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83695

Sigma-Aldrich

Rhodamine 110 chloride

suitable for fluorescence, BioReagent, ≥99.0% (UV)

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About This Item

Empirical Formula (Hill Notation):
C20H14N2O3 · HCl
CAS Number:
13558-31-1
Molecular Weight:
366.80
Beilstein:
4631860
EC Number:
236-944-7
MDL number:
MFCD00042009
UNSPSC Code:
12171500
PubChem Substance ID:
57652964
NACRES:
NA.32

product line

BioReagent

Quality Level

200

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

SMILES string

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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General description

Rhodamine 110 or R110 is a triphenylmethane dye and emits a strong green-fluorescent light. The high fluorescence is attributed to the presence of amino groups as electron donating groups. Rhodamine 110 has excitation and emission maximum at 502.4/521.6 nm, respectively.

Application

Rhodamine 110 is used for the determination of protease activity with accurate kinetic parameters. It is used to measure caspase activity in cells with induced apoptosis.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Samantha Forster et al.
PloS one, 7(3), e33253-e33253 (2012-04-04)
Fluorescent tracer dyes represent an important class of sub-cellular probes and allow the examination of cellular processes in real-time with minimal impact upon these processes. Such tracer dyes are becoming increasingly used for the examination of membrane transport processes, as
Simeonika Rangełowa-Jankowska et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(13), 2449-2452 (2011-07-14)
The first observation of strong directional surface-plasmon-coupled emission (SPCE) of Rhodamine 110 in silica nanofilms deposited on silver nanolayers is reported. The preparation of the material is described in detail. The intensity of SPCE exceeds 10 times that of free
Soichiro Ijiri et al.
Electrophoresis, 32(24), 3499-3509 (2011-12-20)
We describe a highly sensitive CE with laser-induced fluorescence (LIF) detection for the analysis of N-linked oligosaccharides in glycoproteins using rhodamine 110 as a fluorescence derivatization reagent. One CE separation is performed using a fused-silica capillary and neutral pH buffer
Stanislav Kalinin et al.
The Review of scientific instruments, 83(9), 096105-096105 (2012-10-02)
We present a fast hardware photon correlator implemented in a field-programmable gate array (FPGA) combined with a compact confocal fluorescence setup. The correlator has two independent units with a time resolution of 4 ns while utilizing less than 15% of
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