| Molecular Formula | C19H33O5P |
| Molar Mass | 356.44 |
| Density | 1.046±0.06 g/cm3(Predicted) |
| Melting Point | 122 °C |
| Boling Point | 417.0±33.0 °C(Predicted) |
| Storage Condition | Room Temprature |
| MDL | MFCD00227871 |
| Physical and Chemical Properties | White or yellowish crystalline powder. Melting point 159-161 °c. The number of grams dissolved in 0.6 of the following solvents at 20 ° C. Is: acetone 27, methanol 62, benzene 33, chloroform 50, n-hexane 0.01, ethyl acetate 20, water. |
| Use | The product is a phosphorus-containing hindered phenol antioxidant and has good extraction resistance. Especially suitable for polyester anti-aging. It is generally added prior to polycondensation as it is a catalyst for polycondensation of the polyester. Can also be used for polyamide as a light stabilizer, and has anti-Oxygen effect. There is a synergistic effect in combination with an ultraviolet absorber. The general dosage of 0.3-1.0. The product is also useful as a stabilizer for dimethyl terephthalate in storage and transport. The toxicity of the product is low. Mice oral LD50>5000mg/kg. |
| Hazard Symbols | Xi - Irritant![]() |
Antioxidant 1222, chemically known as 2,2'-Methylenebis(4-methyl-6-tert-butylphenol), is a commonly used phenolic antioxidant. It is primarily employed in polymer materials (such as plastics, rubber, synthetic fibers, etc.) to prevent degradation and aging caused by oxidation during processing and use.
Author:
Native , LV , Qian Jianhua
Abstract:
The antioxidant calcium salt was synthesized from domestic 2, 6-di-tert-butylphenol with paraformaldehyde, triethyl phosphite, hydrated sodium hydroxide and calcium chloride in four steps. The structure of each step product is dominated by NMR, IR and elemental analysis.Key words:
DOI:
CNKI:SUN:JXSY.0.1996-03-005
cited:
year:
1996
Who & ie = utf-8 & SC _f_para = SC _hilght = person "target ="_blank "> Yao Ruo
Abstract:
In this paper, 2, 6-di-tert-butylphenol is reacted with formaldehyde and dimethylamine to form N, n-dimethyl-3, 5-, di-tert-butyl-4-hydroxybenzylamine by Mannich reaction, the product is then reacted with a diethyl phosphonate to give the title compound. Its IR and ~ 1HNMR are consistent with the structure. The product is a hindered antioxidant, suitable for polyester fiber, polypropylene fiber and polyvinyl chloride fiber.
Key words:
Antioxidant diethyl phosphate synthesis Antioxidant
year:
1990