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4-Hydroxythiophenol, 97%
CAS: 637-89-8 | C6H6OS | 126.17 g/mol
| Catalog Number | Quantity |
|---|---|
| ALFL04429.06 | 5 g |
Catalog number ALFL04429.06
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Quantity:
5 g
Specifications
Chemical Name or Material4-Hydroxythiophenol
CAS637-89-8
Health Hazard 1H302+H312+H332-H314
Health Hazard 2GHS H Statement
H314-H318-H302
Causes severe skin burns and eye damage.
Causes serious eye damage.
Harmful if swallowed.
H314-H318-H302
Causes severe skin burns and eye damage.
Causes serious eye damage.
Harmful if swallowed.
Health Hazard 3P260-P264b-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c
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4-Hydroxythiophenol is used to improve charge separation in PbSe quantum dots (QDs) as sensitizers for TiO2. It helps in the activation of neocarzinostatin-chromophore. Also used as a resin monomer in the study of the different gold nanocrystal core-resin shell structures
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Hydroxythiophenol is used to improve charge separation in PbSe quantum dots (QDs) as sensitizers for TiO2. It helps in the activation of neocarzinostatin-chromophore. Also used as a resin monomer in the study of the different gold nanocrystal core-resin shell structures
Solubility
Soluble in water.
Notes
Air Sensitive. Store at 4°C. Incompatible with air and oxidizing agents.
4-Hydroxythiophenol is used to improve charge separation in PbSe quantum dots (QDs) as sensitizers for TiO2. It helps in the activation of neocarzinostatin-chromophore. Also used as a resin monomer in the study of the different gold nanocrystal core-resin shell structures
Solubility
Soluble in water.
Notes
Air Sensitive. Store at 4°C. Incompatible with air and oxidizing agents.
RUO – Research Use Only
General References:
- Shaowei Chen. 4-Hydroxythiophenol-Protected Gold Nanoclusters in Aqueous Media.J. Am. Chem. Soc.1999, 15 (22), 7551-7557.
- Hiroshi Sugiyama; Tsuyoshi Fujiwara; Isao Saito. Activation of neocarzinostatin-chromophore by 4-hydroxythiophenol: Intramolecular radical trapping of biradical intermediate.Tetrahedron Letters.1994, 35 8825-8828.