1-Naphthalenesulfonic acid,3,3'-[(3,3'-dimethyl[1,1'-biphenyl]-4,4'-diyl)bis(azo)]bis[4-amino-,disodium salt


Chemical Name: 1-Naphthalenesulfonic acid,3,3'-[(3,3'-dimethyl[1,1'-biphenyl]-4,4'-diyl)bis(azo)]bis[4-amino-,disodium salt
CAS Number: 992-59-6
Product Number: AG003O2Q(AGN-PC-0W94JU)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Properties
MP:
>250℃
Storage:
-10 ℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
724.718g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
5
Exact Mass:
724.115g/mol
Monoisotopic Mass:
724.115g/mol
Topological Polar Surface Area:
233A^2
Heavy Atom Count:
50
Formal Charge:
0
Complexity:
1250
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



1-Naphthalenesulfonic acid, 3,3'-[(3,3'-dimethyl[1,1'-biphenyl]-4,4'-diyl)bis(2,1-diazenediyl)]bis[4-amino-, sodium salt (1:2) is commonly used in chemical synthesis as a versatile reagent. Its unique molecular structure enables it to participate in various reaction pathways, making it a valuable tool for organic chemists. This compound can serve as a coupling agent in the synthesis of azo dyes and pigments, allowing for precise control over the color and properties of the final product. Additionally, it can function as a linker in the construction of complex organic molecules, facilitating the formation of intricate molecular architectures. Its water-soluble sodium salt form enhances its solubility in aqueous environments, enabling its application in a wide range of synthetic procedures.