Buy 1cP-LSD 100mcg Blotters

Product Overview

1cP-LSD (1-Cyclopropionyl-d-lysergic acid diethylamide, CAS 2527-09-5) supplies researchers with a high-purity N1-cyclopropanecarbonyl lysergamide reference standard for serotonin receptor pharmacology research, N1-acyl lysergamide prodrug characterization studies, and forensic toxicology analytical method development within controlled laboratory environments. Researchers looking to buy 1cP-LSD for laboratory applications will find UltraRawz’s HPLC-verified blotter format suitable for comparative 5-HT₂A receptor binding studies, LC-MS/MS method development distinguishing 1cP-LSD from structurally related N1-acyl lysergamide homologues, N1-cyclopropanecarbonyl hydrolysis kinetics research, and fluorescence-based HPLC analytical method validation. 1cP-LSD represents one of the most analytically interesting N1-acyl LSD analogues because the cyclopropanecarbonyl acyl group — a constrained ring structure — produces distinct spectroscopic signatures and potentially different hydrolysis kinetics compared to linear acyl chain homologues such as 1P-LSD (propionyl) and 1B-LSD (butanoyl). For research use only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications.

1cP-LSD differs from 1P-LSD by the replacement of the linear propionyl group (-CO-CH₂-CH₃) with a cyclopropanecarbonyl group (-CO-cyclopropyl) at the N1 position. This acyl group substitution increases molecular weight by 12 Da (1P-LSD MW 379.50 vs 1cP-LSD MW 391.47 g/mol) and produces characteristic NMR cyclopropyl ring proton signals that enable unambiguous identification independent of mass spectrometric data. In published in-vitro hydrolysis research examining N1-acyl lysergamide prodrug behavior, the ring strain of the cyclopropanecarbonyl group has been proposed to influence esterase-mediated deacylation kinetics relative to linear acyl chain analogues — making 1cP-LSD a valuable comparative reference compound for pharmacokinetic research examining structure-dependent metabolic conversion rates. 1cP-LSD for sale at UltraRawz ships worldwide with discreet packaging from our US and Netherlands warehouses.

1cP-LSD is available at ultrarawz.com/shop in standard blotter format (100μg per blotter) in multiple quantity tiers. Each batch is HPLC-verified at ≥98% purity with batch-specific COA documentation. The complete N1-acyl lysergamide reference panel at UltraRawz includes 1P-LSD, 1B-LSD, 1V-LSD “Valerie”, 1D-LSD, AL-LAD, LSZ, and 1cP-AL-LAD — browse all at ultrarawz.com — Lysergamides.

Chemical Identity & Classification

1cP-LSD carries CAS number 2527-09-5, molecular formula C₂₃H₂₇N₃O₂ (note: contains cyclopropyl ring reducing H count vs 1P-LSD C₂₃H₂₉N₃O₂), and molecular weight 391.47 g/mol. Systematic IUPAC designation: 1-(cyclopropylcarbonyl)-N,N-diethyl-d-lysergamide. Laboratory synonyms: 1-cyclopropionyl-LSD, 1cP-LSD, cyclopropionyl-LSD. Structurally classified as an N1-cyclopropanecarbonyl ergoline lysergamide — tetracyclic ergoline scaffold, N,N-diethyl amide at C-8, cyclopropanecarbonyl at N1. The cyclopropyl ring in the acyl group produces characteristic NMR multiplets at δ 0.7–1.1 ppm (cyclopropyl CH₂ protons) and δ 1.8–2.0 ppm (cyclopropyl CH) that are diagnostically distinct from linear alkyl chain signals in 1P-LSD, 1B-LSD, and 1V-LSD spectra. Protonated molecular ion [M+H]⁺: m/z 392. Mass delta from 1P-LSD: +12 Da (cyclopropyl vs n-propyl, molecular formula difference C₃H₄ vs C₃H₆).

