432202
氯化罗丹明 110
Dye content ≥75 %
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关于此项目
经验公式（希尔记法）:
C20H14N2O3 · HCl
化学文摘社编号:
分子量:
366.80
Beilstein:
4631860
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47
表单
powder or crystals
质量水平
组成
Dye content, ≥75%
mp
>300 °C (lit.)
λmax
496 nm
应用
diagnostic assay manufacturing
hematology
histology
储存温度
room temp
SMILES字符串
Cl.Nc1ccc2c(OC3=CC(=N)C=CC3=C2c4ccccc4C(O)=O)c1
InChI
1S/C20H14N2O3.ClH/c21-11-5-7-15-17(9-11)25-18-10-12(22)6-8-16(18)19(15)13-3-1-2-4-14(13)20(23)24;/h1-10,21H,22H2,(H,23,24);1H
InChI key
JNGRENQDBKMCCR-UHFFFAOYSA-N
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一般描述
罗丹明110氯化物（R110）是一种激光级染料。
应用
罗丹明110氯化物已被用于合成罗丹明110十八烷基酯（R110C18）。
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)
Yan Liang et al.
Journal of the American Chemical Society, 132(18), 6306-6308 (2010-04-20)
Access to native protein structure depends on precise polypeptide folding and assembly pathways. Identifying folding missteps that may lead to the nearly 40 protein misfolding diseases could feature prominently in the development of intervention strategies. Accordingly, we have investigated the
Marisa Ninivaggi et al.
Clinical chemistry, 58(8), 1252-1259 (2012-06-06)
The calibrated automated thrombogram (CAT) assay in plasma is a versatile tool to investigate patients with hypo- or hypercoagulable phenotypes. The objective was to make this method applicable for whole blood measurements. Thin-layer technology and the use of a rhodamine
Ke Liu et al.
Analytica chimica acta, 651(1), 85-90 (2009-09-08)
The ability to quickly measure flow parameters in microfluidic devices is critical for micro total analysis system (microTAS) applications. Macrofluidic methods to assess flow suffer from limitations that have made conventional methods unsuitable for the flow behavior profiling. Single molecule
Ana Virel et al.
Analytical chemistry, 84(5), 2380-2387 (2012-02-14)
By site directed mutagenesis, we have produced recombinant mutants of human and mouse prethrombin-2 which are able to convert themselves autocatalytically into α-thrombin. We also have created a new method to amplify the signal of bioanalytical assays based on the
Tatyana G Terentyeva et al.
Bioconjugate chemistry, 22(10), 1932-1938 (2011-09-13)
Commonly used fluorogenic substrate analogues for the detection of protease activity contain two enzyme-cleavable bonds conjugated to the fluorophore. Enzymatic cleavage follows a two-step reaction with a monoamide intermediate. This intermediate shows fluorescence at the same wavelength as the final
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