| Identification | More | [Name]
Iron(III) p-toluenesulfonate | [CAS]
77214-82-5 | [Synonyms]
Iron(III)p-toluenesulfonate
Benzenesulfonic acid, 4-methyl-, iron(3+) salt
IRON(III)-PARA-TOLUENESULPHONATE
4-Methyl-benzolsulfonsure, Eisen Salz
p-Toluenesulfonic acid, ferric salt
Iron (III) tris(4-methylbenzenesulfonate)
Iron(Ⅲ)p-toluenesulfonate | [EINECS(EC#)]
420-960-8 | [Molecular Formula]
C21H21FeO9S3 | [MDL Number]
MFCD01766290 | [Molecular Weight]
569.43 | [MOL File]
77214-82-5.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS05 | [Signal word ]
Danger | [Hazard statements ]
H318 | [Precautionary statements ]
P280-P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
R41:Risk of serious damage to eyes. | [Safety Statements ]
S24:Avoid contact with skin .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S39:Wear eye/face protection . | [TSCA ]
TSCA listed | [REACH Registrations]
Active | [HS Code ]
2904100090 |
| Hazard Information | Back Directory | [Chemical Properties]
Iron (III) p-toluenesulfonate, also known as Iron p-toluenesulfonate, is a red or orange solid powder. It is an oxidising agent for solid-state capacitors, readily soluble in water, ethanol and n-butanol, and is polymerised with EDOT in specific proportions to manufacture solid-state capacitors.
 | [Uses]
Iron(III) p-toluenesulfonate is a conductive compound used as a dopant or a conductive coating in vapor phase polymerized conductive polymers. | [Application]
Iron(III) p-toluenesulfonate, Fe(OTs)3·6H2O, is an inexpensive, versatile and commercially available catalyst for the allylation of acetals using allyltrimethylsilane to yield homoallyl ethers in moderate to good yields[1]. | [Preparation]
Iron(III) p-toluenesulfonate is prepared by reacting p-toluenesulphonic acid (PTS) with iron(III) hydroxide (Fe(OH)₃) under specific conditions. | [References]
[1] Spafford, M. J., Anderson, E. D., Lacey, J. R., Palma, A. C., Mohan, R. S. (2007). Iron(III) p-toluenesulfonate catalyzed synthesis of homoallyl ethers from acetals and aldehydes. Tetrahedron Letters, 48 49, Pages 8665-8667. https://doi.org/10.1016/j.tetlet.2007.10.026
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