Welcome to LookChem.com Sign In|Join Free
  • or
Rhodamine 110 is a green fluorescent cationic dye characterized by its red to bordeaux crystals or crystalline powder appearance. It has excitation and emission maxima of 496 and 520 nm, respectively. When combined with a hydrolytic substrate, such as proteinase or peptidase substrates, it serves as a highly sensitive detection reagent in fluorescence-based enzyme assays. Additionally, Rhodamine 110 has been utilized in a fluorescence quenching method for determining trace nitrite and as a probe for cytochrome P450 activity.

13558-31-1

Post Buying Request

13558-31-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13558-31-1 Usage

Uses

Used in Biotechnology and Pharmaceutical Industry:
Rhodamine 110 is used as a fluorescent dye for flow cytometric measurements, specifically as APand exopeptidase substrates. This application allows for the sensitive detection and analysis of various biological processes and interactions.
Used in Analytical Chemistry:
Rhodamine 110 is employed in a fluorescence quenching method for determining trace nitrite levels. This method is valuable for environmental monitoring and assessing the presence of nitrite contaminants in various samples.
Used in Enzyme Assays:
As a highly sensitive detection reagent, Rhodamine 110 is used in fluorescence-based enzyme assays, particularly when incorporated with hydrolytic substrates like proteinase or peptidase substrates. This application aids in the study of enzyme activity and function.
Used in Cytochrome P450 Activity Studies:
Rhodamine 110 serves as a probe for cytochrome P450 activity, a crucial enzyme family involved in the metabolism of drugs and other substances. This application helps researchers understand the role of these enzymes in various biological processes and their potential interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 13558-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13558-31:
(7*1)+(6*3)+(5*5)+(4*5)+(3*8)+(2*3)+(1*1)=101
101 % 10 = 1
So 13558-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H14N2O3/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)/p-1/b21-11+

13558-31-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma

  • (83695)  Rhodamine110chloride  BioReagent, suitable for fluorescence, ≥99.0% (UV)

  • 13558-31-1

  • 83695-250MG

  • 878.67CNY

  • Detail

13558-31-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name rhodamine 110

1.2 Other means of identification

Product number -
Other names Rhodamine 110 chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13558-31-1 SDS

13558-31-1Synthetic route

rhodamine B
81-88-9

rhodamine B

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

Conditions
ConditionsYield
With fluorinated BiVO4 In water at 20℃; UV-irradiation;
rhodamine B
81-88-9

rhodamine B

A

N,N,N’-triethylrhodamine

N,N,N’-triethylrhodamine

B

N-ethylrhodamine

N-ethylrhodamine

C

N-ethyl-N'-ethylrhodamine
2768-89-0

N-ethyl-N'-ethylrhodamine

D

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

Conditions
ConditionsYield
With BiOI/Fe MIL-88B In water for 2h; Catalytic behavior; Kinetics; Mechanism; Reagent/catalyst; Time; Wavelength; Irradiation;
pivaloyl chloride
3282-30-2

pivaloyl chloride

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

N,N'-bis-pivaloyl rhodamine

N,N'-bis-pivaloyl rhodamine

Conditions
ConditionsYield
With triethylamine In dichloromethane91%
acetic anhydride
108-24-7

acetic anhydride

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

N,N'-bis-acetyl rhodamine
3086-43-9

N,N'-bis-acetyl rhodamine

Conditions
ConditionsYield
With pyridine89%
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

propionic acid anhydride
123-62-6

propionic acid anhydride

N,N'-bis-propionyl rhodamine

N,N'-bis-propionyl rhodamine

Conditions
ConditionsYield
With pyridine In dichloromethane83%
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

isobutyryl chloride
79-30-1

isobutyryl chloride

N,N'-bis-isobutyl rhodamine

N,N'-bis-isobutyl rhodamine

Conditions
ConditionsYield
With triethylamine In dichloromethane83%
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

trifluoroacetic acid
76-05-1

trifluoroacetic acid

N,N' bis-triflouroacetyl rhodamine

N,N' bis-triflouroacetyl rhodamine

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide for 16h;76%
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

6-aminohexanoic acid
60-32-2

6-aminohexanoic acid

2-(6-(2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)hexanamido) benzenaminium 2,2,2-trifluoroacetate

2-(6-(2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)hexanamido) benzenaminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
8-Aminooctanoic acid
1002-57-9

