4486-05-9

Basic information

• Product Name: BINDSCHEDLER'S GREEN
• Synonyms: 4,4'-BIS(DIMETHYLAMINO) DIPHENYLAMINE;[4-[[4-(dimethylamino)phenyl]imino]cyclohexa-2,5-dien-1-ylidene]dimethylammonium chloride;[4-(4-dimethylaminophenyl)iminocyclohexa-2,5-dien-1-ylidene]-dimethylazanium chloride;[4-(4-dimethylaminophenyl)iminocyclohexa-2,5-dien-1-ylidene]-dimethyl-azanium chloride;BINDSCHEDLERS GREEN, INDICATOR GRADE;N1-(4-(Dimethylamino)phenyl)-N4,N4-dimethylbenzene-1,4-diamine;BINDSCHEDLER GREEN;BINDSCHEDLER'S GREEN
• CAS NO: 4486-05-9
• Molecular Formula: C₁₆H₂₀N₃*Cl
• Molecular Weight: 289.8
• EINECS: 224-773-0
• Mol File: 4486-05-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BINDSCHEDLER'S GREEN(CAS DataBase Reference)
• NIST Chemistry Reference: BINDSCHEDLER'S GREEN(4486-05-9)
• EPA Substance Registry System: BINDSCHEDLER'S GREEN(4486-05-9)

Safety Data

• Hazardous Substances Data: 4486-05-9(Hazardous Substances Data)

Usage

General Description

BINDSCHEDLER'S GREEN is a chemical compound commonly used in histology and microbiology to stain fungal cell walls. It is a mixture of aniline blue and fluorescent brighteners, and it emits a green fluorescence when exposed to ultraviolet light. BINDSCHEDLER'S GREEN is used to differentiate between fungal and plant cell walls, making it an essential tool in research and diagnostics. Its ability to selectively bind to fungal cell walls makes it an important tool in the study of plant-fungus interactions and fungal diseases. Overall, BINDSCHEDLER'S GREEN plays a crucial role in the identification and study of fungal structures and is an important tool in the field of biology and medicine.

InChI:InChI=1/C16H20N3/c1-18(2)15-9-5-13(6-10-15)17-14-7-11-16(12-8-14)19(3)4/h5-12H,1-4H3/q+1

Upstream product

• 637-31-0 4,4'-bis(dimethylamino)diphenylamine 
• 76-83-5 trityl chloride 
• 615-93-0 2,5-Dichloro-1,4-benzoquinone 
• 527-17-3 Duroquinone 
• 697-91-6 2,6-dichloro-1,4-benzoquinone 
• 84-58-2 2,3-dicyano-5,6-dichloro-p-benzoquinone 
• 64-17-5 ethanol 
• 71-43-2 benzene 
• 106-51-4 p-benzoquinone 
• 118-75-2 chloranil 
• 1990-18-7 tetrakis-(4-dimethylamino-phenyl)-hydrazine 
• 121-69-7 N,N-dimethyl-aniline 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 32047-95-3 N,N-bis-(4-dimethylamino-phenyl)-acetamide 

Downstream Products

• 366-29-0 N,N,N',N'-tetramethylbenzidine 
• 106-51-4 p-benzoquinone 
• 637-31-0 4,4'-bis(dimethylamino)diphenylamine 

Relevant articles and documents

Reactions of Leuco Bindschedler's Green with Some p-Benzoquinones in Acetone

The rate of reaction between Leuco Bindschedler's Green (BGH) and some p-benzoquinone derivatives (Q's) in acetone was followed spectrophotometrically by means of the stopped-flow technique.The reaction was found to proceed reversibly.The rate data and the activation parameters for the forward and backward reactions were estimated.The rates were susceptible to the oxidation-reduction potentials of the Q's.The absorption spectra observed at low temperatures indicated that three kinds of intermediates were involved.Radicals formed during the reaction were detected by the ESR method.The results have been discussed in relation to those previously obtained for systems involving Leuco Crystal Violet (LCV) and Leuco Malachite Green (LMG).