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N-Dansyl ethylamine, also known as 5-dimethylaminonaphthalene-1-sulfonyl ethylamine, is a chemical compound with the molecular formula C12H16N2O2S. It is a fluorescent derivatization reagent commonly used in analytical chemistry for the detection and quantification of primary amines, amino acids, and peptides. The dansyl group, derived from 5-dimethylaminonaphthalene-1-sulfonic acid, is a well-known chromophore that exhibits strong fluorescence upon excitation, making it an ideal label for sensitive and selective detection. N-Dansyl ethylamine is particularly useful in high-performance liquid chromatography (HPLC), thin-layer chromatography (TLC), and other separation techniques, as it allows for the visualization and quantification of amines in complex mixtures. Its properties include a melting point of 65-67°C and a maximum absorption wavelength of 330 nm, with a fluorescence emission maximum at 540 nm.

5282-88-2

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5282-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5282-88-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5282-88:
(6*5)+(5*2)+(4*8)+(3*2)+(2*8)+(1*8)=102
102 % 10 = 2
So 5282-88-2 is a valid CAS Registry Number.

5282-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-DANSYL ETHYLAMINE

1.2 Other means of identification

Product number -
Other names -

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:5282-88-2 SDS

5282-88-2Downstream Products

5282-88-2Relevant academic research and scientific papers

Use of an isotactic-propylene/hexene copolymer as a new, versatile, soluble support

Hicks, Abbey,Lin, Binhong,Osburn, Philip L.,Hobbs, Christopher E.

, p. 600 - 605 (2014)

The use of isotactic-poly(propylene-co-hexene) (iPPH) as new polymeric scaffold for synthesis as well as a phase-selective, soluble polymer support for homogeneous catalysis is described. It was possible to functionalize olefin-terminated iPPH using stand

Convergent preparation and photophysical characterization of dimaleimide dansyl fluorogens: Elucidation of the maleimide fluorescence quenching mechanism

Guy, Julia,Caron, Karine,Dufresne, Stephane,Michnick, Stephen W.,Skene,Keillor, Jeffrey W.

, p. 11969 - 11977 (2008/03/13)

Dimaleimide fluorogens are being developed for application to fluorescent protein labeling. In this method, fluorophores bearing two maleimide quenching groups do not fluoresce until both maleimide groups have undergone thiol addition reactions with the C

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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