2,2'-Thiodi(4-tert-octylphenol) Chemical Properties

Melting point:

133-135°C

Boiling point:

524.8±50.0 °C(Predicted)

Density 

1.05±0.1 g/cm3(Predicted)

pka

8.86±0.50(Predicted)

form 

powder to crystal

color 

White to Almost white

CAS DataBase Reference

3294-03-9(CAS DataBase Reference)

NIST Chemistry Reference

2,2'-Thiobis[4-(1,1,3,3-tetramethylbutyl)phenol](3294-03-9)

EPA Substance Registry System

Phenol, 2,2'-thiobis[4-(1,1,3,3-tetramethylbutyl)- (3294-03-9)

Safety Information

Risk Statements 

36/37/38

Safety Statements 

26-36/37/39

HS Code 

2930.90.2900

2,2'-Thiodi(4-tert-octylphenol) Usage And Synthesis

Chemical Properties

Hops are perennial climbing vines that grow wild and also are cultivated extensively in several central European countries, North America, Brazil and Australia. It has shoots up to 10 m (33 ft) in length, opposite leaves, greenish-yellow flowers (June to September) and ovoidal fruits surrounded by a calix. Hops have male and female flowers on separate plants. The part used is the

Occurrence

The hop plant is a perennial that is cultivated throughout the world.

Uses

Hops traditionally have been used as an analgesic, an anthelmintic, a sedative/ hypnotic to treat insomnia, and for attention defi cit–hyperactivity disorder. It is also used to treat menopausal symptoms and to wean patients off conventional sedative prescriptions.

2,2'-Thiodi(4-tert-octylphenol)(3294-03-9)Related Product Information

• o-Cresol
• 2-Thiobarbituric acid
• tert-Butanol
• 2-tert-Butylphenol
• tert-Butyldimethylsilyl chloride
• Octylphenol
• Sodium thiosulfate pentahydrate
• Thioacetamide
• 4-tert-Butylphenol
• p-Cresol
• Thioacetic acid
• Xylenol
• 4-tert-Octylphenol
• 4-Butylphenol
• N-(n-Butyl)thiophosphoric triamide
• Phenol
• Phenol Red
• 3-Aminophenol