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Iso-OMPA (Tetraisopropyl pyrophosphoramide) is a selective, covalent, and irreversible butylcholinesterase (BuChE) inhibitor for studying BuChE-related diseases.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $93 | - | In Stock | |
| 5 mg | $228 | - | In Stock | |
| 10 mg | $372 | - | In Stock | |
| 25 mg | $745 | - | In Stock | |
| 50 mg | $1,180 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $253 | - | In Stock |
| Description | Iso-OMPA (Tetraisopropyl pyrophosphoramide) is a selective, covalent, and irreversible butylcholinesterase (BuChE) inhibitor for studying BuChE-related diseases. |
| In vitro | Iso-OMPA exhibited IC₅₀ values of 694.7 μM (brain), 10.56 μM (liver), and 9.84 μM (muscle) for propionylthiocholine iodide (PSCh) in the brain, liver, and muscle tissues of the brown shrimp Penaeus aztecus, respectively [1]. For butyrylthiocholine iodide (BSCh), Iso-OMPA showed IC₅₀ values of 12.49 μM (liver) and 11.42 μM (muscle) in the liver and muscle tissues of P. aztecus, with corresponding Ki values of 0.2019 μM (liver) and 0.6612 μM (muscle) [1]. Iso-OMPA (100 μM, treated for 30 minutes) increased the sensitivity of isolated bronchial preparations from Homo sapiens to acetylcholine [2]. |
| In vivo | Iso-OMPA (0.6 and 1.9 mg/kg, subcutaneous injection, single dose) only slightly inhibited rat plasma cholinesterase (CarbE) activity at the low dose, while significantly inhibiting its activity at the high dose; however, no obvious inhibitory effect was observed on mouse plasma CarbE activity [3]. |
| Synonyms | Tetraisopropyl pyrophosphoramide |
| Molecular Weight | 342.36 |
| Formula | C12H32N4O3P2 |
| Cas No. | 513-00-8 |
| Smiles | O=P(OP(=O)(NC(C)C)NC(C)C)(NC(C)C)NC(C)C |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (233.67 mM), Sonication is recommended. H2O: 8 mg/mL (23.37 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 3.3 mg/mL (9.64 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO
DMSO
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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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