Skip to main content

Solvent Yellow 56

ADVERTISEMENT
Identification
Molecular formula
C18H18N4O2
CAS number
11097-12-2
IUPAC name
N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide
State
State

Solvent Yellow 56 is typically in a solid state at room temperature.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.00
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.00
General information
Molecular weight
282.36g/mol
Molar mass
281.3500g/mol
Density
1.1000g/cm3
Appearence

Solvent Yellow 56 is an orange-red crystalline powder.

Comment on solubility

Solubility of N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide

N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide, a compound known for its complex structure, presents an intriguing profile regarding its solubility in various solvents. The solubility characteristics of this compound can be explored through several key points:

  • Polar Solvents: Generally, compounds featuring acetyl functional groups tend to exhibit some level of solubility in polar solvents such as water or methanol. This is due to the presence of hydrogen-bonding capabilities.
  • Non-Polar Solvents: The presence of the bulky tolylazo group might enhance solubility in non-polar solvents like ethyl acetate or cyclohexane, facilitating interactions between the compound and the solvent.
  • Temperature Effects: Increased temperature typically results in increased solubility for many organic compounds, including this one. Thus, heating the solvent can be beneficial for dissolution.
  • pH Sensitivity: The solubility can also be influenced by the pH of the solution. It is essential to assess the pH level, particularly in acidic or basic conditions, to determine the solubility behavior.

In summary, while N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide may show varying solubility in different environments, its overall behavior can be attributed to its unique chemical structure and the interactions it forms with different solvents. It is crucial to approach solubility testing with the understanding that the right conditions can significantly influence results.

Interesting facts

Exploring N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide

N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide is a fascinating chemical compound known for its unique properties and applications in various fields. Here are some intriguing facts that highlight its significance:

  • Colorimetric Applications: This compound is often utilized in the field of analytical chemistry due to its ability to form colored complexes. This property allows for the quantification of certain metal ions via spectrophotometric methods.
  • Dye Chemistry: The presence of the azo group (—N=N—) in its structure makes this compound an effective dye, especially in textile and printing industries. Azo dyes are known for their vibrant colors and stability, making them popular choices for coloring materials.
  • Biological Relevance: Compounds with similar structures have been studied for their effects in biological systems. Some azo compounds exhibit antimicrobial properties, which has spurred research into their potential as therapeutic agents.
  • Synthetic Versatility: N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide can be synthesized through various methods, allowing chemists to modify its structure for specific applications. This versatility is crucial for developing new materials in pharmacology and dye technology.
  • Research Impact: The exploration of such compounds can lead to significant advancements in numerous scientific fields, including materials science, biochemistry, and pharmacology. Understanding their mechanisms and interactions can open doors to innovative applications.

As we continue to study compounds like N-acetyl-N-[2-methyl-4-(o-tolylazo)phenyl]acetamide, we uncover their potential to advance technology and improve lives. Each compound adds a unique piece to the vast puzzle of chemical science, and this one is no exception.

Synonyms
Diacetazotol
83-63-6
Diacetotoluide
Pellidol
Diacetylaminoazotoluene
N,N-Diacetyl-o-aminoazotoluene
Dermagan
Epithelone
Pellidole
Diamazo
Dimazon
Periphermin
Dermagen
Epidermol
Granulin
4-o-Tolylazo-o-diacetotoluide
Periphermine
4''-(ortho-Tolylazo)-ortho-diacetoluidide
NSC 6509
N-acetyl-N-[2-methyl-4-[(2-methylphenyl)diazenyl]phenyl]acetamide
4'-(o-Tolylazo)-o-diacetotoluidide
N,N-Diacetyl-o-tolylazo-o-toluidine
o-Diacetotoluidide, 4''-(o-tolylazo)-
Acetamide, N-acetyl-N-[2-methyl-4-[(2-methylphenyl)azo]phenyl]-
N-Acetyl-N-(2-methyl-4-((2-methylphenyl)azo)phenyl)acetamide
U1925T7L3Z
NSC-6509
4''-(o-Tolylazo)-o-diacetotoluide
4''-(o-Tolylazo)-o-diacetotoluidide
Acetamide, N-acetyl-N-(2-methyl-4-((2-methylphenyl)azo)phenyl)-
WLN: 1VNV1&R B DNUNR B
N-acetyl-N-{2-methyl-4-[(2-methylphenyl)diazenyl]phenyl}acetamide
N-acetyl-N-{2-methyl-4-[(1E)-2-(2-methylphenyl)diazen-1-yl]phenyl}acetamide
EINECS 201-490-0
N-(4-o-Tolylazo-o-tolyl)diacetamide
BRN 0686326
N-Acetyl-N-[2-methyl-4-[(2-methylphenyl)azo]phenyl]acetamide
UNII-U1925T7L3Z
MFCD00026179
Orange G (Salt/Mix)
DIACETAZOTOL [MI]
3-16-00-00387 (Beilstein Handbook Reference)
Acid orange 10 (Salt/Mix)
C.I. Orange G (Salt/Mix)
Acidal Fast Orange (Salt/Mix)
SCHEMBL12848332
SCHEMBL14582013
CHEBI:81046
DTXSID30871563
DTXSID70878298
NSC6509
NSC7221
YIEDSISPYKQADU-UHFFFAOYSA-N
HY-B2187
N,N-Diacetyl-o-tolyazo-o-toluidine
NSC-7221
AKOS024257947
AKOS024332194
4-Diacetamido-2',3-dimethylazobenzene
CS-7499
AS-60082
DA-62831
2,3'-Dimethyl-4'-(diacetylamino)azobenzene
D0063
NS00010144
C17380
D87593
Q27155006
N-Acetyl-N-(2-methyl-4-[(2-methylphenyl)diazenyl]phenyl)acetamide #
ACETAMIDE, N-ACETYL-N-(2-METHYL-4-(2-(2-METHYLPHENYL)DIAZENYL)PHENYL)-