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Triethylamine is the chemical compound with the formula N(CH 2 CH 3) 3, commonly abbreviated Et 3 N. Like triethanolamine and tetraethylammonium , it is often abbreviated TEA. [ 8 ] [ 9 ] It is a colourless volatile liquid with a strong fishy odor reminiscent of ammonia .
Odor threshold value (OTV) (also aroma threshold value (ATV), Flavor threshold) is defined as the most minimal concentration of a substance that can be detected by a human nose. Some substances can be detected when their concentration is only few milligrams per 1000 tonnes, which is less than a drop in an Olympic swimming pool. Odor threshold ...
Sheath cleaning is a hygienic process occasionally needed by male horses, both geldings and stallions, wherein a caretaker, groom or veterinarian checks the horse's sheath, the pocket of skin that protects the penis of the horse when it is not in use for urination (or, in the case of stallions, breeding). [1]
Accidents happen, but if you have a young pet, they happen a lot.
Odour activity value (OAV) is a measure of importance of a specific compound to the odour of a sample (e.g. food). It is calculated as the ratio between the concentration of individual substance in a sample and the threshold concentration of this substance (odour threshold value, the minimal concentration that can be detected by human nose).
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.
DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.
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]