5-hydroxy Thiabendazole structure
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Common Name | 5-hydroxy Thiabendazole | ||
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CAS Number | 948-71-0 | Molecular Weight | 217.25 | |
Density | 1.535g/cm3 | Boiling Point | 525.6ºC at 760mmHg | |
Molecular Formula | C10H7N3OS | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 271.7ºC | |
Symbol |
GHS07, GHS09 |
Signal Word | Warning |
Use of 5-hydroxy Thiabendazole5-Hydroxythiabendazole (5-OHTBZ) is a biomarker of Thiabendazole (HY-B0263) exposure[1]. |
Name | 5-Hydroxy Thiabendazole |
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Synonym | More Synonyms |
Description | 5-Hydroxythiabendazole (5-OHTBZ) is a biomarker of Thiabendazole (HY-B0263) exposure[1]. |
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Related Catalog | |
References |
Density | 1.535g/cm3 |
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Boiling Point | 525.6ºC at 760mmHg |
Molecular Formula | C10H7N3OS |
Molecular Weight | 217.25 |
Flash Point | 271.7ºC |
Exact Mass | 217.03100 |
PSA | 90.04000 |
LogP | 2.39200 |
Index of Refraction | 1.783 |
Storage condition | 0-6°C |
~% 5-hydroxy Thiab... CAS#:948-71-0 |
Literature: Xenobiotica, , vol. 26, # 7 p. 765 - 778 |
Precursor 1 | |
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DownStream 1 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Multi-residue Determination of Polar Veterinary Drugs in Livestock and Fishery Products by Liquid Chromatography/Tandem Mass Spectrometry.
J. AOAC Int. 98(1) , 230-47, (2015) Residues of 37 polar veterinary drugs belonging to six families (quinolones, tetracyclines, macrolides, lincosamides, sulfonamides, and others) in livestock and fishery products were determined using ... |
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Evidence for cytochrome P4501A2-mediated protein covalent binding of thiabendazole and for its passive intestinal transport: use of human and rabbit derived cells.
Chem. Biol. Interact. 127(2) , 109-24, (2000) Thiabendazole (TBZ), an anthelmintic and fungicide benzimidazole, was recently demonstrated to be extensively metabolized by cytochrome P450 (CYP) 1A2 in man and rabbit, yielding 5-hydroxythiabendazol... |
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In vitro and in silico identification and characterization of thiabendazole as a mechanism-based inhibitor of CYP1A2 and simulation of possible pharmacokinetic drug-drug interactions.
Drug Metab. Dispos. 37 , 1286-1294, (2009) Thiabendazole (TBZ) and its major metabolite 5-hydroxythiabendazole (5OH-TBZ) were screened for potential time-dependent inhibition (TDI) against CYP1A2. Screen assays were carried out in the absence ... |
2-(1,3-thiazol-4-yl)-3H-benzimidazol-5-ol |