(S)-(+)-Ibuprofen
Suppliers
Names
[ CAS No. ]:
51146-56-6
[ Name ]:
(S)-(+)-Ibuprofen
[Synonym ]:
(2S)-2-(4-Isobutylphenyl)propanoic acid
(S)-(+)-4-Isobutyl-α-methylphenylacetic Acid
(S)-2-(4-Isobutylphenyl)propanoic acid
Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (αS)-
(+)-(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
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
MSDS
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
Precursor & DownStream
Precursor
DownStream
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%
Articles
Nat. Chem. Biol. 3(5) , 268-273, (2007)
The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc...
SAAD Dig. 29 , 70-81, (2013)
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...