T5535
Thiabendazole
powder, suitable for plant cell culture, BioReagent
Sinónimos:
2-(4-Thiazolyl)benzimidazole
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Fórmula empírica (notación de Hill):
C10H7N3S
Número CAS:
Peso molecular:
201.25
NACRES:
NA.72
PubChem Substance ID:
UNSPSC Code:
10171502
EC Number:
205-725-8
MDL number:
Beilstein/REAXYS Number:
611403
Servicio técnico
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Permítanos ayudarleNombre del producto
Thiabendazole, BioReagent, suitable for plant cell culture, powder
product line
BioReagent
form
powder
technique(s)
cell culture | plant: suitable
color
light yellow
antibiotic activity spectrum
fungi
application(s)
agriculture
mode of action
enzyme | inhibits
SMILES string
c1ccc2[nH]c(nc2c1)-c3cscn3
InChI
1S/C10H7N3S/c1-2-4-8-7(3-1)12-10(13-8)9-5-14-6-11-9/h1-6H,(H,12,13)
InChI key
WJCNZQLZVWNLKY-UHFFFAOYSA-N
Gene Information
human ... CYP2C9(1559)
General description
Chemical structure: imidazole
Application
Thiabendazole, a metal chelator and helminth-specific fumarate reductase inhibitor, is used primarily as an anthelmintic to control infections by helminth organisms. It is also used to control mold and fungal growth in plants.
Other Notes
Keep container tightly closed in a dry and well-ventilated place.Keep in a dry place.Storage class (TRGS 510): Non Combustible Solids
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Neonicotinoid insecticides are associated with a decline in the diversity and distribution of bees and wasps (Hymenoptera: Aculeata). The effects of neonicotinoids on the metamorphosis of aculeates have never been addressed in detail; however, recent evidence suggests that neonicotinoids induce
Stuart Dashper et al.
Antimicrobial agents and chemotherapy, 54(3), 1311-1314 (2009-12-30)
Porphyromonas gingivalis is a major pathogen of chronic periodontitis and exists in a biofilm on the surface of the tooth root. Oxantel, a cholinergic anthelmintic and fumarate reductase inhibitor, significantly inhibited biofilm formation by P. gingivalis and disrupted established biofilms