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N,N′-diisopropyl-p-phenylenediamine

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Identification
Molecular formula
C12H18N2
CAS number
101-72-4
IUPAC name
N4-isopropyl-N1-phenyl-benzene-1,4-diamine
State
State

At room temperature, N,N′-diisopropyl-p-phenylenediamine is a solid compound, highlighting its relatively high melting point compared to many other organics.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
376.00
Boiling point (Kelvin)
649.15
General information
Molecular weight
190.29g/mol
Molar mass
0.0000g/mol
Density
1.0077g/cm3
Appearence

N,N′-diisopropyl-p-phenylenediamine is typically a dark-colored, crystalline solid. It can appear as an amorphous powder depending on its formulation and purity.

Comment on solubility

Solubility of N4-isopropyl-N1-phenyl-benzene-1,4-diamine

The solubility of N4-isopropyl-N1-phenyl-benzene-1,4-diamine can be influenced by several factors, including its structure and the intermolecular interactions it can engage in. This compound exhibits specific characteristics that determine its solubility behavior:

  • Polarity: As an organic amine, the presence of amine groups contributes to moderate polarity, which typically enhances solubility in polar solvents like water, but may also allow for reasonable solubility in non-polar solvents depending on the overall molecular structure.
  • Hydrogen bonding: The amine groups are capable of forming hydrogen bonds, which can increase the solubility in polar solvents, thus aiding dissolution in certain aqueous environments.
  • Temperature Effects: As with many organic compounds, solubility can be significantly affected by temperature. Generally, increased temperature may lead to increased solubility.
  • Concentration Dependencies: The compound may display different solubility limits at various concentrations, particularly in relation to its saturation point in the solvent.

In summary, while the solubility of N4-isopropyl-N1-phenyl-benzene-1,4-diamine is nuanced and contingent on molecular interactions, it is essential to consider the interplay of polarity, hydrogen bonding, and environmental conditions when evaluating its dissolution behavior. As stated, "The key to understanding solubility lies in the balance of interactions." This principle resonates through the study of such compounds.

Interesting facts

Interesting Facts about N4-isopropyl-N1-phenyl-benzene-1,4-diamine

N4-isopropyl-N1-phenyl-benzene-1,4-diamine is a fascinating compound with a structure that holds significant potential in various fields such as organic chemistry and materials science. Here are some engaging aspects to consider:

  • Structure and Stability: The presence of isopropyl and phenyl groups enhances the stability and versatility of this diamine, making it essential for building specific organic molecules.
  • Diverse Applications: Compounds like this one are pivotal in the synthesis of various functional materials, including polymers and dyes. They serve as intermediates in manufacturing processes.
  • Active Research Area: Due to its intricate structure, N4-isopropyl-N1-phenyl-benzene-1,4-diamine has become an interesting subject in the research of organic electronics, pesticides, and pharmaceuticals.
  • Biological Significance: Some diamines exhibit biological activity, and chemists are investigating the possible therapeutic uses of compounds structurally related to this one.
  • Environmental Considerations: Understanding the behavior of such amines is critical in assessing their environmental impact and in designing greener synthetic pathways.

In summary, N4-isopropyl-N1-phenyl-benzene-1,4-diamine is not just a simple structure; it represents a confluence of organic chemistry’s potential in addressing modern challenges, including material innovation and biological sciences. Its journey from laboratory synthesis to practical application is a prime example of how chemical compounds can shape the future.

