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(R)-(-)-IBUPROFEN

(R)-(-)-IBUPROFEN Structure
  • ₹0
  • Product name: (R)-(-)-IBUPROFEN
  • CAS: 51146-57-7
  • MF: C13H18O2
  • MW: 206.29
  • EINECS:
  • MDL Number:MFCD00069290
  • Synonyms:(R)-(-)-2-(4-ISOBUTYLPHENYL)-PROPIONIC ACID;(R)-(-)-IBUPROFEN;(-)-Ibuprophen;Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (R)-;Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (αR)-;l-Ibuprofen;R-(-)-p-Isobutylhydratropic acid;(aR)-a-Methyl-4-(2-methylpropyl)benzeneacetic Acid
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :41-42°C
Boiling point :305.14°C (rough estimate)
Density :1.0176 (rough estimate)
refractive index :1.5290 (estimate)
storage temp. :Sealed in dry,2-8°C
solubility :Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly)
form :White crystalline powder.
pka :4.41±0.10(Predicted)
color :Colourless to Pale Beige Oil
Water Solubility :369.3mg/L(25 ºC)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Ibuprofen is a non-steroidal anti-inflammatory drug with diverse biochemical actions, most notably inhibiting COX-1 and COX-2 (IC50s = 2.6 and 1.53 μM, respectively). It is commonly synthesized as a racemic mixture of (S) and (R) isomers . (R)-Ibuprofen is an enantiomer that is generally not considered a COX inhibitor and is instead thought to be involved in pathways of lipid metabolism as it is incorporated into triglycerides along with fatty acids. The (R) enantiomer can, however, inhibit NF-κB activation (IC50 = 121.8 μM) in response to T-cell stimulation as well as block superoxide formation, β-glucuronidase release, and LTB4 generation by stimulated neutrophils (IC50 values range from 40-100 μM). 50-60% of (R)-ibuprofen is inverted to (S)-ibuprofen in humans after oral administration.

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