| Identification | More | [Name]
4-Diazodiphenylamine sulfate | [CAS]
4477-28-5 | [Synonyms]
1,4-DIAZODIPHENYLAMINE HYDROGEN SULFATE
4-AMINO-DIPHENYLAMINE, DIAZONIUM SALT
4-AMINODIPHENYLAMINE DIAZONIUM SULFATE
4-DIAZODIPHENYLAMINE SULFATE
4-(N-PHENYLAMINO)BENZENEDIAZONIUM HYDROGENSULFATE
4-(PHENYLAMINO)BENZENEDIAZONIUM SULFATE
AZOIC DIAZO NO 22
CI 37240
DIAZO S
DIPHENYLAMINE-4-DIAZONIUM SULFATE
FAST BLUE SALT R
P-AMINODIPHENYLAMINE DIAZONIUM SULFATE
P-(PHENYLAMINO)BENZENEDIAZONIUM SULFATE
VARIAMINE BLUE RT SALT
4-(phenylamino)-benzenediazoniusulfate(1:1)
AcnaBlueRTSalt
BluebaseRT
BlueSaltNR
C.I.AzoicDiazoComponent22(37240)
DaitoBlueSaltVR | [EINECS(EC#)]
224-756-8 | [Molecular Formula]
C24H22N8O4S | [MDL Number]
MFCD00011895 | [Molecular Weight]
518.55 | [MOL File]
4477-28-5.mol |
| Chemical Properties | Back Directory | [Boiling point ]
623.17℃[at 101 325 Pa] | [density ]
1.512[at 20℃] | [vapor pressure ]
0Pa at 25℃ | [solubility ]
1 M HCl: 10 mg/mL | [Colour Index ]
37240 | [form ]
solid | [Water Solubility ]
21.24g/L at 20℃ | [Major Application]
diagnostic assay manufacturing
hematology
histology | [InChI]
1S/C12H10N3.H2O4S/c13-15-12-8-6-11(7-9-12)14-10-4-2-1-3-5-10;1-5(2,3)4/h1-9,14H;(H2,1,2,3,4)/q+1;/p-1 | [InChIKey]
FMRQRWPEQSPSDG-UHFFFAOYSA-M | [SMILES]
OS([O-])(=O)=O.N#[N+]c1ccc(Nc2ccccc2)cc1 | [LogP]
1.28 at 23℃ | [CAS DataBase Reference]
4477-28-5(CAS DataBase Reference) | [EPA Substance Registry System]
4477-28-5(EPA Substance) |
| Safety Data | Back Directory | [WGK Germany ]
3
| [TSCA ]
TSCA listed | [HS Code ]
2927.00.5000 | [REACH Registrations]
Active | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Aquatic Acute 1
Eye Dam. 1
Muta. 2
Skin Irrit. 2 |
| Hazard Information | Back Directory | [Uses]
4-Aminodiphenylamine sulfate (Variamine Blue RT sulfate) is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells. | [Flammability and Explosibility]
Notclassified | [Purification Methods]
Dissolve 10g of the dye in 100mL of hot water. Sodium dithionite (0.4g) is then added, followed by active carbon (1.5g) and is filtered hot. To the colourless or slightly yellow filtrate a solution of saturated NaCl is added, and the mixture is cooled. The needles are filtered off, washed with cold water, dried at room temperature, and stored in a dark bottle (light sensitive). [Anderson & Steedly J Am Chem Soc 76 5144 1954, Erdey Chem Analyst 48 106 1959, Beilstein 16 H 602, 16 I 371, 16 II 307, 16 III 575. ] | [References]
[1] Sultana M, et al. A review on experimental chemically modified activated carbon to enhance dye and heavy metals adsorption[J]. Cleaner engineering and technology, 2022, 6: 100382. |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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Maya High Purity Chemicals
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