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N,N-Diethyl-p-phenylenediamine

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Identification
Molecular formula
C10H16N2
CAS number
93-05-0
IUPAC name
N4,N4-diethylbenzene-1,4-diamine
State
State

At room temperature, N,N-Diethyl-p-phenylenediamine is typically in a solid state, either as a crystalline solid or powder.

Melting point (Celsius)
38.00
Melting point (Kelvin)
311.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
164.24g/mol
Molar mass
164.2430g/mol
Density
0.9861g/cm3
Appearence

N,N-Diethyl-p-phenylenediamine is typically a white to light brown crystalline solid. It may appear in powdered form or as crystalline granules, which are often used in analytical chemistry applications such as water testing.

Comment on solubility

Solubility of N4,N4-diethylbenzene-1,4-diamine

N4,N4-diethylbenzene-1,4-diamine is a unique compound with solubility characteristics influenced by its chemical structure. Understanding its solubility is crucial for applications in various fields, including organic synthesis and materials science.

The solubility of this compound can be analyzed considering the following factors:

  • Polarity: The presence of amine groups can introduce some degree of polarity, assisting in solubility in polar solvents.
  • Hydrophobic regions: The diethyl groups contribute to hydrophobic character, which may limit solubility in highly polar solvents.
  • Solvent interactions: It demonstrates better solubility in organic solvents, such as ethanol or acetone, compared to aqueous solutions.

In essence, while N4,N4-diethylbenzene-1,4-diamine finds a more favorable solubility scenario in non-polar solvents, it may exhibit limited solubility in water. As noted, “the *nature of the solvent* can dramatically influence solubility.”

For researchers and chemists working with this compound, it's essential to consider these aspects to optimize formulations and reactions.

Interesting facts

Interesting Facts about N4,N4-diethylbenzene-1,4-diamine

N4,N4-diethylbenzene-1,4-diamine, often referred to in the industry as a *diamine*, is a fascinating compound with a variety of applications across different fields. Here are some intriguing aspects to consider:

  • Structure and Stability: The compound features a benzene ring substituted with two ethyl groups and two amine groups, creating a stable structure that exhibits interesting chemical reactivity.
  • Building Block for Polymers: It plays a crucial role as a precursor in the synthesis of polymers, especially in the manufacturing of polyamides and other high-performance materials.
  • Use in Dyes: This compound is also used in the synthesis of various dyes and pigments, where its ability to form stable complexes is of great advantage.
  • Biological Significance: Due to the presence of amine groups, N4,N4-diethylbenzene-1,4-diamine can act as a biological probe, aiding in the study of physiological processes.

Furthermore, the compound's versatility is reflected in its use in various research domains, from synthetic organic chemistry to material science. It is truly a testament to how intricate chemical structures can lead to myriad beneficial applications.

As a fascinating side note, compounds like N4,N4-diethylbenzene-1,4-diamine expand our understanding of chemical interactions, inspiring chemists to explore even deeper into the world of organic synthesis.

Synonyms
93-05-0
N,N-DIETHYL-P-PHENYLENEDIAMINE
N,N-Diethyl-1,4-phenylenediamine
4-Amino-N,N-diethylaniline
N1,N1-Diethylbenzene-1,4-diamine
p-Aminodiethylaniline
4-(Diethylamino)aniline
Diethylaminoaniline
p-Amino-N,N-diethylaniline
N,N-Diethyl-4-aminoaniline
p-(Diethylamino)aniline
N,N-Diethyl-1,4-benzenediamine
Diethyl-p-phenylenediamine
p-Phenylenediamine, N,N-diethyl-
Diethyl-para-phenylenediamine
para-Aminodiethylaniline
1,4-Benzenediamine, N,N-diethyl-
N,N-Diethyl 4-phenylenediamine
4-N,4-N-diethylbenzene-1,4-diamine
N,N-diethylbenzene-1,4-diamine
CCRIS 4620
NSC 147488
HSDB 5281
N,N-Diethyl-para-phenylenediamine
0QQA4DFV2J
EINECS 202-214-1
1,4-Benzenediamine, N1,N1-diethyl-
DTXSID2025058
NSC-147488
4-(N,N-diethylamino)aniline
MLS002454419
DTXCID205058
EC 202-214-1
n1,n1-diethyl-1,4-benzenediamine
DIETHYL-P-PHENYLENEDIAMINE, N,N-
SMR001372013
N,N-Diethyl-1,4-phenylenediamine; >98%
N,N-DIETHYL-P-PHENYLENEDIAMINE [HSDB]
UNII-0QQA4DFV2J
MFCD00007861
N,N-diethyl p-phenylenediamine
pAminodiethylaniline
N4,N4-diethylbenzene-1,4-diamine
4-Amino-N,N-diethylaniline, dist.
p-Diethylaminoaniline
4-diethylaminoaniline
paraAminodiethylaniline
p(Diethylamino)aniline
Diethylpphenylenediamine
4(Diethylamino)aniline
pAminoN,Ndiethylaniline
4AminoN,Ndiethylaniline
N,NDiethyl4aminoaniline
Diethylparaphenylenediamine
aniline, 4-diethylamino-
N,NDiethyl4phenylenediamine
cid_7120
N,NDiethyl1,4benzenediamine
SCHEMBL33781
N,NDiethylparaphenylenediamine
pPhenylenediamine, N,Ndiethyl
N,N-diethyl-p-phenylendiamine
p-Phenylenediamine,N-diethyl-
WLN: ZR DN2&2
(4-aminophenyl)-diethyl-amine
PARAAMINO-DIETHYLANILINE
4-(N,N-diethylamino)-aniline
1,4Benzenediamine, N,Ndiethyl
PPD 89
4-(N,N-diethyl-amino)-aniline
CHEMBL1452158
BDBM89017
QNGVNLMMEQUVQK-UHFFFAOYSA-
N,N-diethyl-1,4-diamino-benzene
N,N-Diethyl-benzene-1,4-diamine
Tox21_200888
NSC147488
STK122955
AKOS000101559
N,N-Diethyl-p-phenylenediamine, 97%
CS-W010827
FS-4085
CAS-93-05-0
NCGC00091343-01
NCGC00091343-02
NCGC00091343-03
NCGC00258442-01
DB-057362
D0518
NS00003411
EN300-33900
D89670
Q3032706
F0001-2236
202-214-1
InChI=1/C10H16N2/c1-3-12(4-2)10-7-5-9(11)6-8-10/h5-8H,3-4,11H2,1-2H3