
Tris(2-aminoethyl)amine is the organic compound with the formula N(CH 2 CH 2 NH 2) 3.This colourless liquid is soluble in water and is highly basic, consisting of a tertiary amine center and three pendant primary amine groups.
teaa, triethylamine/acetate buffer. Identifiers CAS Number. ... 161.24 g/mol Boiling point: 164.5 °C (328.1 °F; 437.6 K) Solubility in water. Soluble Hazards
Triethylaluminium ignites on contact with air and will ignite and/or decompose on contact with water, and with any other oxidizer [13] —it is one of the few substances sufficiently pyrophoric to ignite on contact with cryogenic liquid oxygen. The enthalpy of combustion, Δ c H°, is –5105.70 ± 2.90 kJ/mol [14] (–22.36 kJ/g).
tert-Butylamine (also erbumine and other names) is an organic chemical compound with the formula (CH 3) 3 CNH 2.It is a colorless liquid with a typical amine-like odor. tert-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and isobutylamine.
DCM is produced by treating either chloromethane or methane with chlorine gas at 400–500 °C. At these temperatures, both methane and chloromethane undergo a series of reactions producing progressively more chlorinated products. In this way, an estimated 400,000 tons were produced in the US, Europe, and Japan in 1993. [12] CH 4 + Cl 2 → CH ...
Steric effects make triisopropylamine difficult to synthesise and unlike less hindered tertiary amines (such as triethylamine) it cannot be produced by the alkylation of ammonia with alcohol; attempts to do so stall at diisopropylamine. It can be prepared from diisopropylamine on the laboratory scale: [2]
Ethanolamine is the second-most-abundant head group for phospholipids, substances found in biological membranes (particularly those of prokaryotes); e.g., phosphatidylethanolamine. It is also used in messenger molecules such as palmitoylethanolamide , which has an effect on CB1 receptors.