1cP-LSD (N1-(cyclopropylmethanoyl)-lysergic acid diethylamide) is an acylated derivative of Lysergic acid diethylamide (LSD). It is structurally comparable to many other Lysergamides, like ALD-52 and 1P-LSD. Like most derivatives of Lysergamides, its origin and history are relatively unknown. We do know that 1cP-LSD was first synthesized in the Netherlands in 2019.
1cP-LSD is a semisynthetic compound of the Lysergamide class. 1cP-LSD gets its name from the cyclopropionyl group bound to the nitrogen of the polycyclic indole group. The cyclopropionyl group consists of a carbonyl ring with the chemical formula C3H6 bound to an amino group.
1cP-LSD’s structure contains a polycyclic group featuring a bicyclic hexahydro indole bound to a bicyclic quinoline group. Like many Lyssergamides on the market, an N,N-diethyl carboxamide is bound at the carbon eight of the quinoline.
1cP-LSD is almost identical to 1P-LSD. The difference is in the alkylcarbonyl group that has the empirical formula C4H7O, whereas the cyclopropylcarbonyl group corresponds to a molecular formula of C4H5O. However, calling the cyclopropyl an alkyl radical is incorrect.
Chemical Name: 1‐cyclopropanecarbonyl‐(8ß)-N,N-diethyl-6-(prop-2-enyl)-9,10-didehydroergoline-8-carboxamide hemi-L-tartrate
Chemical Class: Lysergamide.
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