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Merck
CN

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

经验公式(希尔记法):
C9H12FN · HCl
CAS号:
分子量:
189.66
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

certified reference material

表单

liquid

特点

(Snap-N-Spike®)

包装

ampule of 1 mL

制造商/商品名称

Cerilliant®

drug control

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

浓度

1.0 mg/mL in methanol (as free base)

技术

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

应用

forensics and toxicology

包装形式

single component solution

储存温度

−20°C

SMILES字符串

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

InChI key

GKWYMWZWSCKSMT-UHFFFAOYSA-N

一般描述

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.

法律信息

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

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产品编号
说明
价格

警示用语:

Danger

危险分类

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

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

49.5 °F

闪点(°C)

9.7 °C

法规信息

监管及禁止进口产品

分析证书(COA)

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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
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
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
Chih-Sheng Jhang et al.
Electrophoresis, 33(19-20), 3073-3078 (2012-09-25)
A novel drug-screening system, consisting of paper spray-MS (PS-MS) and a CE-ESI-MS method was developed. This system can be easily switched either to PS-MS for rapidly screening samples or to the traditional CE-ESI-MS method for separation and to obtain detailed

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