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Details

Stereochemistry RACEMIC
Molecular Formula C3H8OS2
Molecular Weight 124.225
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMERCAPROL

SMILES

OCC(S)CS

InChI

InChIKey=WQABCVAJNWAXTE-UHFFFAOYSA-N
InChI=1S/C3H8OS2/c4-1-3(6)2-5/h3-6H,1-2H2

HIDE SMILES / InChI
Molecular Formula C3H8OS2
Molecular Weight 124.225
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:03:29 UTC 2023
Edited
by admin
on Fri Dec 15 15:03:29 UTC 2023
Record UNII
0CPP32S55X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMERCAPROL
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USP   VANDF   WHO-DD   WHO-IP  
INN  
Official Name English
DIMERCAPROL [VANDF]
Common Name English
DIMERCAPROL [WHO-IP]
Common Name English
2,3-DITHIOPROPANOL
Common Name English
2,3-DIMERCAPTOPROPANOL
Systematic Name English
2,3-DITHIOPROPAN-1-OL
Common Name English
DIMERCAPROLUM [WHO-IP LATIN]
Common Name English
DITHIOGLYCERINE
Systematic Name English
DIMERCAPROL [USP MONOGRAPH]
Common Name English
DIMERCAPROL [HSDB]
Common Name English
DIMERCAPROL [ORANGE BOOK]
Common Name English
1,2-DITHIOGLYCEROL
Systematic Name English
DITHIOGLYCEROL
Systematic Name English
Dimercaprol [WHO-DD]
Common Name English
1,2-DIMERCAPTO-3-PROPANOL
Systematic Name English
BAL
Brand Name English
DIMERCAPROL [MI]
Common Name English
DIMERCAPROL [JAN]
Common Name English
DICAPTOL
Common Name English
2,3,-DIMERCAPTO-1-PROPANOL
Common Name English
3-HYDROXY-1,2-PROPANEDITHIOL
Systematic Name English
PANOBAL
Common Name English
NSC-4646
Code English
dimercaprol [INN]
Common Name English
SULFACTIN
Common Name English
DIMERSOL
Common Name English
NSC-39515
Code English
ANTOXOL
Common Name English
DIMERCAPROL [EP MONOGRAPH]
Common Name English
DIMERCAPROL [MART.]
Common Name English
1-PROPANOL, 2,3-DIMERCAPTO
Common Name English
Classification Tree Code System Code
WHO-VATC QV03AB09
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
LIVERTOX NBK548426
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
NDF-RT N0000175472
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 4.2
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
NCI_THESAURUS C62357
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
NDF-RT N0000175473
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
WHO-ATC V03AB09
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
Code System Code Type Description
EVMPD
SUB07165MIG
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
WIKIPEDIA
Dimercaprol
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
NCI_THESAURUS
C47494
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
DIMERCAPROL
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY Description: A clear, colourless or slightly yellow liquid, with an unpleasant, mercaptan-like odour. Miscibility. Miscible with 20 parts of water; miscible with ethanol (~750 g/l) TS and methanol R.Category: Antidote for arsenic, gold, and mercury poisoning. Storage: Dimercaprol should be kept in a small, well-filled and tightly closed container, protected from light, and stored at atemperature not exceeding 5?C. Definition: Dimercaprol contains not less than 98.5% w/w and not more than 101.5% w/w of C3H8OS2. Identity tests: A. Mix 0.05 mL of cobalt(II) chloride (30 g/l) TS with 5 mL of water and add 0.05 mL of the test liquid; a yellowbrowncolour is produced.B. Dissolve 0.1 mL in 4 mL of water and add a few drops of lead acetate (80 g/l) TS; a yellow precipitate is formed.
CAS
59-52-9
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
PUBCHEM
3080
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
INN
1614
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
FDA UNII
0CPP32S55X
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
CHEBI
64198
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
DAILYMED
0CPP32S55X
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
HSDB
4004
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
DRUG CENTRAL
3150
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
MESH
D004112
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
ChEMBL
CHEMBL1597
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
SMS_ID
100000082658
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
DRUG BANK
DB06782
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-433-7
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID5040461
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
RXCUI
3445
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY RxNorm
NSC
4646
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
MERCK INDEX
m4501
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY Merck Index
NSC
39515
Created by admin on Fri Dec 15 15:03:29 UTC 2023 , Edited by admin on Fri Dec 15 15:03:29 UTC 2023
PRIMARY
Related Record Type Details
Structure of DIMERCAPROL, (S)-
ENANTIOMER -> RACEMATE
Structure of DIMERCAPROL, (R)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of DIMERCAPROL
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