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Laurocapram

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Catalog No. T2A2509Cas No. 59227-89-3
Alias Tranzone, N-Lauryl caprolactam, N-Dodecylcaprolactam, N-0252, Azone

Laurocapram (N-Lauryl caprolactam) is a percutaneous enhancer. Upon application to the skin, laurocapram interacts with lipids in the stratum corneum and may enhance the ability of the skin to absorb a hydrophilic chemical.

Laurocapram

Laurocapram

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Purity: 98.91%
Catalog No. T2A2509Alias Tranzone, N-Lauryl caprolactam, N-Dodecylcaprolactam, N-0252, AzoneCas No. 59227-89-3
Laurocapram (N-Lauryl caprolactam) is a percutaneous enhancer. Upon application to the skin, laurocapram interacts with lipids in the stratum corneum and may enhance the ability of the skin to absorb a hydrophilic chemical.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 g$29In StockIn Stock
5 g$42-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:98.91%
Appearance:Solid
Color:White
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Product Introduction

Laurocapram AI Summary
Laurocapram enhances the permeation of theophylline through human skin from water with an enhancement ratio of 2.5, but shows a lower enhancement ratio of 0.6 when the permeation is from an isopropyl myristate (IPM) suspension. Additionally, Laurocapram exhibits antiviral activity against SARS-CoV-2 by inhibiting the virus-induced cytotoxicity in VERO-6 cells, with an inhibition rate of -0.29% at a concentration of 10 µM after 48 hours of exposure to 0.01 MOI SARS-CoV-2 virus and an IC50 value greater than 20000 nM. Furthermore, the compound inhibits the SARS-CoV-2 3CL-Pro protease by 23.87% at a 20 µM concentration..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Laurocapram (N-Lauryl caprolactam) is a percutaneous enhancer. Upon application to the skin, laurocapram interacts with lipids in the stratum corneum and may enhance the ability of the skin to absorb a hydrophilic chemical.
SynonymsTranzone, N-Lauryl caprolactam, N-Dodecylcaprolactam, N-0252, Azone
Chemical Properties
Molecular Weight281.48
FormulaC18H35NO
Cas No.59227-89-3
SmilesC(CCCCCCCCCCC)N1C(=O)CCCCC1
Relative Density.0.906-0.926
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (177.63 mM), Sonication is recommended.
H2O: 100 mg/mL (355.27 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.11 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
DMSO/H2O
1mg5mg10mg50mg
1 mM3.5527 mL17.7633 mL35.5265 mL177.6325 mL
5 mM0.7105 mL3.5527 mL7.1053 mL35.5265 mL
10 mM0.3553 mL1.7763 mL3.5527 mL17.7633 mL
20 mM0.1776 mL0.8882 mL1.7763 mL8.8816 mL
50 mM0.0711 mL0.3553 mL0.7105 mL3.5527 mL
100 mM0.0355 mL0.1776 mL0.3553 mL1.7763 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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