2163-77-1 Usage
Description
3-amino-4-hydroxyphenylarsonic acid, also known as p-arsanilic acid, is a chemical compound derived from the arsenic compound arsanilic acid. It possesses antimicrobial properties and is used as a feed additive in the poultry industry to promote growth and prevent disease.
Used in Poultry Industry:
3-amino-4-hydroxyphenylarsonic acid is used as a feed additive for promoting growth and preventing disease in poultry. Its antimicrobial properties help to maintain the health of the animals and improve their overall well-being.
However, the use of 3-amino-4-hydroxyphenylarsonic acid has raised concerns about the potential for arsenic residues to accumulate in poultry meat and eggs, posing health risks for consumers. This has led to efforts to regulate and limit its use in food production.
Additionally, the compound has been studied for its potential environmental impact, as it can leach into soil and water systems, contributing to arsenic contamination. This highlights the need for responsible use and management of 3-amino-4-hydroxyphenylarsonic acid to minimize its negative effects on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 2163-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2163-77:
(6*2)+(5*1)+(4*6)+(3*3)+(2*7)+(1*7)=71
71 % 10 = 1
So 2163-77-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H8AsNO4/c8-5-3-4(7(10,11)12)1-2-6(5)9/h1-3,9H,8H2,(H2,10,11,12)
2163-77-1Relevant articles and documents
Substituted phenylarsonic acids; structures and spectroscopy
Lloyd, Nicholas C.,Morgan, Hugh W.,Nicholson, Brian K.,Ronimus, Ron S.
, p. 2443 - 2450 (2008/09/20)
Full NMR and ESI-MS spectra, and differential scanning calorimeter data are presented for 15 substituted phenylarsonic acids, including two new fluoro-substituted examples. X-ray crystal structure determinations of five examples (phenylarsonic acid and the 4-fluoro-, 4-fluoro-3-nitro-, 3-amino-4-hydroxy- and 3-amino-4-methoxy-substituted derivatives) were determined and the H-bonding crystal-packing patterns analysed.