Search results
Results from the WOW.Com Content Network
Dimethylamphetamine has weaker stimulant effects than amphetamine or methamphetamine and is considerably less addictive [1] and less neurotoxic compared to methamphetamine. [ 2 ] [ 3 ] However, it still retains some mild stimulant effects and abuse potential, [ 4 ] and is a Schedule I controlled drug.
In 2016, Michigan reported an increase in incidents following the formation of the Midland County Methamphetamine Protocol Team in 2015. However, many of the cases reported involved meth users making small amounts of the drug using a crude and dangerous "one-pot method". These small operations were for both personal use and for sale to others. [25]
Methamphetamine is a Class "A" or Schedule 1 controlled drug under the Misuse of Drugs Act 1975. [20] The maximum penalty for production and distribution is imprisonment for life. While in theory a doctor could prescribe it for an appropriate indication, this would require case-by-case approval by the director-general of public health.
Dimethyl sulfone (DMSO 2) is an organosulfur compound with the formula (CH 3) 2 SO 2. It is also known by several other names including methyl sulfone and (especially in alternative medicine) methylsulfonylmethane (MSM). [4] This colorless solid features the sulfonyl functional group and is the simplest of the sulfones. It is relatively inert ...
Diagnostic impurities are the naphthalenes 1-benzyl-methylnaphthalene and 1,3-dimethyl-2-phenylnaphthalene, [108] arising in the Nagai and Leuckart routes, and cis-or trans-1,2-dimethyl-3-phenylaziridine, ephedrine, or erythro-3,4-dimethyl- 5-phenyloxazolidine, arising in the Nagai and Emde routes; these are absent in the reductive amination ...
For premium support please call: 800-290-4726 more ways to reach us
An assortment of several designer drugs. Designer drugs are structural or functional analogues of controlled substances that are designed to mimic the pharmacological effects of the parent drug while avoiding detection or classification as illegal.
STP was first synthesized and tested in 1963 by Alexander Shulgin, who was investigating the effect of 4-position substitutions on psychedelic amphetamines. [3]In mid-1967, tablets containing 20 mg (later 10 mg) of STP were widely distributed in the Haight-Ashbury District of San Francisco under the name of STP, having been manufactured by underground chemists Owsley Stanley and Tim Scully.