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13558-31-1

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13558-31-1 Usage

Description

Rhodamine 110 is a green fluorescent cationic dye with excitation and emission maxima of 496 and 520 nm, respectively. When incorporated with a hydrolytic substrate (e.g., proteinase or peptidase substrates), it can be used as a highly sensitive detection reagent in fluorescence-based enzyme assays. Rhodamine 110 has also been used in a fluorescence quenching method for determining trace nitrite and as a probe for cytochrome P450 activity.

Chemical Properties

red to bordeaux crystals or crystalline powder

Uses

Different sources of media describe the Uses of 13558-31-1 differently. You can refer to the following data:
1. Rhodamine 110 is a fluorescent dye used as AP- and exopeptidase substrates for flow cytometric measurements.
2. Rhodamine 110 is a fluorescent dye used as AP- and exopeptidase substrates for flow cytometric measurements. Dyes and metabolites.

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

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  • 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

13558-31-1Relevant articles and documents

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.

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

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.

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.

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.

Tandem photocatalytic oxidation of Rhodamine B over surface fluorinated bismuth vanadate crystals

Liu, Shengwei,Yin, Kai,Ren, Wanshu,Cheng, Bei,Yu, Jiaguo

, p. 17759 - 17767 (2012)

BiVO4 crystals with monoclinic-phase and controllable morphologies were synthesized by NaF-mediated hydrothermal processes using Bi(NO3)3 and V2O5 as precursors. The NaF added as a structural controller not only affected the crystal evolution processes of BiVO4 crystals, but also enabled the in situ surface fluorination of the as-synthesized BiVO4 crystals. Interestingly, the photocatalytic oxidation reactions of RhB occurred in a stepwise manner over fluorinated BiVO4 photocatalyst, that is, a faster de-ethylation process (conversion of RhB into rhodamine) followed by a relatively slower mineralization process, involving the destruction of the conjugated structure in rhodamine. Surface fluorination favored the RhB adsorption and hole transfer between RhB molecules and BiVO4 photocatalyst, thus progressively enhancing the initial direct hole transfer mediated de-ethylation process. In contrast, surface fluorination exerts compromised effects on the ·O 2- mediated mineralization process, enhancing surface RhB adsorption versus retarding electron transfer from BiVO4 photocatalyst to O2 giving rise to ·O2-, and consequently, moderate surface fluorine coverage is required to balance the aforementioned conflicting effects and achieve the higher mineralization rate. The present study not only demonstrates that the photocatalytic efficiency can be modified by tuning photogenerated active species and photocatalytic reaction processes, but also provides new insights into the fluorination effects on the semiconductor photocatalysis.

Piezocatalytic performance of Na0.5Bi0.5TiO3 nanoparticles for degradation of organic pollutants

Chen, Lirong,Hao, Xihong,Li, Yong,Lu, Chunxiao,Shi, Lu,Zhang, Qiwei,Zhang, Tiejun

, (2021/11/16)

Piezocatalysis has been considered as a promising technology in water pollution treatment. In this work, a series of piezoelectric Na0.5Bi0.5TiO3 (NBT) nanoparticles were prepared by hydrothermal method using different titanium sources as titanium precursors. The piezocatalytic performances of the NBT nanoparticles were investigated by the degradation of Rhodamine B (RhB) with the concentration of 10 mg/L under ultrasonic vibration. It is found that the NBT nanoparticles prepared by using anatase titanium oxide as titanium precursor show optimum piezocatalytic activity and the rate constant of 0.022 min?1 is achieved for RhB. The initial RhB concentration, ultrasonic power, particles size and specific surface area of NBT materials play an important role in optimizing the piezocatalytic performance. Moreover, the NBT nanoparticles show a satisfactory stability and reusability for the piezocatalytic degradation. The piezocatalytic mechanism of NBT nanoparticles was elucidated by the identification of free radicals and intermediates in the degradation process. The work provides a guidance to design and develop new high-performance piezocatalysts.

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