8-Aminooctanoic acid

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

2-(8-(2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)octanamido) benzenaminium 2,2,2-trifluoroacetate

2-(8-(2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)octanamido) benzenaminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
p-aminomethylbenzoic acid
56-91-7

p-aminomethylbenzoic acid

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

2-(4-((2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)methyl)benzamido) benzenaminium 2,2,2-trifluoroacetate

2-(4-((2-(6-amino-3-iminio-3H-xanthen-9-yl)benzamido)methyl)benzamido) benzenaminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

hydrazine hydrate
7803-57-8

hydrazine hydrate

propionaldehyde
123-38-6

propionaldehyde

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

7-aminoheptanoic acid
929-17-9

7-aminoheptanoic acid

6-amino-9-(2-((7-oxo-7-(2-propylhydrazinyl)heptyl)carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

6-amino-9-(2-((7-oxo-7-(2-propylhydrazinyl)heptyl)carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With sodium cyanoborohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

hydrazine hydrate
7803-57-8

hydrazine hydrate

propionaldehyde
123-38-6

propionaldehyde

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

6-amino-9-(2-((2-oxo-2-((4-(2-propylhydrazine-1-carbonyl)phenyl)amino)ethyl) carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

6-amino-9-(2-((2-oxo-2-((4-(2-propylhydrazine-1-carbonyl)phenyl)amino)ethyl) carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With sodium cyanoborohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
methyl 4-(aminomethyl)benzoate hydrochloride
6232-11-7

methyl 4-(aminomethyl)benzoate hydrochloride

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

hydrazine hydrate
7803-57-8

hydrazine hydrate

propionaldehyde
123-38-6

propionaldehyde

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

6-amino-9-(2-((2-oxo-2-((4-(2-propylhydrazine-1-carbonyl)benzyl)amino)ethyl) carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

6-amino-9-(2-((2-oxo-2-((4-(2-propylhydrazine-1-carbonyl)benzyl)amino)ethyl) carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With sodium cyanoborohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid
p-aminomethylbenzoic acid
56-91-7

p-aminomethylbenzoic acid

rhodamine 110 hydrochloride salt
13558-31-1

rhodamine 110 hydrochloride salt

hydrazine hydrate
7803-57-8

hydrazine hydrate

propionaldehyde
123-38-6

propionaldehyde

N-ethyl-N,N-diisopropylamine
7087-68-5

N-ethyl-N,N-diisopropylamine

6-amino-9-(2-((4-(2-propylhydrazine-1-carbonyl)benzyl)carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

6-amino-9-(2-((4-(2-propylhydrazine-1-carbonyl)benzyl)carbamoyl)phenyl)-3H-xanthen-3-iminium 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With sodium cyanoborohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid

13558-31-1Downstream Products

13558-31-1Relevant academic research and scientific papers

Photocatalysis through Excitation of Adsorbates. 3. Effect of Electron Acceptors on the Efficiency of Interfacial Charge Separation

Takizawa, Takuo,Watanabe, Tadashi,Honda, Kenichi

, p. 51 - 55 (1980)

Charge separation in photoexcited rhodamine B-CdS-electron acceptor systems was investigated photochemically and photoelectrochemically, by using acceptors with different standard reduction potentials (E0red.).The formal quantum efficiency (FQE) of N-deethylation of the dye after photoinduced electron injection into CdS (in photochemical suspension systems) and sensitized photocurrents flowing through a single-crystal CdS membrane separating the dye from an acceptor (in photoelectrochemical systems) were measured as a function of concentration of acceptors.Both FQE and sensitized photocurrents reflect the efficiency of charge separation between the dye and acceptors.Results indicate that charge separation occurs only in the presence of CdS and its efficiency rises as E0red. of the acceptor is more positive.The effectiveness of the present systems for photoinduced charge separation is discussed.