Chemical & Physical Characteristics

1cP-LSD is supplied in blotter substrate format (100μg per blotter unit). Active compound properties: highly photosensitive ergoline scaffold with characteristic UV absorption at ~254 nm (indole chromophore) and fluorescence emission at 445 nm (excitation 325 nm). DMSO solubility: ≥10 mg/mL equivalent. Methanol and acidified methanol: soluble. logP: ~2.5 (calculated — cyclopropyl group slightly increases lipophilicity vs propionyl). The cyclopropyl ring in the acyl group imparts greater conformational rigidity than linear acyl chains — a structural property that may influence the binding geometry at the esterase active site during N1-acyl deacylation, making 1cP-LSD particularly interesting as a prodrug hydrolysis kinetics research tool. Extreme photosensitivity: like all lysergamides, 1cP-LSD requires amber/red laboratory lighting during all handling operations and strict UV exclusion storage.

Purity & Analytical Verification

Production lots certify ≥98% purity by gradient HPLC (C18 reverse-phase, acetonitrile/0.1% formic acid gradient, UV 254 nm, area normalization). Identity confirmed by: ¹H NMR (CDCl₃) — cyclopropyl CH₂ signals at δ ~0.7–1.1 ppm and cyclopropyl CH at δ ~1.8–2.0 ppm confirm cyclopropanecarbonyl N1-substitution; these signals are completely absent in 1P-LSD (propionyl CH₂ at δ ~2.4 ppm) and other linear acyl chain analogues. LC-MS/MS identity: [M+H]⁺ m/z 392; fragment at m/z 324 (loss of cyclopropanecarbonyl, 68 Da — distinguished from 1P-LSD neutral loss of 56 Da propionyl). HPLC-FLD: excitation 325 nm, emission 445 nm (ergoline fluorescence confirmation). Karl Fischer water content: <0.5% w/w. Blotter content uniformity: 10-blotter CV% <5%. COA available at support@ultrarawz.com.

Quality Control & Batch Integrity

Each 1cP-LSD production batch undergoes photosensitivity-aware quality verification procedures: HPLC purity under amber lighting conditions, ¹H NMR identity confirmation (cyclopropyl signal verification), LC-MS/MS molecular ion and cyclopropanecarbonyl neutral loss confirmation, HPLC-FLD fluorescence response calibration, blotter content uniformity testing (10-blotter CV% <5%), and visual blotter appearance inspection. Cold chain handling maintained throughout production and fulfillment. Batch photostability testing confirms UV degradation susceptibility as a release criterion. Retained reference blotters per batch maintained under optimal cold/dark storage for stability monitoring.

Safety, Handling & Laboratory Precautions

Handle exclusively under amber or red laboratory lighting — standard white laboratory lighting causes measurable photodegradation of the ergoline scaffold during handling. Required PPE: nitrile gloves (double-glove), lab coat, safety glasses. Serotonin receptor agonist — prevent all dermal contact. Blotter handling: use clean forceps — do not handle with bare fingers (dermal absorption risk). Stock solution extraction from blotters: extract in acidified methanol (0.1% formic acid), vortex 15 minutes, centrifuge to clarify. Return to cold dark storage immediately after use. Spill: collect blotters with forceps, absorb any solution with inert material, sealed container, dispose per institutional chemical waste procedures.

Packaging, Labeling & Storage

1cP-LSD blotters are packaged in foil-sealed opaque pouches with desiccant, in discreet external packaging. Labels specify compound name, CAS 2527-09-5, lot number, purity, dose per blotter, and research use notice. Critical storage — stricter than most NPS compounds: -20°C or below long-term (>2 weeks); ≤4°C (refrigerator) short-term active use (max 1 week). ALL light sources excluded — UV and visible light. Sealed in opaque foil pouch at all times when not in active analytical use. Inert gas headspace (N₂ or Ar) recommended for long-term storage of opened units. Avoid pH >8 conditions. Under recommended conditions, compound integrity maintained for lot expiry period on COA.

