Antioxidant BHT 264
CAS:128-37-0
Purity:99%
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Product Details
Flammability and Explosibility |
Nonflammable |
Synthesis |
a, first raw material diphenylamine 50.0g into a reaction vessel equipped with a stirrer, reflux condenser, heated to diphenylamine added to melt;After completely melted, a mixed catalyst prepared from 1.5 g of magnesium chloride and 1.5 g of anhydrous stannous chloride was added, and heating and stirring were continued for mixing; b. After step a is mixed uniformly, 80.5 g of α-methylstyrene is added dropwise, and the dropwise addition time is 0.5 h. After the dropwise addition is completed, the reaction temperature is controlled to be 130-140° C., and the reaction is completed at this temperature for 1 h. The reaction is completed. ; c, after the end of the reaction, the resulting reaction solution was cooled, then add 60 of petroleum ether 140g and methanol 5g mixed solvent, dropped to 25 ± 2 °C cooling crystallization; d, after the end of crystallization, followed by filtration, petroleum ether and water washing, and then dried at 45 °C for 14 hours, dried to obtain the antioxidant 4,4 '- bis (α, α- dimethyl benzyl) diphenylamine . The product obtained in this example was white crystal with a yield of 85% and a purity of 98.24% |
Application |
Diphenylamine antioxidant CAPOX 445, 4, 4'-Bis (alpha, alpha-dimethylbenzyl) diphenylamine, is a highly effective non-discoloring aromatic amine type antioxidant finding utility as a thermal stabilizer in a wide variety of applications, including polyolefins, styrenics, polyols, hot melt adhesives, lubricants and polyamides. Excellent performance at processing temperatures, and strong synergy with other types of antioxidants such as phenolics and phosphites, makes CAPOX 445 an excellent choice as a component of your thermal stabilizer package. |
Industrial uses |
This product is one of the few kinds of antioxidant, which is non-toxic, tasteless, light colored. The anti- oxygen effect is similar America in Uniroyal. It is widely used in various kinds of elastomers. It can be used in polyethylene, polypropylene, polyvinyl chloride and other color master batch. It can also be used as antioxidant in polyurethane foam, rubber wire, cable, food package and adhesive, especially in neoprene colorful cable's jacket for its excellent resistance to heat, light, and aging. In polyether this product can be used as light-resistant and anti-aging antioxidant, also as antioxidant for lubricating oil.It is especially effective to be used in neoprene acrylate rubber, polyether polyalcohol for its resistance to aging caused by high temperature and light. When used together with sulfur-contained antioxidant, it has operational effect. |
InChI:InChI=1/C30H31N/c1-29(2,23-11-7-5-8-12-23)25-15-19-27(20-16-25)31-28-21-17-26(18-22-28)30(3,4)24-13-9-6-10-14-24/h5-22,31H,1-4H3
The conversion of diphenylamine (DPA) an...
Alkylation of diphenylamine was carried ...
A practical approach to the synthesis of...
The invention discloses a method for ant...
The invention relates to a preparation m...
The invention relates to a composition c...
diphenylamine
isopropenylbenzene
bis[4-(2-phenyl-2-propyl)phenyl]amine
Conditions | Yield |
---|---|
With
zinc(II) chloride;
In
ethanol; 1,2-dichloro-ethane;
at 185 ℃;
Solvent;
Temperature;
Reagent/catalyst;
regioselective reaction;
Flow reactor;
|
89% |
diphenylamine;
With
tin(ll) chloride; magnesium chloride;
Heating;
isopropenylbenzene;
at 130 - 140 ℃;
for 1.5h;
Reagent/catalyst;
Temperature;
|
85% |
With
2-methylbenzene-1,4-diol;
In
toluene;
at 60 - 125 ℃;
Inert atmosphere;
|
38.5 g |
diphenylamine
isopropenylbenzene
bis[4-(2-phenyl-2-propyl)phenyl]amine
4-(α,α-dimethylbenzyl)diphenylamine
Conditions | Yield |
---|---|
With
Al-MSU-G;
at 90 ℃;
for 6h;
Further Variations:;
Reagents;
Temperatures;
reaction time;
Product distribution;
|
97.2% |
With
acid-treated clay catalyst Engelhard F-24;
In
o-xylene;
at 89.9 ℃;
for 12h;
Product distribution;
Irradiation;
other alkylating agent, var. catalyst, var. temp, var. solvent, var. time, also without sonication, and in air, also reused catalysts;
|
diphenylamine
isopropenylbenzene
2,4-dimethyl-1-heptene
N-phenyl-1-naphthylamine
N,N-bis(4-nitrophenyl)-N',N'-bis[4-(2-phenyl-2-isopropyl)phenyl]-1,4-phenylenediamine
N,N-bis(4-aminophenyl)-N',N'-bis[4-(2-phenyl-2-isopropyl)phenyl]-1,4-phenylenediamine
C39H33N3O2S
C45H43N3O4S