ChemicalBook--->CAS DataBase List--->121-59-5

121-59-5

121-59-5 Structure

121-59-5 Structure
IdentificationBack Directory
[Name]

CARBARSONE
[CAS]

121-59-5
[Synonyms]

kutan
ameban
Arsuran
AMABEVAN
NSC32868
NSC-32868
NSC 32868
ARSAMBIDE
FENARSONE
HISTOCARB
Carbasone
aminarson
carbarson
carb-o-sep
aminoarson
amebarsone
pentarsone
CARBARSONE
AMebarsene
AMINARSONE
AMIBIARSON
LEUCARSONE
P-ARSONOPHENYLUREA
Carbarsone (200 mg)
CARBARSONE USP/EP/BP
n-carbamylarsanilicacid
n-carbamoyl-arsanilicaci
n-carbamoylarsanilicacid
UREIDOBENZENEARSONICACID
p-Ureidophenylarsonicacid
p-ureido-benzenearsonicaci
4-ureidophenylarsonic acid
ARSANILICACID,N-CARBAMOYL-
4-Ureidobenzenearsonic Acid
P-UREIDOBENZENEARSONIC ACID
4-ureido-1-phenylarsonicacid
p-carbaminophenylarsonicacid
kyselinan-karbamylarsanilova
carbaminophenyl-p-arsonicacid
PARA-UREIDOBENZENEARSONICACID
P-CARBAMIDOBENZENEARSONIC ACID
4-carbamylaminophenylarsonicacid
P-CARBAMYLAMINOPHENYLARSONIC ACID
[4-(carbamoylamino)phenyl]arsonic acid
4-[(Aminocarbonyl)amino]phenylarsonicacid
(4-((aminocarbonyl)amino)phenyl)-arsonicaci
(4-((aminocarbonyl)amino)phenyl)arsonicacid
Arsonic acid, [4-[(aminocarbonyl)amino]phenyl]-
[EINECS(EC#)]

204-484-6
[Molecular Formula]

C7H9AsN2O4
[MDL Number]

MFCD00025427
[MOL File]

121-59-5.mol
[Molecular Weight]

260.08
Chemical PropertiesBack Directory
[Melting point ]

174°
[form ]

solid
[pka]

3.78±0.10(Predicted)
[EPA Substance Registry System]

Carbarsone (121-59-5)
Hazard InformationBack Directory
[Uses]

insecticide, cholinesterase inhibitor
[General Description]

White powder or solid.
[Air & Water Reactions]

Slightly soluble in water.
[Reactivity Profile]

An acidic salt of an amide. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.
[Fire Hazard]

Flash point data for CARBARSONE are not available; however, CARBARSONE is probably combustible.
[Definition]

ChEBI: [4-(carbamoylamino)phenyl]arsonic acid is a member of ureas.
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Water-->4-Nitroaniline-->4-Aminophenylarsonic acid-->Sodium cyanate-->NITARSONE-->ARSINE-->Cyanogen bromide-->Potassium cyanate
Safety DataBack Directory
[Safety Profile]

Poison by ingestion. Moderately toxic by intraperitoneal route. Questionable carcinogen with experimental tumorigenic data. See also ARSENIC COMPOUNDS. When heated to decomposition it emits very toxic fumes of As and NOx
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