CAS 139-65-1
:4,4′-Diaminodiphenyl sulfide
Description:
4,4′-Diaminodiphenyl sulfide, also known as benzidine sulfide, is an organic compound characterized by its structure, which features two amino groups (-NH2) attached to a diphenyl sulfide backbone. This compound is typically a solid at room temperature and is known for its potential use in the synthesis of dyes and pigments, particularly in the textile industry. It exhibits moderate solubility in organic solvents but is generally insoluble in water. The presence of amino groups makes it a versatile intermediate in organic synthesis, allowing for various chemical reactions, including coupling reactions. However, it is important to note that 4,4′-Diaminodiphenyl sulfide is associated with health risks, including potential carcinogenicity, which necessitates careful handling and regulation in industrial applications. Safety data sheets recommend using appropriate personal protective equipment when working with this compound to mitigate exposure risks. Overall, while it has useful applications, its safety profile requires stringent precautions.
Formula:C12H12N2S
InChI:InChI=1S/C12H12N2S/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8H,13-14H2
InChI key:InChIKey=ICNFHJVPAJKPHW-UHFFFAOYSA-N
SMILES:S(C1=CC=C(N)C=C1)C2=CC=C(N)C=C2
Synonyms:- 4,4'-Di(Aminophenyl) Sulfide
- 4,4'-Diaminodiphenyl Sulfide
- 4,4'-Sulfanediyldianiline
- 4,4'-Thiodianiline
- 4,4′-Diaminodiphenyl thioether
- 4,4′-Diaminophenyl sulfide
- 4,4′-Thiobis[aniline]
- 4,4′-Thiobis[benzenamine]
- 4-(Aminophenylthio)phenylamine
- 4-Aminophenyl Sulfide
- 4-Aminophenylthioether
- ASD
- Aniline, 4,4′-thiodi-
- Benzenamine, 4,4′-thiobis-
- Bis(4-Aminophenyl) Sulfide
- Bis(P-Aminophenyl)Sulfide
- Di(p-aminophenyl) sulfide
- NSC 6191
- Thioaniline
- Thiodi-P-Phenylenediamine
- [4-[(4-Aminophenyl)thio]phenyl]amine
- p,p'-Diaminodiphenyl Sulfide
- p,p-Thiodianiline
- See more synonyms
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Found 18 products.
Bis(4-aminophenyl) Sulfide
CAS:Formula:C12H12N2SPurity:>98.0%(T)(HPLC)Color and Shape:White to Brown powder to crystalMolecular weight:216.30GB 31604.52-2021 Primary Aromatic Amine Mixtures 36 1000 µg/mL in Acetonitrile
CAS:Controlled Product- 101-14-4
- 101-77-9
- 101-80-4
- 106-47-8
- 106-50-3
- 108-45-2
- 119-90-4
- 119-93-7
- 120-71-8
- 1208-52-2
- 137-17-7
- 139-65-1
- 60-09-3
- 615-05-4
- 62-53-3
- 6582-52-1
- 838-88-0
- 87-62-7
- 90-04-0
- 91-59-8
- 91-94-1
- 92-67-1
- 92-87-5
- 95-53-4
- 95-68-1
- 95-69-2
- 95-80-7
- 97-56-3
- 99-55-8
Color and Shape:Mixture4-Aminophenylthioether 10 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C12H12N2SColor and Shape:ColourlessMolecular weight:216.30GB/T 17592-2011 Azo Dyes Mixture 128 1000 µg/mL in Acetonitrile
CAS:Controlled Product- 101-14-4
- 101-77-9
- 101-80-4
- 106-47-8
- 106-50-3
- 119-90-4
- 119-93-7
- 120-71-8
- 137-17-7
- 139-65-1
- 60-09-3
- 615-05-4
- 62-53-3
- 838-88-0
- 87-62-7
- 90-04-0
- 91-59-8
- 91-94-1
- 92-67-1
- 92-87-5
- 95-53-4
- 95-68-1
- 95-69-2
- 95-80-7
- 97-56-3
- 99-55-8
Color and Shape:Colourless4-Aminophenylthioether
CAS:Controlled ProductFormula:C12H12N2SColor and Shape:NeatMolecular weight:216.304,4'-Thiodianiline
CAS:<p>Applications 4,4'-Thiodianiline is a carcinogenic aromatic amine used in the textile industry. It can also be used to modify electrodes in solar cells. Dyes and metabolites, Environmental Testing.<br>References Kawakami, Tsuyoshi, et al.: Kankyo Kagaku, 22(4), 197-204 (2012);Yang, Shuiping, et al.: Analytical Chem., 81(15), 6070-6079 (2009);Yildiz, Huseyin B., et al.: Adv. Funct. Mat., 18(21), 3497-3505 (2008)<br></p>Formula:C12H12N2SColor and Shape:NeatMolecular weight:216.304,4′-Diaminodiphenyl sulfide
CAS:Formula:C12H12N2SPurity:98%Color and Shape:White to pale reddish yellow powderMolecular weight:216.3Bis(4-aminophenyl) sulfide
CAS:<p>Bis(4-aminophenyl) sulfide is a hydroxylated derivative of aminophenol. It is used as a chemical intermediate in the production of dyes and pharmaceuticals. Bis(4-aminophenyl) sulfide has been shown to be carcinogenic in rats, but not in mice. The carcinogenicity may be due to the formation of reactive oxygen species that results from the hydroxyl group on this compound. This chemical also reacts with deionized water to produce hydrogen sulfide gas and sulfuric acid, which can corrode metals and other materials. Bis(4-aminophenyl) sulfide has been used as an optical dye for Raman spectroscopy, where it emits light at 514 nm when irradiated with laser light.</p>Formula:C12H12N2SPurity:Min. 95%Molecular weight:216.3 g/mol
