Sodium 4-Aminophenylarsonate Chemical Properties

Water Solubility 

Soluble in water

form 

powder to crystal

color 

Tetrahydrate: white, crystalline powder

Odor

odorless

Merck 

14,8578

EPA Substance Registry System

Sodium arsanilate (127-85-5)

Safety Information

Risk Statements 

26/27/28

Safety Statements 

26-36/37/39

RIDADR 

2473

RTECS 

CF9625000

HS Code 

2920.90.2000

HazardClass 

6.1(b)

PackingGroup 

III

Hazardous Substances Data

127-85-5(Hazardous Substances Data)

Toxicity

LD50 scu-rat: 75 mg/kg BIZEA2 184,360,27

Sodium 4-Aminophenylarsonate Usage And Synthesis

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.

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