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グレード
certified reference material
形状
liquid
特徴
(Snap-N-Spike®)
包装
ampule of 1 mL
メーカー／製品名
Cerilliant®
drug control
psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)
濃度
1.0 mg/mL in methanol (as free base)
テクニック
gas chromatography (GC): suitable
liquid chromatography (LC): suitable
アプリケーション
forensics and toxicology
フォーマット
single component solution
保管温度
−20°C
SMILES記法
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
詳細
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.
法的情報
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
アプリケーション
関連製品
製品番号
詳細
価格
シグナルワード
Danger
危険有害性情報
危険有害性の分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
保管分類コード
3 - Flammable liquids
WGK
WGK 1
引火点(°F)
49.5 °F
引火点(℃)
9.7 °C
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
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
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
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
Chromatograms
application for HPLCライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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