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Bromadiolone

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Identification
Molecular formula
C11H12Br2N2O2
CAS number
28772-56-7
IUPAC name
1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione
State
State

At room temperature, Bromadiolone is in a solid state and is quite stable under normal conditions. It does not have any significant vapor pressure and thus is not expected to be found in the gas phase under ambient conditions.

Melting point (Celsius)
350.00
Melting point (Kelvin)
623.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
347.95g/mol
Molar mass
347.9540g/mol
Density
2.6480g/cm3
Appearence

Bromadiolone appears as a white to off-white crystalline powder. Its physical form can be described as a fine powder which may clump together due to its crystalline nature. Additionally, under certain lighting conditions, it might exhibit a slight yellow tint.

Comment on solubility

Solubility of 1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione

The solubility of 1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione can be influenced by various factors, including temperature, the presence of solvents, and electrolyte concentrations. Understanding its solubility characteristics can provide insights into its potential applications and functionality.

  • Solvent Compatibility: This compound typically exhibits varying degrees of solubility in organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO). However, its solubility in water is generally low due to its complex structure.
  • Temperature Effects: Increasing temperature often enhances solubility in organic solvents, allowing for increased interaction between the solvent molecules and the compound.
  • Ionization: The presence of bromine atoms may affect the compound’s ability to ionize in solution, which in turn can influence its solubility profile.

In summary, while 1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione may not be highly soluble in water, its solubility in organic solvents can be significant, making it suitable for various chemical reactions and formulations. As always, conducting solubility tests in your specific conditions is recommended to obtain accurate results.

Interesting facts

Interesting Facts about 1,3-Dibromo-5,5-dimethyl-imidazolidine-2,4-dione

1,3-Dibromo-5,5-dimethyl-imidazolidine-2,4-dione, often simply referred to as a dibrominated derivative of imidazolidine, holds particular significance in organic chemistry. Here are some fascinating insights into this compound:

  • Biological Activity: This compound has shown potential in various biological applications. Its bromine substituents can play a crucial role in the reactivity and interaction with biological systems, making it a subject of study for medicinal chemistry.
  • Versatile Reactivity: The presence of the imidazolidine ring gives the compound an ability to participate in numerous chemical reactions, including cycloadditions and substitutions. This versatility is valuable in synthetic organic chemistry.
  • Applications in Synthesis: It is often utilized as an intermediary in the synthesis of more complex molecules. Chemists appreciate its ability to serve as a building block in pharmaceutical and agrochemical synthesis.
  • Environmental Chemistry: The behavior of brominated compounds in the environment is a subject of interest, particularly in the study of persistence and toxicity. Understanding the fate of such compounds can aid in assessing environmental impacts.
  • Structural Diversity: The unique structure of 1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione allows it to adopt different conformations, which can affect its reactivity and interaction with other chemical species.

In summary, 1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione not only showcases intriguing chemical properties but also highlights key areas of interest in both industrial applications and environmental studies. As chemists continue to explore its potential, the compound remains a valuable piece of the chemical puzzle.

Synonyms
1,3-Dibromo-5,5-dimethylhydantoin
77-48-5
Dibromantin
1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione
Dibromantine
Take Charge Orange
N,N'-Dibromodimethylhydantoin
DBDMH
1,3-Dibromo-5,5-dimethyl-2,4-imidazolidinedione
5,5-Dimethyl-1,3-dibromohydantoin
NSC 33305
2,4-Imidazolidinedione, 1,3-dibromo-5,5-dimethyl-
UNII-V9R5F9I7MZ
EINECS 201-030-9
V9R5F9I7MZ
HYDANTOIN, 1,3-DIBROMO-5,5-DIMETHYL-
EPA Pesticide Chemical Code 006317
BRN 0146024
DTXSID3035341
AI3-23671
N,N'-dibromo-5,5-dimethylhydantoin
MFCD00003189
NSC-33305
Dibromo-5,5-dimethylhydantoin
DTXCID1015341
EC 201-030-9
5-24-05-00374 (Beilstein Handbook Reference)
NSC33305
1,3-dibromo-5,5-dimethyl-imidazolidine-2,4-dione
1,3-Dibromo-5,5-dimethylhydantoine
1,3-DIBROMO-5,5-DIMETHYLIMIDAZOLIDIN-2,4-DIONE
C5H6Br2N2O2
1,3-Dibromo-5,5-dimethylhydantoin (DBDMH)
TakeCharge Orange
DisinfectantTablets
Disinfectant Tablets
1,3-dibromo-5,5-dimethyl hydantoin
5,3-dibromohydantoin
dibromodimethylhydantoin
dibromo-dimethylhydantoin
dibromodimethyl hydantoin
DIBROMANTIN [MI]
dibromo-dimethyl hydantoin
SCHEMBL2790
CHEMBL3184055
5,5-dimethy-1,3-dibromohydantoin
1,3-dibromo 5,5-dimethylhydantoin
1,3-dibromo-5,5 dimethylhydantoin
1.3-dibromo-5,5-dimethylhydantoin
2, 1,3-dibromo-5,5-dimethyl-
2,4-dibromo-5,5-dimethylhydantoin
BCP16411
HY-Y0786
STR01390
1,3-dibrom-5,5-dimethyl-hydantoin
Hydantoin,3-dibromo-5,5-dimethyl-
Tox21_300158
1,3-dibromo 5,5-dimethylhydantoine
1,3 dibromo-5,5 dimethyl hydantoin
1,3-dibromo -5,5-dimethylhydantoin
1,3-dibromo-5,5-dimethyl-hydantoin
AKOS009031396
AC-4444
CAS-77-48-5
NCGC00164069-01
NCGC00164069-02
NCGC00254227-01
1,3-Dibromo-5,5-dimethylhydantoin, 98%
CS-0015767
D1265
NS00004807
EN300-19692
D72511
Hydantoin, 1,3-dibromo-5,5-dimethyl- (8CI)
1,3-dibromo-5,5-dimethylimidazoline-2,4-dione
1,3-dibromo-5,5-dimethyl 2,4-imidazolidinedione
A839113
Q2078816
1,3-bis(bromanyl)-5,5-dimethyl-imidazolidine-2,4-dione
201-030-9