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Merck
CN

22680

Sigma-Aldrich

喹啉黄

for microscopy (Hist.), mixture of mono- and disulfonic acid sodium salt

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别名:
酸性黄 3
CAS号:
颜色索引号:
47005
UNSPSC代码:
12171500
NACRES:
NA.47

等级

for microscopy (Hist.)

质量水平

形式

powder

溶解性

H2O: 0.1 g/10 mL

εmax

≥350 at 283-293 nm in water
≥450 at 407-417 nm in water

应用

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

InChI

1S/C18H11NO8S2.2Na/c20-17-11-3-1-2-4-12(11)18(21)15(17)13-6-5-9-7-10(28(22,23)24)8-14(16(9)19-13)29(25,26)27;;/h1-8,15H,(H,22,23,24)(H,25,26,27);;/q;2*+1/p-2

InChI key

FZUOVNMHEAPVBW-UHFFFAOYSA-L

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Iatrogenic xanthoderma.
Nancy V Bruckner
Journal of the American Academy of Dermatology, 58(5), 895-896 (2008-04-22)
A L Goldberg
Journal - Association of Official Analytical Chemists, 68(3), 477-479 (1985-05-01)
A sensitive, reproducible method that uses an Extrelut QE column and liquid chromatography (LC) in the reverse phase mode is described for the determination of 2-(2-quinolinyl)-1H-indene-1,3-[2H]-dione and other organic-soluble matter found in D&C Yellow No. 10. With this method the
Sensitization potentials of D & C Yellow No. 10 and D & C Yellow No. 11 dyes.
J E Weaver
Journal of the American Academy of Dermatology, 9(4), 605-606 (1983-10-01)
Adrian Weisz et al.
Journal of mass spectrometry : JMS, 37(10), 1025-1033 (2002-10-11)
Several positional isomers of 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione mono- and disulfonic acids prepared as reference materials for development of analytical methods involved in FDA certification of D&C Yellow No. 10 (Quinoline Yellow) were found consistently to show [MH + 14](+) ions when their
A Weisz et al.
Journal of mass spectrometry : JMS, 31(6), 676-680 (1996-06-01)
The isomeric 2-, 3-, 5-, 6- and 8-quinolinylphthalimides give rise to different electron impact ionization mass spectra, which permit easy distinction. The specific fragmentation process are rationalized in terms of proximity effects and stabilization of cyclic ion structures. Collision-induced dissociation

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