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orcinol (Synonyms: 5-Methylresorcinol, 5-Methylresorcin, 5-Methyl-1,3-benzenediol, 3,5-ToluenediolOrcin, 3,5...)

Catalog No. T3748 Copy Product Info
Purity: 99.93%
🥰Excellent
orcinol (5-Methylresorcin) is anxiolytic agent without sedative effect.

orcinol

Copy Product Info
🥰Excellent
Catalog No. T3748
Synonyms 5-Methylresorcinol, 5-Methylresorcin, 5-Methyl-1,3-benzenediol, 3,5-ToluenediolOrcin, 3,5-Dihydroxytoluene

orcinol (5-Methylresorcin) is anxiolytic agent without sedative effect.

orcinol
Cas No. 504-15-4
Pack SizePriceUSA StockGlobal StockQuantity
1 g$31-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.93%
Appearance:Solid
Color:White to Yellow
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Product Introduction

orcinol AI Summary
orcinol exhibits a range of biological activities, including antibacterial, antifungal, antioxidant, and phytogrowth-inhibitory effects. It inhibits Bacillus subtilis PCI219 spore germination with an IC50 of 16,800,000 nM and has noteworthy antibacterial activity against Staphylococcus epidermidis and Staphylococcus aureus with an EC50 of 4030 nM. The compound also shows phytogrowth-inhibitory activity against Amaranthus hypochondriacus and Echinochloa crusgalli, with IC50 values ranging from 1,000,000 nM to over 8,100,000 nM. In antioxidant assays, orcinol scavenges DPPH free radicals with an IC50 of 800 nM. It inhibits tyrosinase activity, with inhibition percentages ranging from 28.0% to 63.0% across different assays, indicating potential for skin whitening applications. However, it shows lower potency in inhibiting bovine brain phosphoinositide-specific phospholipase C gamma 1 (PI-PLCgamma1), with an IC50 greater than 250 µg/mL, and minimal activity against alpha-glucosidase, with an IC50 greater than 100,000 nM. The compound also demonstrates antifungal activity, with variable inhibition of Bipolaris leersiae conidial germination, reaching 80% inhibition at 500 ppm. Its antifouling activity is evident against Bugula neritina larvae, with 10% inhibition at 25 µg/mL. Physicochemical properties of orcinol include a LogP value of 1.27, a pKa of 9.3, and a consistent LogD of 1.27..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
orcinol (5-Methylresorcin) is anxiolytic agent without sedative effect.
Synonyms5-Methylresorcinol, 5-Methylresorcin, 5-Methyl-1,3-benzenediol, 3,5-ToluenediolOrcin, 3,5-Dihydroxytoluene
Chemical Properties
Molecular Weight124.14
FormulaC7H8O2
Cas No.504-15-4
SmilesCC1=CC(O)=CC(O)=C1
Relative Density.1.2900 g/cm3
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: 45 mg/mL (362.49 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (16.11 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
1mg5mg10mg50mg
1 mM8.0554 mL40.2771 mL80.5542 mL402.7711 mL
5 mM1.6111 mL8.0554 mL16.1108 mL80.5542 mL
10 mM0.8055 mL4.0277 mL8.0554 mL40.2771 mL
20 mM0.4028 mL2.0139 mL4.0277 mL20.1386 mL
50 mM0.1611 mL0.8055 mL1.6111 mL8.0554 mL
100 mM0.0806 mL0.4028 mL0.8055 mL4.0277 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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

You can also refer to dose conversion for different animals. More Dose Conversion

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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