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Fomepizole hydrochloride (4-Methylpyrazole), a potent, orally active inhibitor of cytochrome P450 (CYP2E1) and a competitive inhibitor of alcohol dehydrogenase, prevents the conversion of methanol and ethylene glycol into toxic metabolites. It has potential as an antidote for poisoning by ethylene glycol or methanol.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 7-10 days | 7-10 days | |
| 50 mg | $1,980 | 7-10 days | 7-10 days | |
| 100 mg | $2,500 | 7-10 days | 7-10 days |
| Description | Fomepizole hydrochloride (4-Methylpyrazole), a potent, orally active inhibitor of cytochrome P450 (CYP2E1) and a competitive inhibitor of alcohol dehydrogenase, prevents the conversion of methanol and ethylene glycol into toxic metabolites. It has potential as an antidote for poisoning by ethylene glycol or methanol. |
| Synonyms | 4-Methylpyrazole hydrochloride |
| Molecular Weight | 118.56 |
| Formula | C4H7ClN2 |
| Cas No. | 56010-88-9 |
| Smiles | Cl.N1=CC(=CN1)C |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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