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Merck
CN

V900710

Antipyrine

Vetec, reagent grade, 98%

Synonym(s):

2,3-Dimethyl-1-phenyl-3-pyrazolin-5-one, Phenazone

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About This Item

Empirical Formula (Hill Notation):
C11H12N2O
CAS Number:
Molecular Weight:
188.23
EC Number:
200-486-6
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
157775
MDL number:
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InChI key

VEQOALNAAJBPNY-UHFFFAOYSA-N

InChI

1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3

SMILES string

CN1N(C(=O)C=C1C)c2ccccc2

grade

reagent grade

product line

Vetec

assay

98%

mp

109-111 °C (lit.)

Gene Information

human ... PTGS1(5742)

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1


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Line Mathiesen et al.
PloS one, 15(6), e0233979-e0233979 (2020-06-04)
Exposure to maternal stress during pregnancy can have adverse effects on the fetus, which has potential long-term effects on offspring´s development and health. We investigated the kinetics and metabolism of the hormones and amino acids: cortisol, cortisone, tryptophan and serotonin
Gro Klitgaard Povlsen et al.
BMC neuroscience, 14, 34-34 (2013-03-19)
Upregulation of vasoconstrictor receptors in cerebral arteries, including endothelin B (ETB) and 5-hydroxytryptamine 1B (5-HT(1B)) receptors, has been suggested to contribute to delayed cerebral ischemia, a feared complication after subarachnoid hemorrhage (SAH). This receptor upregulation has been shown to be
Joy Eliaerts et al.
Drug testing and analysis, 9(10), 1480-1489 (2016-12-16)
Traditionally, fast screening for the presence of cocaine in unknown powders is performed by means of colour tests. The major drawbacks of these tests are subjective colour evaluation depending on the operator ('50 shades of blue') and a lack of
Factors influencing antipyrine elimination.
I H Stevenson
British journal of clinical pharmacology, 4(3), 261-265 (1977-06-01)
Antipyrine as a model drug to study hepatic drug-metabolizing capacity.
H E Poulsen et al.
Journal of hepatology, 6(3), 374-382 (1988-06-01)

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