| Weight | 188.23 g/mol |
|---|---|
| Formula | C11H12N2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
antipyrine (60-80-0)
Phenazone · Pyramidone · Anodynin
Score:
#2175 in Biology
,
#2677 in Chemistry
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- Estimation of plasma phosphatase by determination of hydrolysed phenol with amino-antipyrine. (Journal of Clinical Pathology, 1954)
- Measurement of local cerebral blood flow with iodo [14C] antipyrine (American Journal of Physiology-heart and Circulatory Physiology, 1978)
- Determination of blood glucose using 4-amino phenazone as oxygen acceptor. (Journal of Clinical Pathology, 1969)
- Measurement of Regional Cerebral Blood Flow with Antipyrine-[14C] in Awake Cats (Journal of Applied Physiology, 1969)
- Transfer across the perfused human placenta of antipyrine, sodium and leucine. (American Journal of Obstetrics and Gynecology, 1972)
- The estimation of antipyrine in biological materials. (Journal of Biological Chemistry, 1949)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Phenazone
- Pyramidone
- Anodynin
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SMILESCC1=CC(=O)N(N1C)C2=CC=CC=C2
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InChIKeyVEQOALNAAJBPNY-UHFFFAOYSA-N
- Pubchem - antipyrine
- Wikipedia - antipyrine
Phenazone (INN and BAN; also known as phenazon, antipyrine (USAN), or analgesine) is an analgesic, a nonsteroidal anti-inflammatory drug (NSAID) and an antipyretic. It was first synthesized by Ludwig Knorr in 1887. Phenazone is synthesized by condensation of phenylhydrazine and ethyl acetoacetate under basic conditions and methylation of the resulting intermediate compound 1-phenyl-3-methylpyrazolone with dimethyl sulfate or methyl iodide.
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antipyrine
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