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Sodium 4-Aminophenylarsonate

Sodium 4-Aminophenylarsonate Structure
Sodium 4-Aminophenylarsonate
  • CAS No.127-85-5
  • Chemical Name:Sodium 4-Aminophenylarsonate
  • CBNumber:CB3111606
  • Molecular Formula:C6H6AsNNa2O3
  • Formula Weight:261.02
  • MOL File:127-85-5.mol
Sodium 4-Aminophenylarsonate Property
  • Water Solubility Soluble in water
  • form powder to crystal
  • color Tetrahydrate: white, crystalline powder
  • Odor odorless
  • Merck 14,8578
  • FDA UNII UC2409302Q
  • EPA Substance Registry System Sodium arsanilate (127-85-5)
Safety
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordDanger
  • Hazard statements H410-H400-H331-H350-H301
  • Precautionary statements P273-P391-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501-P273-P391-P501-P264-P270-P301+P310-P321-P330-P405-P501
Sodium 4-Aminophenylarsonate Price More Price(1)
  • Brand: TCI Chemicals (India)
  • Product number: A0531
  • Product name : Sodium 4-Aminophenylarsonate
  • Purity: 
  • Packaging: 25G
  • Price: ₹2900
  • Updated: 2022/05/26
  • Buy: Buy

Sodium 4-Aminophenylarsonate Chemical Properties,Usage,Production

  • Definition ChEBI: Sodium arsanilate is an organoarsonic acid salt and an organic sodium salt. It has a role as an antisyphilitic drug. It contains an arsanilate(1-).
  • General Description A white crystalline, odorless powder. Slightly denser than water. Contact may irritate skin, eyes, and mucous membranes. May be toxic by ingestion. Used to make other chemicals.
  • Air & Water Reactions Soluble in water.
  • Health Hazard TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
  • Fire Hazard Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
  • Pharmaceutical Applications Bechamp,teaching medicinal chemistry at the University of Montpellier, synthesised in 1863 a compound from aniline and arsenic acid, which became known later as Atoxyl. The name Atoxyl stems from its decreased toxicity. Bechamp characterised his compound as an anilide.
    In 1905, Thomas and Breinl showed that Atoxyl was effective in the treatment of trypanosomas, mainly Trypanosoma brucei gambiense-the cause of the African sleeping sickness, which was the main health problem around that time in Africa. Nevertheless, very high doses were required to show any pronounced effect, and as a result severe side effects such as blindness and damage to the optical nerve were common issues.
    Inspired by this research, Ehrlich hired the chemist Bertheim in 1905. Bertheim revised the structure of Atoxyl and the correct chemical formula was assigned. Atoxyl was identified as an p-anilinyl arsenic acid derivative on the basis of its properties to reduce Tollen’s reagent [Ag(NH3)2]+ to metallic silver and its potential use to synthesise the corresponding diazo dye.
  • Safety Profile Poison by subcutaneous route. Can cause blindness. When heated to decomposition it emits very toxic fumes of As and NOx.
Sodium 4-Aminophenylarsonate Preparation Products And Raw materials
Raw materials
Preparation Products
Sodium 4-Aminophenylarsonate Suppliers
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Sodium 4-Aminophenylarsonate Spectrum
127-85-5, Sodium 4-AminophenylarsonateRelated Search:
  • Semimetal Compounds
  • Classes of Metal Compounds
  • As (Arsenic) Compounds
  • Organometallics
  • 有机类
  • 化工
  • Classes of Metal Compounds
  • Semimetal Compounds
  • As (Arsenic) Compounds
  • C6H6AsNNa2O3
  • C6H7AsNNaO3
  • C6H7AsNNaO3xH2O
  • 芳官酸,AS-(4-氨基苯基)-,钠盐(1:1)
  • 4-氨基苯胂酸钠盐
  • 4-胺苯胂酸钠盐
  • 对氨基苯胂酸钠
  • 4-氨基苯胂酸钠
  • 127-85-5
  • Sodium 4-Aminophenylarsonate USP/EP/BP
  • sodium:(4-aminophenyl)-hydroxyarsinate
  • 4-AMINOPHENYLARSONIC ACID SODIUM SALT
  • 4-AMINOBENZENEARSONIC ACID SODIUM SALT
  • 4-Aminobenzenearsonic Acid Sodium Salt p-Arsanilic Acid Sodium Salt Atoxyl 4-Aminophenylarsonic Acid Sodium Salt Sodium Arsanilate Sodium Hydrogen 4-Aminophenylarsonate
  • Chebi:36049
  • 4-AMINOPHENYLARSONIC ACID SODIUM SALT HYDRATE
  • Arsonic acid, (4-aminophenyl)-, monosodium salt
  • 4-Arsanilic Acid Sodium
  • sodium hydrogen 4-aminophenylarsonate
  • Arsanilic acid，monosodium salt
  • ATOXYL
  • trypoxyl
  • sonate
  • sodiump-arsanilate
  • sodiump-aminophenylarsonate
  • sodiump-aminobenzenearsonate
  • sodiumarsonilate
  • sodiumaniline-arsonate[qr]
  • sodiumanilarsonate[qr]
  • sodiumanilarsonate
  • sodium-analinearsonate
  • sodiumaminophenylarsonate[qr]
  • sodiumaminophenolarsonate[qr]
  • sodiumaminophenolarsonate
  • sodiumaminarsonate
  • soamin
  • protoxyl
  • pro-gensodium
  • pigletpro-genv[qr]
  • pigletpro-genv
  • nuarsol
  • nci-c61176
  • nci-61176[qr]
  • monosodium(4-aminophenyl)arsonate
  • arsinosolvin
  • arsanilicacidsodiumsalt
  • arsanilicacid,sodiumsalt[qr]
  • arsamin
  • anhydroussodiumarsanilate[qr]

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