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Key Documents

I1892

Supelco

Ibuprofen sodium salt

≥98% (GC)

Synonyme(s) :

α-Methyl-4-(isobutyl)phenylacetic acid

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About This Item

Formule linéaire :
C13H17O2Na
Numéro CAS:
Poids moléculaire :
228.26
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Pureté

≥98% (GC)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Solubilité

H2O: 100 mg/mL, clear to slightly hazy

Application(s)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

[Na+].CC(C)Cc1ccc(cc1)C(C)C([O-])=O

InChI

1S/C13H18O2.Na/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15;/h4-7,9-10H,8H2,1-3H3,(H,14,15);/q;+1/p-1

Clé InChI

PTTPUWGBPLLBKW-UHFFFAOYSA-M

Informations sur le gène

Description générale

Ibuprofen belongs to the class of non-steroidal anti-inflammatory drugs, widely used for the treatment of mild to moderate pain and several forms of arthritis.

Application

Ibuprofen sodium salt may be used as a model drug to study the intercalation mechanism via ion exchange reaction between ibuprofen and a biocompatible hydrotalcite compound.
Ibuprofen sodium salt may be used as an analytical reference standard for the qualification of the analyte in wastewaters using high-performance liquid chromatography (HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Actions biochimiques/physiologiques

Cyclooxygenase (COX) inhibitor that has greater activity against COX-1 than against COX-2.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

David J Pérez et al.
European journal of pharmacology, 814, 18-27 (2017-08-02)
There are many chronic diseases related with inflammation. The chronic inflammation can produce other problems as cancer. Therefore, it is necessary to design drugs with better anti-inflammatory activity than those in the clinic. Likewise, these could be used in chronic
Mixed supramolecular hemimicelles aggregates and magnetic carrier technology for solid phase extraction of ibuprofen in environmental samples prior to its HPLC-UV determination
Beiraghi A, et al.
Chemical Engineering Science, 108(3), 103-110 (2014)
Intercalation compounds of hydrotalcite-like anionic clays with antiinflammatory agents?I. Intercalation and in vitro release of ibuprofen
Ambrogi V, et al.
International Journal of Pharma Research & Review, 220, 23-32 (2001)
Emanuele Mauri et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 146, 143-149 (2019-11-15)
Ibuprofen (IBU) is a non-steroidal anti-inflammatory drug (NSAID) commonly used in the treatment of pain, fever and inflammation. However, the administration of IBU in its free carboxylic acid form is strongly dependent on its limited solubility in aqueous solution. This
Fareeha Batool et al.
Materials (Basel, Switzerland), 11(4) (2018-04-13)
Ibuprofen (IBU) has been shown to improve periodontal treatment outcomes. The aim of this study was to develop a new anti-inflammatory scaffold by functionalizing an electrospun nanofibrous poly-ε-caprolactone membrane with IBU (IBU-PCL) and to evaluate its impact on periodontal inflammation

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