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N-Phenylnaphthalen-1-amine

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Identification
Molecular formula
C16H13N
CAS number
92-29-5
IUPAC name
N-phenylnaphthalen-1-amine
State
State

At room temperature, N-Phenylnaphthalen-1-amine is a solid, typically found in its crystalline form.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
219.29g/mol
Molar mass
219.2860g/mol
Density
1.1660g/cm3
Appearence

N-Phenylnaphthalen-1-amine appears as a yellow crystalline powder. It is aromatic and may have a distinct smell characteristic of aromatic amines.

Comment on solubility

Solubility of N-phenylnaphthalen-1-amine

N-phenylnaphthalen-1-amine, also known as 1-amino-2-phenylnaphthalene, exhibits interesting solubility characteristics that are essential for various applications in chemistry and industry.

When assessing its solubility, consider the following factors:

  • Polar vs. Nonpolar Solvents: N-phenylnaphthalen-1-amine is primarily a nonpolar compound. Therefore, it tends to be more soluble in nonpolar solvents such as toluene or hexane.
  • Water Solubility: This compound is generally insoluble in water due to its hydrophobic character, which diminishes its ability to interact with polar water molecules.
  • Temperature Effects: Solubility can also be influenced by temperature; typically, nonpolar substances become more soluble in organic solvents at elevated temperatures.
  • Functional Groups: The presence of the amino group (-NH2) might suggest possible interactions with polar solvents, but overall, its nonpolar characteristics prevail.

In summary, N-phenylnaphthalen-1-amine demonstrates a preference for solubility in nonpolar environments, showcasing the classic principle of "like dissolves like." Its incompatibility with water highlights the importance of choosing the right solvent for applications involving this compound.

Interesting facts

Interesting Facts about N-phenylnaphthalen-1-amine

N-phenylnaphthalen-1-amine, a polycyclic aromatic amine, has garnered interest in both organic chemistry and materials science due to its unique structure and properties. Here are some engaging facts about this compound:

  • Structure and Bonding: This compound features a naphthalene core linked to a phenyl group, showcasing a fascinating interaction of aromatic systems through π-π stacking.
  • Applications in Dyes: N-phenylnaphthalen-1-amine is frequently used as an intermediate in the synthesis of various dyes and pigments, highlighting its importance in the textile and paint industries.
  • Biological Significance: Compounds like N-phenylnaphthalen-1-amine have been studied for their potential biological activities. Some derivatives have displayed anti-cancer properties in preliminary studies, making them of interest for medicinal chemistry.
  • Electronic Properties: Due to its conjugated system, this compound exhibits semiconducting properties in certain contexts. This feature makes it a candidate for use in organic electronics, including organic light-emitting diodes (OLEDs).
  • Toxicity Considerations: As with many aromatic amines, N-phenylnaphthalen-1-amine can pose health risks, emphasizing the need for careful handling and use in laboratory settings.

A notable quote in the world of chemistry is, "The essence of chemistry is not in the compounds themselves, but in their potential applications." N-phenylnaphthalen-1-amine vividly illustrates this idea through its diverse roles and functionalities across multiple domains.

In conclusion, N-phenylnaphthalen-1-amine is not just another chemical compound; it serves as a bridge linking chemistry with practical applications in industries ranging from textiles to electronics. Its continuing study and exploration may reveal even more exciting uses in the future.

Synonyms
N-PHENYL-1-NAPHTHYLAMINE
90-30-2
N-phenylnaphthalen-1-amine
1-Anilinonaphthalene
PANA
Antioxidant PAN
N-(1-Naphthyl)aniline
Neozone A
Nonox A
Phenylnaphthylamine
Aceto PAN
1-Naphthalenamine, N-phenyl-
N-Phenyl-alpha-naphthylamine
Vulkanox PAN
Phenyl-1-naphthylamine
1-Naphthylamine, N-phenyl-
Additin 30
N-1-Naphthylaniline
Amoco 32
Antigene PAN
Naphthalen-1-yl-phenyl-amine
1-naphthylphenylamine
alpha-Naphthylphenylamine
N-Fenyl-1-aminonaftalen
Naugard PANA
Nocrac PA
Nonox AN
N-Phenyl-1-naphthalenamine
N-Phenyl-1-aminonaphthalene
NSC 2622
1-(n-phenylamino)naphthalene
Fenyl-alpha-naftylamin
C.I. 44050
CCRIS 4701
Fenyl-alpha-naftylamin [Czech]
DTXSID2025892
HSDB 7232
N-Fenyl-1-aminonaftalen [Czech]
N-Phenyl-1-napthyl Amine
EINECS 201-983-0
BRN 2211174
CHEBI:34876
AI3-00528
n-phenyl-1-napthylamine
NSC-2622
Phenyl-alpha-naphthylamine
.alpha.-Naphthylphenylamine
.alpha.-Phenylnaphthylamine
5I112077IN
Phenyl-.alpha.-naphthylamine
MLS002415761
MLS002637634
CHEMBL170408
DTXCID605892
N-Phenyl-.alpha.-naphthylamine
EC 201-983-0
4-12-00-03015 (Beilstein Handbook Reference)
SMR000112177
Antigene PA
CAS-90-30-2
N-Phenylnaphthylamine
Irganox L 05
1-N-phenylnaphthylamine
1-(Phenylamino)naphthalene
Algerite
N-phenyl-N-(1-naphthyl)amine
UNII-5I112077IN
N1Naphthylaniline
Neozon A
1Anilinonaphthalene
Fenylalphanaftylamin
phenyl naphthylamine
Phenyl1naphthylamine
NFenyl1aminonaftalen
MFCD00003878
N(1Naphthyl)aniline
ALGERITE POWDER
alphaNaphthylphenylamine
1-phenylaminonaphthalene
3s0b
NPhenylalphanaphthylamine
1Naphthylamine, Nphenyl
1-Naphthyl phenyl amine
N-phenyl-l-naphthylamine
alpha-naphthyl-phenylamine
Fenyl-.alpha.-naftylamin
1Naphthalenamine, Nphenyl
Naphthalenamine, N-phenyl-
WLN: L66J BMR
SCHEMBL19796
BIDD:ER0663
ALPHA-PHENYLNAPTHYLAMINE
1-Naphthaleneamine, N-phenyl-
SCHEMBL7751770
NSC2622
1-NAPHTHYLAMINE,N-PHENYL-
HMS2270J09
Tox21_202073
Tox21_303075
BDBM50504083
STK182583
AKOS003386028
CS-W010472
HY-W009756
NCGC00091327-01
NCGC00091327-02
NCGC00091327-03
NCGC00091327-04
NCGC00256930-01
NCGC00259622-01
1-NAPHTHYLAMINE, N-PHENYL-[HSDB]
AS-17486
1-NAPHTHYLAMINE, N-PHENYL- [HSDB]
DB-000338
NS00010304
P0197
EN300-365758
N-Phenyl-1-naphthylamine, reagent grade, 98%
SR-01000868875
SR-01000868875-2
Q10859671
201-983-0