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Hubei Langyou International Trading Co., LtdLocal Anesthetic Drugs 99%min Levobupivacaine 27262-47-1 For Surgical Anaesthesia//file1.lookchem.com/cas/reactions/2021/07/08/5382240.png
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Local Anesthetic Drugs 99%min Levobupivacaine 27262-47-1 For Surgical Anaesthesia CAS NO.27262-47-1

Min.Order Quantity:
10 Gram
Purity:
99%
Port:
Wuhan
Payment Terms:
T/T,MoneyGram

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Product Details

Keywords

  • 99% Levobupivacaine hydrochloride
  • 1-Butyl-N-(2,6-dimethylphenyl)-piperidine-2-carboxamide
  • API Manufacturer

Quick Details

  • ProName: Local Anesthetic Drugs 99%min Levobupi...
  • CasNo: 27262-47-1
  • Molecular Formula: C18H28N2O
  • Appearance: White Powder
  • Application: It Can Be Used As Pharmaceutical Inte...
  • DeliveryTime: 2-4 days after confirming your payment...
  • PackAge: 100g/ bag, 2 kg/ bag, 25kg/ carton or ...
  • Port: Wuhan
  • ProductionCapacity: 10000 Metric Ton/Month
  • Purity: 99%
  • Storage: Store in sealed containers at cool & d...
  • Transportation: By DHL, TNT, FedEx, HKEMS, UPS, Etc
  • LimitNum: 10 Gram

Superiority

advantages:

hubei xinrunde chemical co., ltd is a renowned pharmaceutical manufacturer. we can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. never stop striving to offer our best service is our philosophy. we have flexible and untraceable payment terms. as a leading manufacture, our products have been exported to germany, norway, poland, finland, spain, uk, france, russia, usa, brazil, mexico, australia, japan, korea, thailand, indonesia, uruguay and many other countries.

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Details

product name:levobupivacaine
cas no:27262-47-1
assay:99% above
molecular weight:288.428
density:1.0 0.1 g/cm3
boiling point:423.4 45.0 c at 760 mmhg
molecular formula:c18h29cln2o
melting point:254c (dec.)(lit.)
flash point:209.9/28.7 c
appearance:white powder


description:


the bupivacaine molecule is a racemic compound.levobupivacaine is the s-enantiomer of bupivacaine and is thought to have less cardiotoxic potential than the r-enantiomer.the pharmacokinetic parameters of levobupivacaine are similar to those of bupivacaine.

levobupivacaine has been studied in surgical anaesthesia and for pain management.it can be used for local infiltration,epidural,intrathecal and peripheral nerve blocks.for epidural analgesia it can be given with clonidine.double-blind comparisons of levobupivacaine and bupivacaine show that their anaesthetic effects are similar.
levobupivacaine (rinn) is a local anaesthetic drug belonging to the amino amide group. it is the s-enantiomer of bupivacaine.


the hydrochloride salt of levobupivacaine, an amide derivative with anesthetic property. levobupivacaine reversibly binds voltage-gated sodium channels to modulate ionic flux and prevent the initiation and transmission of nerve impulses (stabilizing neuronal membrane), thereby resulting in analgesia and anesthesia. in comparison with racemic bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action.

levobupivacaine is an amide-type local anaesthetic. levobupivacaine acts via blockade of voltage-sensitive ion channels in neuronal membranes, preventing transmission of nerve impulses. localised and reversible anaesthesia is produced by interference with the opening of the sodium channel, which inhibits conduction of the action potential in nerves involved in sensory and motor activity and sympathetic activity. [1] levobupivacaine displaces 3h-btx from sodium channels of rat brain synaptosomes with ic50 of 2.9 μm and hill coefficients of 1.2. when cell membrane is held at -80 mv, -70 mv, -60 mv or -100 mv, levobupivacaine shows tonic inhibition of sodium channel in gh3 cells with ic50s of 132.1, 37.6, 21.6 and 264 μm, respectively. [2] levobupivacaine depresses action potential of isolated axon in vitro. levobupivacaine (1mm) depresses action potential amplitude and maximal rate of rise of action potential (dv/dtmax) in the crayfish giant axons with value of 88 and 81 respectively, after perfusion for 15 min. [3] levobupivacaine also displays activity on cardiac ion channels. in isolated ventricular myocytes, the apparent affinity for inactivated state of the sodium channel is 4.8 μm for levobupivacaine, with a calculated kd of 39μm. on inhibition of cardiac delayed rectifier potassium channels (hkv1.5), the steady-state block for levobupivacaine (20 μm) is 31%, with a calculated kd of 27.3 μm. levobupivacaine may also inhibit cardiac calcium channels. 10 μm levobupivacaine produces a 50% decrease in contractile force of guinea-pig papillary muscles.


levobupivacaine applications:

clinical use
compared to bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action. it is approximately 13 percent less potent (by molarity) than racemic bupivacaine and has a longer motor block onset time.

indications
levobupivacaine is indicated for local anaesthesia including infiltration, nerve block, ophthalmic, epidural and intrathecal anaesthesia in adults; and infiltration analgesia in children.

contraindications
levobupivacaine is contraindicated for iv regional anaesthesia (ivra).


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