S2380
苏丹黑 B
practical grade
别名:
Ceres黑色 BN, 溶剂黑 3, 脂肪黑 HB
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关于此项目
经验公式（希尔记法）:
C29H24N6
化学文摘社编号:
分子量:
456.54
UNSPSC Code:
12171500
EC Number:
224-087-1
Beilstein/REAXYS Number:
723248
MDL number:
SMILES string
CC1(C)Nc2cccc3c(ccc(N1)c23)\N=N\c4ccc(\N=N\c5ccccc5)c6ccccc46
InChI
1S/C29H24N6/c1-29(2)30-26-14-8-13-22-25(17-18-27(31-29)28(22)26)35-34-24-16-15-23(20-11-6-7-12-21(20)24)33-32-19-9-4-3-5-10-19/h3-18,30-31H,1-2H3/b33-32+,35-34+
InChI key
YCUVUDODLRLVIC-VPHDGDOJSA-N
grade
practical grade
mp
120-124 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Muta. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Neutrophil dysplasia demonstrated on Sudan black B staining.
Barbara J Bain
American journal of hematology, 85(9), 707-707 (2010-07-28)
Israd H Jaafar et al.
Acta biomaterialia, 7(4), 1588-1598 (2010-12-15)
Immunofluorescence imaging on polymeric biomaterials is often inhibited by autofluorescence and other optical phenomena. This often limits the analysis that can be performed on cells that are in contact with these materials. This study outlines a method that will quench
Toshiko Ozawa et al.
Dental materials journal, 28(3), 290-294 (2009-08-11)
This study compared the effectiveness of three obturation techniques for oval-shaped canals. Roots of 42 extracted teeth with oval canals were randomly divided into three groups: (1) ProTaper canal preparation and single cone obturation with matching gutta-percha point; (2) ProTaper
V C Oliveira et al.
Histology and histopathology, 25(8), 1017-1024 (2010-06-17)
Interference by autofluorescence is one of the major concerns of immunofluorescence analysis of in situ hybridization-based diagnostic assays. We present a useful technique that reduces autofluorescent background without affecting the tissue integrity or direct immunofluorescence signals in brain sections. Using
Yan Sun et al.
Archives of pathology & laboratory medicine, 135(10), 1335-1342 (2011-10-06)
Renal tissue emits intense autofluorescence, making it difficult to differentiate specific immunofluorescence signals and thus limiting its application to clinical biopsy material. To identify and minimize autofluorescence of renal tissue and demonstrate a simple, efficient method to reduce autofluorescence using
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