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Triethylamine is prepared by the alkylation of ammonia with ethanol: [10]. NH 3 + 3 C 2 H 5 OH → N(C 2 H 5) 3 + 3 H 2 O. The pK a of protonated triethylamine is 10.75, [4] and it can be used to prepare buffer solutions at that pH.
Refrigerant concentration limit / immediately dangerous to life or health in parts per million (volume per volume) and grams per cubic meter Molecular mass in atomic mass units Normal boiling points for pure substances, bubble and dew points for zeotropic blends, or normal boiling point and azeotropic temperature for the azeotropic blends, at ...
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
This is a list of the various reported boiling points for the elements, with recommended values to be used elsewhere on Wikipedia. For broader coverage of this topic, see Boiling point . Boiling points, Master List format
Triethylenetetramine (TETA and trien), also known as trientine when used medically, is an organic compound with the formula [CH 2 NHCH 2 CH 2 NH 2] 2.The pure free base is a colorless oily liquid, but, like many amines, older samples assume a yellowish color due to impurities resulting from air oxidation.
Triethylphosphite is prepared by treating phosphorus trichloride with ethanol in the presence of a base, typically a tertiary amine: [1] PCl 3 + 3 EtOH + 3 R 3 N → P(OEt) 3 + 3 R 3 NH + 3 Cl −. In the absence of the base, the reaction of ethanol and phosphorus trichloride affords diethylphosphite ((EtO) 2 P(O)H). Of the many related ...
Like other simple aliphatic amines, ethylamine is a weak base: the pK a of [CH 3 CH 2 NH 3] + has been determined to be 10.8 [8] [9] Ethylamine undergoes the reactions anticipated for a primary alkyl amine, such as acylation and protonation. Reaction with sulfuryl chloride followed by oxidation of the sulfonamide give diethyldiazene, EtN=NEt. [10]