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Ropivacaine Hydrochloride Powder CAS 132112-35-7 - China Suppliers and Factory for Local Anesthetic Drug
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Ropivacaine Hydrochloride Powder CAS 132112-35-7 - China Suppliers and Factory for Local Anesthetic Drug

Ropivacaine Hydrochloride - High-Quality Pharmaceutical Ingredient

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English Name: Ropivacaine Hydrochloride

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CAS No.: 132112-35-7

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Molecular Formula: C17H26N2O.ClH.H2O

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Molecular Weight: 328.88

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EINECS No.: 663-286-1

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As a leading China supplier and factory of pharmaceutical ingredients, we are proud to offer Ropivacaine Hydrochloride, a highly regarded local anesthetic used in various medical applications. Our product meets stringent quality standards, ensuring reliability and effectiveness. By choosing our Ropivacaine Hydrochloride, you can be confident in sourcing premium-grade materials from trusted suppliers in China. Explore our offerings and experience the exceptional quality that sets us apart in the pharmaceutical industry.

    Functions

    Ropivacaine is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain.
    Ropivacaine is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains.
    Ropivacaine is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer.
    Ropivacaine may also be used for purposes not listed in this medication guide.
    Ropivacaine is indicated for local anaesthesia including infiltration, nerve block, epidural and intrathecal anaesthesia in adults and children over 12 years. It is also indicated for peripheral nerve block and caudal epidural in children 1-12 years for surgical pain. It is also sometimes used for infiltration anaesthesia for surgical pain in children.
    Ropivacaine is often coadministered for epidural analgesia, for example in pregnant women during labour.

    Application

    Ropivacaine Clinical Use
    Ropivacaine is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer. Ropivacaine is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain.
    Ropivacaine is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains. Ropivacaine may also be used for purposes not listed in this medication guide.
    Tetracaine HCl Synthesis
    Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction.
    Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

    Details

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    Frequently Asked Questions

    What is Ropivacaine and how does it work?
    Ropivacaine is a local anesthetic drug belonging to the amino amide group. It works by blocking the nerve impulses that send pain signals to your brain, providing effective pain relief and numbing in targeted areas.
    What are the primary clinical applications of Ropivacaine?
    Ropivacaine is commonly used as a local anesthesia for spinal blocks (epidurals) during surgical procedures, C-sections, or to manage labor pain. It is also suitable for infiltration, nerve blocks, and intrathecal anesthesia.
    Can Ropivacaine be used for pediatric patients?
    Yes. Ropivacaine is indicated for local anesthesia in children over 12 years. Additionally, it can be used for peripheral nerve blocks and caudal epidurals in children aged 1 to 12 years to manage surgical pain.
    Is Ropivacaine safe for epidural analgesia during labor?
    Yes, Ropivacaine is frequently coadministered for epidural analgesia to ease pain in pregnant women during labor.
    How is Tetracaine HCl synthesized?
    Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The process involves forming an ethyl ester via acid-catalyzed esterification, followed by base-catalyzed transesterification by boiling the ethyl ester with excess 2-dimethylaminoethanol in the presence of sodium ethoxide.