Synonyms
101-72-4
N-Isopropyl-N'-phenyl-p-phenylenediamine
IPPD
N-isopropyl-N'-phenyl-1,4-phenylenediamine
Cyzone
N1-Isopropyl-N4-phenylbenzene-1,4-diamine
4-Anilino-N-isopropylaniline
4-Isopropylaminodiphenylamine
Antigen 3c
Nonox ZA
Antioxidant 4010NA
Antioxidant IP
Santoflex IP
4-(ISOPROPYLAMINO)DIPHENYLAMINE
Diaphen FP
Cyzone IP
Diafen FP
Orflex PP
Antigene 3C
Flexzone 3C
Elastozone 34
1,4-Benzenediamine, N-(1-methylethyl)-N'-phenyl-
Santoflex 36
Antioxidant 40NA
Ozonon 3C
Ipognox 44
Permanax 115
Nocrack 810NA
N-isopropyl-N'-phenylbenzene-1,4-diamine
Antioxidant 4010 NA
Nocrac 810NA
S-IP
ASM 4010MA
N-(1-Methylethyl)-N'-phenyl-1,4-benzenediamine
4010 NA
NCI-C56304
N-2-Propyl-N'-phenyl-p-phenylenediamine
4010NA
p-Phenylenediamine, N-isopropyl-N'-phenyl-
N-Phenyl-N'-isopropyl-p-phenylenediamine
N-Fenyl-N'-isopropyl-p-fenylendiamin
N-Isopropyl-N'-fenyl-p-fenylendiamin
N-Phenyl-N'-isopropyl-1,4-phenylenediamine
NSC 41029
para-Isopropylaminodiphenylamine
CCRIS 4833
Akrochem antioxidant pd1
NA 4010
CHEBI:63569
HSDB 5342
Santoflex IPPD
Dusantox IPPD
Permanax IPPD
Permanex IPPD
N-Isopropyl-N'-phenyl-para-phenylenediamine
EINECS 202-969-7
1-N-phenyl-4-N-propan-2-ylbenzene-1,4-diamine
BRN 2213195
Vulkanox 4010NA
DTXSID1025485
0M7PSL4100
N-Fenyl-N'-isopropyl-p-fenylendiamin [Czech]
N-Isopropyl-N'-fenyl-p-fenylendiamin [Czech]
NSC-41029
N-Isopropyl-N'-phenyl-4-phenylenediamine
p-(Isopropylamino)diphenylamine
DTXCID705485
EC 202-969-7
1,4-Benzenediamine, N1-(1-methylethyl)-N4-phenyl-
NCGC00091826-01
p-Phenylenediamine, N-isopropyl-N'-phenyl
4-(ISOPROPYLAMINO)DIPHENYLAMINE [HSDB]
N-ISOPROPYL-N'-PHENYL PARAPHENYLENEDIAMINE
N1-phenyl-N4-(propan-2-yl)benzene-1,4-diamine
CAS-101-72-4
SMR000826283
N-Fenyl-N'-isopropyl-p-fenylendiamin (czech)
N-ISOPROPYL-N'-FENYL-P-FENYLENDIAMIN (CZECH)
UNII-0M7PSL4100
Flexizone GH
Black rubber mix
Flexone 3c
lsopropyl 0 PPD
Anto H
Vanox 3C
Phenylcyclohexyl PPD
ACCINOX ZA
DIAFEN PP
AO-CD
4AnilinoNisopropylaniline
Enamine_001818
NAUGARD I 4
ANTO "H
WLN: 1YMR DMR
N-Isopropyl-N/'-phenyl-1,4-phenylenediamine
4Isopropylaminodiphenylamine
Epitope ID:161749
VULKANOX 4020NA
N,N`Diphenylpphenylenediamine
Oprea1_357975
SCHEMBL38820
VULKANOX 4010 NA
paraIsopropylaminodiphenylamine
4-isopropylamino-diphenylamine
MLS002152911
MLS006011580
4(Isopropylamino)diphenylamine
NFenylN'isopropylpfenylendiamin
NIsopropylN'fenylpfenylendiamin
Benzenediamine, N-(1-methylethyl)-N'-phenyl-, 1,4-
SCHEMBL8585221
CHEMBL1449018
N2PropylN'phenylpphenylenediamine
OUBMGJOQLXMSNT-UHFFFAOYSA-
NIsopropylNphenyl4phenylenediamine
NPhenylN'isopropylpphenylenediamine
810NA
HMS1399C14
HMS3016N21
NCI C56304
NIsopropylN'phenyl4phenylenediamine
NPhenylN`cyclohexylpphenylenediamine
ALBB-024373
NSC41029
Tox21_111169
Tox21_201424
Tox21_303202
1, N-(1-methylethyl)-N'-phenyl-
4-isopropylamino-1-phenylaminobenzene
MFCD00026348
MSK165255
NIsopropylN'phenylparaphenylenediamine
pPhenylenediamine, NisopropylN'phenyl
NPhenylN'isopropyl1,4phenylenediamine
AKOS001025457
DB14195
PS-7762
NCGC00091826-02
NCGC00091826-03
NCGC00257032-01
NCGC00258975-01
[4-(isopropylamino)-phenyl]-phenyl-amine
N-isopropyl-N\'-phenyl-p-phenylenediamine
1,4Benzenediamine, N(1methylethyl)N'phenyl
1ST165255
MSK165255-1000
CS-0196455
N-Isopropyl-N'-fenyl-p-fenylendiamin(Czech)
NS00008626
P0327
EN300-02412
N'-phenyl-N-propan-2-ylbenzene-1,4-diamine
Benzenediamine, N(1methylethyl)N'phenyl, 1,4
F71245
N-(1-Methylethyl)-N-phenyl-1,4-benzenediamine
N-Isopropyl-N'-phenyl-p-phenylenediamine (IPPD)
1ST165255-1000
N-Isopropyl-N-Phenyl-1 pound not4-Phenylenediamine
Q21009595
Z56821893
N-Isopropyl-N'-phenyl-p-phenylenediamine Solution in Toluene, 1000?g/mL
N-Isopropyl-N'-phenyl-p-phenylenediamine Solution in Toluene, 1000mug/mL
202-969-7
InChI=1/C15H18N2/c1-12(2)16-14-8-10-15(11-9-14)17-13-6-4-3-5-7-13/h3-12,16-17H,1-2H3