Interesting facts
Interesting Facts about 7-hydroxy-8-(4-phenylazophenyl)azo-naphthalene-1,3-disulfonic acid
7-hydroxy-8-(4-phenylazophenyl)azo-naphthalene-1,3-disulfonic acid, often abbreviated as an azo dye, is a fascinating compound with numerous applications in various fields. Here are some engaging insights about this remarkable substance:
- Azo Dye Chemistry: As a member of the azo dye family, this compound contains the characteristic azo functional group (–N=N–), which is responsible for its vivid coloration. This feature makes azo dyes invaluable in textiles and food industries.
- Versatile Applications: This compound is primarily used in the synthesis of dyes and pigments. Its ability to produce bright shades allows it to be utilized in:
- Textile dyeing
- Printing inks
- Cosmetics
- Food coloring
- Environmental Awareness: The use of azo dyes has raised concerns regarding their impact on human health and the environment. Some azo dyes can degrade into problematic amines, which can be toxic or carcinogenic. Researchers are continuously working to develop safer alternatives and explore eco-friendly dyeing processes.
- Scientific Research: The structural properties of this compound make it a subject of interest in various scientific studies focused on the effects of dyes on biological systems, as well as in materials science, where its unique properties can be harnessed for new technologies.
- Color Changes: The solutions of azo compounds often show striking color changes when they undergo chemical transformations, making them useful indicators in analytical chemistry.
In summary, 7-hydroxy-8-(4-phenylazophenyl)azo-naphthalene-1,3-disulfonic acid is more than just a compound; it represents a blend of chemistry, artistry, and environmental consideration. Its rich history and ongoing relevance in modern science keep it at the forefront of chemical research and application.
Synonyms
Oxanal Scarlet A
Ponceau PSNR
Scarlet MOO
Brilliant Croceine
Eriosin Red GR
Fenazo Red XG
Crocein Scarlet N
Croceine Acid Red
Croceine Scarlet M
Hispacid Scarlet M
Kiton Scarlet MOO
Paper Scarlet WEG
Acid Fast Red RN
Erionyl Red E-GR
Airedale Scarlet MO
Brilliant Red EMBL
Croceine Scarlet SS
Acilan Croceine MOO
Brilliant Croceine M
Brilliant Croceine P
Acid Red 2 Zh
Croceine Scarlet 3B
Brilliant Croceine Scarlet M
Brilliant Scarlet LC
Croceine Scarlet MOO
Brilliant Croceine MO
Brilliant Red 2EMBL
Kiton Fast Scarlet A
Acidal Bright Croceine
Brilliant Croceine 3B
Calcocid Scarlet MOON
Croceine Scarlet MOON
Brilliant Croceine LBH
Brilliant Croceine MOO
Brilliant Croceine SWW
Curol Brilliant Red G
Paper Scarlet A Extra
Wood Stain Scarlet NS
Brilliant Croceine 3BM
Acid Leather Red PSNR
Brilliant Croceine MOOL
Eniacid Brilliant Scarlet
Atul Croceine Scarlet MOO
Crocein Scarlet MOO
Brilliant Croceine 3BA-CF
Java Brilliant Scarlet MOO
Vondacid Light Scarlet MOO
Brilliant Croceine Scarlet N
Brilliant Scarlet R
Amacid Brilliant Croceine 3BA
Croceine Brilliant Scarlet 3BC
Croceine Brilliant Scarlet 3BS
C.I. Acid Red 73
Tertracid Brilliant Croceine MOO
Hidacid Brilliant Crocein Scarlet
EINECS 246-826-7
7-Hydroxy-8-((4-(phenylazo)phenyl)azo)naphthalene-1,3-disulphonic acid
NSC-7832
NSC-47724
C.I. 27290
SOLVENT RED 69
Brilliant Scarlet R (VAN)
7-hydroxy-8-[[4-(phenylazo)phenyl]azo]naphthalene-1,3-disulphonic acid
NSC 7832
EINECS 226-502-1
NSC 47724
Erionyl Red EGR
Baumwollscharlach extra
CI Solvent Red 69
crocein scarlet MOO.3B
Brilliant Croceine 3BACF
ACID RED 73 [INCI]
D&C Red No. 13, Ext.
CI 27290 [INCI]
Sodium 6hydroxy5(4phenylazophenylazo)naphthalene2,4disulphonate
7Hydroxy8((4(phenylazo)phenyl)azo)1,3naphthalindisulfonsaure, Dinatriumsalz
1,3Naphthalenedisulfonic acid, 7hydroxy8((4(phenylazo)phenyl)azo), disodium salt
7Hydroxy8((4(phenylazo)phenyl)azo)1,3naphthalenedisulfonic acid, disodium salt
1,3-Naphthalenedisulfonic acid, 7-hydroxy-8-((E)-2-(4-((E)-2-phenyldiazenyl)phenyl)diazenyl)-, sodium salt (1:2)
1,3Naphthalenedisulfonic acid, 7hydroxy8(2(4(2phenyldiazenyl)phenyl)diazenyl), sodium salt (1:2)
246-826-7
25317-39-9
C.I. Acid Red 73, disodium salt
Paper Scarlet R
Woodstain Scarlet
Ext D and C Red No. 13
NSC7832
7-hydroxy-8-[(4-phenyldiazenylphenyl)diazenyl]naphthalene-1,3-disulfonic acid
7-hydroxy-8-{[4-(phenyldiazenyl)phenyl]diazenyl}naphthalene-1,3-disulfonic acid
Brilliant Crocein (C.I. 27290)
1, 7-hydroxy-8-[[4-(phenylazo)phenyl]azo]-, disodium salt
7-Hydroxy-8-((4-(phenyldiazenyl)phenyl)diazenyl)-1,3-naphthalenedisulfonic acid
7-Hydroxy-8-{[4-(phenyldiazenyl)phenyl]diazenyl}-1,3-naphthalenedisulfonic acid
woodstain scarlet free acid
SCHEMBL110351
acid red 73 (free acid form)
CHEMBL1976160
CHEBI:87190
DTXSID90859908
IMFORQFZCYFVDA-BSDCMEITSA-N
PIEQFSVTZMAUJA-UHFFFAOYSA-N
DTXSID701043670
NSC47724
7-HYDROXY-8-[[4-(PHENYLAZO)PHENYL]AZO]NAPHTHALENE-1,3-DISULFONIC ACID
NS00083458
Q27159435
1,3-Naphthalenedisulfonic acid, {7-hydroxy-8-[[4-(phenylazo)phenyl]azo]-,} disodium salt
7-Hydroxy-8-((E)-{4-[(E)-phenyldiazenyl]phenyl}diazenyl)naphthalene-1,3-disulfonic acid-
7-hydroxy-8-[(E)-[4-[(E)-phenylazo]phenyl]azo]naphthalene-1,3-disulfonic acid
7-Hydroxy-8-[(E)-{4-[(E)-phenyldiazenyl]phenyl}diazenyl]-1,3-naphthalenedisulfonic acid
1379505-49-3
Solubility of 7-hydroxy-8-(4-phenylazophenyl)azo-naphthalene-1,3-disulfonic acid
The solubility of 7-hydroxy-8-(4-phenylazophenyl)azo-naphthalene-1,3-disulfonic acid is influenced by various factors due to its complex structure. This compound features multiple functional groups that affect its interactions with solvents.
Key Factors Influencing Solubility:
Furthermore, this compound can exhibit hydrophobic interactions due to its naphthalene moiety and phenyl groups, which may limit its solubility in highly polar solvents under certain conditions. Consequently, one could characterize its solubility behavior as a complex interplay of the structural components and the surrounding medium.
In conclusion, while it possesses the potential for solubility in polar solvents, particularly water, various conditions need to be optimized for maximum dissolution efficiency: