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经验公式(希尔记法):
C12H15N3O4S
化学文摘社编号:
分子量:
297.33
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8394880
产品名称
Albendazole sulfone, VETRANAL®, analytical standard
Quality Level
InChI
1S/C12H15N3O4S/c1-3-6-20(17,18)8-4-5-9-10(7-8)14-11(13-9)15-12(16)19-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
SMILES string
CCCS(=O)(=O)c1ccc2[nH]c(NC(=O)OC)nc2c1
InChI key
CLSJYOLYMZNKJB-UHFFFAOYSA-N
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)
forensics and toxicology
pharmaceutical (small molecule)
format
neat
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Application
Albendazole sulfone may be used as a reference standard in the determination of albendazole sulfone in plasma samples using high-performance liquid chromatography (HPLC) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Albendazole sulfone is a nonactive metabolite of albendazole sulfoxide (ABZSO).
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - STOT RE 2 Oral
target_organs
Adrenal gland,spleen,male reproductive organs,Blood
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Simultaneous determination of albendazole sulfoxide enantiomers and albendazole sulfone in plasma.
Lanchote LV, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 709(2), 273-279 (1998)
Victoria Miró et al.
Xenobiotica; the fate of foreign compounds in biological systems, 50(4), 408-414 (2019-07-16)
Combinations of bioactive phytochemicals with synthetic compounds have been suggested as promissory tools for the improvement of nematode control in livestock. Bioactive phytochemicals may interfere with the activity of drug-metabolizing enzymes and delay the metabolic conversion of anthelmintics into less
Francesca Accioni et al.
Journal of agricultural and food chemistry, 67(1), 520-530 (2018-12-06)
In this work, a restricted access volatile supramolecular solvent (RAM-VOL-SUPRAS) directly synthesized in milk is proposed for the first time for the simultaneous extraction and cleanup of benzimidazole anthelmintic drugs in milk meant for human consumption. The RAM-VOL-SUPRAS was formed
Jessica D Schulz et al.
Antimicrobial agents and chemotherapy, 63(4) (2019-02-13)
Albendazole is an effective anthelmintic intensively used for decades. However, profound pharmacokinetic (PK) characterization is missing in children, the population mostly affected by helminth infections. Blood microsampling would facilitate PK studies in pediatric populations but has not been applied to
Constant Edi et al.
PLoS neglected tropical diseases, 13(5), e0007325-e0007325 (2019-05-21)
A single co-administered dose of ivermectin (IVM) plus diethylcarbamazine (DEC) plus albendazole (ALB), or triple-drug therapy, was recently found to be more effective for clearing microfilariae (Mf) than standard DEC plus ALB currently used for mass drug administration programs for
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