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Details

Stereochemistry RACEMIC
Molecular Formula C17H16F6N2O.ClH
Molecular Weight 414.773
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEFLOQUINE HYDROCHLORIDE

SMILES

Cl.[H][C@@]1(CCCCN1)[C@@H](O)C2=C3C=CC=C(C3=NC(=C2)C(F)(F)F)C(F)(F)F

InChI

InChIKey=WESWYMRNZNDGBX-YLCXCWDSSA-N
InChI=1S/C17H16F6N2O.ClH/c18-16(19,20)11-5-3-4-9-10(15(26)12-6-1-2-7-24-12)8-13(17(21,22)23)25-14(9)11;/h3-5,8,12,15,24,26H,1-2,6-7H2;1H/t12-,15+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C17H16F6N2O
Molecular Weight 378.3122
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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 15:24:53 UTC 2023
Edited
by admin
on Fri Dec 15 15:24:53 UTC 2023
Record UNII
5Y9L3636O3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEFLOQUINE HYDROCHLORIDE
EP   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN  
Official Name English
MEFLOQUINE HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
MEFLOQUINE HYDROCHLORIDE [MART.]
Common Name English
RO-215998001
Code English
MEFLOQUINE HYDROCHLORIDE [WHO-IP]
Common Name English
MEFLOQUINI HYDROCHLORIDUM [WHO-IP LATIN]
Common Name English
NSC-157387
Code English
MEFLOQUINE HCL
Common Name English
MEFLOQUINE HYDROCHLORIDE [USP-RS]
Common Name English
4-QUINOLINEMETHANOL, .ALPHA.-2-PIPERIDINYL-2,8-BIS(TRIFLUOROMETHYL)-, MONOHYDROCHLORIDE, (R*,S*)- (±)-
Common Name English
DL-ERYTHRO-.ALPHA.-2-PIPERIDYL-2,8-BIS(TRIFLUOROMETHYL)-4-QUINOLINEMETHANOL MONOHYDROCHLORIDE
Common Name English
MEFLOQUINE HYDROCHLORIDE [VANDF]
Common Name English
RO-21-5998/001
Code English
MEFLOQUINE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
Mefloquine hydrochloride [WHO-DD]
Common Name English
RO-21-5998
Code English
WR-142490
Code English
LORIAM
Brand Name English
LARIAM
Brand Name English
MEFLOQUINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
MEFLOQUINE HYDROCHLORIDE [EP IMPURITY]
Common Name English
MEFLOQUINE HYDROCHLORIDE [USAN]
Common Name English
MEFLOQUINE HYDROCHLORIDE [JAN]
Common Name English
RO 21-5998/001
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 18687
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
NCI_THESAURUS C271
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
FDA ORPHAN DRUG 26287
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
Code System Code Type Description
USAN
W-48
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
DRUG BANK
DBSALT000311
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
CAS
51773-92-3
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
EVMPD
SUB14492MIG
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
PUBCHEM
65329
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
NSC
157387
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID1047819
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
NCI_THESAURUS
C47600
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL416956
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
SMS_ID
100000076533
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
DAILYMED
5Y9L3636O3
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
FDA UNII
5Y9L3636O3
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
RS_ITEM_NUM
1379059
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
RXCUI
82130
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
257-412-0
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
MERCK INDEX
m7142
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY Merck Index
WHO INTERNATIONAL PHARMACOPEIA
MEFLOQUINE HYDROCHLORIDE
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY Description: A white to slightly yellow, crystalline powder. Solubility: Very slightly soluble in water; freely soluble in methanol R; soluble in ethanol (~750 g/L) TS; sparingly soluble in dichloromethane R. Category: Antimalarial. Storage: Mefloquine hydrochloride should be kept in a tightly closed container, protected from light. Additional information: Mefloquine hydrochloride may exhibit polymorphism. It melts at about 260 ?C, with decomposition. Requirement: Mefloquine hydrochloride contains not less than 99.0% and not more than 101.0% of C17H16F6N2O,HCl, calculated with reference to the anhydrous substance.
Related Record Type Details
ENANTIOMER -> RACEMATE
Related Record Type Details
IMPURITY -> PARENT
IMPURITY -> PARENT
MEFLOQUINE HYDROCHLORIDE Impurity A. In the chromatogram obtained with solution (1) the following impurities, if present, are eluted at the following relative retention with reference to mefloquine (retention time about 3.9 minutes): impurity A about 0.9. In the chromatogram obtained with solution (1):the area of any peak corresponding to impurity A is not greater than the area of the principal peak in the chromatogram obtained with solution (2) (0.2%).
IMPURITY -> PARENT
MEFLOQUINE HYDROCHLORIDE Impurity B. In the chromatogram obtained with solution (1) the following impurity, if present, is eluted at the following relative retention with reference to mefloquine (retention time about 3.9 minutes): impurity B about 7.4.
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY