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| Parbendazole Basic information |
Product Name: | Parbendazole | Synonyms: | PARBENDAZOLE;(4-butyl-1h-benzimidazol-2-yl)-carbamicacidmethylester;(5-butyl-1h-benzimidazol-2-yl)-carbamicacimethylester;5-butyl-2-benzimidazolecarbamicacimethylester;helmatac;methyl5-butyl-2-benzimidazolecarbamate;n-(butyl-5,benzimidazolyl)-2,carbamatedemethyle;pbdz | CAS: | 14255-87-9 | MF: | C13H17N3O2 | MW: | 247.29 | EINECS: | 238-133-3 | Product Categories: | | Mol File: | 14255-87-9.mol | |
| Parbendazole Chemical Properties |
Melting point | 255-257°C | Boiling point | 390.33°C (rough estimate) | density | 1.1214 (rough estimate) | refractive index | 1.5700 (estimate) | storage temp. | Keep in dark place,Sealed in dry,2-8°C | solubility | DMSO (Slightly, Heated), Methanol (Slightly, Heated) | pka | 11.66±0.10(Predicted) | form | neat | color | White to Off-White | Water Solubility | <0.1 g/100 mL at 18 ºC | Stability: | Stable. Incompatible with strong oxidizing agents. | InChIKey | YRWLZFXJFBZBEY-UHFFFAOYSA-N | EPA Substance Registry System | Parbendazole (14255-87-9) |
Hazard Codes | Xn | Risk Statements | 63-22 | Safety Statements | 36/37 | WGK Germany | 3 | RTECS | DD6495000 | HS Code | 2933997500 | Toxicity | LD50 in mice, rats (g/kg): >4 orally, both species (Actor) |
| Parbendazole Usage And Synthesis |
Chemical Properties | solid | Uses | Antiparasitic | Uses | Parbendazole is a benzimidazole carbamate and a potent inhibitor of microtubule assembly and functions. | Definition | ChEBI: N-(6-butyl-1H-benzimidazol-2-yl)carbamic acid methyl ester is a carbamate ester and a member of benzimidazoles. | General Description | Crystals or fine white powder. | Air & Water Reactions | Insoluble in water. | Reactivity Profile | Parbendazole is a carbamate ester-amine. Amines behave as chemical bases. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. | Health Hazard | ACUTE/CHRONIC HAZARDS: When heated to decomposition Parbendazole emits toxic fumes. | Fire Hazard | Flash point data for Parbendazole are not available; however, Parbendazole is probably combustible. |
| Parbendazole Preparation Products And Raw materials |
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