Intended Research Use & Market Positioning

1cP-LSD is positioned for: forensic toxicology laboratories developing LC-MS/MS methods that must discriminate between N1-acyl lysergamide homologues (1P-LSD, 1cP-LSD, 1B-LSD, 1V-LSD) in biological and seized material matrices; prodrug hydrolysis kinetics research examining the effect of cyclopropyl ring strain on N1-acyl deacylation rates versus linear acyl chain homologues; 5-HT₂A and 5-HT₁A receptor binding affinity studies comparing N1-cyclopropanecarbonyl versus N1-linear acyl substitution effects on receptor interaction profiles; HPLC-FLD method development for trace-level lysergamide quantitation in biological matrices; and SAR programs examining acyl group structural constraints on lysergamide prodrug behavior. Browse the full lysergamide panel at ultrarawz.com — Lysergamides.

Ordering, Availability & Fulfillment

1cP-LSD is available in blotter format (100μg per blotter) in multiple quantity tiers — see variants above. Cold chain handling during dispatch. Payment methods: Bitcoin (BTC), bank transfer, Apple Pay (US), Zelle (US), Revolut (Europe), gift cards — full details at ultrarawz.com/payment. Orders processed same day, discreet tamper-evident packaging. Worldwide shipping from US and Netherlands. Delivery: 2–5 days (US/EU); 5–10 days international. COA and institutional pricing: support@ultrarawz.com or WhatsApp +1 (567) 457-7456. Track at ultrarawz.com/track-order.

Legal & Regulatory Disclaimer

1cP-LSD (CAS 2527-09-5) is supplied strictly for laboratory research purposes only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications. Legal status varies significantly by jurisdiction — N1-acyl LSD analogues are controlled in multiple countries. Purchasers are solely responsible for verifying compliance with all applicable regulations prior to ordering. UltraRawz supplies this compound exclusively to qualified research professionals for legitimate laboratory research purposes.

Frequently Asked Questions

Q: What is the key analytical difference between 1cP-LSD and 1P-LSD?
A: Three distinguishing features: (1) MW difference — 1cP-LSD 391.47 vs 1P-LSD 379.50 g/mol (+12 Da, cyclopropyl vs n-propyl); (2) LC-MS/MS neutral loss — 1cP-LSD loses 68 Da (cyclopropanecarbonyl) vs 1P-LSD loses 56 Da (propionyl); (3) ¹H NMR — 1cP-LSD shows cyclopropyl CH₂ multiplets at δ 0.7–1.1 ppm absent in 1P-LSD spectra.

Q: Why does the cyclopropyl group make 1cP-LSD analytically interesting?
A: The cyclopropyl ring is conformationally constrained compared to linear alkyl chains. This rigidity may influence esterase active site binding geometry during N1-acyl deacylation — making 1cP-LSD vs 1P-LSD a useful paired reference set for prodrug hydrolysis kinetics research examining acyl group structural effects on metabolic conversion rates.

Q: What storage conditions are required?
A: -20°C or below long-term; ≤4°C short-term (max 1 week). ALL light excluded — ergoline scaffold is extremely photosensitive. Sealed in opaque foil pouch. More stringent than most NPS compounds.

Q: What purity does UltraRawz 1cP-LSD achieve?
A: ≥98% HPLC area normalization. COA with HPLC chromatogram, NMR, and blotter uniformity data on request.

Q: How is 1cP-LSD extracted from blotters for analytical work?
A: Extract in acidified methanol (0.1% formic acid), vortex 15 minutes, centrifuge to clarify, dilute to working concentration. Under amber lighting throughout procedure.

Q: What related lysergamides does UltraRawz carry?
A: Full N1-acyl panel: 1P-LSD, 1B-LSD, 1V-LSD “Valerie”, 1D-LSD, AL-LAD, LSZ, 1cP-AL-LAD. Browse at ultrarawz.com — Lysergamides.

Q: Do you ship internationally?
A: Yes, worldwide from US and Netherlands. Legal status of N1-acyl lysergamides varies by country — verify before ordering. See shipping & delivery.