Bupivacaine hydrochloride structure
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Common Name | Bupivacaine hydrochloride | ||
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CAS Number | 18010-40-7 | Molecular Weight | 324.889 | |
Density | N/A | Boiling Point | 423.4ºC at 760 mmHg | |
Molecular Formula | C18H29ClN2O | Melting Point | 107.5 to 108ºC | |
MSDS | N/A | Flash Point | 209.9ºC |
Use of Bupivacaine hydrochlorideBupivacaine Hydrochloride is a local anaesthetic drug belonging to the amino amide group.Target: OthersBupivacaine hydrochloride is an effective local anesthetic agent. It has a rapid onset time, a high frequency of surgical anesthesia, a long duration, and a low incidence of side effects [1]. Median doses of bupivacaine (in milligrams per kilogram) producing asystole in protocol 1 were for 17.7 for saline, 27.6 for 10% Intralipid, 49.7 for 20% Intralipid, and 82.0 for 30% Intralipid (P < 0.001 for differences between all groups). Differences in mean +/- SE concentrations of bupivacaine in plasma (in micrograms per milliliter) were significant (P < 0.05) for the difference between saline (93.3 +/- 7.6) and 30% Intralipid (212 +/- 45). In protocol 2, lipid infusion increased the dose of bupivacaine required to cause death in 50% of animals by 48%, from 12.5 to 18.5 mg/kg. The mean lipid:aqueous ratio of concentrations of bupivacaine in a plasma-Intralipid mixture was 11.9 +/- 1.77 (n = 3) [2]. |
Name | bupivacaine hydrochloride (anhydrous) |
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Synonym | More Synonyms |
Description | Bupivacaine Hydrochloride is a local anaesthetic drug belonging to the amino amide group.Target: OthersBupivacaine hydrochloride is an effective local anesthetic agent. It has a rapid onset time, a high frequency of surgical anesthesia, a long duration, and a low incidence of side effects [1]. Median doses of bupivacaine (in milligrams per kilogram) producing asystole in protocol 1 were for 17.7 for saline, 27.6 for 10% Intralipid, 49.7 for 20% Intralipid, and 82.0 for 30% Intralipid (P < 0.001 for differences between all groups). Differences in mean +/- SE concentrations of bupivacaine in plasma (in micrograms per milliliter) were significant (P < 0.05) for the difference between saline (93.3 +/- 7.6) and 30% Intralipid (212 +/- 45). In protocol 2, lipid infusion increased the dose of bupivacaine required to cause death in 50% of animals by 48%, from 12.5 to 18.5 mg/kg. The mean lipid:aqueous ratio of concentrations of bupivacaine in a plasma-Intralipid mixture was 11.9 +/- 1.77 (n = 3) [2]. |
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Related Catalog | |
References |
Boiling Point | 423.4ºC at 760 mmHg |
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Melting Point | 107.5 to 108ºC |
Molecular Formula | C18H29ClN2O |
Molecular Weight | 324.889 |
Flash Point | 209.9ºC |
Exact Mass | 324.196838 |
PSA | 32.34000 |
LogP | 4.70940 |
Storage condition | 2-8°C |
Hazard Codes | T+: Very toxic; |
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Risk Phrases | R26/27/28 |
Safety Phrases | 22-36/37/39-45 |
RIDADR | UN 2811 6.1/PG 2 |
RTECS | TK6125000 |
Packaging Group | II |
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Inhibition of murine cardiomyocyte respiration by amine local anesthetics.
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