H-002

Haloperidol-D₄ solution

100 μg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant^®

• Formule empirique (notation de Hill): C₂₁D₄H₁₉ClFNO₂
• Numéro CAS: 136765-35-0
• Poids moléculaire : 379.89
• Numéro CE : 200-659-6
• Numéro MDL: MFCD00673279
• Code UNSPSC : 41116107
• ID de substance PubChem : 329815099
• Nomenclature NACRES : NA.24

Propriétés

• Qualité: certified reference material
• Niveau de qualité: 300
• Forme: liquid
• Caractéristiques: Snap-N-Spike^®/Snap-N-Shoot^®
• Conditionnement: ampule of 1 mL
• Fabricant/nom de marque: Cerilliant^®
• Concentration: 100 μg/mL in methanol
• Technique(s): gas chromatography (GC): suitable; liquid chromatography (LC): suitable
• Application(s): clinical testing
• Format: single component solution
• Température de stockage: −20°C
• Chaîne SMILES: FC1=C([2H])C([2H])=C(C(CCCN2CCC(O)(C3=CC=C(Cl)C=C3)CC2)=O)C([2H])=C1[2H]
• InChI: 1S/C21H23ClFNO2/c22-18-7-5-17(6-8-18)21(26)11-14-24(15-12-21)13-1-2-20(25)16-3-9-19(23)10-4-16/h3-10,26H,1-2,11-15H2/i3D,4D,9D,10D
• Clé InChI: LNEPOXFFQSENCJ-AKPGVGPLSA-N

Description

Description générale

Haloperidol, sold under the trade name Haldol^®, is a typical antipsychotic which functions as a dopamine inverse agonist. This internal standard is suitable for quantitation of haloperidol levels in urine, serum, or plasma by LC/MS or GC/MS for urine drug testing, clinical toxicology, or forensic analysis. This butyrophenone analog is used to treat schizophrenia and delirium.

Application

• Production and NMR analysis of the human ibuprofen metabolite 3-hydroxyibuprofen.: This study discusses the use of preparative thin-layer chromatography (TLC) plates for the production and subsequent NMR analysis of the ibuprofen metabolite 3-hydroxyibuprofen. The method ensures the isolation and purification of the metabolite for detailed structural analysis (Neunzig et al., 2012).


• Preparative thin-layer chromatographic separation and subsequent gas chromatographic-mass spectrometric analysis of monoacylglycerols derived from butter oil by fungal degradation.: This research employs preparative TLC plates to separate monoacylglycerols from butter oil, followed by gas chromatographic-mass spectrometric analysis. The study highlights the efficiency of TLC in compound isolation for further analysis (Liu and Kinderlerer, 1999).
• Impurities in drugs IV: Indomethacin.: This research uses preparative TLC plates to identify and isolate impurities in the drug Indomethacin, underscoring the role of TLC in ensuring drug purity and safety (Curran et al., 1980).

Informations légales

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Haldol is a registered trademark of Johnson & Johnson

Snap-N-Shoot is a registered trademark of Cerilliant Corporation

Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Informations sur la sécurité

• Pictogrammes: GHS02,GHS06,GHS08
• Mention d'avertissement: Danger
• Mentions de danger: H225 - H301 + H311 + H331 - H370
• Conseils de prudence: P210 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P311
• 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 2
• Point d'éclair (°F): 49.5 °F - closed cup
• Point d'éclair (°C): 9.7 °C - closed cup