AL-LAD Relives because LL is a Fucking Genius
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Recent email I got, Idk where he finds the time…..
“After years of process development, we have finally managed to produce AL-LAD!
For the last couple of years, AL-LAD has been almost entirely unavailable. Yet it always remained a highly desirable and much demanded product. It is almost legendary in status due to its unique properties, and it is recognised as being the first legal lysergamide to reach the RC market.
We have been slaving away trying to prepare this compound via a new route (avoiding LSD as the precursor) for the last few years. And after MUCH blood, sweat and tears, our hard work has come to fruition. We have successfully developed a new route to AL-LAD and isolated the first commercial batch of product. Although the process is far from efficient; with low yields and a high cost price, we are happy that AL-LAD has been resurrected.
We are now offering AL-LAD 150mcg Blotters – available for immediate dispatch. Please see latest catalogues below for prices. AL-LAD L-tartrate is available on request only.
Given the rarity and relatively high wholesale cost of this product, we recommend this be marketed as premium product for the most avid researchers! We therefore suggest a retail price around double that of 1P-LSD and 1cP-LSD.”
And a week after that ….
“Last week we provided an important update detailing the launch of AL-LAD, you can read it here. We chose not to clutter that email with further details and updates, so this email will serve as our official October newsletter.
In our quest for the perfect MXE analogue, we are pleased to announce the release of another dissociative product, DMXE (deoxymethoxetamine, 3-Me-2’-oxo-PCE hydrochloride). This molecule is structurally very similar to MXE, with only the methoxy replaced with methyl (oxygen removed and hence the ‘deoxy’).
As with each iteration of our MXE analogues, we get closer and closer to the original. And whilst DMXE has it’s own unique and special flavour, it is extremely similar to MXE. As we demonstrated with 3-Me-PCP, the 3-MeO group can be substituted with methyl without loss of potency or significant alteration of pharmacological profile. We are pleased to see that the 2’-oxo compounds follow the same SAR, from the several we have synthesised, including DMXE.”
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