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Dinoseb

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Identification
Molecular formula
C7H6N2O5
CAS number
88-85-7
IUPAC name
2-methyl-4,6-dinitro-phenol
State
State

At room temperature, Dinoseb is in a solid state. It is crystalline and typically colored yellow to orange.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
378.70
Boiling point (Kelvin)
651.85
General information
Molecular weight
240.19g/mol
Molar mass
240.1920g/mol
Density
1.5300g/cm3
Appearence

Dinoseb typically appears as a yellow to orange crystalline solid. It is known for its intense coloration, which can range from bright yellow to orange depending on the specific purity and form.

Comment on solubility

Solubility of 2-methyl-4,6-dinitro-phenol

The solubility of 2-methyl-4,6-dinitro-phenol (often abbreviated as DNOC) presents an interesting case in the study of phenolic compounds. This specific compound is known for its unique chemical structure which significantly influences its solubility behavior.

Solubility Characteristics

  • Solvent Interaction: 2-methyl-4,6-dinitro-phenol is generally soluble in organic solvents such as ethanol and acetone, but it exhibits limited solubility in water.
  • Polar vs. Nonpolar: Its solubility can be described as more favorable in nonpolar environments due to its hydrophobic character, which arises from the presence of nitro groups.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, suggesting that thermal energy can facilitate the dissolution process.

It's important to note that solubility does not remain constant across conditions. Here are some factors influencing the solubility of 2-methyl-4,6-dinitro-phenol:

  1. pH of the solution: The solubility can vary with changes in pH, as phenolic compounds can ionize under certain conditions, affecting water solubility.
  2. Presence of other solutes: The interaction with other solutes can enhance or hinder the solubility of DNOC, demonstrating the complexities of chemical solubility.
  3. Structural Variants: Substituents on the phenolic ring can either increase or decrease overall solubility, an aspect worth exploring when discussing isomer variations.

In summary, the solubility of 2-methyl-4,6-dinitro-phenol is characterized by its ability to dissolve in organic solvents while maintaining a certain resistance in aqueous environments. The interplay of molecular interactions, environmental conditions, and chemical structures plays a significant role in determining its solubility, making it a fascinating compound for further research.

Interesting facts

Interesting Facts about 2-methyl-4,6-dinitro-phenol

2-methyl-4,6-dinitro-phenol, often abbreviated as DN(2)M, is a fascinating chemical compound due to its unique structure and various applications. Here are some key points that highlight its significance:

  • Versatile Applications: This compound is primarily known for its use as an intermediate in the synthesis of other chemical products, particularly in the manufacturing of herbicides and pesticides. Its nitro groups contribute to its reactivity, making it an essential reagent in organic synthesis.
  • Structure and Properties: The presence of both methyl and dinitro functional groups introduces intriguing geometric properties to the molecule. The arrangement of these groups affects its reactivity and makes it a compound of study in the realms of chemistry and pharmacology.
  • Research Interest: Scientists have investigated 2-methyl-4,6-dinitro-phenol for its antibacterial and antifungal properties. The compound's potential to inhibit certain biological processes makes it a subject of interest for pharmaceutical research.
  • Environmental Considerations: Like many nitro compounds, 2-methyl-4,6-dinitro-phenol raises environmental concerns due to its potential toxicity and the persistence in ecosystems. Therefore, researchers are also focusing on ways to mitigate its environmental impact.
  • Historical Context: Understanding the evolution of chemical compounds like 2-methyl-4,6-dinitro-phenol tells a story about the development of materials over time. As chemistry has advanced, so has our knowledge of safe handling and application methods for such reactive substances.

As evidenced by these points, 2-methyl-4,6-dinitro-phenol serves as much more than just a chemical formula; it encapsulates the evolving nature of chemical research and its applications in real-world scenarios. The exploration of its properties and effects continues to shape the landscape of modern chemistry.

