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2,6-Di-tert-butyl-4-methylphenol (2,6-Di-tert-butyl-4-methylphenol)

Bargaining 10-21 09:11 Update

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2,6-Di-tert-butyl-4-methylphenol

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2,6-Di-tert-butyl-4-methylphenol
3,5-Di-tert-butyl-4-hydroxytoluene
Butylhydroxytoluene
Phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-
2,6-Di-tert-butyl-p-cresol
4-hydroxy-3,5-di-tert-butylphenylacetic acid
3,5-di-t-butyl-4-hydroxyphenyl-acetic acid
2,6-di-tert-butyl-4-methyl-phenol
Naugard BHT
2,6-Di-Tert-Butyl-4-Methylphenol
4-methyl-2,6-di-tert-butylphenol
2,6-di-t-butyl-p-methyl phenol

+Expand -Stow

128-37-0

C15H24O

220.35

2907199090

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Nature Description

White or light yellow crystals. Melting point 71 ℃, boiling point 265 ℃, relative density 1.048(20/4 ℃), refractive index 1.4859(75℃). Solubility under normal temperature in the following: methanol 25, ethanol 25-26, isopropyl alcohol 30, mineral oil 30, acetone 40, petroleum ether 50, benzene 40, lard (40-50 ℃)40-50, corn oil and soybean oil 40-50. It is insoluble in water, 10NaOH solution, glycerol and propylene glycol. Odorless, tasteless, with good thermal stability.

1.048

265oC

69-71oC

127oC

不溶

Product Applications

Used for organic synthesis; Plastic additives; Used as rubber, plastic antioxidant, gasoline, transformer oil, turbine oil, animal and vegetable oil, food and other antioxidant; BHT is widely used oil-soluble antioxidant at home and abroad. Although it is highly toxic, it has strong antioxidant capacity, good heat resistance and stability..

Production method

After isobutyl alcohol is vaporized, dehydration reaction is carried out in the presence of catalyst to generate isobutene, which is obtained by alkylating reaction with P-cresol. KG, ton isobutyl alcohol (95)1400 p-Cresol (80)1000

Security

Dangerous Goods Marking： Xn

Safety instructions： S26: in case of contact with eyes, rinse with plenty of water immediately and send it to the doctor for diagnosis and treatment. S37/39: use suitable gloves and goggles or mask.