Interesting facts
Interesting Facts About (4-aminophenyl)arsonic Acid
(4-aminophenyl)arsonic acid, commonly known as monosodium methanearsonate, is an intriguing organoarsenic compound that has garnered attention for its unique properties and applications. Here are some key points to consider:
- Biodiversity Impact: This compound has been researched for its role in agriculture as a herbicide. Its effectiveness against certain weeds makes it a valuable tool for crop management.
- Contamination Studies: Due to the presence of arsenic, understanding the environmental impact of this compound is crucial. Researchers often study its behavior in soil and water ecosystems to assess contamination risks.
- Novel Therapeutics: There is ongoing research into the potential use of (4-aminophenyl)arsonic acid in medicinal chemistry. Arsenic compounds have been explored in the treatment of various diseases, showcasing the duality of their utility and toxicity.
- Historical Significance: Arsenic compounds like this one have been used traditionally in medicine, albeit with caution due to their poisonous nature. The evolution of the understanding of such compounds reflects a significant chapter in the history of chemistry.
- Analytical Challenges: Detecting (4-aminophenyl)arsonic acid in samples can be challenging due to its complex nature. Advanced analytical techniques, such as mass spectrometry, are often employed to ensure accurate quantification.
In summary, (4-aminophenyl)arsonic acid presents a fascinating case study in the balance of benefits and risks that organoarsenic compounds offer. As researchers continue to explore its properties, the compound remains a subject of significant scientific interest.
Synonyms
ARSANILIC ACID
p-Arsanilic acid
98-50-0
(4-Aminophenyl)arsonic acid
4-Arsanilic acid
4-AMINOPHENYLARSONIC ACID
4-Aminobenzenearsonic acid
Atoxylic acid
p-Aminobenzenearsonic acid
p-Anilinearsonic acid
Aminophenylarsine acid
Pro-Gen
Arsonic acid, (4-aminophenyl)-
p-Aminophenylarsonic acid
Antoxylic acid
Progen 90
Pro-Gen 227 premix
R-Sonic
4-Aminophenylarsonsaeure
Arsanilsaeure
Arsanilic acid-100
(p-Aminophenyl)arsonic acid
Acido arsanilico
Acide arsanilique
p-Aminophenylarsine acid
Acidum arsanilicum
Benzenearsonic acid, p-amino-
UDX9AKS7GM
CHEBI:49477
DTXSID8035138
4-Aminophenylarsonsaure
NSC-2023
ARSANILIC ACID [MI]
ARSANILIC ACID [INN]
ARSANILIC ACID [HSDB]
MLS000028390
ARSANILIC ACID [MART.]
ARSANILIC ACID [USP-RS]
ARSANILIC ACID [WHO-DD]
DTXCID6015138
NSC2023
ARSANILIC ACID [GREEN BOOK]
Arsonic acid, As-(4-aminophenyl)-
ARSANILIC ACID [USP IMPURITY]
ARSANILIC ACID [USP MONOGRAPH]
NCGC00093366-03
NCGC00093366-05
SMR000058589
ARSANILIC ACID (MART.)
ARSANILIC ACID (USP-RS)
Acid, Arsanilic
ARSANILIC ACID (USP IMPURITY)
ARSANILIC ACID (USP MONOGRAPH)
CAS-98-50-0
Kyselina arsanilova
Kyselina arsanilova [Czech]
Acide p-arsanilique
Acide p-arsanilique [French]
HSDB 432
Acide arsanilique [INN-French]
Acido arsanilico [INN-Spanish]
Acidum arsanilicum [INN-Latin]
UNII-UDX9AKS7GM
NSC 2023
p Aminophenylarsonic Acid
EINECS 202-674-3
4 Aminobenzenearsonic Acid
Acid, p-Aminophenylarsonic
Acid, 4-Aminobenzenearsonic
BRN 1102334
arsanilic-acid
pArsanilic acid
RSonic
AI3-16308
4Arsanilic acid
Arsanilic acid [USP:INN:BAN]
Acide parsanilique
pAnilinearsonic acid
Arsanilic acid100
MFCD00007819
anilarsinate de sodium
ProGen 227 premix
4Aminophenylarsonsaeure
pAminophenylarsine acid
Opera_ID_36
pAminophenylarsonic acid
pAminobenzenearsonic acid
4Aminobenzenearsonic acid
p-Aminophenylarsinic acid
(4Aminophenyl)arsonic acid
Epitope ID:137484
Benzenearsonic acid, pamino
WLN: ZR D-AS-QQO
Arsanilic acid (USP/INN)
PRO-GEN 90
Pesticide Code: 129005
4-16-00-01190 (Beilstein Handbook Reference)
MLS001076469
Arsonic acid, (4aminophenyl)
SCHEMBL160507
CHEMBL351769
P-AMINOPHENYLARSENIC ACID
HMS2093B12
HMS2231G15
HMS3374J04
Pharmakon1600-01505652
Tox21_111204
Tox21_301443
NSC759173
AKOS004114712
Tox21_111204_1
CCG-213501
DB03006
NSC-759173
NCGC00093366-02
NCGC00093366-04
NCGC00255544-01
FA168641
NCI60_001697
SBI-0206819.P001
DB-057730
A0530
NS00079207
D02988
E78960
AB00441338_10
L023959
Q704203
SR-01000721896
SR-01000721896-2
BRD-K24179883-001-16-7
p-Arsanilic acid, VETRANAL(TM), analytical standard
Arsanilic acid, United States Pharmacopeia (USP) Reference Standard
202-674-3
Solubility of (4-Aminophenyl)arsonic Acid
(4-Aminophenyl)arsonic acid, a compound containing both an amino group and an arsonic acid functional group, displays interesting solubility characteristics. Solubility can be influenced by various factors, including:
The presence of the arsonic acid group typically renders this compound more polar, allowing it to engage in hydrogen bonding with water, thus implying increased solubility. However, it's crucial to note that the actual solubility can vary based on the specific conditions under which the compound is tested. As a guiding principle, one can say: “Solubility is a reflection of the balance between molecular interactions.”
Ultimately, understanding the solubility of (4-aminophenyl)arsonic acid is essential for its practical applications and handling in various chemical environments.