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Chemodex
Ropivacaine hydrochloride monohydrate
Product Details | |
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Synonyms | LEA 103; Naropin; (S)-Ropivacaine hydrochloride monohydrate |
Product Type | Chemical |
Properties | |
Formula | C17H26N2O . HCl . H2O |
MW | 274.4 . 36.5 . 18.0 |
CAS | 132112-35-7 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥98% (T) |
Appearance | White to off-white powder. |
Solubility | Soluble in DMSO (25mg/mL), DMF (15mg/ml), ethanol (15mg/ml), methanol or water (2mg/ml). |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | VSHFRHVKMYGBJL-UHFFFAOYSA-N |
Smiles | CC1=CC=CC(C)=C1NC(C2CCCCN2CCC)=O.O.Cl |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +4°C |
Long Term Storage | +4°C |
Use/Stability | Stable for at least 2 years after receipt when stored at +4°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
Ropivacaine is a long-acting amide local anaesthetic agent. Ropivacaine is a potent and reversible blocker of sodium channels in nerve fibers. It is a pure S(-)enantiomer and less lipophilic than racemic sodium channel blockers, such as bupivacaine and is less likely to penetrate large myelinated motor fibres, resulting in a relatively reduced motor blockade. Thus, ropivacaine has a greater degree of motor sensory differentiation, which could be useful when motor blockade is undesirable. The reduced lipophilicity is also associated with decreased potential for central nervous system toxicity and cardiotoxicity.
(1) R.D. Wang, et al.; Exp. Opin. Pharmacother. 2, 2051 (2001) (Review) | (2) T.G. Hansen; Exp. Rev. Neurother. 4, 781 (2004) (Review) | (3) G. Kuthiala & G. Chaudhary; Indian J. Anaesth. 55, 104 (2011) (Review)