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Sodium dodecyl sulfate

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Catalog No. T20075Cas No. 151-21-3
Alias Sodium lauryl sulfate, Sodium dodecylsulfate, SDS, NSC-402488, NSC402488, NSC 402488, Natrium laurylsulfuricum, Laurylsulfuric acid sodium salt, Anticerumen

Sodium dodecyl sulfate(Sodium lauryl sulfate) is a pharmaceutical excipient that is biologically inactive and improves the stability, solubility and processability of pharmaceutical preparations.

Sodium dodecyl sulfate

Sodium dodecyl sulfate

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Purity: 99.75%
Catalog No. T20075Alias Sodium lauryl sulfate, Sodium dodecylsulfate, SDS, NSC-402488, NSC402488, NSC 402488, Natrium laurylsulfuricum, Laurylsulfuric acid sodium salt, AnticerumenCas No. 151-21-3
Sodium dodecyl sulfate(Sodium lauryl sulfate) is a pharmaceutical excipient that is biologically inactive and improves the stability, solubility and processability of pharmaceutical preparations.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 g$39-In Stock
1 mL x 10 mM (in DMSO)$29-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.75%
Appearance:Solid
Color:White
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Product Introduction

Sodium dodecyl sulfate AI Summary
Sodium dodecyl sulfate exhibits a diverse range of biological activities. It demonstrates a dose-dependent hemolytic effect on rat red blood cells, with hemolysis increasing from 12.25% at 1 mM concentration to 62.66% at 5 mM. In antimicrobial studies, it shows significant activity against various strains of Escherichia coli, including multidrug-resistant strains, with Minimum Inhibitory Concentration (MIC) values ranging from 62.5 µg/mL to 128.0 µg/mL. It also exhibits antibacterial activity against Enterobacter cloacae, Enterococcus faecalis, Proteus mirabilis, and methicillin-resistant Staphylococcus aureus, and antifungal activity against Candida species. Additionally, it has potent anti-inflammatory properties by inhibiting IL1alpha release in a reconstituted human epidermis model. In terms of cytotoxicity, Sodium dodecyl sulfate is highly potent against human HepG2/C3A cells with an IC50 value of 0.222 nM, and it shows lesser toxicity against mouse RAW264.7 and human HCT116 cells, with IC50 values greater than 100,000 nM. The compound also presents impacting activities against Steinernema feltiae in nematicidal assays and induces membrane permeabilization. Biosurfactant properties are indicated by its ability to lower surface tension, with a critical micelle concentration (CMC) of 8.2 mM and activity in oil displacement assays. Furthermore, it displays significant inhibition of full-length human soluble epoxide hydrolase phosphatase activity, stabilizing the phosphatase domain while showing weaker activity against the hydrolase domain. Sodium dodecyl sulfate's broad spectrum of activities position it as a potential candidate for therapeutic applications involving antimicrobial, anti-inflammatory, and cytotoxic properties..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Sodium dodecyl sulfate(Sodium lauryl sulfate) is a pharmaceutical excipient that is biologically inactive and improves the stability, solubility and processability of pharmaceutical preparations.
SynonymsSodium lauryl sulfate, Sodium dodecylsulfate, SDS, NSC-402488, NSC402488, NSC 402488, Natrium laurylsulfuricum, Laurylsulfuric acid sodium salt, Anticerumen
Chemical Properties
Molecular Weight288.38
FormulaC12H25NaO4S
Cas No.151-21-3
SmilesO=S([O-])(OCCCCCCCCCCCC)=O.[Na+]
Relative Density.1.03 g/cm3 at 20℃
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 60 mg/mL (208.06 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4676 mL17.3382 mL34.6765 mL173.3823 mL
5 mM0.6935 mL3.4676 mL6.9353 mL34.6765 mL
10 mM0.3468 mL1.7338 mL3.4676 mL17.3382 mL
20 mM0.1734 mL0.8669 mL1.7338 mL8.6691 mL
50 mM0.0694 mL0.3468 mL0.6935 mL3.4676 mL
100 mM0.0347 mL0.1734 mL0.3468 mL1.7338 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:
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2 Enter the in vivo formulation:
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%
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