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Details

Stereochemistry ACHIRAL
Molecular Formula 3C6H2Br3O.Bi
Molecular Weight 1198.355
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BISMUTH TRIBROMOPHENATE

SMILES

[Bi+3].[O-]C1=C(Br)C=C(Br)C=C1Br.[O-]C2=C(Br)C=C(Br)C=C2Br.[O-]C3=C(Br)C=C(Br)C=C3Br

InChI

InChIKey=SAOHCOFTVLEOCB-UHFFFAOYSA-K
InChI=1S/3C6H3Br3O.Bi/c3*7-3-1-4(8)6(10)5(9)2-3;/h3*1-2,10H;/q;;;+3/p-3

HIDE SMILES / InChI
Molecular Formula C6H2Br3O
Molecular Weight 329.791
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula Bi
Molecular Weight 208.9804
Charge 3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2000
172
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:46:48 GMT 2025
Edited
by admin
on Mon Mar 31 17:46:48 GMT 2025
Record UNII
5K96Y7WG8T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4,6-TRIBROMOPHENOL BISMUTH(3+) SALT (3:1)
Preferred Name English
BISMUTH TRIBROMOPHENATE
MI   VANDF   WHO-DD  
Common Name English
SIGMAFORM
Common Name English
BISMUTH TRIBROMOPHENATE [MI]
Common Name English
XEROFORM
Common Name English
BISMUTH TRIBROMOPHENATE [VANDF]
Common Name English
DRESSING,XEROFORM [VANDF]
Common Name English
TRIS(2,4,6-TRIBROMOPHENOXY)BISMUTHINE
Systematic Name English
Bismuth tribromophenate [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
Code System Code Type Description
FDA UNII
5K96Y7WG8T
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
MERCK INDEX
m2561
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY Merck Index
SMS_ID
100000092804
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
CHEBI
47696
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
CAS
5175-83-7
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
NCI_THESAURUS
C87256
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID6063729
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
PUBCHEM
78852
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
EVMPD
SUB13095MIG
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
RXCUI
47180
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY RxNorm
ECHA (EC/EINECS)
225-958-9
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
DAILYMED
5K96Y7WG8T
Created by admin on Mon Mar 31 17:46:48 GMT 2025 , Edited by admin on Mon Mar 31 17:46:48 GMT 2025
PRIMARY
Related Record Type Details
Structure of 2,4,6-TRIBROMOPHENOL
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of BISMUTH CATION
ACTIVE MOIETY
Structure of 2,4,6-TRIBROMOPHENOL
ACTIVE MOIETY
NIH
NCATS
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