Skip to main content

Bronopol

ADVERTISEMENT
Identification
Molecular formula
C3H6BrNO4
CAS number
52-51-7
IUPAC name
2-ethyl-2-nitro-propane-1,3-diol
State
State

At room temperature, Bronopol is in a solid state, presenting as a crystallized powder.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.00
Boiling point (Celsius)
208.70
Boiling point (Kelvin)
481.90
General information
Molecular weight
199.04g/mol
Molar mass
199.0380g/mol
Density
1.8750g/cm3
Appearence

Bronopol typically appears as a white or slightly yellow crystalline powder. It is known for being stable in solid form under normal conditions but may discolor with light exposure.

Comment on solubility

Solubility of 2-ethyl-2-nitro-propane-1,3-diol

2-ethyl-2-nitro-propane-1,3-diol presents an interesting case when it comes to solubility. The solubility of this compound can be influenced by several factors:

  • Polar Functional Groups: The presence of hydroxyl (-OH) groups in its structure enhances its ability to form hydrogen bonds with water, which typically increases solubility.
  • Hydrophobic Character: The ethyl group contributes some hydrophobic characteristics that may limit its solubility in water.
  • Solvent Choice: In polar solvents, the compound is expected to have better solubility, whereas non-polar solvents may provide limited solubility.

In summary, the solubility of 2-ethyl-2-nitro-propane-1,3-diol can be described as moderate in aqueous solutions due to the balance between polar and non-polar influences in its molecular structure. It is important to note that the exact solubility may vary depending on temperature and the presence of other solutes.


Interesting facts

Exploring 2-ethyl-2-nitro-propane-1,3-diol

2-ethyl-2-nitro-propane-1,3-diol, a notable organic compound, piques the interest of chemists and researchers due to its unique structural features and potential applications. Here are some fascinating insights:

  • Versatile Applications: This compound has gained attention in various fields, including pharmaceuticals and agriculture, primarily due to its properties that can influence biological activities.
  • Nitro Group Importance: The presence of the nitro group (–NO2) is crucial as it often enhances the reactivity of organic compounds, making it vital for the synthesis of other chemicals.
  • Alcohol Functionality: With hydroxyl groups (–OH) in its structure, 2-ethyl-2-nitro-propane-1,3-diol exemplifies the role of alcohols in organic chemistry, often acting as solvents and intermediates in reactions.
  • Structural Features: The 2-ethyl branching contributes to its sterics, influencing how the compound interacts with other substances, thereby affecting its reactivity and compatibility.
  • Importance of Stereochemistry: The chiral centers in the compound can signify the importance of stereochemistry in determining the efficacy and selective interactions of the compound in biological systems.

As we delve deeper into the chemical landscape, the multifaceted properties of 2-ethyl-2-nitro-propane-1,3-diol offer rich avenues for exploration, encouraging scientists to investigate its potential benefits further.


“Understanding the underpinning chemistry of compounds like 2-ethyl-2-nitro-propane-1,3-diol not only broadens our scientific knowledge but also encapsulates the essence of innovation in chemical research.”

Synonyms
2-ETHYL-2-NITRO-1,3-PROPANEDIOL
597-09-1
2-Nitro-2-ethyl-1,3-propanediol
1,3-Propanediol, 2-ethyl-2-nitro-
2-Ethyl-2-nitropropanediol
NSC 2024
EINECS 209-893-3
UNII-5243OT5I3L
BRN 1705448
DTXSID7041417
AI3-02257
5243OT5I3L
NSC-2024
DTXCID5021417
4-01-00-02550 (Beilstein Handbook Reference)
ETHYL-2-NITRO-1,3-PROPANEDIOL, 2-
2Ethyl2nitropropanediol
2Ethyl2nitropropane1,3diol
2Nitro2ethyl1,3propanediol
1,3Propanediol, 2ethyl2nitro
209-893-3
yadiskicboyxfs-uhfffaoysa-n
2-Ethyl-2-nitropropane-1,3-diol
NEPD
NSC2024
MFCD00024813
dimethylol nitropropane
1, 2-ethyl-2-nitro-
SCHEMBL635431
CHEMBL3185030
ALBB-035692
Tox21_301742
AKOS024319393
NCGC00255422-01
CAS-597-09-1
DB-053445
NS00034223
Q27260956