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H-002

Supelco

Haloperidol-D4 solution

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

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About This Item

Empirical Formula (Hill Notation):
C21D4H19ClFNO2
CAS Number:
136765-35-0
Molecular Weight:
379.89
EC Number:
200-659-6
MDL number:
MFCD00673279
UNSPSC Code:
41116107
PubChem Substance ID:
329815099
NACRES:
NA.24

grade

certified reference material

Quality Level

300

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

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

storage temp.

−20°C

SMILES string

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

InChI key

LNEPOXFFQSENCJ-AKPGVGPLSA-N

Related Categories

General description

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).



Legal Information

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

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Description
Pricing

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Danger

Hazard Classifications

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

target_organs

Eyes

wgk_germany

WGK 2

flash_point_f

closed cup

flash_point_c

closed cup

Certificates of Analysis (COA)

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Articles

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Analysis of 20 pharmaceutical compounds in calf serum using Supel™ Swift HLB SPE cartridge for cleanup and LC-MS determination and another commercially available HLB cartridge for comparison.

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