4-Hydroxythiophenol, 97%, Thermo Scientific Chemicals
4-Hydroxythiophenol, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Hydroxythiophenol, 97%, Thermo Scientific Chemicals

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Quantity:
25 g
5 g
Catalog number L04429.14
also known as L04429-14
Price (USD)/ Each
170.00
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Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
170.00
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4-Hydroxythiophenol, 97%, Thermo Scientific Chemicals
Catalog numberL04429.14
Price (USD)/ Each
170.00
-
Add to cart
Chemical Identifiers
CAS637-89-8
IUPAC Name4-sulfanylphenol
Molecular FormulaC6H6OS
InChI KeyBXAVKNRWVKUTLY-UHFFFAOYSA-N
SMILESOC1=CC=C(S)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White or colorless to cream to yellow
Assay (GC)≥96.0%
FormCrystalline or low melting/fused solid or clear liquid as melt
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.
RUO – Research Use Only

General References:

  1. Shaowei Chen. 4-Hydroxythiophenol-Protected Gold Nanoclusters in Aqueous Media.J. Am. Chem. Soc.1999, 15 (22), 7551-7557.
  2. 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.