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Supelco

Ketoprofen-d3

VETRANAL®, analytical standard

Synonym(s):

2-(3-Benzoylphenyl)propionic acid-(methyl-d3)

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About This Item

Empirical Formula (Hill Notation):
C16D3H11O3
CAS Number:
159490-55-8
Molecular Weight:
257.30
MDL number:
MFCD08063452
UNSPSC Code:
41116107
PubChem Substance ID:
329754286
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

[2H]C([2H])([2H])C(C(O)=O)c1cccc(c1)C(=O)c2ccccc2

InChI

1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)/i1D3

InChI key

DKYWVDODHFEZIM-FIBGUPNXSA-N

Related Categories

Application

Ketoprofen-d3 has been used as a surrogate analytical standard for the determination of ketoprofen in sewage sludge samples by QuEChERS (quick, easy, cheap, effective, rugged and safe) extraction with on-line solid-phase extract purification and pre-concentration, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS).
It may be used as an analytical standard for the determination of ketoprofen in compost from sewage sludge by ultrasound-assisted extraction (UAE) and salt-assisted liquid–liquid extraction (SALLE), followed by ultrahigh performance liquid chromatography (UHPLC) coupled to MS/MS.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

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Description
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pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD9385
BCCC7051
BCBX5289
BCBS5216V
SZBF166XV

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Jaber Assaf et al.
Journal of pharmaceutical and biomedical analysis, 145, 414-422 (2017-07-22)
Investigations on the photochemical stability of pharmaceutical substances are mandatory in drug development and licensing as photo-induced degradation of an active pharmaceutical ingredient (API) may not only lead to decreased API concentrations but also to toxic or reactive products. Thus
C Roos et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 142, 387-395 (2019-07-16)
Oral administration of drug products is the preferred administration route. In recent decades there has been an increase in drug candidates with low solubility and/or low permeability. To increase the possibility of oral administration for the poorly permeating drugs, the
C Roos et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 132, 222-230 (2018-09-30)
The number of highly lipophilic active pharmaceutical ingredients (APIs) in pharmaceutical development has been constantly increasing over recent decades. These APIs often have inherent issues with solubility and dissolution, limiting their oral bioavailability. Traditionally, a reduction in particle size to
Melissa M Melough et al.
Journal of agricultural and food chemistry, 65(24), 5049-5055 (2017-06-06)
Furocoumarins are a class of photoactive compounds found in several plant species and may be responsible for the observed association between consumption of citrus products and the risk of skin cancer. Furocoumarin contents of several foods have been reported previously
Kristina Kotnik et al.
Chemosphere, 147, 114-123 (2016-01-15)
This study investigates the environmental fate of eight benzophenone derivatives (the pharmaceutical ketoprofen, its phototransformation products 3-ethylbenzophenone and 3-acetylbenzophenone, and five benzophenone-type UV filters) by evaluating their photolytic behaviour. In addition, the genotoxicity of these compounds and the produced photodegradation
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