A4382
4-Aminoantipyrine
reagent grade
Synonyme(s) :
4-Amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one, Ampyrone
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A propos de cet article
Formule empirique (notation de Hill) :
C11H13N3O
Numéro CAS:
Poids moléculaire :
203.24
UNSPSC Code:
51384603
NACRES:
NA.31
PubChem Substance ID:
EC Number:
201-452-3
Beilstein/REAXYS Number:
181635
MDL number:
Service technique
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reagent grade
Quality Level
assay
≥97% (HPLC)
form
powder
mp
105-110 °C (lit.)
solubility
water: 50 mg/mL
SMILES string
CN1N(c2ccccc2)C(=O)C(N)=C1C
InChI
1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3
InChI key
RLFWWDJHLFCNIJ-UHFFFAOYSA-N
Application
Reagent for glucose determination in the presence of phenol and peroxidase.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Protocoles
Enzymatic assay of lipase type XIII from Pseudomonas sp. using a coupled enzyme system of glycerol kinase and glycerophosphate oxidase (EC 3.1.1.3)
Amjad H El-Sheikh et al.
Talanta, 83(2), 667-673 (2010-11-30)
Molecularly imprinted polymer (MIP) may not selectively recognize small template of limited number of functional groups, such as 2-chlorophenol (2-CP). In this work, a novel method was proposed to improve the recognition ability of the molecularly imprinted solid phase extraction
Qihui Wang et al.
Journal of hazardous materials, 186(2-3), 1076-1081 (2010-12-21)
In this work, the immobilization of 4-aminoantipyrine onto bentonite was carried out and it was then used to investigate the adsorption behavior of Cr(III), Hg(II) and Pb(II) ions from aqueous solutions. The separation and preconcentration conditions of analytes were investigated
Mohammad Sayed Alam et al.
Bioorganic & medicinal chemistry, 20(13), 4103-4108 (2012-05-26)
4-Aminoantipyrine (4-amino-1,5-dimethyl-2-phenylpyrazole-3-one) and its analogues have been found to be compounds of interest for their anti-inflammatory, analgesic, antiviral, antipyretic, antirheumatic and antimicrobial activities. In the present study, Schiff base analogues of 4-aminoantipyrine were synthesized by the condensation reaction with substituted
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| A4382-100G | 04061835326211 |
| A4382-10G | 04061835326228 |
| A4382-250G | 04061835326235 |
| A4382-25G | 04061835326242 |
| A4382-50G | 04061835326259 |