AlibendolCAS# 26750-81-2 |
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Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 26750-81-2 | SDF | Download SDF |
| PubChem ID | 71916 | Appearance | Powder |
| Formula | C13H17NO4 | M.Wt | 251.28 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | DMSO : ≥ 100 mg/mL (397.96 mM) H2O : 0.91 mg/mL (3.62 mM; Need ultrasonic) *"≥" means soluble, but saturation unknown. | ||
| Chemical Name | 2-hydroxy-N-(2-hydroxyethyl)-3-methoxy-5-prop-2-enylbenzamide | ||
| SMILES | COC1=C(C(=CC(=C1)CC=C)C(=O)NCCO)O | ||
| Standard InChIKey | UMJHTFHIQDEGKB-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C13H17NO4/c1-3-4-9-7-10(13(17)14-5-6-15)12(16)11(8-9)18-2/h3,7-8,15-16H,1,4-6H2,2H3,(H,14,17) | ||
| 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. |
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| 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. |
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| 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. | ||
| Description | Alibendol is an antispasmodic,choleretic, and cholekinetic.
Target: Others
administration of alibendol in beagle dogs, observed retention times were approximately 5.0 min for alibendol. The within-run precision showed RSD values between 5.83 and 16.96 %. The between-run RSD values varied from 6.73 to 17.99 % at the LLOQ [1]. References: | |||||
Alibendol Dilution Calculator
Alibendol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.9796 mL | 19.8981 mL | 39.7962 mL | 79.5925 mL | 99.4906 mL |
| 5 mM | 0.7959 mL | 3.9796 mL | 7.9592 mL | 15.9185 mL | 19.8981 mL |
| 10 mM | 0.398 mL | 1.9898 mL | 3.9796 mL | 7.9592 mL | 9.9491 mL |
| 50 mM | 0.0796 mL | 0.398 mL | 0.7959 mL | 1.5918 mL | 1.9898 mL |
| 100 mM | 0.0398 mL | 0.199 mL | 0.398 mL | 0.7959 mL | 0.9949 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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Alibendol is an antispasmodic,choleretic, and cholekinetic. Target: Others administration of alibendol in beagle dogs, observed retention times were approximately 5.0 min for alibendol. The within-run precision showed RSD values between 5.83 and 16.96 %. The between-run RSD values varied from 6.73 to 17.99 % at the LLOQ
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Metal-Free Thermal Activation of Molecular Oxygen Enabled Direct alpha-CH2-Oxygenation of Free Amines.[Pubmed:29182340]
J Org Chem. 2018 Jan 5;83(1):260-266.
Direct oxidation of alpha-CH2 group of free amines is hard to achieve due to the higher reactivity of amine moiety. Therefore, oxidation of amines involves the use of sophisticated metallic reagents/catalyst in the presence or absence of hazardous oxidants under sensitive reaction conditions. A novel method for direct C-H oxygenation of aliphatic amines through a metal-free activation of molecular oxygen has been developed. Both activated and unactivated free amines were oxygenated efficiently to provide a wide variety of amides (primary, secondary) and lactams under operationally simple conditions without the aid of metallic reagents and toxic oxidants. The method has been applied to the synthesis of highly functionalized amide-containing medicinal drugs, such as O-Me-Alibendol and -buclosamide.