Synonyms
2-Methyl-4,6-dinitrophenol
4,6-DINITRO-O-CRESOL
DNOC
534-52-1
Antinonnin
Dinitrocresol
Dinitro
Sinox
Winterwash
Antinonin
Arborol
Capsine
Degrassan
Dekrysil
Dinitrol
Dinurania
Ditrosol
Effusan
Elgetol
Hedolit
Hedolite
Kresamone
Nitrador
Nitrofan
Prokarbol
Raphatox
Sandolin
Selinon
Trifocide
Detal
Dillex
Dinoc
Elipol
Extrar
Lipan
Rafex
Dinitrodendtroxal
2,4-Dinitro-6-methylphenol
6-Methyl-2,4-dinitrophenol
Sandolin A
3,5-Dinitro-2-hydroxytoluene
Krezotol 50
Elgetol 30
Trifrina
Dnok
Kresonite-E
Rafex 35
Dn-dry mix no. 2
Effusan 3436
Chemsect DNOC
Dwunitro-o-krezol
2,4-Dinitro-o-cresol
K III
2-methyl-4,6-dinitro-phenol
K IV
4,6-Dinitrokresol
Oranz viktoria
Phenol, 2-methyl-4,6-dinitro-
Le dinitrocresol-4,6
Zahlreiche bezeichnungen
4,6-Dinitro-o-kresol
4,6-Dinitro-o-cresolo
Rcra waste number P047
o-Cresol, 4,6-dinitro-
ENT 154
C.I. 10310
DTXSID1022053
CHEBI:39349
1604ZJR09T
NSC-2082
NCGC00091775-03
Kreozan
Flavin-Samdoz
Neudorff DN 50
DTXCID902053
DNOK [Czech]
Caswell No. 390
Oranz viktoria [Czech]
DNOC [BSI:ISO]
Dwunitro-o-krezol [Polish]
4,6-Dinitrokresol [Dutch]
o-Cresol, 4,6,-dinitro-
4,6-Dinitro-o-cresol; 2,4-Dinitro-6-methylphenol; 2,4-Dinitro-o-cresol; 2-Methyl-4,6-dinitrophenol
CAS-534-52-1
DNOC (pesticide)
CCRIS 6822
4,6-Dinitro-o-kresol [Czech]
LE dinitrocresol-4,6 [French]
HSDB 1596
Zahlreiche bezeichnungen [German]
4,6-Dinitro-o-cresolo [Italian]
Dinitro-o-cresol, solid
Toluene, 3,5-dinitro-2-hydroxy-
NSC 2082
EINECS 208-601-1
UN1598
DNOC [ISO]
RCRA waste no. P047
EPA Pesticide Chemical Code 037507
BRN 2054389
Dinitrosol
4,6-Dinitro-2-methylphenol
Elgetox
Detol
Dinok
UNII-1604ZJR09T
Dinitro Cresol
AI3-00154
AI3-01567
Flavin-Sandoz
4,6-Dinitrocresol
Dinitro-ortho-cresol
o-Cresol,6-dinitro-
DNOC [HSDB]
DINITROCRESOL [MI]
EC 208-601-1
NCIOpen2_004211
SCHEMBL20734
Dinitromethyl cyclohexyltrienol
WLN: WNR BQ C1 ENW
4,6 DINITRO-O-CRESOL
4,6-DNOC
CHEMBL419564
NSC2082
DINITRO-O-CRESOL [MART.]
DNOC 100 microg/mL in Methanol
Phenol, 2-methyl, 4,6-dinitro-
Phenol, 2-methyl-4,6-dinitro-,
AAA53452
DNOC 10 microg/mL in Acetonitrile
Tox21_300327
Tox21_400068
MFCD00007105
STK295371
DNOC 100 microg/mL in Acetonitrile
AKOS000120494
NCGC00091775-01
NCGC00091775-02
NCGC00091775-04
NCGC00091775-05
NCGC00254265-01
AC-13097
DNOC, PESTANAL(R), analytical standard
D0828
NS00007710
EN300-20395
C18653
Dinitro-o-cresol, solid [UN1598] [Poison]
2-Methyl-4,6-dinitrophenol, analytical standard
A829601
Q209437
2-Methyl-4,6-dinitrophenol 1000 microg/mL in Methanol
Z104478022
InChI=1/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H