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DNP-BETA-ALANINE, also known as 2,4-dinitrophenyl-beta-alanine, is a synthetic chemical compound derived from beta-alanine, an amino acid. It is characterized by the presence of a 2,4-dinitrophenyl group attached to the beta-carbon of the alanine molecule. DNP-BETA-ALANINE is primarily used as a reagent in various biochemical and analytical applications, such as enzyme assays and the determination of amino acid composition in proteins. DNP-BETA-ALANINE is known for its ability to form a yellow-colored complex with copper ions, which can be utilized for colorimetric analysis. Due to its reactivity and potential applications in research, it is an important tool in the field of biochemistry and molecular biology.

3185-97-5

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3185-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3185-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3185-97:
(6*3)+(5*1)+(4*8)+(3*5)+(2*9)+(1*7)=95
95 % 10 = 5
So 3185-97-5 is a valid CAS Registry Number.

3185-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,4-dinitroanilino)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(2,4-dinitrophenylamino)propionic acid

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:3185-97-5 SDS

3185-97-5Relevant academic research and scientific papers

Quinoxaline-phosphonic acid derivatives

-

, (2008/06/13)

The disclosure relates to quinoxaline derivatives of Formula I wherein R1, R4, R5, R6, R7 and R8 are as defined in the disclosure, as well as their production and use in medicinal agents.

Pyrrolylquinoxalinediones: A new class of AMPA receptor antagonists

Lubisch,Behl,Hofmann

, p. 2887 - 2892 (2007/10/03)

Pyrrolylquinoxalinediones were synthesized and their affinities for the AMPA receptor were determined. Most compounds showed moderate to good affinities. The acetic acid derivative 8b exhibited a K(i) value of 70 nM and was equipotent to NBQX 1. Structure activity relationships are discussed. Selected compounds were tested for their potency to inhibit AMPA induced lethal convulsions in mice. In this in vivo model the compounds showed improved potency compared with NBQX.

Direct Cleavage of Peptides from a Solid Support into Aqueous Buffer. Application in Simultaneous Multiple Peptide Synthesis

Bray, Andrew M.,Maeji, N. Joe,Valerio, Robert M.,Campbell, Rhonda A.,Geysen, H. Mario

, p. 6659 - 6666 (2007/10/02)

A method of simultaneous multiple peptide synthesis which integrates synthesis, side-chain deprotection, cleavage, and purification so as to afford peptide solutions suitable for immediate biological testing is described.The approach utilizes a novel dike

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