637-31-0

Usage

Uses

Used in Histology and Cytology:
Bindschedler's Green is used as a staining agent for visualizing plant cell walls, enabling the differentiation of different types of plant tissues due to its binding affinity with cellulose and lignin components.
Used in Detection of Lipid Peroxidation:
In addition to its primary application in histology, Bindschedler's Green is also utilized in the detection of lipid peroxidation in cells and tissues, serving as a valuable tool in studying oxidative stress and related cellular processes across various scientific and medical fields.

Upstream product

• 807306-71-4 3,7-bis(dimethylamine)phenothiazonium 
• 60-29-7 diethyl ether 
• 7732-18-5 water 
• 1990-18-7 tetrakis-(4-dimethylamino-phenyl)-hydrazine 
• 7647-01-0 hydrogenchloride 
• 13916-80-8 Bis-<4-dimethylamino-phenyl>-nitrosamin 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 20491-92-3 2,4,6-trimethoxyphenol 
• 2316-27-0 C₁₆H₂₂N₃ 
• 109-72-8 n-butyllithium 
• 100-23-2 N,N-Dimethyl-4-nitroaniline 
• 861572-35-2 bis-(4-dimethylamino-phenyl)-trityl-amine 
• 4486-05-9 Bindschedler's Green 

Downstream Products

• 2877-78-3 [1,4]benzoquinone-(4-dimethylamino-phenylimine)-methylimine 
• 55087-74-6 4,4’-bis(dimethylamino)triphenylamine 
• 13916-80-8 Bis-<4-dimethylamino-phenyl>-nitrosamin 
• 2150-58-5 phenol blue 
• 4486-05-9 Bindschedler's Green 
• 1990-18-7 tetrakis-(4-dimethylamino-phenyl)-hydrazine 
• 67697-66-9 3-(1-ethyl-2-methyl-3-indolyl)-3-[N-(4-dimethylaminophenyl)-N-(4-dimethylamino)phenylamino]phthalide 
• 937042-88-1 N-(2,6-diisopropylphenyl)-9-di(p-dimethylaminophenyl)aminoperylene-3,4-dicarboximide 
• 2316-27-0 C₁₆H₂₂N₃ 
• 1135975-57-3 N-(2,6-diisopropylphenyl)-1,6-di(pyridine-4-thio)-9-di(p-dimethylaminophenyl)-aminoperylene-3,4-dicarboximide 
• 1135975-55-1 N-(2,6-diisopropylphenyl)-1,6-diphenylthio-9-di(p-dimethylaminophenyl)-aminoperylene-3,4-dicarboximide 
• 78496-45-4 7-[4-(diethylamino)phenyl]-7-bis[4-(dimethylamino)phenyl]amino furo[3,4-b]pyrazine-5(7H)-one 
• 55586-94-2 3-[4-(diethylamino)-2-methylbenzoyl]-2-pyridinecarboxylic acid 
• 78496-05-6 7-[4-(diethylamino)-2-methylphenyl]-7-{bis[4-(dimethylamino)phenyl]amino}furo[3,4-b]pyridine-5(7H)-one 

Relevant academic research and scientific papers

Incorporation of ring nitrogens into diphenylamine antioxidants: Striking a balance between reactivity and stability

The incorporation of nitrogen atoms into the aryl rings of conventional diphenylamine antioxidants enables the preparation of readily accessible, air-stable analogues, several of which have temperature-independent radical-trapping activities up to 200-fold greater than those of typical commercial diphenylamines. Amazingly, the nitrogen atoms raise the oxidation potentials of the amines without greatly changing their radical-trapping (H-atom transfer) reactivity.

SUBSTITUTED DIARYLAMINES AND USE OF SAME AS ANTIOXIDANTS

The present invention relates to substituted heteroaromatic dianlamine compounds of Formula I and II, their pharmaceutically acceptable salts, and compositions thereof useful as antioxidants, wherein each of X, Y and Z are independently a carbon or nitrogen atom; R1 and R2 are each independently a hydrogen or an electron donating group, but are not both hydrogen, and wherein R1 and R2 are each bonded to a carbon atom in their own respective aryl ring.

Preparation of diarylamines by the addition of 4-(N,N-dimethylamino)phenyllithium to nitroarenes

The addition of 4-(N,N-dimethylamino)phenyllithium to nitroarenes in THF (-78°C) affords the corresponding diarylamines in one-pot and the reaction appears to be general in scope. A 'nitroso'-based mechanism is proposed for this novel nitroreductive N-arylation reaction.

Diphenylamino and indolyl substituted pyromellitides

This invention relates to 3,7-bis(disubstituted aminophenyl- or indolyl)-3,7-bis(diphenylamino)pyromellitides, 3,5-bis(disubstituted aminophenyl- or indolyl)-3,5-bis(diphenylamino)pyromellitides and mixtures thereof useful as color formers, particularly in carbonless duplicating and thermal marking systems, which are prepared by the interaction of 2,5-bis(disubstituted aminophenyl- or indolyl)carbonyl-1,4-benzenedicarboxylic acids or 2,4-bis(disubstituted aminophenyl- or indolyl)carbonyl-1,5-benzenedicarboxylic acids and mixtures thereof with diphenylamines.