CE-123 99% purity Nootropic Powder 1000mg
CE-123 White dosing spoon 50mg.
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Buy CE-123 Nootropic Powder
This modafinil analog shows a unique enhancing effect on memory acquisition on day one after a single administration before training at various drug concentrations.
A second dose on day two before training shows an enhancing effect only at 1 mg/kg, the same as for the retrieval phase.
A dose-dependent effect on cognition, learning and memory consolidation was reported previously for classical psychostimulants, as well as for modafinil.
Alex wimFeb 27, 2019, 15:17This product does works well with high and low dopamine variation, focus is at the meeting.
Jun 5, 2019, 06:03
Does CE -123 have the wakefullness effect as modafinil.
Also does it have a stimulating mental effect to help with attention span. Thank yoi.Jun 5, 2019, 13:20
CE-123 enhanced cognitive flexibility at very low dosages without producing impulsive responding even at higher dosages and therefore may be suitable for further testing of its cognition-enhancing properties in different behavioral paradigms.
If you are asking about my personal feedback hell yea I like research CE-123
However, please review the rules available below
Jun 3, 2019, 05:14
Sorry in advance for my English.
Question: How did you synthesize this drug? If so far there is almost no information, for example: pubchem or any other database.
There are only a couple of articles on the Internet about this substance.
P.S. I am not saying to tell the secrets of your store, I just want to buy it, but these questions bother meJun 3, 2019, 11:13
Synthesis of 5-((Benzhydrylsulfinyl)methyl)thiazole (CE-123)
5-((Benzhydrylthio)methyl)thiazole (21.09 g, 71 mmol) was dissolved in 50 ml of glacial acetic acid. Then, 8.19 ml (71 mmol) of 30% H2O2 was dropped into the solution and stirred for 12 h. The acid solution was neutralized with 5% sodium bicarbonate in an ice-bath. Reaction products were extracted (3×) from the neutral solution with 150 ml of ethyl acetate. Organic extracts were collected, combined, dried over Na2SO4, and filtered off. Then, the solvent was separated under reduced pressure to obtain a brownish solid which was suspended in 400 ml of diethyl ether and stirred under reflux for 2 h. The etheric solution was slowly cooled +4°C and the resulting product was filtered under reduced pressure and washed (3×) with 50 ml of cold diethyl ether and dried under high vacuum overnight to obtain 13.178 g of a white powdered product (yield 59.2%).