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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

CAS# 152628-03-0

4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

2D Structure

Catalog No. BCC8713----Order now to get a substantial discount!

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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid: 5mg $17 In Stock
4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid: 10mg Please Inquire In Stock
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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid: 100mg Please Inquire Please Inquire
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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid: 500mg Please Inquire Please Inquire
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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

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Chemical Properties of 4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

Cas No. 152628-03-0 SDF Download SDF
PubChem ID 10262831 Appearance Powder
Formula C12H14N2O2 M.Wt 218.3
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 7-methyl-2-propyl-3H-benzimidazole-5-carboxylic acid
SMILES CCCC1=NC2=C(C=C(C=C2N1)C(=O)O)C
Standard InChIKey XWAJTVCEILFDGU-UHFFFAOYSA-N
Standard InChI InChI=1S/C12H14N2O2/c1-3-4-10-13-9-6-8(12(15)16)5-7(2)11(9)14-10/h5-6H,3-4H2,1-2H3,(H,13,14)(H,15,16)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid Dilution Calculator

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4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid Molarity Calculator

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Preparing Stock Solutions of 4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.5809 mL 22.9043 mL 45.8085 mL 91.617 mL 114.5213 mL
5 mM 0.9162 mL 4.5809 mL 9.1617 mL 18.3234 mL 22.9043 mL
10 mM 0.4581 mL 2.2904 mL 4.5809 mL 9.1617 mL 11.4521 mL
50 mM 0.0916 mL 0.4581 mL 0.9162 mL 1.8323 mL 2.2904 mL
100 mM 0.0458 mL 0.229 mL 0.4581 mL 0.9162 mL 1.1452 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid

The Inhibition of Mild Steel Corrosion in 1 N HCl by Imidazole Derivatives.[Pubmed:24061751]

Acta Chim Slov. 2010 Jun;57(2):497-304.

The inhibition effect of imidazole derivatives 4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid (MPBI) and 1,4'-Dimethyl-2'-propyl-1H,3'H-2,5'-dibenzimidazole (DPBI) against mild steel corrosion in 1 N HCl solutions were evaluated using conventional weight loss, potentiodynamic polarization, linear polarization and electrochemical impedance spectroscopy. The weight loss results showed that both are excellent corrosion inhibitors, electrochemical polarizations data revealed the mixed mode of inhibition and the results of electrochemical impedance spectroscopy have shown that the change in the impedance parameters, charge transfer resistance and double layer capacitance, with the change in concentration of the inhibitor is due to the adsorption of the molecule leading to the formation of a protective layer on the surface of mild steel. The inhibition action of these compounds was, assumed to occur via adsorption on the steel surface through the active centres contained of the molecule.

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