83695
氯化罗丹明 110
suitable for fluorescence, BioReagent, ≥99.0% (UV)
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经验公式（希尔记法）:
C20H14N2O3 · HCl
化学文摘社编号:
分子量:
366.80
UNSPSC Code:
12171500
NACRES:
NA.32
PubChem Substance ID:
EC Number:
236-944-7
Beilstein/REAXYS Number:
4631860
MDL number:
产品名称
氯化罗丹明 110, suitable for fluorescence, BioReagent, ≥99.0% (UV)
InChI key
JNGRENQDBKMCCR-UHFFFAOYSA-N
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
SMILES string
Cl.Nc1ccc2c(OC3=CC(=N)C=CC3=C2c4ccccc4C(O)=O)c1
product line
BioReagent
assay
≥99.0% (UV)
form
crystals
mp
>300 °C (lit.)
solubility
ethanol: soluble
methanol: soluble
fluorescence
λex 498 nm; λem 520 nm in methanol
suitability
suitable for fluorescence
Quality Level
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Application
罗丹明110被用于测定具有准确的动力学参数的蛋白酶活性。它被用于测量诱导细胞凋亡的半胱天冬酶活性。
General description
罗丹明110或R110是一种三苯甲烷染料，可发射出强烈的绿色荧光。能发出高强度荧光是由于存在作为给电子基团的氨基。罗丹明110的最大激发光谱和发射光谱分别为502.4/521.6521.6 nm。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Xian Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(8), 1667-1672 (2003-05-09)
A simple and sensitive fluorescence quenching method for the determination of trace nitrite has been developed. The method is based on the reaction of Rhodamine 110 with nitrite in acidic medium to form a new compound, which has much lower
P-O Gendron et al.
Journal of fluorescence, 18(6), 1093-1101 (2008-04-24)
Rhodamine derivatives are popular, photostable fluorophores that are used in a number of fluorescent based techniques, including fluorescence correlation spectroscopy (FCS). Indeed, in FCS, both rhodamine 6G (R6G) and rhodamine 110 (R110) are used as calibration standards to determine the
Melissa M Yatzeck et al.
Bioorganic & medicinal chemistry letters, 18(22), 5864-5866 (2008-07-04)
A derivative of rhodamine 110 has been designed and assessed as a probe for cytochrome P450 activity. This probe is the first to utilize a 'trimethyl lock' that is triggered by cleavage of an ether bond. In vitro, fluorescence was
Aya Shibata et al.
Bioorganic & medicinal chemistry letters, 18(7), 2246-2249 (2008-03-25)
We have developed a new fluorescent probe for biological thiol. The probe was synthesized by the modification of the 2,4-dinitrobenzenesulfonyl group with rhodamine 110. The selective detection of thiol species such as cysteine or glutathione was achieved in biological conditions.
Sambashiva Banala et al.
ACS chemical biology, 7(2), 289-293 (2011-10-27)
A caged rhodamine 110 derivative for the specific labeling of SNAP-tag fusion proteins is introduced. The caged rhodamine 110 derivative permits the labeling of cell surface proteins in living cells and of intracellular proteins in fixed cells. The probe requires
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