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1cP-AL-LAD (1-cyclopropanecarbonyl-6-allyl-6-nor-lysergic acid diethylamide) is a novel lysergamide derivative structurally related to AL-LAD, 1P-LSD, and 1cP-LSD. Recognized in chemical and pharmacological research as an N1-cyclopropanoylated prodrug standard, this compound serves as an essential reference material for spectroscopic profiling, mass spectrometry fragment analysis, and receptor-binding affinity studies.
Featuring an N1-cyclopropanecarbonyl substitution combined with an N6-allyl moiety on the ergoline core, this compound displays distinct chromatographic retention behaviors and targeted hydrolysis profiles. These unique structural characteristics allow research teams to precisely evaluate enzymatic cleavage rates, binding kinetics, and chemical stability under controlled laboratory environments.
Chemical Identification & Technical Specifications
Accurate structural data and certified chemical metrics are required for high-precision analytical research. Below are the core technical specifications for this reference material:
| Product Name | 1cP-AL-LAD |
| Systematic / Alternative Name | 1-cyclopropanecarbonyl-6-allyl-6-nor-lysergic acid diethylamide, 1cP-AL-LAD |
| Full IUPAC Description | (8β)-1-(cyclopropanecarbonyl)-N,N-diethyl-6-(prop-2-en-1-yl)-9,10-didehydroergoline-8-carboxamide |
| Molecular Formula | C₂₆H₃₁N₃O₂ |
| Molar Mass | 417.55 g/mol |
| Availability Status | In Stock – Ready for Immediate Worldwide Dispatch |
*All orders include complete analytical certificates of analysis (CoA) verifying batch purity and structural integrity prior to shipment.
Why Choose 1cP-AL-LAD? Molecular Dynamics & Structural Value
The chemical architecture of 1cP-AL-LAD pairs an N1-cyclopropanecarbonyl group with an N6-allyl substitution. The cyclopropyl ring imparts distinct steric density and electronic properties at the indole position compared to straight-chain acyl modifications (such as propionyl or butyryl), serving as a crucial reference point in structure-activity relationship (SAR) studies.
These unique molecular attributes make this compound an outstanding addition for analytical laboratories evaluating N-alkylated and N-acylated lysergamides:
Standard AL-LAD Framework
Features an un-substituted N1 indole nitrogen with an N6 allyl group, exhibiting baseline chromatographic elution parameters.
1cP-Acylated Modification
Incorporates a cyclopropanecarbonyl acyl group at N1, altering lipophilicity, mass spectral fragmentation pathways, and enzymatic stability.
Maintain project consistency by securing pure, verified batches directly through our dedicated online portal.
Lab-Tested Quality & Research Reliability
High-precision research requires uncompromised material standards. Every batch of 1cP-AL-LAD is subjected to rigorous testing via Nuclear Magnetic Resonance (NMR) spectroscopy and High-Performance Liquid Chromatography (HPLC) to confirm high purity and exact molecular composition.
Our streamlined supply chain guarantees vacuum-sealed, moisture-resistant protective packaging and prompt, tracked delivery to authorized institutions.
All compounds are supplied exclusively for forensic, academic, and analytical research applications. Direct human or veterinary application is strictly prohibited.
Key Product Highlights
1cP-AL-LAD
(8β)-1-(cyclopropanecarbonyl)-N,N-diethyl-6-(prop-2-en-1-yl)-9,10-didehydroergoline-8-carboxamide
Lysergamide Derivative
C₂₆H₃₁N₃O₂
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100% Fully Batch-Tested with CoA
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