AL-LAD Blotter Paper


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AL-LAD is an alkenated / alkylenated analogue of (6-nor-)LSD, Al lad for sale or differently put a ‘homologue’ of DMT, that has a slightly lower potency in practice and somewhat shorter duration of effects than LSD although it showed higher potency in theory.
It gained recognition after Alexander Shulgin described the substance in the book TIHKAL, although David Nichols and Albert Hofmann described AL-LAD 12 years before that in an article. However until recently AL-LAD has not been known to have been available on the market. Buy Al-Lad Blotter paper online
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Because it is not an alkyl analogue it bypasses UK drug analogue laws. In this early stage of availability on the market AL-LAD for sale is quickly gaining popularity, having a lot of the virtues of LSD and even advantages over it, although opinions and reactions always vary as per YMMV.
Until recently history of use in humans was quite limited, and positive reports do not guarantee physical safety. If it has remotely the therapeutic index LSD has it should be considered physically quite safe, but has not yet been proven


AL-LAD is one of several lysergamides that have been modified at the N6-position. The synthesis of AL-LAD was first described in 1976. The substance was also synthesized by Hoffman and Nichols using a modified procedure published in 1985. Like LSD, AL-LAD induces hyperthermia in rabbits. When tested in the isolated rat uterus preparation, AL-LAD was found to have a more potent contractile effects than LSD. The first investigation of the hallucinogen-like activity of AL-LAD was conducted by Hoffman and Nichols, who found that AL-LAD produced full substitution in rats trained to discriminate 0.08 mg/kg LSD tartrate. Furthermore, the potency of AL-LAD in the drug discrimination paradigm (ED50 = 13 nmol/kg) exceeded that of LSD (ED50 = 46 nmol/kg). Receptor binding studies revealed that AL-LAD had high affinity for 5-HT2A receptors labeled with [3H]ketanserin (Ki = 8.1 nM) and ([125I]-R-DOI (Ki = 3.4 nM) in rat frontal cortex homogenates. Subsequently, it was shown that AL-LAD displayed slightly lower affinity than LSD for D1 (K0.5 = 189 nM vs. [3H]SCH-23390) and D2 (K0.5 12.3 nM vs. [3H]spiperone in the presence of ketanserin) dopaminergic receptors.

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AL-LAD Blotter Paper