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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6Br2N2O2
Molecular Weight 285.921
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-DIBROMO-5,5-DIMETHYLHYDANTOIN

SMILES

CC1(C)N(Br)C(=O)N(Br)C1=O

InChI

InChIKey=VRLDVERQJMEPIF-UHFFFAOYSA-N
InChI=1S/C5H6Br2N2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3

HIDE SMILES / InChI

Molecular Formula C5H6Br2N2O2
Molecular Weight 285.921
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of geminal difluorides by oxidative desulfurization-difluorination of alkyl aryl thioethers with halonium electrophiles in the presence of fluorinating reagents and its application for 18F-radiolabeling.
2010-09-17
Effectiveness of 1,3-dibromo-5,5 dimethylhydantoin on reduction of Escherichia coli O157:H7- and Salmonella-inoculated fresh meat.
2009-01
Lewis acid catalyzed benzylic bromination.
2008-09-01
Short intermolecular N-Br...O=C contacts in 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione.
2007-07
Quantification of dibromodimethylhydantoin disinfectants in water by chemiluminescent method.
2007-03
An efficient, stereoselective synthesis of the hydroxyethylene dipeptide isostere core for the HIV protease inhibitor A-792611.
2006-07-07
An efficient chemoenzymatic approach to (S)-gamma-fluoroleucine ethyl ester.
2005-03-18
Facile exchange of glycosyl S,S-acetals to their O,O-acetals and preparation of glycofuranosides from acyclic glycosyl S,S-acetals under metal-free reaction conditions in the presence of 1,3-dibromo-5,5-dimethylhydantoin.
2005-02-28
Highly efficient catalytic aerobic oxidations of benzylic alcohols in water.
2005-01-21
Cetylpyridinium tetrachlorozincate as standard for tenside titration. Analytical methods with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in respect to environmental and economical concern, part 19.
2004-08
Determination of iodine values using 1,3-dibromo-5,5-dimethylhydantoin (DBH) and ethyl acetate as solvent. Analytical methods with DBH in respect to environmental and economical concern, part 18.
2004-08
Hypohalites and related oxidants as chemiluminescence reagents: a review.
2004-04-21
Synthesis of fluorinated analogs of myristic acid as potential inhibitors of Egyptian armyworm (Spodoptera littoralis) delta11 desaturase.
2003-08
Determination of iodine values using 1,3-dibromo-5,5-dimethylhydantoin (DBH) without the employment of chlorinated hydrocarbons. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 17.
2002-08
Determination of organically bound iodine by reductive mineralization with aluminium powder. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 16.
2002-07
1,3-Dibromo-5,5-dimethylhydantoin (DBH) as oxidant and precipitant for drug identification according to PH. EUR Analytical methods of pharmacopoeias with DBH in respect of environmental and economical concern, Part 15(1).
2002-06
Application of 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of bromine gas or bromine water decolorization for drug identification according to PH. EUR. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 14.
2002-05
Determination of selenium sulfide using 1,3-dibromo-5,5-dimethylhydantoin (DBH). Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern Part 11.
2002-04-15
Determination of propylthiouracil using 1,3-dibromo-5,5-dimethylhydantoin (DBH): analytical methods of pharmacopeias with DBH in respect to environmental and economical concern: part 9.
2002-04-15
Determination of iodine values according to Hanus using 1,3-dibromo-5,5-dimethylhydantoin (DBH): analytical methods of pharmacopeias with DBH: part 7.
2002-04-01
Replacement of cyanogen bromide solution PH. EUR. with 1,3-dibromo-5,5-dimethylhydantoin (DBH). Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 13.
2002-04
Colour reactions of PH. EUR. for identification of drugs using 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of elemental bromine. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 10.
2002-03
Determination of iron limiting values according to PH. EUR. using 1,3-dibromo-5,5-dimethylhydantoin (DBH) instead of elemental bromine. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern. Part 8.
2002-01
Determination of phenol and resorcinol using 1,3-dibromo-5,5-dimethylhydantoin (DBH) analogous to the Koppeschaar reaction. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 6.
2001-10
Identification of lactate. Analytical methods of pharmacopoeias with DBH in respect to environmental and economical concern, Part 4.
2001-07
Determination of iodide with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in comparison with the ICl-method. Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern. Part 3.
2001-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:12:11 GMT 2025
Edited
by admin
on Mon Mar 31 21:12:11 GMT 2025
Record UNII
V9R5F9I7MZ
Record Status Validated (UNII)
Record Version
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Name Type Language
1,3-DIBROMO-5,5-DIMETHYLHYDANTOIN
Systematic Name English
DIBROMANTIN
MI  
Preferred Name English
DIBROMANTINE
Common Name English
DBH
Common Name English
1,3-DIBROMO-5,5-DIMETHYLIMIDAZOLIDINE-2,4-DIONE
Systematic Name English
NSC-33305
Code English
5,5-DIMETHYL-1,3-DIBROMOHYDANTOIN
Systematic Name English
1,3-DIBROMO-5,5-DIMETHYLIMIDAZOLIDIN-2,4-DIONE
Systematic Name English
DBDMH
Common Name English
N,N'-DIBROMODIMETHYLHYDANTOIN
Systematic Name English
DIBROMANTIN [MI]
Common Name English
N,N'-DIBROMO-5,5-DIMETHYLHYDANTOIN
Systematic Name English
HYDANTOIN, 1,3-DIBROMO-5,5-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
Food Contact Sustance Notif, (FCN No.) FCN NO. 1118
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 1190
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 453
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 792
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 775
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
EPA PESTICIDE CODE 6317
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 334
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 357
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Food Contact Sustance Notif, (FCN No.) FCN NO. 1102
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
Code System Code Type Description
FDA UNII
V9R5F9I7MZ
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
RXCUI
2368732
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-030-9
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
DAILYMED
V9R5F9I7MZ
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
CFR
21 CFR 176.300
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
CAS
77-48-5
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
MESH
C056578
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
MERCK INDEX
m4292
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY Merck Index
PUBCHEM
6479
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID3035341
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
WIKIPEDIA
DBDMH
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
NSC
33305
Created by admin on Mon Mar 31 21:12:11 GMT 2025 , Edited by admin on Mon Mar 31 21:12:11 GMT 2025
PRIMARY
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