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[2] [6] [7] [1] Hamilton Morris has further supported these findings with his own self-experimentation. [7] [6] According to Morris, the psychedelic effects of bufotenin are a cross between those of DMT and 5-MeO-DMT. [7] [6] Morris has stated that bufotenin may in fact be the psychedelic with the longest history of human entheogenic use. [7] [6]
Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin, a succinate salt, is chemical compound which is claimed by its manufacturer, the Russian company Pharmasoft Pharmaceuticals, to have antioxidant and actoprotector properties, [2] [3] but these purported properties of emoxypine have not been proven. [4]
Butyrophenone is an organic compound with the formula C 6 H 5 C(O)C 3 H 7. It is a colorless liquid. It is a colorless liquid. The butyrophenone structure—a ketone flanked by a phenyl ring and a butyl chain —forms the basis for many other chemicals containing various substituents .
2-Butyne (dimethylacetylene, crotonylene or but-2-yne) is an alkyne with chemical formula CH 3 C≡CCH 3. Produced artificially, it is a colorless, volatile, pungent liquid at standard temperature and pressure .
Butyne is an alkyne that contains 4 carbon and 6 hydrogen. It contains one triple bond and has two isomeric organic chemical compounds: 1-Butyne (ethylacetylene)
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.
Ethyl butylacetylaminopropionate is an insect repellent whose trade name is IR3535 and was developed and commercialized by Merck KGaA (Germany). It is a colorless and odorless oil with a good skin feel in final products, and it is biodegradable. [1] [2] [3]
Bromoform can be absorbed into the body by inhalation and through the skin. The substance is irritating to the respiratory tract, the eyes, and the skin, and may cause effects on the central nervous system and liver, resulting in impaired functions. Its LD 50 is 7.2 mmol/kg in mice, or 1.8 g/kg. The International Agency for Research on Cancer ...
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