32595
4-甲酰氨基安替吡啉
VETRANAL®, analytical standard
别名:
N-(1,5-二甲基-3-氧代-2-苯基-2,3-二氢-1H-吡唑-4-基)甲酰胺
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经验公式（希尔记法）:
C12H13N3O2
化学文摘社编号:
分子量:
231.25
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
216-808-3
Beilstein/REAXYS Number:
217665
MDL number:
产品名称
4-甲酰氨基安替吡啉, VETRANAL®, analytical standard
InChI key
WSJBSKRPKADYRQ-UHFFFAOYSA-N
InChI
1S/C12H13N3O2/c1-9-11(13-8-16)12(17)15(14(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3,(H,13,16)
SMILES string
CN1N(C(=O)C(NC=O)=C1C)c2ccccc2
grade
analytical standard
product line
VETRANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
pharmaceutical
format
neat
Quality Level
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Application
4-Formylaminoantipyrine may be used as an analytical reference standard for the determination of the analyte in:
- Aqueous samples by ultra-high performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS).
- Groundwater, surface water and wastewater samples by online mixed-bed multilayer solid-phase extraction (SPE) and HPLC combined with tandem mass spectrometry (MS/MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
4-Formylaminoantipyrines are grouped under the class of biodegradable organic micropollutants (OMPs).
Legal Information
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
Integrating organic micropollutant removal into tertiary filtration: Combining PAC adsorption with advanced phosphorus removal.
Altmann J, et al.
Water Research, 84, 58-65 (2015)
Multiresidue analytical method for the simultaneous determination of 72 micropollutants in aqueous samples with ultra high performance liquid chromatography-high resolution mass spectrometry.
Wode F, et al.
Journal of Chromatography A, 1270, 118-126 (2012)
K Matsuyama et al.
Journal of pharmacobio-dynamics, 6(11), 821-828 (1983-11-01)
The effect of phenobarbital (PB) and 3-methylcholanthrene (3-MC) on the metabolic behavior of aminopyrine (AM) was studied using an isolated hepatocyte system prepared from male Wistar rats. The formation of 4-formylaminoantipyrine (FAA) was increased after pretreatment with PB, but not
K Inoue et al.
Journal of chromatography, 274, 201-208 (1983-05-13)
Aminopyrine and its metabolites, including 3-hydroxymethyl-2-methyl-4-dimethylamino-1-phenyl-3-pyrazoline-5-one which is a hydroxylated metabolite of aminopyrine, were separated on a reversed-phase (C8) Radial-Pak column using a mobile phase of methanol-triethylamine-water (30:1:69) adjusted to pH 5.40 with acetic acid. Detection of the peak was
I Carretero et al.
The Analyst, 120(6), 1729-1732 (1995-06-01)
A rapid solid-phase extraction (SPE) procedure was developed for the quantitative isolation of three important antipyrine (dipyrone) metabolites from human plasma: 4-formylaminoantipyrine (FAA), 4-aminoantipyrine (AA) and 4-methylaminoantipyrine (MAA). Separation and quantitation were performed using micellar liquid chromatography (MLC) with a
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