U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C15H22N2O.ClH
Molecular Weight 282.809
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEPIVACAINE HYDROCHLORIDE

SMILES

Cl.CN1CCCCC1C(=O)NC2=C(C)C=CC=C2C

InChI

InChIKey=RETIMRUQNCDCQB-UHFFFAOYSA-N
InChI=1S/C15H22N2O.ClH/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);1H

HIDE SMILES / InChI

Molecular Formula C15H22N2O
Molecular Weight 246.348
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:17:18 UTC 2023
Edited
by admin
on Fri Dec 15 17:17:18 UTC 2023
Record UNII
4VFX2L7EM5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEPIVACAINE HYDROCHLORIDE
EP   GREEN BOOK   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
Common Name English
MEPIVACAINE HYDROCHLORIDE [USP-RS]
Common Name English
MEPIVACAINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
MEPIVACAINE HYDROCHLORIDE [USP IMPURITY]
Common Name English
MEPIVACAINE HYDROCHLORIDE [GREEN BOOK]
Common Name English
(±)-1-METHYL-2',6'-PIPECOLOXYLIDIDE MONOHYDROCHLORIDE
Common Name English
POLOCAINE
Brand Name English
2-PIPERIDINECARBOXAMIDE, N-(2,6-DIMETHYLPHENYL)-1-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
MEPIVACAINE HYDROCHLORIDE [MI]
Common Name English
MEPIVACAINE MONOHYDROCHLORIDE
Common Name English
OPTOCAIN
Brand Name English
ISOCAINE HYDROCHLORIDE
Brand Name English
SCANDONEST PLAIN
Brand Name English
Mepivacaine hydrochloride [WHO-DD]
Common Name English
NSC-758674
Code English
ARESTOCAINE HYDROCHLORIDE
Brand Name English
2-PIPERIDINECARBOXAMIDE, N-(2,6-DIMETHYLPHENYL)-1-METHYL-, MONOHYDROCHLORIDE, (±)-
Common Name English
MEPIVACAINE HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
MEPIVACAINE HYDROCHLORIDE [VANDF]
Common Name English
(±)-MEPIVACAINE HYDROCHLORIDE
Common Name English
MEPIVACAINE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
MEPIVACAINE HYDROCHLORIDE [MART.]
Common Name English
MEPIVACAINE HCL
Common Name English
MEPIVACAINE HYDROCHLORIDE [JAN]
Common Name English
SCANDICAIN
Brand Name English
CARBOCAINE
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
Code System Code Type Description
CHEBI
6759
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
CAS
38423-99-3
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
SUPERSEDED
EVMPD
SUB03158MIG
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
NSC
758674
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
SMS_ID
100000090134
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
CAS
1722-62-9
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID4031566
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
DRUG BANK
DBSALT000478
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
ChEMBL
CHEMBL1087
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
CHEBI
6760
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
RXCUI
203185
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY RxNorm
MERCK INDEX
m7196
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY Merck Index
FDA UNII
4VFX2L7EM5
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
ECHA (EC/EINECS)
217-023-9
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
CAS
16452-56-5
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
SUPERSEDED
RS_ITEM_NUM
1387002
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
NCI_THESAURUS
C47602
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
PUBCHEM
66070
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
DAILYMED
4VFX2L7EM5
Created by admin on Fri Dec 15 17:17:18 UTC 2023 , Edited by admin on Fri Dec 15 17:17:18 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
USP
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
Related Record Type Details
IMPURITY -> PARENT
not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent), and not more than one of the peaks has an area greater than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.1 per cent);
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent), and not more than one of the peaks has an area greater than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.1 per cent);
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
color comparison
EP
IMPURITY -> PARENT
not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent), and not more than one of the peaks has an area greater than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.1 per cent);
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
not more than twice the area of the principal peak in the chromatogram obtained with reference solution (b) (0.2 per cent), and not more than one of the peaks has an area greater than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.1 per cent);
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY