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1655-48-7

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1655-48-7 Usage

General Description

DNP-DL-GLUTAMIC ACID is a chemical compound derived from glutamic acid, which is a naturally occurring amino acid in the body and also found in certain foods. DNP, or 2,4-dinitrophenol, is an industrial chemical that has been used in the past for weight loss and as a pesticide. When DNP is combined with DL-glutamic acid, it forms a crystalline substance with potential pharmaceutical applications. DNP-DL-GLUTAMIC ACID may have potential as a treatment for neurodegenerative diseases, as well as being used in the synthesis of certain drugs and pharmaceuticals. Additionally, DNP-DL-GLUTAMIC ACID may have applications in the field of chemistry and biochemistry as a research tool. However, it is important to note that DNP is a toxic chemical and should only be handled by trained professionals in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 1655-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1655-48:
(6*1)+(5*6)+(4*5)+(3*5)+(2*4)+(1*8)=87
87 % 10 = 7
So 1655-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O8/c15-10(16)4-3-8(11(17)18)12-7-2-1-6(13(19)20)5-9(7)14(21)22/h1-2,5,8,12H,3-4H2,(H,15,16)(H,17,18)

1655-48-7SDS

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 2-(2,4-dinitroanilino)pentanedioic acid

1.2 Other means of identification

Product number -
Other names n-(2,4-dinitrophenyl)glutamicacid

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:1655-48-7 SDS

1655-48-7Relevant articles and documents

Kinetic study and analytical application of the hexadecyltrimethylammonium bromide-catalyzed reaction of 1-fluoro-2,4-dinitrobenzene with amines

Wong,Connors

, p. 146 - 150 (2007/10/02)

Arylation of amines by reaction with 1-fluoro-2,4-dinitrobenzene is catalyzed by micelles of cetrimonium bromide. This catalysis has been exploited to reduce the analysis time in the spectrophotometric determination of amines as their dinitrophenyl derivatives. The kinetics of the catalysis were studied for the five amines: alanine, phenylalanine, aniline, 4-methylaniline, and 4-methoxyaniline. The dependence of rate constant on surfactant concentration can be quantitatively accounted for by Berezin's model, in which uptake of the amine and the 1-fluoro-2,4-dinitrobenzene by the micelle is described as a partitioning phenomenon for both species. An alternative model is developed in which one reactant partitions into the micellar phase and the other binds to the micelle with 1:1 stoichiometry; the two models are formally equivalent. Intrinsic catalytic rate constants and binding constants were evaluated. About one-third to one-half of the maximum observed micellar acceleration is attributed to a true micellar catalysis, the remainder being ascribed to an increase in local reactant concentrations in the micelle.

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