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Details

Stereochemistry ACHIRAL
Molecular Formula C8H4O4.2C6H5Hg
Molecular Weight 719.5
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLMERCURIC PHTHALATE

SMILES

[Hg+]C1=CC=CC=C1.[Hg+]C2=CC=CC=C2.[O-]C(=O)C3=CC=CC=C3C([O-])=O

InChI

InChIKey=QFHSQCRSFKLKMT-UHFFFAOYSA-L
InChI=1S/C8H6O4.2C6H5.2Hg/c9-7(10)5-3-1-2-4-6(5)8(11)12;2*1-2-4-6-5-3-1;;/h1-4H,(H,9,10)(H,11,12);2*1-5H;;/q;;;2*+1/p-2

HIDE SMILES / InChI

Molecular Formula C8H4O4
Molecular Weight 164.115
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C6H5Hg
Molecular Weight 277.69
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Phenylmercuric borate is classified as antimicrobial preservative. It is bactericidal against many Gram-positive and Gram-negative species. Fungicidal activity has been demonstrated against Candida albicans and Aspergillus niger. Phenylmercuric borate (PHB) is very rapidly incorporated into the cells of Escherichia coli. On the membrane, an important part of PHB seems to be associated with the ribosomes and particularly to the ribosomal proteins. Phenylmercuric borate solution is indicated for the treatment of tonsillitis, otitis, vulvovaginitis, furuncles, anthrax and ulcers, pyoderma, impetus, gingivitis and stomatitis. The regular hand disinfection with a liquid soap containing phenylmercuric borate enhanced urinary excretion of mercury indicating an increase in total daily absorption of the toxic metal. The additional amounts of mercury absorbed through the use of mercury contained in skin disinfectants are potentially dangerous for human.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Merfen

Approved Use

indicated for the treatment of wounds, burns, ulcers, forúncles, anthrax, abscesses, pyodermitis, tinyes, vulvitis, vaginitis, vulvovaginitis.
Primary
Merfen

Approved Use

indicated for the treatment of tonsillitis, otitis, vulvovaginitis, furuncles, anthrax and ulcers, pyoderma, impetus, gingivitis and stomatitis.
Primary
Merfen

Approved Use

indicated for the treatment of wounds, burns, ulcers, forúncles, anthrax, abscesses, pyodermitis, tinyes, vulvitis, vaginitis, vulvovaginitis.
PubMed

PubMed

TitleDatePubMed
[Sterilization of suturing silk with 1:10 000 diluted phenylmercuric borate solution].
1956
[Use of phenylmercuric borate in parenteral solutions].
1958 Dec
Studies on the mode of action of phenylmercuric borate on Escherichia coli. I. Structural localization and kinetics of incorporation.
1978 Jun
Antimicrobial activity of seven metallic compounds against penicillinase producing and non-penicillinase producing strains of Neisseria gonorrhoeae.
1986 Jun
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Apply a thin layer of 0.04% ointment on the affected skin area
Route of Administration: Topical
In Vitro Use Guide
Phenylmercuric borate inhibited 90% of all tested penicillinase (beta lactamase) producing strains of Neisseria gonorrhoeae (PPNG) and non-PPNGstrains at concentrations of 5 mg/l.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:15:17 GMT 2023
Edited
by admin
on Fri Dec 15 15:15:17 GMT 2023
Record UNII
FKL5QS2STU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYLMERCURIC PHTHALATE
Common Name English
MERCURY, (.MU.-(1,2-BENZENEDICARBOXYLATO(2-)-O1:O2))DIPHENYLDI-
Systematic Name English
NSC-4816
Code English
MERSOLITE 37
Brand Name English
Code System Code Type Description
CAS
84-70-8
Created by admin on Fri Dec 15 15:15:17 GMT 2023 , Edited by admin on Fri Dec 15 15:15:17 GMT 2023
PRIMARY
NSC
4816
Created by admin on Fri Dec 15 15:15:17 GMT 2023 , Edited by admin on Fri Dec 15 15:15:17 GMT 2023
PRIMARY
PUBCHEM
16682927
Created by admin on Fri Dec 15 15:15:17 GMT 2023 , Edited by admin on Fri Dec 15 15:15:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID101018974
Created by admin on Fri Dec 15 15:15:17 GMT 2023 , Edited by admin on Fri Dec 15 15:15:17 GMT 2023
PRIMARY
FDA UNII
FKL5QS2STU
Created by admin on Fri Dec 15 15:15:17 GMT 2023 , Edited by admin on Fri Dec 15 15:15:17 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE