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

Details

Stereochemistry RACEMIC
Molecular Formula C19H15O4.Na
Molecular Weight 330.3098
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of WARFARIN SODIUM

SMILES

[Na+].CC(=O)CC(C1=CC=CC=C1)C2=C([O-])C3=CC=CC=C3OC2=O

InChI

InChIKey=KYITYFHKDODNCQ-UHFFFAOYSA-M
InChI=1S/C19H16O4.Na/c1-12(20)11-15(13-7-3-2-4-8-13)17-18(21)14-9-5-6-10-16(14)23-19(17)22;/h2-10,15,21H,11H2,1H3;/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C19H15O4
Molecular Weight 307.32
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
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 15:06:25 UTC 2023
Edited
by admin
on Fri Dec 15 15:06:25 UTC 2023
Record UNII
6153CWM0CL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
WARFARIN SODIUM
EP   MART.   ORANGE BOOK   USP   VANDF   WHO-DD   WHO-IP  
Common Name English
WARFARIN SODIUM [USP MONOGRAPH]
Common Name English
WARFARIN SODIUM [VANDF]
Common Name English
SODIUM WARFARIN
Common Name English
WARFARIN SODIUM [ORANGE BOOK]
Common Name English
COUMADIN
Brand Name English
JANTOVEN
Brand Name English
2H-1-BENZOPYRAN-2-ONE, 4-HYDROXY-3-(3-OXO-1-PHENYLBUTYL)-, SODIUM SALT
Common Name English
WARFARIN SODIUM SALT [MI]
Common Name English
Warfarin sodium [WHO-DD]
Common Name English
ZOOCOUMARIN SODIUM SALT
Common Name English
WARFARIN SODIUM [WHO-IP]
Common Name English
WARFARIN SODIUM [MART.]
Common Name English
PROTHROMADIN
Common Name English
ALDOCUMAR
Common Name English
3-(α-Acetonylbenzyl)-4-hydroxycoumarin sodium salt
Common Name English
APO-WARFARIN
Brand Name English
WARFARIN SODIUM SALT
MI  
Common Name English
WARFARIN SODIUM [EP MONOGRAPH]
Common Name English
ATHROMBIN
Brand Name English
WARFARINUM NATRICUM [WHO-IP LATIN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45597
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
EPA PESTICIDE CODE 86003
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
NCI_THESAURUS C263
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
Code System Code Type Description
SMS_ID
100000092049
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
CAS
129-06-6
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-929-4
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
EVMPD
SUB05128MIG
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
ALANWOOD
warfarin-sodium
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
PUBCHEM
16204922
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
NCI_THESAURUS
C1658
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
CHEBI
10034
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
WARFARIN SODIUM
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY Description: A white, amorphous or crystalline powder; odourless. Solubility: Soluble in less than 1 part of water and in ethanol (~750 g/l) TS; slightly soluble in ether R. Category: Anticoagulant. Storage: Warfarin sodium should be kept in a well-closed container, protected from light. Labelling: The designation on the container of Warfarin sodium should state whether the substance is in the amorphous or the crystalline, clathrate form. Additional information: Warfarin sodium is discoloured by light. Even in the absence of light, it is gradually degraded on exposureto a humid atmosphere, the decomposition being faster at higher temperatures.Definition: Warfarin sodium contains not less than 98.0% and not more than 102.0% of C19H15NaO4, calculated with reference to the anhydrous and 2-propanol-free substance.
ChEMBL
CHEMBL1464
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
DAILYMED
6153CWM0CL
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
MERCK INDEX
m11506
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID7035010
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
DRUG BANK
DBSALT000278
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
FDA UNII
6153CWM0CL
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY
RXCUI
114194
Created by admin on Fri Dec 15 15:06:25 UTC 2023 , Edited by admin on Fri Dec 15 15:06:25 UTC 2023
PRIMARY RxNorm
Related Record Type Details
SOLVATE->ANHYDROUS
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
USP
PARENT -> SALT/SOLVATE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (UV)
EP
SOLVATE->ANHYDROUS
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity C = 0.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurity by the corresponding correction factor: impurity B = 0.5
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
UNSPECIFIED
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY