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Dansyl-aniline, also known as A662475, is a fluorescently labeled derivative of aniline. It is a synthetic compound that exhibits unique properties due to its fluorescent nature, making it suitable for various applications across different industries.

34532-47-3

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34532-47-3 Usage

Uses

Used in Dye Manufacturing:
Dansyl-aniline is used as a dye intermediate for the production of various dyes. Its fluorescent properties allow for the creation of dyes with distinct characteristics, enhancing the color and performance of the final products.
Used in Pharmaceutical Industry:
Dansyl-aniline serves as a key component in the development of medicinal compounds. Its fluorescent properties enable the tracking and detection of specific molecules within biological systems, aiding in drug discovery and development processes.
Used in Resin and Varnish Production:
Dansyl-aniline is utilized as a raw material in the manufacturing of resins and varnishes. Its incorporation into these materials can improve their performance, such as enhancing their durability and resistance to environmental factors.
Used in Perfumery:
Dansyl-aniline is employed in the creation of perfumes, where its fluorescent properties can contribute to the development of unique and long-lasting fragrances.
Used in Rubber Vulcanization:
Dansyl-aniline is used as a vulcanizing agent for rubber, improving the rubber's strength, elasticity, and resistance to wear and tear.
Used as a Solvent:
Dansyl-aniline also functions as a solvent in various chemical processes, facilitating reactions and improving the efficiency of the overall process.

Check Digit Verification of cas no

The CAS Registry Mumber 34532-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,3 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34532-47:
(7*3)+(6*4)+(5*5)+(4*3)+(3*2)+(2*4)+(1*7)=103
103 % 10 = 3
So 34532-47-3 is a valid CAS Registry Number.

34532-47-3Downstream Products

34532-47-3Relevant academic research and scientific papers

Fast and sensitive fluorescent detection of inorganic mercury species and methylmercury using a fluorescent probe based on the displacement reaction of arylboronic acid with the mercury species

Neupane, Lok Nath,Park, Joohee,Mehta, Pramod Kumar,Oh, Eun-Taex,Park, Heon Joo,Lee, Keun-Hyeung

, p. 2941 - 2944 (2020)

We present a reaction-based fluorescent probe (1) for Hg2+ and CH3Hg+, based on the displacement reaction of the arylboronic acid with the mercury species. 1 showed promising sensing properties for Hg2+ and CH3Hg+, such as high selectivity and sensitivity, turn-on response, fast response to Hg2+ (3Hg+ (5 min), low detection limits and operation in purely aqueous solutions.

Fluorescent sensing and selective Pb(II) extraction by a dansylamide ion-exchanger

Kavallieratos, Konstantinos,Rosenberg, Jay M.,Chen, Wei-Zhong,Ren, Tong

, p. 6514 - 6515 (2005)

The (bis)dansylated sulfonamide 1,2-C6H4(NHSO2C10H6-5-N(CH3)2)2 (1) extracted Pb(II) selectively from water into 1,2-dichloroethane via an ion-exchange mechanism and showed fluorescence quenching upon Pb(II) extraction. The distribution ratios for metal extraction (determined by ICP-MS) for Pb(II) were 133-1410 times higher than those for other metal cations [Co(II), Ni(II), Cu(II), Zn(II), and Cd(II)] under identical conditions. Fluorescence quenching was observed upon Pb(II) extraction, which was dependent on Pb(II) concentration. The monodansylated control, C6H5NHSO2C10H6-5-N(CH3)2(2), showed neither extraction nor quenching, indicating that the fluorescence effects are a direct result of Pb coordination to 1. The observed selectivity for Pb(II) is ascribed to the formation of a low-coordinate binary Pb(II)-Sulfonamido complex in the organic phase. Copyright

5-(Dimethylamino)-N-(4-ethynylphenyl)-1-naphthalenesulfonamide as a novel bifunctional antitumor agent and two-photon induced bio-imaging probe

Chui,Wang,Chow,Yuen,Wong,Kwok,Cheng,Wong,Tong,Chan,Lau,Lai,Lam,Fabbri,Tao,Gambari,Wong

supporting information; experimental part, p. 3538 - 3540 (2010/08/07)

A novel compound, (5-(dimethylamino)-N-(4-ethynylphenyl)-1- naphthalenesulfonamide), was prepared and characterized; it shows dual functional roles as an effective antitumor and a two-photon induced bio-imaging agent.

Fluorescence modulation in anion sensing by introducing intramolecular H-bonding interactions in host-guest adducts

Chung, Yun Mi,Raman, Balamurali,Kim, Dae-Sik,Ahn, Kyo Han

, p. 186 - 188 (2008/02/08)

Fluorescence signaling in anion binding is modulated from quenching to enhancement by intramolecular H-bonding stabilization of anion-ionophore adducts; the intramolecular H-bonding is suggested to suppress the quenching processes otherwise possible and i

Dansylations of ethylenediamines. Part 1: Analytical reactions of ethylenediamines

Kallmayer, H.-J.,Schwarz, P.

, p. 119 - 122 (2007/10/02)

Dansyl chloride reacts with ethylenediamines A-K to give bisdansyl amides 3a-k, with diethylenetriamine L to give tridansyl amide 4 and with arylethylenediamines M and N to give monodansyl amides 2m,n.The dansylation of arylamines O-Q shows, the dansylati

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