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Levobupivacaine hydrochloride is white crystalline powder, while it's Molecular Formula is C18H28N2O*ClH. Levobupivacaine hydrochloride has been used as an analyte in tandem mass spectrometry. It may be used to test its inhibitory effect on phosphorylation of extracellular signal-regulated kinase (ERK) mediated by capsaicin It may also be used as a component of poly(D,L-lactide-co-glycolide) (PLGA) microparticles for testing its sustainable release by electrospraying technique.
The CAS number of Levobupivacaine hydrochloride is 27262-48-2.
More information of Levobupivacaine hydrochloride 27262-48-2 are:
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Synonyms |
2-Piperidinecarboxamide,1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride, (2S)- (9CI);2-Piperidinecarboxamide, 1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride,(S)-;2',6'-Pipecoloxylidide, 1-butyl-, monohydrochloride, (-)- (8CI);(-)-Bupivacaine monohydrochloride;(S)-(-)-Bupivacaine monohydrochloride;Chirocaine;Popscaine;Levobupivacaine HCL; |
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CAS Number |
27262-48-2 |
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Molecular Formula |
C18H28N2O*ClH |
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Molecular Weight |
324.894 |
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Melting Point |
254 °C (dec.)(lit.) |
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Boiling Point |
423.4 °C at 760 mmHg |
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Flash Point |
209.9 °C |
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HS CODE |
2942000000 |
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PSA |
23.55000 |
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LogP |
4.74080 |
Levobupivacaine was first launched in the US for the production of local anesthesia for surgery and obstetrics and for post-operative pain management. It is the (S)-enantiomer of the long acting, highly potent local anesthetic bupivacaine (Marcaine) that can be prepared by a three step sequence from (S)-pipecolic acid or from (S)-lysine by oxidative deamination and stereospecific ring closure to (S)-pipecolamide core structure. Levobupivacaine exhibits its long-acting local anesthetic effect by blocking neuronal sodium channel ion flow in nerve axons. Clinical studies demonstrated an efficacy and a general profile closely resembling those of the racemic bupivacaine currently in use; however, it produced an enhanced safety profile, in particular substantially reduced (about one-third) cardiotoxicity (less effect on myocardial contractility and QT, prolongation) and CNS depressive side effects. Onset and duration of blockade were also equivalent or even better.
InChI:InChI=1/C18H28N2O.ClH/c1-4-5-12-20-13-7-6-11-16(20)18(21)19-17-14(2)9-8-10-15(17)3;/h8-10,16H,4-7,11-13H2,1-3H3,(H,19,21);1H/t16-;/m0./s1
Articles related to Levobupivacaine hydrochloride:
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Article |
Source |
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Preparation method of levobupivacaine hydrochloride |
- , (2017/07/19) |
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Synthesis method of bupivacaine |
- , (2016/10/10) |
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