Ropivacaine HClCAS# 98717-15-8 |
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Quality Control & MSDS
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Chemical structure
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| Cas No. | 98717-15-8 | SDF | Download SDF |
| PubChem ID | 175804 | Appearance | Powder |
| Formula | C17H27ClN2O | M.Wt | 310.86 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | DMSO : 10 mg/mL (32.17 mM; Need ultrasonic) H2O : 10 mg/mL (32.17 mM; Need ultrasonic) | ||
| Chemical Name | (2S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide;hydrochloride | ||
| SMILES | [Cl-].CCCN1CCCC[C@H]1C(=O)Nc2c(C)cccc2C.[H+] | ||
| Standard InChIKey | NDNSIBYYUOEUSV-RSAXXLAASA-N | ||
| Standard InChI | InChI=1S/C17H26N2O.ClH/c1-4-11-19-12-6-5-10-15(19)17(20)18-16-13(2)8-7-9-14(16)3;/h7-9,15H,4-6,10-12H2,1-3H3,(H,18,20);1H/t15-;/m0./s1 | ||
| 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. | ||
Ropivacaine HCl Dilution Calculator
Ropivacaine HCl Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.2169 mL | 16.0844 mL | 32.1688 mL | 64.3376 mL | 80.4221 mL |
| 5 mM | 0.6434 mL | 3.2169 mL | 6.4338 mL | 12.8675 mL | 16.0844 mL |
| 10 mM | 0.3217 mL | 1.6084 mL | 3.2169 mL | 6.4338 mL | 8.0422 mL |
| 50 mM | 0.0643 mL | 0.3217 mL | 0.6434 mL | 1.2868 mL | 1.6084 mL |
| 100 mM | 0.0322 mL | 0.1608 mL | 0.3217 mL | 0.6434 mL | 0.8042 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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Ropivacaine HCl is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly.
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Crystal structure and physical properties of two polymorphs of ropivacaine HCl.[Pubmed:16447177]
J Pharm Sci. 2006 Mar;95(3):680-8.
The crystal structure of two polymorphs of Ropivacaine HCl have been determined, as well as their relative stability up to 100 degrees C. A geometric restriction for a solid-state transition between the two polymorphs has been identified. The packing density along the H-bonded chains form the basis for a model explaining the kinetic crystallization of the metastable form. The difference in stability and physicochemical properties between the two polymorphs can be attributed to the difference in crystal structure.
Ropivacaine hydrochloride is an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM.
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