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Safety Information

H-052

Supelco

4′-Hydroxydiclofenac solution

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

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About This Item

Empirical Formula (Hill Notation):
C14H11Cl2NO3
CAS Number:
Molecular Weight:
312.15
EC Number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

Quality Level

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

100 μg/mL in acetonitrile

technique(s)

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

application(s)

clinical testing

format

single component solution

storage temp.

−20°C

SMILES string

OC(=O)Cc1ccccc1Nc2c(Cl)cc(O)cc2Cl

InChI

1S/C14H11Cl2NO3/c15-10-6-9(18)7-11(16)14(10)17-12-4-2-1-3-8(12)5-13(19)20/h1-4,6-7,17-18H,5H2,(H,19,20)

InChI key

KGVXVPRLBMWZLG-UHFFFAOYSA-N

General description

A certified solution standard suitable for use in LC/MS or GC/MS applications for clinical toxicology, forensic analysis, or pharmaceutical research. 4′-Hydroxydiclofenac is a major metabolite of diclofenac, a COX-2 inhibitor used for the treatment of minor aches, pains, and fever.

Application

  • Metabolism of non-steroidal anti-inflammatory drugs (NSAIDs): This study examines the biotransformation of 4′-Hydroxydiclofenac by Streptomyces griseolus CYP105A1, emphasizing its relevance in pharmacokinetic research on drug metabolism and enzyme inhibition studies (Yogo et al., 2022).
  • A multi-biomarker approach to assess toxicity of diclofenac and 4-OH diclofenac: Investigates the environmental impact of 4′-Hydroxydiclofenac on molluscs, providing insights into the ecological side-effects of pharmaceutical residues and their metabolites, important for researchers studying drug metabolism and environmental safety (Swiacka et al., 2022).
  • Cytochrome P450 Expression and Chemical Metabolic Activity before Full Liver Development in Zebrafish: Highlights the role of 4′-Hydroxydiclofenac in early developmental stages of liver metabolism in zebrafish, useful for developmental pharmacokinetics and toxicology studies (Nawaji et al., 2020).
  • Different Roles of Human Cytochrome P450 2C9 and 3A Enzymes in Diclofenac 4′- and 5-Hydroxylations: Explores the specific roles of cytochrome P450 enzymes in the metabolism of diclofenac and its major metabolite 4′-Hydroxydiclofenac, offering critical insights for pharmacokinetic research and drug metabolism assays (Miura et al., 2020).

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

WGK

WGK 2

Flash Point(F)

35.6 °F

Flash Point(C)

2 °C

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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