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ChemicalBook--->CAS DataBase List--->1052-38-6

1052-38-6

1052-38-6 Structure

1052-38-6 Structure
IdentificationBack Directory
[Name]

BISMARCK BROWN Y
[CAS]

1052-38-6
[Synonyms]

VESUVIN
VESUVINE
CI 21000
C.I.20000
VESUVINE G
BASIC BROWN
CI NO 21000
BASIC BROWN G
LEATHER BROWN
BASIC BROWN GX
BISMARCK BROWN
BASIC BROWN GXP
EXCELSIOR BROWN
PHENYLENE BROWN
BISMARK BROWN Y
BISMARCK BROWN G
BISMARCK BROWN B
BISMARCK BROWN Y
MANCHESTER BROWN
BASIC BROWN NO 1
Solvent Brown 41
Bismark Brown G/Y
BISMARCK BROWN Y (G)
C.I.Solvent Brown 41
BASIC BROWN G, GX, GXP
Bismark Brown G Base
WCXNNRRUHXJZDQ-LNJOAEQUSA-N
C.I.Basic Brown 1:C.I.21000
Phenylene Brown(C.I. 21000:1)
C.I.Solvent Brown 41:C.I.21000:1
Bismarck brown G base (C.I. 21000:1)
4,6-Bis[(4-aminophenyl)azo]benzene-1,3-diamine
BISMARK BROWN R FOR MICROSCOPY (C.I. No 21010)
4,4’-(1,3-phenylenebis(azo))bis-3-benzenediamine
4,4’-[1,3-phenylenebis(azo)]bis-3-benzenediamine
1,3-Benzenediamine, 4,4-1,3-phenylenebis(azo)bis-
4,4'-(m-Phenylenebisazo)bis(1,3-phenylenediamine)
4,4'-[1,3-phenylenebis(azo)]bisbenzene-1,3-diamine
3-Benzenediamine,4,4’-[1,3-phenylenebis(azo)]bis-1
4,4’-(1,3-phenylenebis(azo))bis(1,3-benzenediamine)
4,4'-(M-PHENYLENEBISAZO)BIS-M-PHENYLENEDIAMINE DIHYDROCHLORIDE
1,3-Benzenediamine, 4,4'-[1,3-phenylenebis(2,1-d iazenediyl)]bis-
[EINECS(EC#)]

213-888-1
[Molecular Formula]

C18H20Cl2N8
[MDL Number]

MFCD00012977
[MOL File]

1052-38-6.mol
[Molecular Weight]

419.31
Chemical PropertiesBack Directory
[Melting point ]

222 C (dec.)
[Boiling point ]

696.4±55.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[vapor pressure ]

0Pa at 25℃
[pka]

3.34±0.10(Predicted)
[Water Solubility ]

18μg/L at 20℃
[EPA Substance Registry System]

1,3-Benzenediamine, 4,4'-[1,3-phenylenebis(azo)]bis- (1052-38-6)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

22-24/25-36-26
[WGK Germany ]

3
Hazard InformationBack Directory
[Definition]

ChEBI: A bis(azo) compound that is 1,1'-(1,3-phenylene)bis(diazene) in which both azene hydrogens are replaced by 2,4-diaminophenyl groups. A metachromatic dye which stains acid mucins yellow. It is also a constituent of Papanicolaou's EA solutions, used for cerv cal, and other smears. Its dihydrochloride salt is also a biological dye known as Bismark brown Y.
[Preparation]

2 Moore’s Nitrous acid?treatment 3 Moore’s Benzene-1,3-diamine dihydrochloride (this product may be based on the double azo dyes as the main component of the mixture, and commodity dye is usually composed of dihydrochloride composition), and made free base.
[Flammability and Explosibility]

Nonflammable
[Properties and Applications]

yellow brown. Soluble in ethanol, acetone and benzene. In concentrated sulfuric acid for brown, dilution after red brown; In concentrated nitric acid for orange solution, to yellow. Dye aqueous solution to join hydrochloric acid don’t change color; Add 10% sodium hydroxide solution have orange precipitation.
Spectrum DetailBack Directory
[Spectrum Detail]

BISMARCK BROWN Y(1052-38-6)MS
BISMARCK BROWN Y(1052-38-6)IR1
BISMARCK BROWN Y(1052-38-6)IR2
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