F1631
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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所有图片(1)
About This Item
线性分子式:
C15H14N3O2 · 0.5 ZnCl4
CAS号:
分子量:
371.89
颜色索引号:
37165
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
组成
Dye content, ≥97%
储存温度
2-8°C
SMILES字符串
[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 key
KIWIFIXMWIMRBZ-UHFFFAOYSA-L
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一般描述
Fast Violet B Salt is a diazonium salt. It is mainly required for cytochemical staining methods, for instance, alkaline phosphatase in leukocytes.
应用
Fast Violet B Salt has been used:
- for alkaline phosphatase staining in cells
- for hexosaminidase staining in cells
- to study lysosomal membrane stability
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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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