For research use only. Not for therapeutic Use.
<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Ropivacaine Hydrochloride (CAS 132112-35-7) <span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">is the hydrochloride salt of ropivacaine, </span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">a local anesthetic of the amide type with analgesic activity. It </span>causes reversible blockade of impulse propagation along nerve fibres by preventing the inward movement of sodium ions through the cell membrane of the nerve fibers.</span></span>
Catalog Number | A000684 |
CAS Number | 132112-35-7 |
Synonyms | LEA-103 HCl; ROPIVACAINE HYDROCHLORIDE MONOHYDRATE; 132112-35-7; Naropin; Ropivacaine hydrochloride hydrate; UNII-V910P86109 |
Molecular Formula | C17H29ClN2O2 |
Purity | ≥95% |
Target | Sodium Channel |
Storage | -20°C |
IUPAC Name | (2S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide;hydrate;hydrochloride |
InChI | InChI=1S/C17H26N2O.ClH.H2O/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;1H2/t15-;;/m0../s1 |
InChIKey | VSHFRHVKMYGBJL-CKUXDGONSA-N |
SMILES | CCCN1CCCCC1C(=O)NC2=C(C=CC=C2C)C.O.Cl |
Reference | 1: Wen XJ, Li XH, Li H, Liang H, Yang CX, Wang HB. CaMK II γ down regulation protects dorsal root ganglion neurons from ropivacaine hydrochloride neurotoxicity. Sci Rep. 2017 Jul 12;7(1):5262. doi: 10.1038/s41598-017-05678-2. PubMed PMID: 28701796; PubMed Central PMCID: PMC5507888.<br /> |