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Ropivacaine hydrochloride monohydrate_Molecular_structure_CAS_132112-35-7)
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Ropivacaine hydrochloride monohydrate

Catalog No. R0283 Name Sigma Aldrich
CAS Number 132112-35-7 Website http://www.sigmaaldrich.com
M. F. C17H29ClN2O2 Telephone 1-800-521-8956
M. W. 328.87736 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 154753

SYNONYMS

IUPAC name
(2S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide hydrate hydrochloride
IUPAC Traditional name
ropivacaine hydrate hydrochloride
Synonyms
(2S)-N-(2,6-dimethylphenyl)-1-propyl-2-piperidinecarboxamide hydrochloride monohydrate
Naropin hydrochloride monohydrate
(S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide hydrochloride monohydrate

DATABASE IDS

MDL Number MFCD00946578
CAS Number 132112-35-7

PROPERTIES

Empirical Formula (Hill Notation) C17H26N2O · HCl · H2O
Optical Purity optical purity: -6 to -10 degree
Purity ≥98% (HPLC)
Apperance white to off-white powder
Solubility DMSO: ≥10 mg/mL
GHS Pictograms GHS05
GHS Signal Word Danger
GHS Hazard statements H318
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P280-P305 + P351 + P338
Risk Statements 41
Safety Statements 26-39
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Local 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.
Description (简体中文)
Biochem/physiol Actions
Local 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.

REFERENCES