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2-(1,3-benzodioxol-5-yl)-3-benzyl-2,3-dihydro-4(1H)-quinazolinone
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2-(1,3-benzodioxol-5-yl)-3-benzyl-2,3-dihydro-4(1H)-quinazolinone

CAS: 33369-31-2

Ref. 3D-FB43263

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Estimated delivery in United States, on Tuesday 2 Jul 2024

Product Information

Name:
2-(1,3-benzodioxol-5-yl)-3-benzyl-2,3-dihydro-4(1H)-quinazolinone
Synonyms:
  • 1,4-Dimethyl-5-p-chlorobenzoylpyrrole-2-acetic acid
  • 1H-pyrrole-2-acetic acid, 5-(4-chlorobenzoyl)-1,4-dimethyl-
  • 5-(4-Chlorobenzoyl)-1,4-dimethyl-1H-pyrrole-2-acetic acid
  • 5-(4-Chlorobenzoyl)-1,4-dimethylpyrrole-2-acetic acid
  • Pyrrole-2-acetic acid, 5-(p-chlorobenzoyl)-1,4-dimethyl-
  • Zomiperac
  • [5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-yl]acetic acid
  • {5-[(4-chlorophenyl)carbonyl]-1,4-dimethyl-1H-pyrrol-2-yl}acetic acid
Description:

Ketorolac is a nonsteroidal anti-inflammatory drug (NSAID) that is used to treat moderate to severe pain. It inhibits prostaglandin synthesis by binding to cyclooxygenase and blocking the conversion of arachidonic acid into prostaglandins. Ketorolac has been shown to be reactive with human serum and may cause anaphylaxis or other hypersensitivity reactions. The drug can also cause increased glomerular filtration rate, which may lead to renal impairment. Ketorolac has been shown in vitro to produce nanoparticulate compositions, which are more stable than conventional formulations and have improved bioavailability.
Ketorolac is often administered as part of combination preparations with analgesics such as acetaminophen or aspirin, or nonsteroidal anti-inflammatory drugs such as ibuprofen, naproxen, or indomethacin.

Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Purity:
Min. 95%
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Hazard Info

UN Number:
EQ:
Class:
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Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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