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Merck
CN

32443

Carboxyibuprofen

VETRANAL®, analytical standard

Synonym(s):

2-[4-(2-Carboxypropyl)phenyl]propionic acid, 3-[4-(1-Carboxyethyl)phenyl]-2-methylpropionic acid

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About This Item

Empirical Formula (Hill Notation):
C13H16O4
CAS Number:
15935-54-3
Molecular Weight:
236.26
UNSPSC Code:
12352100
NACRES:
NA.24
PubChem Substance ID:
329754216
MDL number:
MFCD08063737
Beilstein/REAXYS Number:
5951324

Key Documents

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InChI key

DIVLBIVDYADZPL-UHFFFAOYSA-N

SMILES string

CC(Cc1ccc(cc1)C(C)C(O)=O)C(O)=O

InChI

1S/C13H16O4/c1-8(12(14)15)7-10-3-5-11(6-4-10)9(2)13(16)17/h3-6,8-9H,7H2,1-2H3,(H,14,15)(H,16,17)

grade

analytical standard

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC8466
BCCB0779
BCBW6809
BCBT8174
BCBT0293

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Emilia Waraksa et al.
Journal of separation science, 41(20), 3881-3891 (2018-08-14)
Ibuprofen is widely used in human and veterinary medicine for the treatment of chronic pain as well as rheumatic and musculoskeletal disorders. However, the analgesic and anti-inflammatory properties of Ibuprofen have contributed to frequent drug abuse in equestrian sports. A
Samantha A Whiteside et al.
Journal of medical microbiology, 68(8), 1244-1252 (2019-06-12)
The high incidence of urinary tract infection (UTI) among women and children, in combination with a lack of antibiotic efficacy with regard to pathogen eradication and recurrence prevention, as well as the negative side effects associated with antibiotics, has led
Dolores Camacho-Muñoz et al.
Journal of mass spectrometry : JMS, 52(2), 94-108 (2017-01-07)
This paper presents a multi-residue method for direct enantioselective separation of chiral pharmacologically active compounds in environmental matrices. The method is based on chiral liquid chromatography and tandem mass spectrometry detection. Simultaneous chiral discrimination was achieved with a macrocyclic glycopeptide-based
Aleksandar Lolić et al.
The Science of the total environment, 508, 240-250 (2014-12-08)
The occurrence of seven pharmaceuticals and two metabolites belonging to non-steroidal anti-inflammatory drugs and analgesics therapeutic classes was studied in seawaters. A total of 101 samples covering fourteen beaches and five cities were evaluated in order to assess the spatial
Paula Paíga et al.
Journal of pharmaceutical and biomedical analysis, 106, 61-70 (2014-07-09)
An analytical methodology for the simultaneous determination of seven pharmaceuticals and two metabolites belonging to the non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics therapeutic groups was developed based on off-line solid-phase extraction and ultra-high performance liquid chromatography coupled to tandem mass

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