I found 100mg (actually 105mg or so in the end, due to the starting doses of the drug leaving 10mg more than 2x200mg doses remaining from my original 250mg quantity, and my division of the remainder in rougly half after weighing then splitting by eye into two equal portions) to be about right for this compound.
A LOT less potent than amphetamine or its methylated or ethylated sec. amine homologs, by weight, but much, much smoother. As 'smoothe' in fact as desoxypipradrol, but I prefer this compound to desoxy, the latter has absolutely zero peripheral locomotor or stereotypy-inducing 'noise' present in the effects, but is too long lasting, in any but the 1-2mg doses that are the very maximal dosage range for the functional enhancement I seek in it, camphetamine however does have euphorigenic properties, and I must say, I like it, which for me, concerning psychostimulants is quite unusual.
I definately think I shall get myself another gram or two, although I am hoping the price drops soon. The 250mg was definately a worthwhile aquisition, for the price however, but for larger amounts, a bit pricy. Although definately very nice material.
As currently distributed, do NOT snort it....not if you value your nasal epithethelia, it has to be the fourth most painful material ever to find its way up my nose, the first being molten metallic sodium, with accompanying fused, molten NaOH, from some childhood playing electrolysis (as a kid I never wanted to play with kids toys, high voltage was my action man set, and atomic configurations my lego/mechano
)
Second most painful being Virola theiodora bark, and third being yopo/cohoba snuff made from ground, toasted seeds with the admixture of slaked lime...owch. Insufflation of the current distributed camphetamine comes just behind these, tieing perhaps with the yopo.
What recrystallization method was used to purify this? and is the slight impurity yet known? if it the current batches were produced via the nitroalkene, it would explain the way it burned like fury, and left me, after the effects were tailing off, with a blinder of a residual headache, I don't think it was the drug itself at all which was responsible for this, as it happened only the time I insufflated the first 40mg, and never when it was plugged.
Is the stereochemistry of the current product known? I really would like to know what it looks like under a polariscope, I currently lack the capability to examine the optical properties of such substances though. Would be nice to compare the effects in vivo of the racemate, vs the D and L isomers of camphetamine.