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Merck
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F1631

Sigma-Aldrich

Fast Violet B Salt

Dye content ≥97 %

别名:

4-Amino-5-methoxy-2-methylbenzanilide diazotated zinc double salt, 4-Benzoylamino-2-methoxy-5-methylbenzenediazonium chloride hemi(zinc chloride) salt, Azoic Diazo No. 41

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About This Item

线性分子式:
C15H14N3O2 · 0.5 ZnCl4
CAS号:
14726-28-4
分子量:
371.89
顏色索引編號:
37165
EC號碼:
238-775-4
MDL號碼:
MFCD00083330
分類程式碼代碼:
12171500
PubChem物質ID:
24894789

成份

Dye content, ≥97%

儲存溫度

2-8°C

SMILES 字串

[Cl-].[Cl-].Cl[Zn]Cl.COc1cc(NC(=O)c2ccccc2)c(C)cc1[N+]#N.COc3cc(NC(=O)c4ccccc4)c(C)cc3[N+]#N

InChI

1S/2C15H13N3O2.4ClH.Zn/c2*1-10-8-13(18-16)14(20-2)9-12(10)17-15(19)11-6-4-3-5-7-11;;;;;/h2*3-9H,1-2H3;4*1H;/q;;;;;;+2/p-2

InChI 密鑰

KIWIFIXMWIMRBZ-UHFFFAOYSA-L

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一般說明

Fast Violet B Salt is a diazonium salt. It is mainly required for cytochemical staining methods, for instance, alkaline phosphatase in leukocytes.

應用

Fast Violet B Salt has been used:
  • for alkaline phosphatase staining in cells
  • for hexosaminidase staining in cells
  • to study lysosomal membrane stability

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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Turgeon ML
Clinical Hematology: Theory and Procedures (2005)
Integrated coastal monitoring of a gas processing plant using native and caged mussels.
Brooks S
The Science of the Total Environment, 426, 375-375 (2012)
Beta-glucuronidase and hexosaminidase are marker enzymes for different compartments of the endo-lysosomal system in mussel digestive cells.
Izagirre U
Cell and Tissue Research, 335, 441-441 (2009)
W Cockburn et al.
Analytical biochemistry, 189(1), 95-98 (1990-08-15)
A sensitive, quantitative assay for phosphenolpyruvate carboxylase which utilizes microtiter plates is described. The assay depends upon the production of a colored compound in the reaction between oxaloacetate, the product of the phosphoenolpyruvate reaction, and the dye Fast Violet B.
Jean Rivoal et al.
Analytical biochemistry, 300(1), 94-99 (2001-12-18)
We describe a method for the detection of isoforms of several glycolytic enzymes by activity staining after native PAGE. The staining is based on coupled enzyme assays carried out on the gel after electrophoresis and is linked to the disappearance
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