Diallyl phthalate (DAP) belongs to the class of organic compounds known as benzoic acid esters.
Diallyl phthalates (DAP) are ester derivatives of benzoic acid.
Diallyl phthalate (DAP) is used both for the monomeric and polymeric forms.
CAS Number: 131-17-9
Molecular Formula: C₁₄H₁₄O₄
Molecular Weight: 246.26
Diallyl phthalate (DAP) has been identified in human blood as reported by (PMID: 31557052 ).
Diallyl phthalate (DAP) is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives.
Technically Diallyl phthalate (DAP) is part of the human exposome.
The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health.
An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Description of Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is a phthalate ester.
Phthalate esters are esters of phthalic acid and are mainly used as plasticizers, primarily used to soften polyvinyl chloride.
They are found in a number of products, including glues, building materials, personal care products, detergents and surfactants, packaging, children's toys, paints, pharmaceuticals, food products, and textiles.
Phthalates are hazardous due to their ability to act as endocrine disruptors.
They are being phased out of many products in the United States and European Union due to these health concerns.
As a polymer, Diallyl phthalate (DAP) is used in the production of thermosetting molding powders, casting resins and laminates.
Diallyl phthalate (DAP) is the material of choice for critical, high-performance military and commercial electrical components where long-term reliability is demanded due to its ability to retain its superior insulating properties, even when subjected to extreme environmental conditions of high heat and high humidity over long time periods.
Additionally, Diallyl phthalate (DAP) compounds will resist dimensional change in high-heat soldering environments where competitive materials may warp.
Formula: C6H4(CO2CH2CHCH2)2
Molecular mass: 246.3
Boiling point: 290°C
Melting point: -70°C
Relative density (water = 1): 1.1
Solubility in water, g/100ml at 20°C: 0.015 (very poor)
Vapour pressure, Pa at 25°C: 0.02
Relative vapour density (air = 1): 8.3
Flash point: 166°C c.c.
Auto-ignition temperature: 385°C
Octanol/water partition coefficient as log Pow: 3.23
Diallyl phthalate (DAP) is used as a cross-linking agent in unsaturated polyester resins.
Based on a literature review a significant number of articles have been published on Diallyl phthalate (DAP).
Diallyl phthalate (DAP) resin is a thermosetting resin with a lot of excellent physical properties such as electrical insulation properties, heat resistance, water resistance, chemical resistance, and molding.
In addition to being used in inks and construction materials, Diallyl phthalate (DAP) addresses a wide range of needs in different industries such as electronic and electrical components which require high quality level.
Because of quick-drying, Diallyl phthalate (DAP) is used in organic solvent free UV printing inks.
Diallyl phthalate (DAP) is also adopted electric and electronic parts for high durability in tough high temperature and high voltage environments.
Diallyl phthalate (DAP) is also used in environmentally friendly decorative laminate construction material which does not contain volatile organic compounds (VOC).
Product Description of Diallyl phthalate (DAP):
Catalogue Number: D416055
Chemical Name: Diallyl phthalate (DAP)
Synonyms: 1,2-di-2-Propen-1-yl Ester 1,2-Benzenedicarboxylic Acid; di-2-Propenyl Ester 1,2-Benzenedicarboxylic Acid; Allyl Phthalate; DAP Monomer; DAP-M; DT 170; Daiso DAP Monomer; Dap Tohto DT 170; Dapon R; Dappu; Diallyl phthalate (DAP); NSC 7667
CAS Number: 131-17-9
Molecular Formula: C₁₄H₁₄O₄
Appearance: Clear Colourless Oil
Molecular Weight: 246.26
Storage: 4°C, Light sensitive
Solubility: Chloroform (Slightly), Methanol (Slightly)
Category: Building Blocks; Miscellaneous; Phthalates;
Diallyl Phthalte can be described as polymerizable plasticizer in that it functions as a typical phthalate plasticizer in the uncured states of the compound (such as during mixing and extruding).
Yet contains two allyl groups per molecule that allow cross-linking to increase the cured cross-link density and to lock the plasticizer in place.
Though is not viscous, Diallyl phthalate (DAP) is relatively expensive when compared to the standard phthalate and adipate monomeric plasticizers; and the called-for amount needs to go into the batch instead of being left in a weigh-up container or in a mill pan when the band breaks.
Diallyl phthalate (DAP) solves the handling, weighing, and mixing problems because HallStar uses an amorphous silica carrier that turns the liquid into a free flowing powdered dispersion.
