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Ropivacaine hydrochloride

pharmaceutical raw materials
Ropivacaine hydrochloride structure

Ropivacaine hydrochloride 

structure
  • CAS No:

    98717-15-8

  • Formula:

    C17H26N2O.ClH

  • Chemical Name:

    Ropivacaine hydrochloride

  • Synonyms:

    2-Piperidinecarboxamide,N-(2,6-dimethylphenyl)-1-propyl-,hydrochloride (1:1),(2S)-;2-Piperidinecarboxamide,N-(2,6-dimethylphenyl)-1-propyl-,monohydrochloride,(S)-;2-Piperidinecarboxamide,N-(2,6-dimethylphenyl)-1-propyl-,monohydrochloride,(2S)-;AL 381;Ropivacaine hydrochloride;Naropin;85255-64-7

  • Categories:

    Active Pharmaceutical Ingredients  >  Anesthetic Agents

Description

Ropivacaine hydrochloride is an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM.


An anilide used as a long-acting local anesthetic. It has a differential blocking effect on sensory and motor neurons.

Ropivacaine hydrochloride Basic Attributes

310.86

310.181183

1312995-182-4

35504LBE2T

DTXSID2048379

2933399090

Characteristics

32.34000

4.31930

1

1.044 g/cm3

260-262 °C

410.2ºC at 760 mmHg

201.9ºC

D25 -6.6° (c = 2 in water)

Safety Information

|Danger|H302 (12.24%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P280, P301+P312, P305+P351+P338, P310, P330, and P501|Aggregated GHS information provided by 49 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

Drugs that block nerve conduction when applied locally to nerve tissue in appropriate concentrations. They act on any part of the nervous system and on every type of nerve fiber. In contact with a nerve trunk, these anesthetics can cause both sensory and motor paralysis in the innervated area. Their action is completely reversible. (From Gilman AG, et. al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed) Nearly all local anesthetics act by reducing the tendency of voltage-dependent sodium channels to activate. (See all compounds classified as Anesthetics, Local.)

1 Propyl 2',6' pipecoloxylidide

Ropivacaine hydrochloride Use and Manufacturing

Uses

anesthetic Ropivacaine is such a new type of long-acting amide local anesthetic. Its action lasts for a long time, and it has anesthetic and analgesic effects.

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:310.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:310.1811912
Monoisotopic Mass:310.1811912
Topological Polar Surface Area:32.3
Heavy Atom Count:21
Complexity:308
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • EXCELLA GMBH AND CO KG

    United States United States
    Active
  • FINE CHEMICALS CORP PTY LTD

    United States United States
    Active
  • Shanghai Cenway Int’l Trading Co., Ltd.

    China China
    Active

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