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32443

Supelco

Carboxyibuprofen

VETRANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C13H16O4
Número de CAS:
15935-54-3
Peso molecular:
236.26
Beilstein:
5951324
Número MDL:
MFCD08063737
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
329754216
NACRES:
NA.24

grado

analytical standard

Línea del producto

VETRANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

forensics and toxicology
pharmaceutical (small molecule)

Formato

neat

cadena SMILES

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)

Clave InChI

DIVLBIVDYADZPL-UHFFFAOYSA-N

Aplicación

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

Información legal

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

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Certificados de análisis (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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