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The threshold value is the concentration at which an aroma or taste can be detected (air, water and fat). The recognition threshold or arousal threshold of olfactory neurons is the concentration at which you can identify an odor (air, water and fat). The odour activity value is the concentration divided by the threshold.
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 .
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.
Toxic: a chemical that has a median lethal concentration (LC 50) in air of more than 200 parts per million (ppm) but not more than 2,000 parts per million by volume of gas or vapor, or more than 2 milligrams per liter but not more than 20 milligrams per liter of mist, fume or dust, when administered by continuous inhalation for 1 hour (or less if death occurs within 1 hour) to albino rats ...
The recognition odor threshold is usually a factor of two to five higher than the detection threshold. [22] The measurement of odor concentration is the most widespread method to quantify odors. It is standardized in CEN EN 13725:2003. [23] The method is based on dilution of an odor sample to the odor threshold. The numerical value of the odor ...
The threshold of toxilogical concern (or TTC) is a method for determining the level of exposure to chemicals above which would be considered toxic, [1] in cases where data about such chemicals is scarce or non-existent.
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.
The permethylated derivative of tren has the formula N(CH 2 CH 2 NMe 2) 3. "Me 6 tren" forms a variety of complexes but, unlike tren, does not stabilize Co(III). Related amino-triphosphines are also well developed, such as N(CH 2 CH 2 PPh 2) 3 (m.p. 101-102 °C). This species is prepared from the nitrogen mustard N(CH 2 CH 2 Cl) 3. [7]