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L-005

Supelco

LSD solution

25 μg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®

Synonym(s):

Lysergic acid diethylamide

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About This Item

Empirical Formula (Hill Notation):
C20H25N3O
CAS Number:
Molecular Weight:
323.43
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

Quality Level

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

Narcotic Licence Schedule D (Switzerland); psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)

concentration

25 μg/mL in acetonitrile

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

forensics and toxicology

format

single component solution

storage temp.

2-8°C

SMILES string

O=C(N(CC)CC)[C@@]1([H])CN(C)[C@]2([H])CC3=CNC4=CC=CC(C2=C1)=C43

InChI

1S/C20H25N3O/c1-4-23(5-2)20(24)14-9-16-15-7-6-8-17-19(15)13(11-21-17)10-18(16)22(3)12-14/h6-9,11,14,18,21H,4-5,10,12H2,1-3H3/t14-,18-/m1/s1

InChI key

VAYOSLLFUXYJDT-RDTXWAMCSA-N

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General description

LSD, or lysergic acid diethylamide, is an illicit psychedelic drug with potent hallucinogenic effects such as altered thinking processes, closed- and open-eye visuals, synesthesia and an altered sense of time. This Snap-N-Spike® reference solution is suitable for use in urine drug testing, clinical toxicology, or forensic analysis by LC-MS/MS or GC/MS.

Application


  • LSD Solution for Research Chemicals: Enhancing Scientific Understanding.: LSD solution is a vital research chemical used extensively in scientific studies to investigate the biochemical and pharmacological properties of lysergic acid diethylamide. Its applications span across various fields, including neuroscience, psychology, and pharmacology, providing crucial insights into its effects and mechanisms of action (Walker et al., 1983).

  • LSD Solution for Neurotransmitter Research Applications.: In neurotransmitter research, LSD solution is used to study its impact on serotonin receptors and other neurotransmitter systems. This research helps elucidate the complex neural pathways involved in mood regulation, cognition, and perception, contributing to the development of new therapeutic strategies (Lindstedt et al., 2015).

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

L-005-1ML:
L-005-CC:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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José L Moreno et al.
Psychopharmacology, 225(1), 217-226 (2012-07-31)
In schizophrenia patients, optimal treatment with antipsychotics requires weeks to months of sustained drug therapy. However, single administration of antipsychotic drugs can reverse schizophrenia-like behavioral alterations in rodent models of psychosis. This raises questions about the physiological relevance of such
Jeremy Green et al.
Journal of neuroscience methods, 210(2), 266-271 (2012-08-14)
Zebrafish (Danio rerio) are rapidly becoming an important model organism in neuroscience research, representing an excellent species to study complex social phenotypes. Zebrafish actively form shoals, which can be used to quantify their shoaling behaviors, highly sensitive to various experimental
Emmanuelle A D Schindler et al.
Brain research, 1491, 98-108 (2012-11-06)
The phenethylamine and indoleamine classes of hallucinogens demonstrate distinct pharmacological properties, although they share a serotonin(2A) (5-HT(2A)) receptor mechanism of action (MOA). The 5-HT(2A) receptor signals through phosphatidylinositol (PI) hydrolysis, which is initiated upon activation of phospholipase C (PLC). The
Theresa M Carbonaro et al.
Psychopharmacology, 226(2), 241-246 (2012-10-17)
Serotonergic hallucinogens such as (+)-lysergic acid diethylamide (LSD) and dimethyltryptamine (DMT) produce distinctive visual effects, whereas the synthetic hallucinogen N,N-diisopropyltryptamine (DiPT) is known for its production of auditory distortions. This study compares the discriminative stimulus effects of DiPT to those
George Harrison's inner light.
Guilherme Nogueira M de Oliveira et al.
Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999), 34(4), 517-518 (2013-02-23)

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