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Principaux documents

F-018

Supelco

4-Fluoroamphetamine hydrochloride solution

1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Formule empirique (notation de Hill):
C9H12FN · HCl
Numéro CAS:
Poids moléculaire :
189.66
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material

Forme

liquid

Caractéristiques

(Snap-N-Spike®)

Conditionnement

ampule of 1 mL

Fabricant/nom de marque

Cerilliant®

drug control

psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)

Concentration

1.0 mg/mL in methanol (as free base)

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(F)C=C1.Cl

InChI

1S/C9H12FN.ClH/c1-7(11)6-8-2-4-9(10)5-3-8;/h2-5,7H,6,11H2,1H3;1H

Clé InChI

GKWYMWZWSCKSMT-UHFFFAOYSA-N

Description générale

This Certified Spiking Solution® is suitable for numerous applications in GC/MS or LC/MS testing of 4-fluoroamphetamine from clinical toxicology and urine drug testing to forensic analysis. A fluoro analog of amphetamine, 4-Fluoroamphetamine is sold in the illicit market as a club/designer drug under street names including R2D2, Flux and Flits. The drug produces stimulant and possibly empathogenic or psychoactive effects.

Informations légales

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION 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

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

Point d'éclair (°C)

9.7 °C


Listes réglementaires

Les listes réglementaires sont principalement fournies pour les produits chimiques. Seules des informations limitées peuvent être fournies ici pour les produits non chimiques. L'absence d'indication signifie qu'aucun des composants n'est répertorié. Il incombe à l'utilisateur de s'assurer de l'utilisation sûre et légale du produit.

EU REACH Annex XVII (Restriction List)

CAS No.

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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

D Marona-Lewicka et al.
European journal of pharmacology, 287(2), 105-113 (1995-12-12)
The present study was undertaken to compare the pharmacological properties of p-fluoroamphetamine with those of amphetamine and of other halogenated amphetamines, using several in vivo and in vitro tests. These included substitution testing in (+)-amphetamine (1 mg/kg, 5.4 mu mol/kg
R E Dubin et al.
Progress in neuro-psychopharmacology & biological psychiatry, 9(5-6), 681-685 (1985-01-01)
(+)-Amphetamine (AM) and its fluorinated analogue (+)-2-amino-3-fluoro-1-phenylpropane (fluoroamphetamine, FAM) were compared with regard to their effects on locomotor and exploratory activity in mice. Both drugs caused a reduction in spontaneous exploration, but this effect was more marked with FAM than
T J Danielson et al.
Biochemical pharmacology, 35(24), 4423-4429 (1986-12-15)
The metabolism and some behavioral properties of each of the optical isomers of 2-amino-1-fluoro-3-phenylpropane hydrochloride (fluoroamphetamine, FAM) were examined and compared to those of the optical isomers of amphetamine (AM). Substitution of fluorine into the side-chain of AM increased the
J F McElroy et al.
The Journal of pharmacology and experimental therapeutics, 228(3), 593-599 (1984-03-01)
Serum corticosterone concentrations were measured in rats after injection of fenfluramine (FEN), p-chloroamphetamine (PCA) and p-fluoroamphetamine (PFA), halogenated amphetamine derivatives believed to exert their behavioral and physiological effects through the release and/or depletion of brain serotonin (5-HT). Animals were pretreated
Suad Al-Abri et al.
Clinical toxicology (Philadelphia, Pa.), 52(10), 1292-1295 (2014-10-29)
4-Fluoroamphetamine (4-FA) is a para-substituted phenethylamine-type synthetic stimulant that has in recent years gained popularity through internet blogs and market share according to confiscated drug data. No serious toxicity has previously been reported. We report a case of a young

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