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89717-54-4

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89717-54-4 Usage

General Description

DL-Gamma-ornithine dihydrochloride is a chemical compound that is a salt form of the amino acid ornithine. It is commonly used as a dietary supplement and is believed to have potential benefits for athletic performance and recovery. DL-Gamma-ornithine dihydrochloride is also known for its role in the urea cycle, which is responsible for the breakdown and removal of ammonia from the body. Additionally, it has been studied for its effects on liver function and as a potential treatment for certain metabolic disorders. DL-GAMMA-ORNITHINE DIHYDROCHLORIDE is often included in sports nutrition products and is generally considered safe for consumption when used as directed.

Check Digit Verification of cas no

The CAS Registry Mumber 89717-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,1 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89717-54:
(7*8)+(6*9)+(5*7)+(4*1)+(3*7)+(2*5)+(1*4)=184
184 % 10 = 4
So 89717-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O2/c6-3-4(7)1-2-5(8)9/h4H,1-3,6-7H2,(H,8,9)

89717-54-4SDS

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 4,5-diaminopentanoic acid

1.2 Other means of identification

Product number -
Other names 4,5-Diaminopentanoic acid,4,5-Diaminovaleric 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:89717-54-4 SDS

89717-54-4Relevant articles and documents

Bifunctional Chelating Agents. Part 2. Synthesis of 1-(2-Carboxyethyl)ethylenediaminetetra-acetic Acid by Ring Cleavage of a Substituted Imidazole

Altman, Janina,Shoef, Nurit,Wilchek, Meir,Warshawsky, Abraham

, p. 59 - 62 (2007/10/02)

The synthesis of 1-(2-carboxyethyl)ethylenediaminetetra-acetic acid, a new bifunctional analogue of ethylenediaminetetra-acetic acid (EDTA) is described.This is carried out via ring-opening benzoylation of ethyl imidazol-4-ylpropanoate, hydrogenation and hydrolysis to 4,5-diaminovaleric acid (DL-γ-ornithine) dihydrochloride, and subsequent alkylation.

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