![2-[4′-(1-Hydroxy-2-methylpropyl)phenyl]propionic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F78908-2-4-1-hydroxy-2-methylpropyl-phenyl-propionic-acid.webp&w=3840&q=75)
CAS 53949-53-4: 2-[4′-(1-Hydroxy-2-methylpropyl)phenyl]propionic acid
Formula:C13H18O3
InChI:InChI=1S/C13H18O3/c1-8(2)12(14)11-6-4-10(5-7-11)9(3)13(15)16/h4-9,12,14H,1-3H3,(H,15,16)
InChI key:InChIKey=RMOQYHYFRKTDRI-UHFFFAOYSA-N
SMILES:C(C(O)=O)(C)C1=CC=C(C(C(C)C)O)C=C1
Synonyms:- 2-[4′-(1-Hydroxy-2-methylpropyl)phenyl]propionic acid
- Benzeneacetic acid, 4-(1-hydroxy-2-methylpropyl)-α-methyl-
- 2-[4-(1-Hydroxy-2-methylpropyl)phenyl]propanoic acid
- 4-(1-Hydroxy-2-methylpropyl)-α-methylbenzeneacetic acid
- 1-Hydroxyibuprofen
Sort by
Found 11 products.
Ibuprofen EP Impurity L
CAS:Formula:C13H18O3Color and Shape:White To Off-White SolidMolecular weight:222.281-Hydroxy-ibuprofen
CAS:1-Hydroxy Ibuprofen, a metabolite in P. australis, targets COX-1/COX-2 with IC50s: 13 μM/370 μM.Formula:C13H18O3Color and Shape:SolidMolecular weight:222.28021-Hydroxy Ibuprofen (Ibuprofen Impurity L) (Mixture of Diastereomers)
CAS:Impurity Ibuprofen EP Impurity L Applications 1-Hydroxy Ibuprofen (Ibuprofen EP Impurity L) is a degradation product of Ibuprofen. References Forrest, J., et al.: Clin. Pharmacokinet., 7(2), 93 (1982), Shockcor, J., et al.: Xenobiotica, 26, 189 (1996), Nicholls, A., et al.: Chem. Res. Toxicol., 14, 975 (2001), Holmes, E., et al.: Toxicol. Sci., 87, 1 (2005),Formula:C13H18O3Color and Shape:Off-WhiteMolecular weight:222.28Ibuprofen-1-hydroxy 100 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C13H18O3Color and Shape:Single SolutionMolecular weight:222.282-[4-(1-Hydroxy-2-methylpropyl)phenyl]propanoic Acid (1-Hydroxyibuprofen)
CAS:Controlled ProductFormula:C13H18O3Color and Shape:NeatMolecular weight:222.281-Hydroxy-ibuprofen - Mixture of diastereoisomers
CAS:Ibuprofen is a nonsteroidal anti-inflammatory drug that is used to treat arthritis, rheumatoid arthritis, menstrual cramps and pain. Ibuprofen is a racemic mixture of two enantiomers, ibuprofen and S (+) -ibuprofen. The dextran sulfate method is an analytical method used to determine the concentration of ibuprofen in biological fluids such as human serum or urine. This test can be done by first treating the sample with trifluoroacetic acid (TFA) to convert ibuprofen to its glucuronide conjugate. The glucuronide conjugates are then deproteinized with hydrochloric acid, which converts them into their corresponding carboxylated derivatives. This conversion allows for the separation of ibuprofen from interfering substances using preparative hplc and quantification using mass spectrometry. Toxicity studies have been conducted on bacteria strains and inflammatory bowelFormula:C13H18O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:222.28 g/mol