Mepivacaine manufacturers and suppliers

Mepivacaine suppliers

Properties

Melting point:: 147-151°C

storage temp.: -20°C Freezer

solubility: Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)

form: Solid

pka: pKa 7.73(H2O,t =25±0.2,I=0.01(NaCl)) (Uncertain)

color: White to Off-White

InChI: InChI=1S/C15H22N2O/c1-11-7-6-8-12(2)14(11)16-15(18)13-9-4-5-10-17(13)3/h6-8,13H,4-5,9-10H2,1-3H3,(H,16,18)

InChIKey: INWLQCZOYSRPNW-UHFFFAOYSA-N

SMILES: N1(C)CCCCC1C(NC1=C(C)C=CC=C1C)=O

CAS DataBase Reference: 22801-44-1(CAS DataBase Reference)

EPA Substance Registry System: 2-Piperidinecarboxamide, N-(2,6-dimethylphenyl)-1-methyl- (22801-44-1)

Safety Information

Use

Mepivacaine hydrochloride is available in 1% to 3% solutionsand is indicated for infiltration anesthesia, dental procedures,peripheral nerve block, or epidural block. The onset of anesthesiais rapid, ranging from about 3 to 20 minutes for sensoryblock. Mepivacaine is rapidly metabolized in the liver with50% of the administered dose excreted into the bile asmetabolites. The metabolites are reabsorbed in the intestineand excreted in the kidney with only a small percentage foundin the feces. Less than 5% to 10% of the administered dose isfound unchanged in the urine. The primary metabolic productsare the N-demethylated metabolite and the 3 and 4 phenolicmetabolites excreted as their glucuronide conjugates.

You can find Mepivacaine suppliers, manufacturers, and distributors from countries such as China, United States and the United Kingdom here. Browse to the tetrahydrofuran product information displayed by the supplier, as well as the supplier's contact and capability information.