A comparative study on the efficacy of different probes to predict the photo-activity of nano-titanium dioxide toward biomolecules

Marucco,Carella,Fenoglio

, p. 89559 - 89568 (2015)

TiO2 is a reactive material able to cause the degradation of organic molecules following activation by UV light. This reactivity may be useful, e.g. in environmental or medical applications, but undesired when TiO2 is used as a UV filter in cosmetics and composites since it reduces the photo-stability of the material, and represents a possible pathway of injury. Conventional methods to measure the photo-activity of TiO2 include the degradation of small molecules or dyes. However the suitability of these methods to predict the photo-activity of TiO2 in biological systems is uncertain. This is the first product of a study, conducted within the FP7 EU project SETNanoMetro, that has as a main goal the standardizations of protocols to assess the oxidative potential of TiO2 nanopowders in biofluids. Here, the ability of a series of nano-TiO2 powders exhibiting different crystalline phases to degrade rhodamine B, a dye commonly used in photo-catalysis, and two model biomolecules (linoleic acid and 2-deoxyribose) under simulated sunlight was compared. Electron paramagnetic resonance (EPR) spectroscopy associated to different spin-probes or spin-traps was used to elucidate the reactive species involved in the processes. The results show how the photo-efficiency of TiO2 is affected by the kind of probe and by the presence of species that adsorb at the surface of the nanoparticles underlining the need of appropriate standard operating procedures (SOP) to evaluate the oxidative damage potential of semiconducting nanomaterials.

The upconversion and enhanced visible light photocatalytic activity of Er3+-doped tetragonal BiVO4

Yang, Wei,Tan, Guoqiang,Ren, Huijun,Zhang, Lili,Zhao, Chengcheng,Xia, Ao

, p. 7324 - 7329 (2015)

Er3+-doped BiVO4 with tetragonal structure is prepared by the microwave hydrothermal method. X-ray diffraction and Rietveld refinement demonstrate that the structure is transformed from the monoclinic (C2/c:c3) phase to the tetragonal (I41/amd:2) phase by doping with Er3+ ions. Er3+ doping also influences the morphology change of BiVO4 from irregular flake-like crystal to rod-like crystal, which leads to the increase of the surface areas from 3.25 to 11.96 m2 g-1. Compared with the monoclinic BiVO4, the upconversion of the Er3+-doped tetragonal BiVO4 occurs through the transitions from the 4I15/2 ground state to 4F7/2, 2H11/2, and 4F9/2 states, respectively. The photocatalytic experiment indicates that the tetragonal BiVO4 (8 at.%) with a larger specific surface area (9.88 m2 g-1) shows the best photocatalytic activity under visible light irradiation, which can efficiently improve the degradation rate of RhB up to 97.2% at 150 min. This journal is

Hierarchical BiOI nanostructures supported on a metal organic framework as efficient photocatalysts for degradation of organic pollutants in water

Jahurul Islam,Kim, Hyun Kook,Amaranatha Reddy,Kim, Yujin,Ma, Rory,Baek, Heehyun,Kim, Joonghan,Kim, Tae Kyu

, p. 6013 - 6023 (2017)

Semiconductor-based photocatalysis is a green method for the removal of toxic organic pollutants by decomposition into harmless products. However, traditional single-component semiconductors are unable to reach high degradation efficiencies due to excessive photo charge carrier recombination. The use of hybrid nanocomposite photocatalysts is a promising strategy for overcoming this problem by reducing recombination as well as ensuring that large amounts of solar energy are harvested. Herein, a novel visible-light-active hybrid nanocomposite, BiOI/MIL-88B(Fe), was successfully synthesized through a simple precipitation method. In the BiOI/MIL-88B(Fe) composite, both BiOI and MIL-88B(Fe) have improved charge carrier separation and reduced recombination via a simple Z-scheme mechanism. Photocatalytic degradation of the pollutant RhB was carried out during irradiation of the as-synthesized composites with simulated solar light, and the BiOI/MIL-88B(Fe) (2 wt%) composite was found to exhibit the highest photocatalytic activity among the composites. In addition, colorless phenol and ciprofloxacin (CIP) degradation experiments were also performed to confirm the visible light photocatalytic performance of the BiOI/MIL-88B(Fe) hybrid nanocomposite. Scavenger experiments, PL analysis, NBT transformations, and TA-PL experiments all supported the proposed Z-scheme mechanism of the BiOI/MIL-88B(Fe) composite photocatalyst. Moreover, simple separation from solution provides this 3D composite with good reusability and long-term stability.

