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F1517

Supelco

Fenoprofen calcium salt hydrate

analytical standard, for drug analysis

Synonim(y):

(±)-2-(3-Phenoxyphenyl)propionic acid

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About This Item

Wzór liniowy:
C30H26O6Ca
Numer CAS:
53746-45-5
Masa cząsteczkowa:
522.60
Numer WE:
252-107-9
Numer MDL:
MFCD00242722
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329799683
NACRES:
NA.24

klasa czystości

analytical standard, for drug analysis

Poziom jakości

100

Próba

≥97% (HPLC)

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

ciąg SMILES

O.[Ca].CC(C(O)=O)c1cccc(Oc2ccccc2)c1

InChI

1S/C15H14O3.Ca.H2O.2H/c1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13;;;;/h2-11H,1H3,(H,16,17);;1H2;;

Klucz InChI

JWCQUXFJNIIYQZ-UHFFFAOYSA-N

Zastosowanie

Fenoprofen calcium salt hydrate may be used as an analytical reference standard for the quantification of the analyte in environmental samples using gas chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
This page may contain text that has been machine translated.

Zastosowanie

Numer produktu
Opis
Cennik

Piktogramy

Exclamation mark
GHS07

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

H302 + H312 + H332

Klasyfikacja zagrożeń

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Środki ochrony indywidualnej

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
MKCV3932
MKCP4780
MKCC9461
MKBX3868V
MKBQ1121V

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Sigma-Aldrich

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Sigma-Aldrich

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Zhaoyan Wang et al.
Journal of chromatography. A, 1218(13), 1775-1779 (2011-02-24)
A highly sensitive method for enantioseparation of trace fenoprofen and amino acid derivatives by capillary electrophoresis (CE) with vancomycin as the chiral selector was developed. Several CE techniques, such as the partial filling, large-volume sample stacking with EOF as pump
Frederik André Hansen et al.
Analytica chimica acta, 1143, 109-116 (2021-01-02)
In this work, we investigated for the first time hydrophobic deep eutectic solvents (DES) as supported liquid membrane (SLM) for electromembrane extraction (EME). Camphor, coumarin, DL-menthol, and thymol were used as non-ionic DES components. Different DESs compositions were tested, to
Multiresidue analysis of acidic and polar organic contaminants in water samples by stir-bar sorptive extraction?liquid desorption?gas chromatography?mass spectrometry
Quintana BJ, et al.
Journal of Chromatography A, 1174(1-2), 27-39 (2007)
Josiane Cristófani Poggi et al.
Journal of clinical pharmacology, 46(11), 1328-1336 (2006-10-20)
The objective of the present study was to assess the influence of type 1 and type 2 diabetes mellitus on the enantioselective pharmacodynamics and pharmacokinetics of fenoprofen. Patients with diabetes mellitus type 1 (n = 7) or type 2 (n
Marinko Petrović et al.
Journal of pharmaceutical and biomedical analysis, 39(3-4), 531-534 (2005-06-14)
The gas chromatography (GC) method for enantioseparation of well-known non-steroidal anti-inflammatory drugs ibuprofen, fenoprofen and ketoprofen methyl esters mixture was developed. Best enantioseparation was performed on capillary column with heptakis-(2,3-di-O-methyl-6-O-t-butyldimethyl-silyl)-beta-cyclodextrin stationary phase and hydrogen used as a carrier gas. Initial
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Chromatograms

application for HPLC

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