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Ropivacaine hydrochloride

Ropivacaine hydrochloride Suppliers list
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Products Intro: Product Name:Ropivacaine hydrochloride
CAS:132112-35-7
Purity:99% Package:1KG;10USD|1KG;10USD
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CAS:132112-35-7
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CAS:132112-35-7
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CAS:132112-35-7
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Products Intro: Product Name:Ropivacaine hydrochloride
CAS:132112-35-7
Purity:99% Package:1kilograms;110USD|100kilograms;90USD

Ropivacaine hydrochloride manufacturers

  • Ropivacaine Hcl
  • Ropivacaine Hcl pictures
  • $1.00 / 1g
  • 2024-05-08
  • CAS:132112-35-7
  • Min. Order: 1g
  • Purity: 0.98
  • Supply Ability: 1000
Ropivacaine hydrochloride Basic information
Product Name:Ropivacaine hydrochloride
Synonyms:(S)-1-propyl-2',6'-dimethylanilinoformoxylpiperidine monohydrochloride monohydrate;(S)-1-propyl-2',6'-dimethylanilinoformoxylpiperidine,monohydrochloride,monohydrate;(S)-Ropivaxaine hydrochloride;(S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide hydrochloride;Ropivacaine hydrochloride;(2S)-N-(2,6-Dimethylphenyl)-1-propyl-2-piperidinecarboxamide Hydrochloride Hydrate;LEA-103;(S)-ropivacaine hydrochloride hydrate
CAS:132112-35-7
MF:C17H26N2O.ClH.H2O
MW:328.88
EINECS:663-286-1
Product Categories:Inhibitors;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;API;132112-35-7
Mol File:132112-35-7.mol
Ropivacaine hydrochloride Structure
Ropivacaine hydrochloride Chemical Properties
Melting point 267-269°C
alpha D20 -7.28° (c = 2 in water)
storage temp. 2-8°C
solubility H2O: soluble5mg/mL, clear
form powder
color white to off-white
optical activity[α]/D -9 to -12, c = 1 in methanol
InChIKeyVSHFRHVKMYGBJL-CKUXDGONSA-N
CAS DataBase Reference132112-35-7(CAS DataBase Reference)
Safety Information
Hazard Codes T,Xi
Risk Statements 26/27/28-41
Safety Statements 22-36/37/39-45-39-26
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
HS Code 2933399090
MSDS Information
Ropivacaine hydrochloride Usage And Synthesis
Description(–)-Ropivacaine is a potent and reversible blocker of sodium channels in nerve fibers. In vivo, (–)-ropivacaine induces complete impairment of proprioception, motor function, and nociception in the hindleg of rats when 100 μL of an 8 mM solution is injected percutaneously into the sciatic nerve. (–)-Ropivacaine depresses myocardial contractile force in isolated rat hearts less potently than (±)-ropivacaine, as well as (–)- and (±)-bupivacaine . Formulations containing (–)-ropivacaine have been used as local anesthetics during surgery and childbirth.
Chemical PropertiesWhite Solid
UsesRopivacaine hydrochloride monohydrate has been used as an analyte in tandem mass spectrometry and as an amide-based local anaesthetic to test its effect on breast cancer cell methylation.
UsesAnesthetic (local).
DefinitionChEBI: The monohydrate form of (S)-ropivacaine hydrochloride.
General DescriptionRopivacaine has lidocaine-related structure with tertiary amine side chains.?It is a pure S(-)enantiomer with a propyl group on the piperidine nitrogen atom.
Biochem/physiol ActionsLocal anaesthetic with less cardiotoxicity than bupivacaine; 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.
Ropivacaine hydrochloride Preparation Products And Raw materials
Raw materialsRopivacaine-->Ropivacaine hydrochloride
Tag:Ropivacaine hydrochloride(132112-35-7) Related Product Information
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