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3-Ethyl-2,2-dimethyloctane; 3-Ethyl-2,3-dimethyloctane; 3-Ethyl-2,4-dimethyloctane; 3-Ethyl-2,5-dimethyloctane; 3-Ethyl-2,6-dimethyloctane; 3-Ethyl-2,7-dimethyloctane
2,5-Dimethoxy-4-iodoamphetamine (DOI) is a psychedelic drug and a substituted amphetamine. Unlike many other substituted amphetamines, however, it is not primarily a stimulant . [ 3 ] DOI has a stereocenter and R -(−)-DOI is the more active stereoisomer .
3-Ethyl-2-methylundecane; 3-Ethyl-3-methylundecane; 3-Ethyl-4-methylundecane; 3-Ethyl-5-methylundecane; 3-Ethyl-6-methylundecane; 3-Ethyl-7-methylundecane
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IDNNA (2,5-dimethoxy-4-iodo-N,N-dimethylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. It is also the N,N-dimethyl analog of DOI. IDNNA was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 2.6 mg, and the duration unknown. [1] IDNNA produces few to no effects.
Iodoacetamide (IAA) is an organic compound with the chemical formula I C H 2 CO NH 2.It is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate.
Idoxuridine is available as either a 0.5% ophthalmic ointment or as a 0.1% ophthalmic solution. [3] The dosage of the ointment is every 4 hours during day and once before bedtime. [ 3 ] The dosage of the solution is 1 drop in the conjunctival sac hourly during the day and every 2 hours during the night until definitive improvement, then 1 drop ...
2C-T-2 (2,5-dimethoxy-4-ethylthiophenethylamine) 2C-T-7 (2,5-dimethoxy-4-propyl t hiophenethylamine) DOM (2,5-dimethoxy-4-methylamphetamine), DOM being short for d es o xy m ethyl, referring to the removal of the oxygen atom from the methoxy group on the "4" carbon.