DIALLYL ISOPHTHALATE

DIALLYL ISOPHTHALATE

Product Introduction

DIALLYL ISOPHTHALATE Basic information
Product Name: DIALLYL ISOPHTHALATE
Synonyms: 1,3-Benzenedicarboxylic acid, di-2-propenyl ester;1,3-Benzenedicarboxylicacid,di-2-propenylester;dappu100;Di-2-Propenyl isophthalate;di-2-propenylisophthalate;Diallylm-phthalate;Isophthalic acid, di-(2-propenyl) ester;ISOPHTHALIC ACID DIALLYL ESTER
CAS: 1087-21-4
MF: C14H14O4
MW: 246.26
EINECS: 214-122-9
Product Categories: ester series
Mol File: 1087-21-4.mol
DIALLYL ISOPHTHALATE Structure
 
DIALLYL ISOPHTHALATE Chemical Properties
Melting point -3℃
Boiling point 176-177°C 5mm
density 1.13
vapor pressure 0.155Pa at 25℃
refractive index 1.5230-1.5270
Fp 163 °C
storage temp. 0-10°C
Specific Gravity 1.125 (20/4℃)
Water Solubility 33.8mg/L at 25℃
LogP 3.36 at 25℃
CAS DataBase Reference 1087-21-4(CAS DataBase Reference)
EPA Substance Registry System 1,3-Benzenedicarboxylic acid, di-2-propenyl ester (1087-21-4)
 
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
RTECS CZ4230000
HS Code 29155090
Toxicity mammal (species unspecified),LD50,oral,1700mg/kg (1700mg/kg),Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974.
 
MSDS Information
 
 
DIALLYL ISOPHTHALATE Usage And Synthesis
Uses Diallyl isophthalate (DAIP) has the advantage over the ortho isomer that it polymerizes faster and gives polymers of better heat resistance. The DAIP prepolymer is less stable than the diallyl phthalate prepolymer. Cured moldings from DAIP monomer-prepolymer compositions can be better processed than cured diallyl phthalate moldings because of their greater fluidity. Compositions containing DAIP prepolymers can be used for the production of hard, translucent, abrasive-resistant, and laser-trimmable coatings.
Preparation Diallyl isophthalate (DAIP) is prepared by esterification of isophthalic acid with allyl alcohol:

1087-21-4 synthesis


The polymers of diallyl isophthalate are very similar in preparation, properties and application to the polymers of diallyl phthalate described above. Mouldings based on diallyl isophthalate are more expensive but have enhanced thermal stability (withstanding up to about 220??C for long periods) and resistance to organic solvents.
Flammability and Explosibility Not classified

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