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Dinoseb

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Identification
Molecular formula
C10H12N2O5
CAS number
88-85-7
IUPAC name
2-(1-methylbutyl)-4,6-dinitro-phenol
State
State

At room temperature, Dinoseb is typically a solid. It presents as either orange crystalline form or a reddish-brown solid, depending on its specific formulation or purity.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
240.22g/mol
Molar mass
240.2200g/mol
Density
1.5280g/cm3
Appearence

Dinoseb appears as orange crystals or a reddish-brown solid. It is known for its strong, pungent odor.

Comment on solubility

Solubility of 2-(1-methylbutyl)-4,6-dinitro-phenol

2-(1-methylbutyl)-4,6-dinitro-phenol, often referred to as an organic compound with significant applications, exhibits varied solubility characteristics that are quite interesting.

Generally, the solubility of this compound can be influenced by the following factors:

  • Polarity: The presence of nitro groups (-NO2) and hydroxyl groups (-OH) in the phenolic structure contributes to its polar nature.
  • Solvent Type: This compound is expected to be more soluble in polar solvents such as alcohols or acetone, compared to non-polar solvents like hexane.
  • Temperature: The solubility tends to increase with temperature; thus, heating may help dissolve the compound in the desired solvent.

As with many organic compounds, when evaluating solubility, it’s important to consider:

  1. The degree of hydrogen bonding that may occur with solvents.
  2. The molecule's steric hinderance due to the bulky 1-methylbutyl group affecting solvation.
  3. The balance between hydrophobic and hydrophilic characteristics brought about by functional groups.

In conclusion, understanding the solubility of 2-(1-methylbutyl)-4,6-dinitro-phenol is essential for its practical applications, whether in industrial processes or research endeavors. Further investigation and empirical data are useful for optimizing its use, especially in the context of formulations and reactions.

Interesting facts

Interesting Facts about 2-(1-methylbutyl)-4,6-dinitro-phenol

2-(1-methylbutyl)-4,6-dinitro-phenol, commonly known as a chemical intermediate, has several notable features that make it an interesting subject of study in the field of chemistry. Below are some engaging facts about this compound:

  • Versatile Applications: This compound is primarily utilized in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to serve as a building block in the development of new chemical entities.
  • Structural Significance: The presence of the dinitro groups on the aromatic ring plays a crucial role in its reactivity. These groups are known for enhancing electrophilic substitution reactions, making the compound a valuable intermediate in organic synthesis.
  • Environmental Considerations: As with many nitro compounds, 2-(1-methylbutyl)-4,6-dinitro-phenol raises environmental concerns. Its potential toxicity to aquatic life emphasizes the importance of responsible handling and disposal practices in the laboratory.
  • Research Interest: The compound has garnered attention in research for its biological activities, including potential antifungal and antibacterial properties. Scientists continue to explore these characteristics for possible therapeutic applications.
  • Structure-Activity Relationship (SAR): Understanding how variations in its structure can impact biological activity is a key area of study. This exploration helps chemists in the design and optimization of more effective compounds.

In summary, 2-(1-methylbutyl)-4,6-dinitro-phenol not only serves a purpose in industrial applications but also presents a fascinating subject for both academic and practical chemistry. The ongoing exploration of its properties and applications reflects the ever-evolving nature of chemical science.

Synonyms
Dinosam
Chemox general
4097-36-3
DNOSAP
Dinosame
2-sec-Amyl-4,6-dinitrophenol
Dinosam [ISO]
Dinosame [French]
4,6-Dinitro-o-sec-amylphenol
2,4-Dinitro-6-(1-methylbutyl)phenol
Caswell No. 388
2-(1-Methyl-n-butyl)-4,6-dinitrophenol
Phenol, 2-(1-methylbutyl)-4,6-dinitro-
NSC 21493
2-(1-Methylbutyl)-4,6-dinitrofenol
2-(1-Metil-butil)-4,6-dinitro-fenolo
UNII-J04VBD97F1
2-sec-Amyl-4,6-dinitrophenol (VAN)
EPA Pesticide Chemical Code 037504
BRN 2473527
AI3-19047
2-(1-Methylbutyl)-4,6-dinitrofenol [Dutch]
NSC-21493
2-(1-Metil-butil)-4,6-dinitro-fenolo [Italian]
DTXSID2041882
2-(2-HYDROXY-3,5-DINITROPHENYL)PENTANE
dinitroaminophenyl group
DTXCID0021882
dinitroaminophenol
psozmumwcxlrkx-uhfffaoysa-n
DNAP
2,4-DINITRO-6-PENTAN-2-YL-PHENOL
2,4-dinitro-6-pentan-2-ylphenol
J04VBD97F1
Dinosame [French]
2,4-dinitro-6-s-amylphenol
SCHEMBL118439
WLN: WNR BQ ENW CY3&1
EAA09736
NSC21493
2-(1-Methylbutyl)-4,6-dinitrophenol #
1ST157801
DB-250855
NS00124490
Q27280984