82385-76-0 Usage
Uses
Used in Pharmaceutical Industry:
[Hydroxy(nitroso)amino]acetic acid is used as a reagent in the pharmaceutical industry for its ability to facilitate organic synthesis. Its strong acidic nature aids in the production of various pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Agriculture:
In the agricultural sector, [hydroxy(nitroso)amino]acetic acid is used as a chelating agent for metal ions. This application helps improve the bioavailability and uptake of essential nutrients by plants, thereby enhancing crop growth and yield.
Used in Chemical Manufacturing:
[Hydroxy(nitroso)amino]acetic acid is employed as a key component in the chemical manufacturing industry. Its reactivity and ability to form complexes with metal ions make it a valuable asset in the production of various chemical products and materials.
Used in Medical Applications:
HNAA has potential applications in the treatment of certain medical conditions due to its chelating properties. It can be used to bind and remove toxic metal ions from the body, providing a therapeutic benefit in cases of heavy metal poisoning or other related conditions. However, further research and development are required to fully understand and harness its potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 82385-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82385-76:
(7*8)+(6*2)+(5*3)+(4*8)+(3*5)+(2*7)+(1*6)=150
150 % 10 = 0
So 82385-76-0 is a valid CAS Registry Number.
82385-76-0Relevant academic research and scientific papers
Luk'yanov,Smirnov,Sevost'yanova
, p. 868 - 870 (1996)
Bromination, methylation, and nitration of N-methoxydiazen-N′-oxidoacetic acid derivatives were investigated. The results of the reactions depended significantly on both the type of the starting compound and the electrophilic reagent.
Luk'yanov, O. A.,Smirnov, G. A.,Sevost'yanova, V. V.
, p. 1474 - 1478 (1995)
Methods of synthesis of N-alkyl-N'-alkoxydiazene-N-oxides containing a carbonyl group in the β-position of alkyl or alkoxy radicals were developed. β,β-Dinitro derivatives of N-alkyl-N'-alkoxydiazene-N-oxides were synthesized for the first time via nitration of oximes obtained from the ketones. - Keywords: N-alkyl-N'-alkoxydiazene-N-oxides, ketones, oximes, gem-dinitro derivatives, β,β-dinitro derivatives
AZO AND AZOXY COMPOUND. VII. SYNTHESIS AND PROPERTIES OF DERIVATIVES OF 1-OXIDO-2-ALKOXYDIAZENEACETIC ACIDS
Yandovskii, V. N.,Kuznetsov, V. S.,Tselinskii, I. V.,Frolova, G. M.
, p. 445 - 450 (2007/10/02)
The reaction of nitric oxide with malonic ester and subsequent hydrolysis of the reaction mixture led to the disodium salt of N-nitrosohydroxylaminoacetic acid, the alkylation of which gave 1-oxido-2-alkoxydiazeneacetates.The reaction of these esters (alkylation at the carbon atom, hydrolysis, amidolysis, hydrazinolysis) were investigated.
