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Roxarsone

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Identification
Molecular formula
C6H6AsNO3
CAS number
121-19-7
IUPAC name
2-amino-4-arsoroso-phenol;hydrochloride
State
State

At room temperature, roxarsone is in a solid state.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
263.49g/mol
Molar mass
263.4900g/mol
Density
2.1560g/cm3
Appearence

Roxarsone typically appears as a white to light tan crystalline powder.

Comment on solubility

Solubility of 2-amino-4-arsoroso-phenol;hydrochloride

The solubility of 2-amino-4-arsoroso-phenol;hydrochloride is an important characteristic that influences its application in various chemical and biochemical processes. This compound, which contains both amino and phenolic functional groups, is typically expected to exhibit notable solubility behavior.

Key Points on Solubility:

  • Water Solubility: As a hydrochloride salt, it tends to be more soluble in water compared to its free form due to the ionic nature of the compound.
  • Influence of pH: The solubility can be affected by pH, where varying levels can lead to protonation, thereby enhancing its solubility in acidic environments.
  • Organic Solvents: The presence of hydrophobic phenolic groups may limit solubility in organic solvents, making it less favorable for non-polar solutions.

In conclusion, the overall solubility of 2-amino-4-arsoroso-phenol; hydrochloride highlights its versatility, especially in aqueous solutions, making it suitable for applications in analytical chemistry and pharmaceuticals. Understanding its solubility properties is crucial for optimizing its use in reactions and formulations.

Interesting facts

Interesting Facts About 2-amino-4-arsoroso-phenol; hydrochloride

2-amino-4-arsoroso-phenol; hydrochloride, often referred to simply as a phenolic compound, presents a fascinating intersection of chemistry and biology. Here are some notable insights into this intriguing compound:

  • Chemical Structure: This compound consists of an amino group (-NH2), a hydroxyl group (-OH), and arsenic in its structure, which uniquely positions it among phenolic compounds.
  • Biological Impact: Compounds similar to 2-amino-4-arsoroso-phenol have been studied for their effects on biological systems; such phenolic compounds can exhibit antioxidant, antimicrobial, and potential pharmaceutical properties.
  • Historical Significance: The use of phenols and their derivatives dates back to the 19th century, where they were pivotal in early organic chemistry developments and continue to be integral in various fields today.
  • Environmental Considerations: With the presence of arsenic, this compound raises important environmental considerations. Arsenical compounds must be handled with care due to their toxicity and potential health impacts.
  • Applications: The understanding of compounds like 2-amino-4-arsoroso-phenol extends into various applications, including dye manufacturing and the development of pigments, showcasing its versatility in industrial chemistry.

In conclusion, 2-amino-4-arsoroso-phenol; hydrochloride exemplifies the complex relationship between chemical structure and biological activity, underpinning the necessity for conscientious study in organic and medicinal chemistry. Scientists continually explore such compounds to unlock their potential, while also addressing the necessary precautions linked to any hazardous materials.

Synonyms
OXOPHENARSINE HYDROCHLORIDE
OG8JNR786U
NSC-3087
OXOPHENARSINE HYDROCHLORIDE [MI]
208-682-3
538-03-4
Arsenoxide
Arsphenoxide
Oxiarsolan
Arsenosan
Mapharsen
Metarsen
Fontarsan
Mapharsal
Mapharside
Treparsen
Ehrlich 5
Arseno 39
2-Amino-4-arsenosophenol hydrochloride
3-Amino-4-hydroxy-phenarsine hydrochloride
Oxophenarsine hydrochloride [USP]
3-Amino-4-hydroxyphenyl arsinoxide hydrochloride
3-Amino-4-hydroxyphenylarsine oxide hydrochloride
2-amino-4-arsorosophenol;hydrochloride
Maphersen.RTM.
Maspharside; Metarsen; NSC 627725; Oxiarsolan
Oxophenarsine HCl
Oxophenarsini hydrochloridum
NSC627725
NSC 3087
EINECS 208-682-3
UNII-OG8JNR786U
AI3-04455
Oxophenarsine hydrochloride 3-Amino-4-hydroxyphenyl-arsineoxide hydrochloride
Phenol, monohydrochloride
Phenol, 2-amino-4-arsenoso-, hydrochloride
Phenol, 2-amino-4-arsenoso-, monohydrochloride
SCHEMBL317829
DTXSID50202077
NSC3087
JRIGVWDKYXCHMG-UHFFFAOYSA-N
WLN: ZR BQ E-AS-O &GH
NSC-627725
NS00080184
3-amino-4-hydroxyphenylarsinoxide hydrochloride
2-AMINO-4-ARSENOSOPHENOL MONOHYDROCHLORIDE
Q3287221
OXOPHENARSINE HYDROCHLORIDE 3-AMINO-4-HYDROXYPHENYLARSINEOXIDE HYDROCHLORIDE