4-tert-Butylcatechol, 98%, Thermo Scientific Chemicals
4-tert-Butylcatechol, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-tert-Butylcatechol, 98%, Thermo Scientific Chemicals

数量:
250 g
1000 g
5000 g
製品番号(カタログ番号) A14599.30
または、製品番号A14599-30
価格(JPY)/ Each
-
見積もりを依頼する
数量:
250 g
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化学物質識別子
CAS98-29-3
IUPAC Name4-tert-butylbenzene-1,2-diol
Molecular FormulaC10H14O2
InChI KeyXESZUVZBAMCAEJ-UHFFFAOYSA-N
SMILESCC(C)(C)C1=CC=C(O)C(O)=C1
さらに表示
FormCrystals or powder or crystalline powder or flakes
Appearance (Color)White to cream
Identification (FTIR)Conforms
Melting Point (clear melt)52.0-58.0?C
Assay (GC)≥97.5%
4-tert-Butylcatechol is widely utilized as an inhibitor in polymerization of butadiene, styrene, vinyl acetate and other reactive monomers. It plays an important role in the synthesis of tungsten oxide nanoparticles by nonaqueous sol-gel process. It acts as a stabilizer in the manufacturing of polyurethane foam. It is employed as an antioxidant for synthetic rubber, polymers and oil derivatives. It is also utilized as a purification agent for aminoformate catalysts.

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-Butylcatechol is widely utilized as an inhibitor in polymerization of butadiene, styrene, vinyl acetate and other reactive monomers. It plays an important role in the synthesis of tungsten oxide nanoparticles by nonaqueous sol-gel process. It acts as a stabilizer in the manufacturing of polyurethane foam. It is employed as an antioxidant for synthetic rubber, polymers and oil derivatives. It is also utilized as a purification agent for aminoformate catalysts.

Solubility
Soluble in ether, acetone, alcohol, and methanol. Insoluble in water.

Notes
Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Radical inhibitor and antioxidant.
  2. Rafiee, M. Electrochemical oxidation of 4-tert-butylcatechol in the presence of β-cyclodextrin: Interplay between E and CE mechanisms. Int. J. Chem. Kinet. 2012, 44 (8), 507-513.
  3. Nematollahi, D.; Rafiee, M.; Samadi-Maybodi, A. Mechanistic study of electrochemical oxidation of 4-tert-butylcatechol: A facile electrochemical method for the synthesis of new trimer of 4-tert-butylcatechol. Electrochim. Acta 2004, 49 (15), 2495-2502.