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4-tert-Butylphenol, 99%, Thermo Scientific Chemicals
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Catalog number A15871.0E
also known as A15871-0E
Price (USD)/ Each
130.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
154.00 Save 23.35 (15%)
-
Quantity:
2500 g
Price (USD)/ Each
130.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
154.00 Save 23.35 (15%)
4-tert-Butylphenol, 99%, Thermo Scientific Chemicals
Catalog numberA15871.0E
Price (USD)/ Each
130.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
154.00 Save 23.35 (15%)
-
Chemical Identifiers
CAS98-54-4
IUPAC Name4-tert-butylphenol
Molecular FormulaC10H14O
InChI KeyQHPQWRBYOIRBIT-UHFFFAOYSA-N
SMILESCC(C)(C)C1=CC=C(O)C=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream or pale yellow
FormPowder, flakes, briquettes or lumps
Melting Point (clear melt)97-101?C
Assay (GC)≥98.5%
Identification (FTIR)Conforms
4-tert-butylphenol on condensation with formaldehyde gives calix[5]arene which is used in enzyme mimetics.
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-tert-butylphenol on condensation with formaldehyde gives calix[5]arene which is used in enzyme mimetics.
Solubility
Soluble in water. [8.7 g/L (20°C)]
Notes
Store at room temperature. Keep away from oxidizing agents and acids.
4-tert-butylphenol on condensation with formaldehyde gives calix[5]arene which is used in enzyme mimetics.
Solubility
Soluble in water. [8.7 g/L (20°C)]
Notes
Store at room temperature. Keep away from oxidizing agents and acids.
RUO – Research Use Only
General References:
- C. David Gutsche.; Balram Dhawan.; Kwang Hyun No.; Ramamurthi Muthukrishnan. Calixarenes. 4. The synthesis, characterization, and properties of the calixarenes from p-tert-butylphenol. J. Am. Chem. Soc. 1981, 103 (13),3782-3792 .
- The acid-catalyzed removal of t-butyl groups from phenols (reverse Friedel-Crafts reaction), can be brought about without the need for t-butyl acceptors by using aluminum chloride as catalyst in dichloromethane at ambient temperature: Synth. Commun., 18, 1783 (1988).