Dimethylphenidate was synthesized as a substitute for cocaine. Chemical studies have shown that dimethylphenidate and, according to several studies, has a higher affinity for the dopamine carrier, but much less activity in the norepinephrine receptors, presumably results in greater euphoria with much less side effects than its methylphenidate precursor. It is usually available in the form of a HCl powder intended for oral or nasal administration and as a free base.
| Synonyms | Dimethylphenidate |
|---|---|
| IUPAC | No |
| Formula | No |
| Molecular weight | No |
| CAS | No |
| Appearance | No |
| Purity | > 99 % |
The property properties of Dimethylphenidate are not known yet.
Storage conditions of this chemical: in a cool and dry place. The stability of this chemical compound can last up to 2 years, under the right storage conditions.
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