32544
芬苯达唑砜
VETRANAL®, analytical standard
别名:
(5-苯磺酰基-1H-苯并咪唑-2-基)氨基甲酸甲酯, 5-(苯磺酰基)-2-苯并咪唑氨基甲酸甲酯
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关于此项目
经验公式（希尔记法）:
C15H13N3O4S
化学文摘社编号:
分子量:
331.35
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
703211
产品名称
芬苯达唑砜, VETRANAL®, analytical standard
InChI key
UAFDGCOOJPIAHN-UHFFFAOYSA-N
SMILES string
COC(=O)Nc1nc2cc(ccc2[nH]1)S(=O)(=O)c3ccccc3
InChI
1S/C15H13N3O4S/c1-22-15(19)18-14-16-12-8-7-11(9-13(12)17-14)23(20,21)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
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)
clinical testing
format
neat
Quality Level
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Chemical structure: benzimidazole
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
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1
存储类别
13 - Non Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
S E Marriner et al.
American journal of veterinary research, 42(7), 1143-1145 (1981-07-01)
Pharmacokinetics of oxfendazole and its sulfone metabolite were determined in 6 sheep. Oxfendazole achieved mean peak plasma concentrations of 0.76 micrograms/ml at 30 hours after oral administration of oxfendazole (10 mg/kg of body weight), and concentrations were detectable for up
T G Watson et al.
Research in veterinary science, 38(2), 231-233 (1985-03-01)
The pharmacokinetics of oxfendazole (OFZ) in red deer (Cervus elaphus) was examined. OFZ, administered per os at 4.53 mg kg-1, was extracted in ether from plasma and identified and concentrations estimated by high pressure liquid chromatography. Irrespective of whether the
J Landuyt et al.
Biomedical chromatography : BMC, 7(2), 78-81 (1993-03-01)
A high performance liquid chromatographic (HPLC) method for the determination of the anthelminthic pro-benzimidazole febantel and its major metabolites in lamb plasma has been developed. Samples were extracted after addition of albendazole as internal standard, NH4OH and distilled diethyl ether.
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
P Viviani et al.
Journal of veterinary pharmacology and therapeutics, 41(3), 476-484 (2018-02-22)
Parasitic diseases have a significant impact on livestock production. Nematodicidal drugs, such as fenbendazole (FBZ) or its oxidized metabolite oxfendazole (OFZ), can be used along with the trematodicidal triclabendazole (TCBZ), to broaden the spectrum of anthelmintic activity. However, co-exposure to
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