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Chemical structure of CAS 51146-55-5

2-Hydroxy Ibuprofen

In Stock•Starting at $101 for 50 mg•Purity ≥ 95%
CAS No.51146-55-5
MDL No.MFCD08275592
MFC13H18O3
MW222.28
InChI KeyUJHKVYPPCJBOSG-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
50 mg95%$101In Stock
100 mg95%$163In Stock
250 mg95%$241In Stock
1 g95%$626In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

2-Hydroxyibuprofen is a hydroxy monocarboxylic acid and tertiary alcohol derived from ibuprofen, where the methine proton on the isobutyl group is replaced by a hydroxy group. It functions as a drug metabolite.

CAS No.51146-55-5
Product Name2-Hydroxy Ibuprofen
IrritantIrritant
Signal Word:Warning
HCode:H302-H315-H319-H335-H412
PCode:P261-P264-P264+P265-P270-P271-P273-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

LC-MS-MS determination of ibuprofen, 2-hydroxyibuprofen enantiomers, and carboxyibuprofen stereoisomers for application in biotransformation studies employing endophytic fungi.

Analytical and bioanalytical chemistry • Vol. 399, Issue 2 • 2011
PMID: 21079932DOI: 10.1007/s00216-010-4329-9

Behaviour of pharmaceutical products and biodegradation intermediates in horizontal subsurface flow constructed wetland. A microcosm experiment.

The Science of the total environment • Vol. 394, Issue 1 • 2008
PMID: 18280540DOI: 10.1016/j.scitotenv.2008.01.029

Elimination of pharmaceuticals and personal care products in subsurface flow constructed wetlands.

Environmental science & technology • Vol. 40, Issue 18 • 2006
PMID: 17007145DOI: 10.1021/es0607741

The secretion of ibuprofen metabolites interferes with the capillary chromatography of urinary homovanillic acid and 4-hydroxy-3-methoxymandelic acid in neuroblastoma diagnosis.

Clinical chemistry and laboratory medicine • Vol. 43, Issue 2 • 2005
PMID: 15843212DOI: 10.1515/CCLM.2005.029

Documentation

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