CAS 68239-81-6
:3-Aminophenol sulfate (2:1)
Description:
3-Aminophenol sulfate (2:1), with the CAS number 68239-81-6, is a chemical compound that features a sulfate group attached to a 3-aminophenol structure. This compound typically exhibits characteristics associated with both amines and phenolic compounds, including potential solubility in water and organic solvents, depending on the pH and the presence of other ions. The amino group (-NH2) can participate in hydrogen bonding, enhancing its reactivity and interaction with other chemical species. As a sulfate derivative, it may also exhibit properties related to sulfate esters, such as increased polarity. This compound is often utilized in various applications, including dye manufacturing, pharmaceuticals, and as an intermediate in organic synthesis. Safety data sheets should be consulted for handling and storage guidelines, as compounds containing amines can be hazardous, and appropriate precautions should be taken to mitigate exposure. Overall, 3-Aminophenol sulfate (2:1) is a versatile compound with significant relevance in both industrial and research settings.
Formula:C12H16N2O6S
InChI:InChI=1/2C6H7NO.H2O4S/c2*7-5-2-1-3-6(8)4-5;1-5(2,3)4/h2*1-4,8H,7H2;(H2,1,2,3,4)
InChI key:InChIKey=PACLNJPTGMYEKW-UHFFFAOYSA-N
SMILES:S(=O)(=O)(O)O.NC1=CC(O)=CC=C1
Synonyms:- 269-475-1
- 3-Aminophenol Hemisulfate
- 3-Aminophenol Sulfate (2:1)
- Phenol, 3-Amino-, Sulfate (2:1) (Salt)
- Phenol, 3-amino-, sulfate (2:1)
- m-Aminophenol sulfate
- 3-aminophenol sulfate
- Bis[(3-hydroxyphenyl)ammonium] sulphate
- 3-Aminophenol hemisulfate salt
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Found 3 products.
3-Aminophenol hemisulfate
CAS:Formula:C12H16N2O6SPurity:98%Color and Shape:SolidMolecular weight:316.3302m-Aminophenolsulfate
CAS:<p>m-Aminophenolsulfate is a sulfonated derivative of m-aminophenol. It has been used for wastewater treatment and as an analytical reagent for the determination of p2 group substances, such as sulfa drugs. It is also used in pharmaceutical preparations and human serum. m-Aminophenolsulfate may be activated by hydrochloric acid to form a reactive intermediate (m-aminophenoxy radical) that reacts with electron acceptors such as oxygen or nitrous oxide to generate reactive oxygen species. In this way, m-aminophenolsulfate can act as a broad-spectrum antimicrobial agent against both Gram negative and Gram positive bacteria. The mechanism of this reaction is adsorption on the bacterial cell wall, which leads to cell death through osmotic lysis or disruption of membrane integrity.</p>Formula:C12H16N2O6SPurity:Min. 95%Color and Shape:PowderMolecular weight:316.33 g/mol


