Antioxidant Ehdpp

Product Details
Customization: Available
Certification: CCIC
Environmental Protection: Yes
Manufacturer/Factory, Trading Company
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  • Antioxidant Ehdpp
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Basic Info.

Model NO.
EHDPP
Appearance
Liquid
Boiling Point
389.853ºC at 760 Mmhg(Cal.)Ref.
MW
346.41
Fp
234.101ºC(Cal.)Ref.
Einecs No.
239-716-5
Transport Package
200kg/Drum
Specification
99%
Trademark
DEBORN
Origin
China
HS Code
381220

Product Description

Chemical Name 2-Ethylhexyl Diphenyl Phosphite
Molecular Formula  C20H27O3P
Molecular Weight  346.41
Structure  
Antioxidant Ehdpp
CAS Number  15647-08-2
 
Specification Appearance:                                 liquid
                    Boiling Point:                                389.853ºC at 760 mmHg(Cal.)ref.
                    Flash point:                                  234.101ºC(Cal.)ref.
                    TGA(ºC,% mass loss):                  218           5%
                                                                      236           10%
                                                                      280           50%
                    Solubility(g/100g solvent @25ºC):   Water              -
                                                                        n-Hexane      Soluble
                                                                        Toluene        Soluble
                                                                        Ethanol         Soluble
                                                    
Packing It is packed in drums with net of 50KG.
 
Applications
 Applicable to ABS, PVC, polyurethane, coatings, adhesives and so on.
Antioxidant Ehdpp

 
diphenyl(2-ethylhexyl)phosphite;forstab;forstabk201;Phosphorousacid,2-ethylhexyldiphenylester;2-ETHYLHEXYLDIPHENYLPChemicalbookHOSPHITE;O,O-Diphenyl-O-(2-ethylhexyl)phosphite;diphenylethylhexylphosphite;Phosphorousaciddiphenyl2-ethylhexylester


In the presence of strong bases, the negative ions formed by DEP can undergo nucleophilic addition reactions with unsaturated bonds such as aldehydes and imines to obtain phosphonate compounds. It should be noted that both reaction rate and reaction yield are affected by steric hindrance. Some of these reactions can be well stereoselective under chiral orthogroup induction.

 
 

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