ChemicalBook--->CAS DataBase List--->1087-21-4

1087-21-4

1087-21-4 Structure

1087-21-4 Structure
IdentificationMore
[Name]

DIALLYL ISOPHTHALATE
[CAS]

1087-21-4
[Synonyms]

DIALLYL ISOPHTHALATE
ISOPHTHALIC ACID DIALLYL ESTER
TIMTEC-BB SBB009971
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
Di-amyl phathalate(TMP-511)
Dipropen-2-yl isophthalate
1,3-Benzenedicarboxylic acid diallyl ester
Isophthalic acid diallyl
Allyl Isophthalate
[EINECS(EC#)]

214-122-9
[Molecular Formula]

C14H14O4
[MDL Number]

MFCD00048174
[Molecular Weight]

246.26
[MOL File]

1087-21-4.mol
Chemical PropertiesBack Directory
[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 DataBack Directory
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RTECS ]

CZ4230000
[TSCA ]

TSCA listed
[REACH Registrations]

Active
[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.
Hazard InformationBack Directory
[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]

Notclassified
Spectrum DetailBack Directory
[Spectrum Detail]

DIALLYL ISOPHTHALATE(1087-21-4)MS
DIALLYL ISOPHTHALATE(1087-21-4)1HNMR
DIALLYL ISOPHTHALATE(1087-21-4)13CNMR
DIALLYL ISOPHTHALATE(1087-21-4)IR1
DIALLYL ISOPHTHALATE(1087-21-4)IR2
DIALLYL ISOPHTHALATE(1087-21-4)Raman
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

Diallyl Isophthalate,>97.0%(GC)(1087-21-4)
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