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1-Phenylazonaphthalen-2-ol

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Identification
Molecular formula
C16H12N2O
CAS number
85-86-9
IUPAC name
1-phenylazonaphthalen-2-ol
State
State

At room temperature, 1-Phenylazonaphthalen-2-ol is in a solid state, often found in a crystalline powder form.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
435.00
Boiling point (Kelvin)
708.15
General information
Molecular weight
250.28g/mol
Molar mass
250.2770g/mol
Density
1.3300g/cm3
Appearence

1-Phenylazonaphthalen-2-ol typically appears as an orange to reddish-brown crystalline powder. It is often used as a dye or pigment in various applications.

Comment on solubility

Solubility of 1-phenylazonaphthalen-2-ol

1-phenylazonaphthalen-2-ol, a compound often utilized in various chemical applications, exhibits unique solubility characteristics. Understanding its solubility behavior is essential for its effective use in research and practical applications.

  • Solubility in Water: 1-phenylazonaphthalen-2-ol is not highly soluble in water due to its large aromatic structure which tends to favor non-polar environments.
  • Solubility in Organic Solvents: This compound is generally more soluble in organic solvents such as:
    • Toluene
    • Chloroform
    • Ethanol
    These solvents can stabilize the polar and non-polar parts of the molecule, enhancing solubility.
  • Influence of Temperature: The solubility may increase with temperature as the kinetic energy of the molecules allows for better interactions in the solvent medium.
  • pH Considerations: Changes in pH can affect the ionization of functional groups, which may significantly alter the solubility profile. Generally, neutral to slightly acidic environments foster better solubility.

In conclusion, understanding the solubility of 1-phenylazonaphthalen-2-ol is crucial for applications in dye chemistry, organic synthesis, and analytical chemistry. Remember, *"the right solvent can make all the difference!"*

Interesting facts

Interesting Facts about 1-Phenylazonaphthalen-2-ol

1-Phenylazonaphthalen-2-ol, also known for its vibrant color and unique structural properties, is a fascinating compound within the realm of organic chemistry. Its structure consists of a naphthalene backbone, which provides significant stability and resonance, coupled with an azo group that introduces interesting electronic characteristics. Here are some engaging attributes of this compound:

  • Color and Applications: The presence of the azo group often imparts a vivid coloring property to the compound, making it useful in the dye industry. Azo compounds are known for their bright hues, which are leveraged in textile and paint applications.
  • Reactivity: 1-Phenylazonaphthalen-2-ol can undergo various chemical reactions due to its functional groups. This includes coupling reactions and nucleophilic substitutions, paving the way for developing more complex molecules.
  • Biological Significance: Some azo compounds have drawn attention in medicinal chemistry, where their potential as drug candidates is explored. Their ability to undergo chemical transformations in biological systems can lead to active therapeutic agents.
  • Safety Concerns: While many azo compounds are widely used, some have raised safety concerns due to their potential to form carcinogenic aromatic amines. Understanding the implications of 1-phenylazonaphthalen-2-ol within this context is crucial for safe practices in its applications.

Overall, 1-phenylazonaphthalen-2-ol exemplifies the interplay between structure and function in organic compounds. Its multifaceted applications and implications in various fields make it a compound of significant interest in both academic and industrial settings.

