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Dioctyl sebacate (also di(2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol. It is an oily colorless liquid and is used as a plasticizer , including in the explosive C4 . [ 1 ]
2,5-Dimethoxy-4-hexylamphetamine (DOHx or DOHE) is a non-hallucinogenic serotonin receptor modulator of the phenethylamine, amphetamine, and DOx families. [1] [2] [3 ...
Bis(2-ethylhexyl) phthalate (di-2-ethylhexyl phthalate, diethylhexyl phthalate, diisooctyl phthalate, DEHP; incorrectly — dioctyl phthalate, DIOP) is an organic compound with the formula C 6 H 4 (CO 2 C 8 H 17) 2. DEHP is the most common member of the class of phthalates, which are used as plasticizers.
Bis(2-ethylhexyl) adipate or DEHA or DOA is an organic compound with the formula (CH 2 CH 2 CO 2 C 8 H 17) 2.It is the diester of 2-ethylhexanol and adipic acid.It is a colorless oily liquid.
Medicare does not typically cover ketamine infusions for mental health conditions. However, it may cover Spravato, an FDA-approved drug deriving from ketamine, for treatment-resistant depression.
Dimethoxy-4-amylamphetamine (DOAM) is a lesser-known psychedelic drug and a substituted amphetamine.DOAM was first synthesized by Alexander Shulgin.In his book PiHKAL (Phenethylamines i Have Known And Loved), the minimum dosage is listed as 10 mg, and the duration is unknown.
DOET, also known as 2,5-dimethoxy-4-ethylamphetamine or as 2,5-dimethoxy-4-ethyl-α-methylphenethylamine, is a substituted phenethylamine and amphetamine and is a member of the DOx group of drugs. [ 8 ] [ 6 ] [ 3 ] [ 2 ] It is structurally related to the naturally occurring phenethylamine psychedelic mescaline (3,4,5-trimethoxyphenethylamine).
If there is more than one of the same alkyl group attached to a chain, then the prefixes are used on the alkyl groups to indicate multiples (i.e., di, tri, tetra, etc.) This compound is known as 2,3,3-trimethylpentane. Here three identical alkyl groups attached to carbon atoms 2, 3, and 3.