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M-012

Supelco

(±)-MDA solution

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

Synonyme(s) :

(±)-3,4-Methylenedioxyamphetamine

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About This Item

Formule empirique (notation de Hill):
C10H13NO2
Numéro CAS:
Poids moléculaire :
179.22
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material

Forme

liquid

Caractéristiques

Snap-N-Spike®/Snap-N-Shoot®

Conditionnement

ampule of 1 mL

Fabricant/nom de marque

Cerilliant®

drug control

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

Concentration

1.0 mg/mL in methanol

Technique(s)

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

Application(s)

forensics and toxicology

Format

single component solution

Température de stockage

−20°C

Chaîne SMILES 

NC(C)CC1=CC=C(OCO2)C2=C1

InChI

1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3

Clé InChI

NGBBVGZWCFBOGO-UHFFFAOYSA-N

Description générale

A certified solution standard suitable to use in LC/MS or GC/MS applications for clinical toxicology, forensic analysis, or urine drug testing. MDA, or 3,4-methylenedioxyamphetamine, is an illicit recreational drug of the amphetamine and phenethylamine classes. Also known as tenamphetamine, MDA is abused for its psychedelic and hallucinogenic effects, similar to those of MDMA (Ecstasy).

Application

  • MDA Research Chemical: (±)-MDA solution is extensively used in scientific research to study its pharmacological properties, including its effects on neurotransmitter systems which are critical in understanding substance-related disorders.
  • MDA Enantiomers: The solution includes both enantiomers of MDA, allowing for detailed studies on the differential biological activities of each enantiomer in neuropharmacological research.
  • Synthetic MDA Solution: This synthetic solution is crucial for controlled studies in biochemistry and pharmacology, providing a consistent baseline for experimental reproducibility and validation.
  • MDA Biochemistry Application: Utilized in biochemical assays, (±)-MDA solution helps in the exploration of its metabolic pathways and interactions with biological macromolecules, enhancing the understanding of its pharmacodynamics.
  • MDA Pharmacological Studies: As a key tool in pharmacological research, (±)-MDA solution is used to investigate its potential therapeutic effects and risks, contributing to the development of safety guidelines and therapeutic protocols.

Informations légales

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

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

FlameSkull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organes cibles

Eyes

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

49.5 °F - closed cup

Point d'éclair (°C)

9.7 °C - closed cup


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Cédric M Hysek et al.
PloS one, 7(5), e36476-e36476 (2012-05-11)
This study assessed the effects of the serotonin (5-HT) and norepinephrine (NE) transporter inhibitor duloxetine on the effects of 3,4-methylenedioxy-methamphetamine (MDMA, ecstasy) in vitro and in 16 healthy subjects. The clinical study used a double-blind, randomized, placebo-controlled, four-session, crossover design.
Brandon J Warrick et al.
Journal of medical toxicology : official journal of the American College of Medical Toxicology, 8(1), 65-68 (2011-12-14)
A new generation of designer phenethylamines have emerged and aggressively marketed as "legal highs." The drugs are labeled "not for human consumption" to avoid widespread recognition and prosecution under the existing analog drug laws. The newest generation includes methylone and
Aixin Shi et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 908, 87-93 (2012-11-06)
Piperphentonamine hydrochloride (PPTA) is a new calcium sensitizer. A liquid chromatography-tandem mass spectrometry (LC/MS/MS) method for determination of piperphentonamine and its metabolites M1 and M6 was developed for the first time and applied to a pharmacokinetics study. Protein precipitation was
Han-yi Zhu et al.
Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 31(11), 1858-1862 (2011-12-01)
To investigate the effect of piperphentonamine hydrochloride (PPTA) on cognitive deficits induced by ischemia-reperfusion and explore the possible mechanisms. SD rats were randomly divided into sham-operated group, ischemia-reperfusion group (with saline injection), PPTA-treated groups (2.5, 5, 10 mg/kg) and edaravone-treated
Camilla Montesano et al.
Journal of mass spectrometry : JMS, 48(1), 49-59 (2013-01-11)
This study describes a method for the screening of methylenedioxyamphetamine- and piperazine-derived compounds in urine by liquid chromatography-tandem mass spectrometry. These substances, characterized by possessing common moieties, are screened using precursor ion and neutral loss scan mode and then quantified

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