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Santoflex 77PD

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Identification
Molecular formula
C22H38N2
CAS number
10081-67-1
IUPAC name
N1,N4-bis(1-methylheptyl)benzene-1,4-diamine
State
State

At room temperature, it exists as a waxy or solid material.

Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
286.48g/mol
Molar mass
286.4750g/mol
Density
0.9190g/cm3
Appearence

N1,N4-bis(1-methylheptyl)benzene-1,4-diamine appears as a waxy solid. It can vary in color from light to pale yellow.

Comment on solubility

Solubility of N1,N4-bis(1-methylheptyl)benzene-1,4-diamine

N1,N4-bis(1-methylheptyl)benzene-1,4-diamine is a relatively complex organic compound with unique solubility characteristics. Understanding its solubility entails considering several factors:

  • Polar versus Non-Polar: This compound is primarily non-polar due to its extensive hydrocarbon chains (1-methylheptyl groups). As a result, it exhibits limited solubility in polar solvents such as water.
  • Solvent Compatibility: It is more soluble in non-polar solvents like hexane, toluene, or diethyl ether. This makes it suitable for applications where such solvents are used.
  • Temperature Dependency: Solubility can be affected by temperature; in general, higher temperatures can increase the solubility of organic compounds in organic solvents.
  • Concentration Effects: When dissolved in non-polar solvents, initial concentrations can lead to a varied degree of solubility, with saturation points achievable based on solvent volume.

As a rule of thumb, "like dissolves like" is a key principle in determining solubility. Therefore, N1,N4-bis(1-methylheptyl)benzene-1,4-diamine's solubility aligns with non-polar synergistic solvent systems. Understanding these solubility interactions is crucial for effective application and formulation in chemical processes.

Interesting facts

Interesting Facts about N1,N4-bis(1-methylheptyl)benzene-1,4-diamine

N1,N4-bis(1-methylheptyl)benzene-1,4-diamine, commonly referred to in scientific circles as a novel organic compound, showcases a striking chemical versatility that attracts attention from researchers and industry professionals alike. Here are some fascinating facts about this compound:

  • Unique Structure: The compound features a benzene ring substituted at the 1 and 4 positions with long aliphatic chains, which significantly influence its chemical behavior and interactions.
  • Potential Applications: Its ability to act as an amine makes it a candidate for various applications, especially in the fields of materials science and medicinal chemistry.
  • Polymer Chemistry: Compounds like N1,N4-bis(1-methylheptyl)benzene-1,4-diamine are used in the synthesis of novel polymers, providing unique properties such as improved thermal stability and mechanical strength.
  • Biological Interest: The structural features of this compound may lend themselves to bioactivity, warranting studies into its potential as a pharmaceutical precursor or active ingredient.
  • Research Insight: As noted by leading chemists, "The unique substitution pattern provides insights into reactivity and allows for the exploration of functionalized derivatives."

In summary, N1,N4-bis(1-methylheptyl)benzene-1,4-diamine exemplifies the intricate relationship between molecular structure and chemical function, further emphasizing the importance of detailed compound study in advancing scientific knowledge.

Synonyms
103-96-8
Elastozone 30
N,N'-Bis(1-methylheptyl)-p-phenylenediamine
Tenemene 30
Antozite 1
Santoflex 217
N,N'-Di(2-octyl)-p-phenylenediamine
N,N'-Di-Sec-Octyl-P-Phenylenediamine
N,N'-Bis(2-octyl)-p-phenylenediamine
1-N,4-N-di(octan-2-yl)benzene-1,4-diamine
UOP 288
1,4-Benzenediamine, N,N'-bis(1-methylheptyl)-
N,N'-Di(1-methylheptyl)-p-phenylenediamine
DI-2-OCTYL-P-PHENYLENEDIAMINE
p-Phenylenediamine, N,N'-bis(1-methylheptyl)-
28633-36-5
NSC 56774
N,N'-Bis(1-methylheptyl)-1,4-benzenediamine
0S97TKV89X
N,N'-Di(2-octyl)-para-phenylenediamine
HSDB 5358
EINECS 203-162-2
NSC-56774
1,4-Benzenediamine, N1,N4-bis(1-methylheptyl)-
1,4-Benzenediamine, N,N'-di-sec-octyl-
DI-2-OCTYL-P-PHENYLENEDIAMINE [HSDB]
N,N/'-BIS(1-METHYLHEPTYL)-P-PHENYLENEDIAMINE
UNII-0S97TKV89X
n,n'-di(octan-2-yl)benzene-1,4-diamine
n,n'-bis-(1-methylheptyl)-p-phenylenediamine
NCIOpen2_007505
N,N'-Bis-(1-methylheptyl)-1,4-phenylenediamine
SCHEMBL39138
DTXSID5051523
N,N'Di(2octyl)pphenylenediamine
N,N'Bis(2octyl)pphenylenediamine
1, N,N'-bis(1-methylheptyl)-
N,N'Di(2octyl)paraphenylenediamine
NSC56774
N,N'-Di-sek.-octyl-p-phenylendiamin
AKOS024332348
N,N'Di(1methylheptyl)pphenylenediamine
N,N'-Di-sec-octyl p-phenylene diamine
N,N'Bis(1methylheptyl)pphenylenediamine
N,N'Bis(1methylheptyl)1,4benzenediamine
pPhenylenediamine, N,N'bis(1methylheptyl)
1,4Benzenediamine, N,N'bis(1methylheptyl)
DB-040497
p-Phenylenediamine,N'-bis(1-methylheptyl)-
NS00021462
N~1~,N~4~-bis(1-methylheptyl)-1,4-benzenediamine
p-Phenylenediamine, N,N'-bis(1-methylheptyl)-(8CI)
Q27237187
203-162-2