Visible light photodegradation of rhodamine B over VDF/CTFE copolymer-templated crystalline mesoporous titania

Zi, Guoli,Wang, Yi,Zheng, Kai,Zhao, Huan,Wang, Fuzhi,Zhang, Wenjun,Yan, Zhiying,He, Jiao,Wang, Jiaqiang

, p. 2383 - 2391 (2012)

Mesoporous TiO2 with anatase crystalline structure (MTiO 2/F2319) has been synthesized by using vinylidene fluoride/chlorotrifluoroethylene copolymer (1:9 in mole, F2319) as template. The synthesized mesoporous titania samples were characterized by a combination of various physicochemical techniques, such as X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and N2 adsorption/desorption. It was found that without any external doping, MTiO2/F2319 exhibited significantly higher photocatalytic activities for the degradation of rhodamine B (RhB) dye than P25 TiO2 under visible light irradiation. Furthermore, the UV-Vis absorption maximum of the dye solution exhibited a gradual hypsochromic shift due to de-ethylation and degradation of RhB dye. Springer Science+Business Media B.V. 2012.

Self assembled flower like CdS-ZnO nanocomposite and its photo catalytic activity

Jana,Pal,Chatterjee

, p. 510 - 515 (2014)

Self assembled flower like CdS-ZnO nanocomposite has been synthesized by a facile chemical route and the prepared materials have been investigated as catalyst in the photodegradation of rhodamine B (RhB) in aqueous solution facilitated by the effective charge transfer mechanism in this coupled semiconductor system. CdS has been grown first and then petal-like ZnO has been produced to assemble into a flower like nanostructure. XRD, SEM, TEM, EDX have been employed to study the structural, morphological and compositional details of this unique nanostructure. It is observed that a strong quenching of band-edge emission of CdS following the growth of ZnO petal on it which is evidence for the occurrence of charge transfer between CdS and ZnO. The strong photocatalytic activity of this novel nanostructure on RhB has been investigated in details.

New latent fluorophore for DT diaphorase

Huang, Sheng-Tung,Lin, Yuh-Ling

, p. 265 - 268 (2006)

This study describes the design and synthesis of a novel latent fluorophore 3 for DT diaphorase based on the trimethyl lock effect and characterization of its enzymatic kinetics. Fluorophore 3 is also a sensitive fluorimetric reagent for detecting glucose when coupled with DTD and glucose dehydrogenase.

Fluorescence-Lifetime-Sensitive Probes for Monitoring ATP Cleavage

Hammler, Daniel,Marx, Andreas,Zumbusch, Andreas

, p. 15329 - 15335 (2018)

Adenosine triphosphate (ATP) probes modified with fluorescence dyes that change their fluorescence properties upon cleavage are an interesting tool for monitoring enzymatic ATP turnover. As a readout parameter, fluorescence lifetime is attractive because it is nearly independent of concentration. In our study, we synthesised and investigated fifteen different ATP analogues, in which the fluorophores were attached to the γ-phosphate of ATP. All analogues showed distinctly different fluorescence lifetimes compared to the corresponding values of the free fluorophores. Both increases and decreases in fluorescence lifetime were observed upon attachment to ATP. To shed light on the photophysical processes governing the lifetime changes, we performed photoelectron spectroscopy in air (PESA) to determine HOMO energy levels and time-resolved fluorescence spectroscopy to obtain rate constants. We present evidence that fluorescence quenching in the compounds tested is dynamic and attributed to photoinduced electron transfer (PET), whereas fluorescence lifetime increases are caused by stacking interactions between chromophore and the nucleobase reducing non-radiative relaxation. Finally, we demonstrate that enzymatic cleavage of the ATP analogues presented can be followed by continuous monitoring of fluorescence lifetime changes.

A novel synthetic route for magnetically retrievable Bi2WO 6 hierarchical microspheres with enhanced visible photocatalytic performance

Liu, Zhi,Chen, Feitai,Gao, Yuanpeng,Liu, Yang,Fang, Pengfei,Wang, Shaojie

, p. 7027 - 7030 (2013)

We report a reliable and effective strategy to synthesize magnetically recyclable Bi2WO6 microspheres using Fe3O 4 nanoparticles as supports. The as-prepared hierarchical photocatalyst displays excellent photocatalytic activity and reusability under visible light irradiation. The Royal Society of Chemistry 2013.

Photocatalytic application of nanosized CdS immobilized onto functionalized MWCNTs

Chronopoulos,Karousis,Zhao,Wang,Shinohara,Tagmatarchis

, p. 7429 - 7434 (2014)

Nanosized semiconductor CdS immobilized onto modified multi-walled carbon nanotubes (MWCNTs) carrying poly(amidoamine) dendron units were visualized by HR-TEM. Evidently, spherical CdS nanoparticles 3-5 nm in diameter were identified. Moreover, EDX spectr

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 13558-31-1