- Product Details
Keywords
- 1722-62-9
- Mepivacaine HCL
- Mepivacaine Hydrochloride
Quick Details
- ProName: Mepivacaine Hydrochloride White Crysta...
- CasNo: 1722-62-9
- Molecular Formula: C15H22N2O.ClH
- Appearance: White Crystalline Powder
- Application: Anesthetic (local).
- DeliveryTime: 2-4 days after confirming your payment...
- PackAge: 100g/ bag, 2 kg/ bag, 25kg/ carton or ...
- Port: Wuhan
- ProductionCapacity: 20000 Kilogram/Day
- Purity: 99%
- Storage: Store in sealed containers at cool & d...
- Transportation: By DHL, TNT, FedEx, HKEMS, UPS, Etc
- LimitNum: 100 Gram
Superiority
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Details
Mepivacaine Hydrochloride White Crystalline Powder CAS 1722-62-9
Quick Details:
Other Name:Mepivacaine HCL
Chemical Name:n-(2,6-dimethylphenyl)-1-methyl-2-piperidinecarboxamide hydrochloride;(1-methyl-dl-piperidine-2-carboxylicacid)-2,6-dimethylanilidehydrochloride
CAS:1722-62-9
MF:C15H22N2O.ClH
MW:282.81
EINECS:217-023-9
Assay:99% min
Appearence:White powder or white crystalline powder
Pursope:Local anesthetic drug
Package:1kg/bag;25kg/drum.
Storage:Closed and avoiding light
Usage: Anesthetic (local).
Mepivacaine hydrochloride Description
Mepivacaine is a local anesthetic of the amide type. Mepivacaine has a reasonably rapid onset (more rapid than that of procaine) and medium duration of action (shorter than that of procaine) and is marketed under various trade names including Carbocaine and Polocaine .
Mepivacaine is used in any infiltration and regional anesthesia .
It is supplied as the hydrochloride salt of the racemate, which consists of R(-)-mepivacaine and S(+)-mepivacaine in equal proportions. These two enantiomers have markedly different pharmacokinetic properties.
Application:
Mepivicaine is a local anesthetic of the amide type. Mepivicaine as a reasonably rapid onset and medium duration and is known by the proprietary names as Carbocaine and Polocaine. Mepivicaine is used in local infiltration and regional anesthesia. Systemic absorption of local anesthetics produces effects on the cardiovascular and central nervous systems. At blood concentrations achieved with normal therapeutic doses, changes in cardiac conduction, excitability, refractoriness, contractility, and peripheral vascular resistance are minimal.
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