(S)-(+)-Ibuprofen

Modify Date: 2026-07-01 19:34:38

(S)-(+)-Ibuprofen Structure
(S)-(+)-Ibuprofen structure
Common Name (S)-(+)-Ibuprofen
CAS Number 51146-56-6 Molecular Weight 206.281
Density 1.0±0.1 g/cm3 Boiling Point 319.6±11.0 °C at 760 mmHg
Molecular Formula C13H18O2 Melting Point 49-53ºC
MSDS Chinese USA Flash Point 216.7±14.4 °C

 Use of (S)-(+)-Ibuprofen


(S)-(+)-Ibuprofen is the S-enantiomer of Ibuprofen. Ibuprofen is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50 of 13 μM and 370 μM, respectively.

 Names

Name dexibuprofen
Synonym More Synonyms

 (S)-(+)-Ibuprofen Biological Activity

Description (S)-(+)-Ibuprofen is the S-enantiomer of Ibuprofen. Ibuprofen is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50 of 13 μM and 370 μM, respectively.
Related Catalog

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 319.6±11.0 °C at 760 mmHg
Melting Point 49-53ºC
Molecular Formula C13H18O2
Molecular Weight 206.281
Flash Point 216.7±14.4 °C
Exact Mass 206.130676
PSA 37.30000
LogP 3.72
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.519
InChIKey HEFNNWSXXWATRW-JTQLQIEISA-N
SMILES CC(C)Cc1ccc(C(C)C(=O)O)cc1

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn:Harmful;
Risk Phrases R22;R63
Safety Phrases S36/37-S45
RIDADR 2811.0
WGK Germany 3
Hazard Class 6.1
HS Code 2916399090

 Synthetic Route

 Customs

HS Code 2916399090
Summary 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

 Articles111

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The advantages and limitations of the analgesics available for control of postoperative pain after a dental procedure.

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Pegylation improves the pharmacokinetics and bioavailability of small-molecule drugs hydrolyzable by esterases: a study of phospho-Ibuprofen.

J. Pharmacol. Exp. Ther. 351(1) , 61-6, (2014)

Esterase hydrolysis of drugs can accelerate their elimination, thereby limiting their efficacy. Polyethylene glycol (PEG) covalently attached to drugs (pegylation) is known to improve the efficiency o...

 (S)-(+)-IbuprofenBioassay

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Name: Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
Source: ChEMBL
Target: N/A
External Id: CHEMBL1266185
Name: Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
Source: NCGC
External Id: SNCA-p-activity-luciferase
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
Name: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen
Source: NCGC
Target: N/A
External Id: SMAD3201
Name: uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
Source: Burnham Center for Chemical Genomics
Target: cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id: SBCCG-A764-CF-PAF-Primary-Assay
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ant...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_ANT_FLUO8_1536_1X%INH PRUN
Name: qHTS for Inhibitors of TGF-b
Source: NCGC
Target: Smad3 [Homo sapiens]
External Id: SMAD3101
Name: Inhibition of COX1 by human platelet assay
Source: ChEMBL
Target: Prostaglandin G/H synthase 1
External Id: CHEMBL888935
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 Synonyms

(2S)-2-(4-Isobutylphenyl)propanoic acid
(S)-(+)-4-Isobutyl-α-methylphenylacetic Acid
(S)-2-(4-Isobutylphenyl)propanoic acid
(+)-(S)-Ibuprofen
(+)-ibuprofen
MFCD00069289
Dexibuprofen
(S)-4-Isobutyl-α-methylphenylacetic acid
(2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid
(S)-(+)-Ibuprofen
(S)-(+)-2-(4-isobutylphenyl)propanoic acid
d-Ibuprofen
(S)-(+)-4-Isobutyl-Alpha-Methylphenylacetic Acid
Ibuprofen
(S)-(+)-2-(4-Isobutylphenyl)propionic Acid
(S)-a-Methyl-4-(2-methylpropyl)benzeneacetic acid
(S)-ibuprofen
(2S)-2-[4-(2-Methylpropyl)phenyl]propionic acid
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