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375160

Sigma-Aldrich

(S)-(+)-Ibuprofen

ReagentPlus®, 99%

Sinonimo/i:

S-(+)-IBU, (S)-(+)-2-(4-Isobutylphenyl)propionic acid, (S)-(+)-4-Isobutyl-α-methylphenylacetic acid

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About This Item

Formula condensata:
(CH3)2CHCH2C6H4CH(CH3)CO2H
Numero CAS:
51146-56-6
Peso molecolare:
206.28
Beilstein:
3590022
Numero MDL:
MFCD00069289
Codice UNSPSC:
12352002
ID PubChem:
24863369
NACRES:
NA.22

Livello qualitativo

200

Nome Commerciale

ReagentPlus®

Saggio

99%

Forma fisica

powder

Attività ottica

[α]20/D +59°, c = 2 in ethanol

Punto di fusione

49-53 °C (lit.)

Stringa SMILE

CC(C)Cc1ccc(cc1)[C@H](C)C(O)=O

InChI

1S/C13H18O2/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)/t10-/m0/s1
HEFNNWSXXWATRW-JTQLQIEISA-N

Informazioni sul gene

human ... IL8RA(3577) , PTGS1(5742) , PTGS2(5743)

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Descrizione generale

(S)-(+)-Ibuprofen is the enantiomer associated with the anti-inflammatory action of ibuprofen, which is widely used as a nonsteroidal anti-inflammatory drug in racemic form.

Applicazioni

(S)-(+)-Ibuprofen may be used as a starting material to synthesize hydrogelators with the potential ability to release it via enzyme-mediated hydrolysis.
Enantiomeric form of the anti-inflammatory agent ibuprofen used in pharmacokinetic studies.

Note legali

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

Applicazioni

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCD7027
BCCD5855
BCBT9452
BCBR3849V
BCBQ0296V

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(S)-(+)-Ketoprofen 99%

Sigma-Aldrich

471909

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(S)-(-)-1-Phenylethylamine for the resolution of racemates for synthesis

Sigma-Aldrich

8.07047

(S)-(-)-1-Phenylethylamine

Ibuprofen Arginate ≥98% (HPLC)

Sigma-Aldrich

SML1842

Ibuprofen Arginate

F Jamali et al.
Journal of pharmaceutical sciences, 81(3), 221-225 (1992-03-01)
The influences of absorption rate and dosage size on the pharmacokinetics of ibuprofen (IB) enantiomers were studied in six healthy subjects. Rapidly absorbed solutions (50, 100, 200, 400, 600, and 1200 mg) and regular 600-mg tablets of racemic IB were
Enantioselective determination of ibuprofen in plasma by high-performance liquid chromatography-electrospray mass spectrometry.
Bonato PS, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 796(2), 413-420 (2003)
(S)-(+)-Ibuprofen-based hydrogelators: an approach toward anti-inflammatory drug delivery.
Bhuniya S, et al.
Tetrahedron Letters, 47(40), 7153-7156 (2006)
Youssef Harrak et al.
Journal of medicinal chemistry, 53(18), 6560-6571 (2010-09-02)
Following our previous research on anti-inflammatory drugs (NSAIDs), we report on the design and synthesis of 4-(aryloyl)phenyl methyl sulfones. These substances were characterized for their capacity to inhibit cyclooxygenase (COX-1 and COX-2) isoenzymes. Molecular modeling studies showed that the methylsulfone
Jennifer Manley et al.
The Annals of pharmacotherapy, 41(7), 1227-1232 (2007-05-24)
To evaluate the literature examining prophylactic use of acetaminophen and ibuprofen for prevention of adverse reactions associated with childhood immunization. Articles were identified via MEDLINE/PubMed/EMBASE (1966-March 2007) using the following key terms: vaccination, immunization, diphtheria-tetanus toxoids-whole pertussis (DTwP), diphtheria tetanus-toxoid
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