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Trimipramine

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Catalog No. T21364Cas No. 739-71-9
Alias Surmontil, Stangyl, Rhotrimine

Trimipramine is an antidepressant with an anxiety-reducing sedative component to its action.

Trimipramine
Other Forms of Trimipramine:
Trimipramine maleateT1045521-78-8
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Trimipramine

😃Good
Catalog No. T21364Alias Surmontil, Stangyl, RhotrimineCas No. 739-71-9
Trimipramine is an antidepressant with an anxiety-reducing sedative component to its action.
Pack SizePriceAvailabilityQuantity
25 mg$1,5201-2 weeks
50 mg$1,9801-2 weeks
100 mg$2,5001-2 weeks
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Product Introduction

Bioactivity
Description
Trimipramine is an antidepressant with an anxiety-reducing sedative component to its action.
AliasSurmontil, Stangyl, Rhotrimine
Chemical Properties
Molecular Weight294.43
FormulaC20H26N2
Cas No.739-71-9
Relative Density.0.9912 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: Soluble
H2O: Insoluble

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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2 Enter the in vivo formulation:
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