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Principaux documents

F1517

Supelco

Fenoprofen calcium salt hydrate

analytical standard, for drug analysis

Synonyme(s) :

(±)-2-(3-Phenoxyphenyl)propionic acid

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About This Item

Formule linéaire :
C30H26O6Ca
Numéro CAS:
Poids moléculaire :
522.60
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard, for drug analysis

Niveau de qualité

Essai

≥97% (HPLC)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

Chaîne 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;;

Clé InChI

JWCQUXFJNIIYQZ-UHFFFAOYSA-N

Application

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.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Équipement de protection individuelle

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


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Les clients ont également consulté

Hiroyuki Yamada et al.
Journal of pharmaceutical and biomedical analysis, 56(2), 448-453 (2011-06-28)
The purpose of this study was to develop a sensitive system for detection of crystalline drug substances in intact pharmaceutical tablets by X-ray powder diffractometry (XRPD), using synchrotron X-rays. Fenoprofen calcium dihydrate was used as a model compound. The wavelength
Fernanda Gumilar et al.
European journal of pharmacology, 675(1-3), 32-39 (2011-12-16)
The proposed curative properties of copper(II)-non-steroidal anti-inflammatory drugs (NSAIDs) have led to the development of numerous copper(II)-NSAID complexes with enhanced anti-inflammatory activity. In this work, the antinociceptive and toxic effects of two new coordination complexes: Cu₂(fen)₄(caf)₂ [fen: fenoprofenate anion; caf:
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
Cynthia L Stevenson et al.
Journal of pharmaceutical sciences, 94(9), 1861-1880 (2005-07-30)
Pharmaceutical solids have generally been characterized as either three-dimensional crystals or amorphous solids based on X-ray powder diffraction and modulated temperature differential scanning calorimetry. In contrast, fewer examples of thermotropic and lyotropic liquid crystals, or mesophases, appear in the pharmaceutical
Shirou Itagaki et al.
Pharmaceutical research, 23(6), 1209-1216 (2006-05-27)
Sodium-coupled monocarboxylate transporter 1 (SMCT1) is a Na+-coupled transporter for monocarboxylates. Many nonsteroidal anti-inflammatory drugs (NSAIDs) are monocarboxylates. Therefore, we investigated the interaction of these drugs with human SMCT1 (hSMCT1). We expressed hSMCT1 in a mammalian cell line and in

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