所有图片(1)
About This Item
经验公式（希尔记法）:
C28H18N3NaO6S2
CAS号:
分子量:
579.58
颜色索引号:
50085
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47
推荐产品
产品名称
Azocarmine G,
表单
powder
质量水平
颜色
dark red
溶解性
water: 1 mg/mL, clear, red
ε (消光系数)
210-255 at 510-523 nm in water
应用
diagnostic assay manufacturing
hematology
histology
储存温度
room temp
SMILES字符串
[Na+].[O-]S(=O)(=O)c1ccc(Nc2cc3[n+](-c4ccccc4)c5ccccc5nc3c6ccc(cc26)S([O-])(=O)=O)cc1
InChI
1S/C28H19N3O6S2.Na/c32-38(33,34)20-12-10-18(11-13-20)29-25-17-27-28(22-15-14-21(16-23(22)25)39(35,36)37)30-24-8-4-5-9-26(24)31(27)19-6-2-1-3-7-19;/h1-17H,(H2,32,33,34,35,36,37);/q;+1/p-1
InChI key
LUERODMRBLNCFK-UHFFFAOYSA-M
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一般描述
Azocarmine G is a synthetic dye, commonly used in food and beverages to restore their original appearance, in situations where, the color is affected by processing, storage, packaging and distribution.
Azocarmine G is useful for protein determination in acidic medium. It is indicated by the formation of purple-red complex.
Standard stain for microscopy. Azocarmine G may be used as a reference standard for the determination of the analyte in food and beverages using high-performance liquid chromatography coupled with diode-array detector (HPLC-DAD).
应用
Azocarmine G is a standard stain for microscopy.
It may be also be used as a reference standard in the determination of azocarmine G in food products and beverages using high performance liquid chromatography coupled with diode array detector (HPLC-DAD).
It may be also be used as a reference standard in the determination of azocarmine G in food products and beverages using high performance liquid chromatography coupled with diode array detector (HPLC-DAD).
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Investigation on the determination of proteins by spectrophotometry with azocarmine G.
Wang L L, et al.
Journal of Yunnan University(Natural Sciences Edition), 30(1), 83-83 (2008)
T Takamatsu et al.
Histochemistry, 66(2), 169-180 (1980-01-01)
In Feulgen nuclear staining nonspecific dye-binding due to the "pseudo-plasmal reaction" is intensified in isolated cells with intact cytoplasm, and cannot be eliminated by the post-irradiation method. Fluorescence intensity in the cytoplasm sometimes exceeds that of specific nuclear fluorescence, especially
T Murakami et al.
Archives of histology and cytology, 60(3), 265-274 (1997-08-01)
Sections from the human somatosensory cortex were observed with a light microscope. The neurons were classified into light and dark ones. The light neurons were slightly stained with thionin, luxol fast blue MBS and azocarmine G (80% of all neurons).
T Takamatsu et al.
Histochemistry, 71(2), 161-170 (1981-01-01)
A technique for isolation of cells from paraffin embedded tissue is indispensable for the performance of Feulgen-DNA cytofluorometry in parallel with the definition of histological characteristics. Background fluorescence due to nonspecific dye-binding by a "pseudo-plasmal reaction" is usually found to
M I Benigno et al.
Journal of oral rehabilitation, 28(2), 113-119 (2001-04-12)
The bilaminar zone (BZ) in the human temporomandibular joint (TMJ) of toothed adults (GI) and toothless, elderly humans (GII) were analysed using light and scanning electron microscopy (SEM). In both groups the BZ consists of an upper and a lower
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