English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The aim of the work. Developing the methods of standardization, including identi cation and quantitative assay, of L-lysine 3-methyl-1.2.4-triazole-5-thioacetate an active pharmaceutical ingredient (API) by physico-chemical methods.Research Methods. For identi cation of L-lysine 3-methyl-1.2.4-triazole-5-thioacetate we invited and conducted method of spectroscopic studies. During of operation we selected optimal condition for the analyses of L-lysine 3-methyl-1.2.4-triazole-5-thioacetate in different concentration. We picked up concentration for our results that absorption line must be in the UV area 238 nm.Results and Discussion. The results of the studies show that the absorption characteristic in UV area of L-lysine 3-methyl-1.2.4-triazolyl-5-thioacetate an shoulder of 238 nm.Conclusions. We developed methods to identi cation and quantitative during operation of substance. In further time we have plan to introduce methods of qualitative and quantitative analysis substance to MCQ drugs L-lysine 3-methyl-1.2.4-triazolyl-5-thioacetate.

REGARDING L-LYSINE 3-METHYL-1.2.4-TRIAZOLE-5-THIOACETATE STANDARDIZATION