Chemodex

Ropivacaine hydrochloride monohydrate

CHF 108.00
In stock
CDX-R0123-M05050 mgCHF 108.00
CDX-R0123-M250250 mgCHF 434.00
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Product Details
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
Our product description may differ slightly from the original manufacturers 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.
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Product Specification Sheet
Datasheet Download PDF
Description

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.

Product References

(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)

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