Synonyms
Sudan I
842-07-9
Solvent Yellow 14
1-Phenylazo-2-naphthol
C.I. Solvent Yellow 14
1-(Phenylazo)-2-naphthalenol
Fast Orange
Grasal Orange
Soudan I
Pyronalorange
Carminaph
Dunkelgelb
SUDAN 1
Fettorange lg
Cerotinorange G
Organol Orange
Stearix Orange
Fettorange R
Motiorange R
Scharlach B
Calcogas M
Orange Pel
Fettorange 4a
Grasan Orange R
Sansel Orange G
Ceres Orange R
Enial Orange I
Oleal Orange R
Sudan Orange R
Sudan Orange RA
Atul Orange R
Resinol Orange R
Somalia Orange I
Sudan J
Fat Orange G
Fat Orange I
Fat Orange R
Fat Orange RS
Resoform Orange G
Waxoline Yellow I
Lacquer Orange VG
Waxakol Orange GL
Fat Orange 4A
Fat Soluble Orange
Orange A L'Huile
Calcogas Orange NC
Silotras Orange TR
Waxoline Yellow IM
Waxoline Yellow IP
Waxoline Yellow IS
2-Naphtholazobenzene
Dispersol Yellow PP
Orange Insoluble Olg
2-Naphthalenol, 1-(phenylazo)-
Tertrogras Orange SV
Morton Orange Y
Sudan Orange RA New
1-Benzoazo-2-naphthol
Benzeneazo-beta-naphthol
Plastoresin Orange F4A
Orange Resenole No. 3
Orange 2 Insoluble
1-(phenyldiazenyl)naphthalen-2-ol
Solvent Yellow No. 14
Disperse Yellow 97
Benzene-1-azo-2-naphthol
Fettorange IG
Orange Soluble A L'Huile
1-Benzeneazo-2-naphthol
Orange Resenole 3
2-Naphthol, 1-(phenylazo)-
Orange 3RA Soluble in Grease
2-Hydroxynaphthyl-1-azobenzene
1-Phenylazo-beta-naphthol
2-Hydroxy-1-phenylazonaphthalene
C.I. 12055
ci solvent yellow 14
NCI-C53929
Zlut rozpoustedlova 14
Fat Orange G (VAN)
1-(Phenylazo)-2-naphthol
C.I. Disperse Yellow 97
alpha-Phenylazo-beta-naphthol
CCRIS 174
Zlut rozpoustedlova 14 [Czech]
HSDB 4132
EINECS 212-668-2
NSC 11227
NSC 51524
BRN 0651992
48I7IBB68J
DTXSID4021135
CHEBI:30958
Waxoline Orange EP-FW
NSC-11227
NSC-51524
SUDAN I [IARC]
2-Naphthalenol, 1-(2-phenyldiazenyl)-
1-(2-Hydroxynaphthyl)azobenzene
DTXCID50809767
1-(Phenylazo)-2-hydroxynaphthalene
4-16-00-00228 (Beilstein Handbook Reference)
C.I. SOLVENT YELLOW 14 [HSDB]
SUDAN I (IARC)
1-phenylazo-2-hydroxynaphthalene
1Benzoazo2naphthol
2Naphtholazobenzene
1Phenylazo2naphthol
Benzene1azo2naphthol
Oil Orange R14
1,2-naphthoquinone-1-phenylhydrazone
Benzeneazobetanaphthol
1Phenylazobetanaphthol
Oil Orange 7078V
Oil Orange Z7078
alphaPhenylazobetanaphthol
1(Phenylazo)2naphthalenol
2Naphthol, 1(phenylazo)
2Hydroxynaphthyl1azobenzene
SUDAN ORANGE 220
Calco Oil Orange 7078Y
Calco Oil Orange Z7078
2Hydroxy1phenylazonaphthalene
2Naphthalenol, 1(phenylazo)
PLASTORESIN ORANGE F 4A
1-PHENYLAZO-2-NAPHTHALENOL
2-HYDROXY-1-(PHENYLAZO)NAPHTHALENE
212-668-2
1-phenyldiazenylnaphthalen-2-ol
CI 12055
C16H12N2O
C.I Solvent yellow 14
MFCD00003911
Benzeneazo-.beta.-naphthol
1-Phenylazo-.beta.-naphthol
1-[(E)-Phenyldiazenyl]-2-naphthol
40339-35-3
(E)-1-(phenyldiazenyl)naphthalen-2-ol
WLN: L66J BNUNR& CQ
CAS-842-07-9
1-(2-PHENYLHYDRAZIN-1-YLIDENE)NAPHTHALEN-2-ONE
UNII-48I7IBB68J
C. I. Solvent Yellow 14
Sudangelb
Sudan centn
Sudan 1 100 microg/mL in Acetonitrile
SCHEMBL51451
Sudan I, analytical standard
SCHEMBL333149
2-Naphthalenol, 1-(phenylazo)
CHEMBL1397023
SCHEMBL11876526
SCHEMBL11876532
DTXSID50873448
DTXSID90873447
MSK2401
MRQIXHXHHPWVIL-ISLYRVAYSA-N
MRQIXHXHHPWVIL-UHFFFAOYSA-N
Sudan I, Dye content >=95 %
ZONYAPYTDIVJGG-VLGSPTGOSA-N
1-(Phenyldiazenyl)-2-naphthol #
.alpha.-Phenylazo-.beta.-naphthol
Sudan I (C.I. 12055)
HY-D0024
NSC11227
NSC51524
Tox21_200511
Tox21_300297
s6191
AKOS003581973
AKOS028109814
1-[(Phenyliminio)amino]-2-naphtholate
CS-5362
1-[(Z)-Phenyldiazenyl]naphthalen-2-ol
NCGC00164031-01
NCGC00164031-02
NCGC00164031-03
NCGC00254059-01
NCGC00258065-01
1-(2-phenyldiazen-1-yl)naphthalen-2-ol
AC-34716
DA-58156
NCI60_000270
NCI60_004248
1,2-Naphthalenedione, 1-(phenylhydrazone)
1-[(1E)-2-Phenyldiazenyl]-2-naphthalenol
NS00000074
P0585
EN300-21432
C19525
Q901018
(E)-1-(2-Phenyldiazen-2-ium-1-yl)naphthalen-2-olate
Z104496932
1-[(Z)-2-Phenylhydrazin-1-ylidene]naphthalen-2(1H)-one
71351-99-0