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1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually handled as the hydrochloride. [1] It is typically employed in the 4.0-6.0 pH range. It is generally used as a carboxyl activating agent for the coupling of primary amines to yield amide bonds.
The drug is approximately 73% protein-bound across a plasma range of 7 to 226 ng/mL (28–892 nM). [1] The metabolism of nefopam is hepatic , by N - demethylation and via other routes . [ 1 ] Its terminal half-life is 3 to 8 hours, while that of its active metabolite , desmethylnefopam, is 10 to 15 hours. [ 1 ]
3,4-Methylenedioxy-N-ethylamphetamine (MDEA; also called MDE and colloquially, Eve) is an empathogenic psychoactive drug. MDEA is a substituted amphetamine and a substituted methylenedioxyphenethylamine. MDEA acts as a serotonin, norepinephrine, and dopamine releasing agent and reuptake inhibitor. [1] Possession of MDEA is illegal in most ...
1,4-Butanediol: GHB and Gamma-Butyrolactone: Cyclohexanone: phencyclidine Diethylamine and its salts lysergic acid diethylamide ethyl 3-oxo-4-phenylbutanoate phenylacetone: ethyl-3-(1,3-benzodioxol-5-yl)-2-methyloxirane-2-carboxylate (MDP2P ethyl glycidate) MDMA: Formamide: amphetamine, methamphetamine Formic acid: amphetamine, methamphetamine
Moracizine [1] or moricizine, sold under the trade name Ethmozine, is an antiarrhythmic of class IC. [2] It was used for the prophylaxis and treatment of serious and life-threatening ventricular arrhythmias, [3] but was withdrawn in 2007 for commercial reasons.
[1] [2] It is the α-ethyl analog of MDPEA and MDA and the methylenedioxy analogue of α-ethylphenethylamine. BDB was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage range is listed as 150–230 mg and the duration is listed as 4–8 hours. [3] BDB produces entactogenic, MDMA-like effects. Although pleasant and euphoric ...
Tapentadol, sold under the brand names Nucynta and Palexia among others, is a synthetic opioid analgesic of the benzenoid class with a dual mode of action as a highly selective full agonist of the μ-opioid receptor and as a norepinephrine reuptake inhibitor (NRI). [7]
This is the list of extremely hazardous substances defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. § 11002).The list can be found as an appendix to 40 CFR 355. [1]