Features & Benefits of Diallyl phthalate (DAP):
Eliminates drum disposal
Eliminates need for heating viscous liquid
80% reduction in VOCs compared with Texanol: meets and exceeds international regulations for no VOCs
Improves Handling
Improves Safety
Reduces employee exposure
Reduces waste
Reduces clean up time
Diallyl phthalate (DAP) is a thermosetting resin with a lot of excellent physical properties such as electrical insulation properties, heat resistance, water resistance, chemical resistance, and molding.
In addition to being used in inks and construction materials, Diallyl phthalate (DAP) addresses a wide range of needs in different industries such as electronic and electrical components which require high quality level.
Because of quick-drying, Diallyl phthalate (DAP) is used in organic solvent free UV printing inks.
Diallyl phthalate (DAP) is also adopted electric and electronic parts for high durability in tough high temperature and high voltage environments.
Diallyl phthalate (DAP) is also used in environmentally friendly decorative laminate construction material which does not contain volatile organic compounds (VOC).
Although different values for vapour pressure of Diallyl phthalate (DAP) are given ranging from 0.0049 to 0.155 Pa, the value of 0.0213 Pa is considered as most reliable.
Phthalate esters are esters of phthalic acid and are mainly used as plasticizers, primarily used to soften polyvinyl chloride.
KEYWORDS:
131-17-9, 1 2-di-2-Propen-1-yl Ester 1 2-Benzenedicarboxylic Acid, di-2-Propenyl Ester 1 2-Benzenedicarboxylic Acid, Allyl Phthalate, DAP Monomer, DAP-M, DT 170, Daiso DAP Monomer, Dap Tohto DT 170, Dapon R
Grade:
Technical
Form:
Liquid
Appearance:
liquid
Auto Ignition Temperature:
435 °C (815 °F)
Boiling Point:
157 °C (315 °F)
Color:
colorless, yellow
Flash Point:
166 °C (331 °F)
Melting Point:
-70 °C (-94 °F)
Odor:
characteristic
Partition Coefficient:
Pow: 3.23
pH:
6.9 - 7.3 @ 20 °C (68 °F)
Relative Density:
1.12 @ 20 °C (68 °F)
Relative Vapor Density:
8.3 @ 25 °C (77 °F)
Vapor Pressure:
0.0015980 mmHg @ 25 °C (77 °F)
Diallyl phthalate (DAP) is a widely used crosslinking agent for unsaturated polyesters.
Diallyl phthalate (DAP) or Diallyl phthalate (DAP) polyester blends are used primarily as plasticizers and carriers for adding catalysts and pigments to polyesters and in molding, electrical parts, laminating compounds, and impregnation of metal castings.
Rubber compounds, epoxy formulations, and polyurethane foams may also contain Diallyl phthalate (DAP).
Annual production of Diallyl phthalate (DAP) in the United States exceeds 5,000 pounds; precise figures are not available.
A NTP Carcinogenesis bioassay of Diallyl phthalate (DAP) (99% pure) was conducted by administering 0 (vehicle control), 150, or 300 mg/kg Diallyl phthalate (DAP) in corn oil by gavage, 5 days per week for 103 weeks, to groups of 50 male and 50 female B6C3F1 mice.
Survival rates and mean body weights of dosed mice were not different from those of the controls, and pathological lesions unrelated to proliferative changes were not observed.
Therefore, a maximally tolerated dose for the purposes of carcinogenicity testing may not have been achieved.
The incidences of lymphoma and either lymphoma or leukemia in dosed male mice were no significantly greater than those in the controls according to pairwise comparisons (P=0.051 to P=0.096), but the trend tests were statistically significant by either life table or incidental tumor analysis (P=0.031 to P=0.045).
The incidence of lymphomas in the high-dose male mice was 12/50 (24%) in comparison with 6/50 (12%) in the controls.
Recent historical incidences at the performing laboratory and in the NTP Bioassay Program were 18/120 (15%) and 71/661 (11%), respectively.
Compound Type of Diallyl phthalate (DAP):
Aromatic Hydrocarbon
Cosmetic Toxin
Ester
Ether
Food Toxin
Household Toxin
Industrial/Workplace Toxin
Organic Compound
Phthalate
Plasticizer
Synthetic Compound
Diallyl phthalate (DAP) is used in electrical parts, laminating compounds, and impregnation of metal castings.
Diallyl phthalate (DAP) is also found in rubber compounds, epoxy formulations, and polyurethane foams.
Diallyl phthalate (DAP) is imported for use as a primary plasticiser for electrical insulation materials, flexible fibreglass topcoat laminates, adhesives and injection moulding materials.
Diallyl phthalate (DAP) is distributed also to various institutions and laboratories for analytical, pharmaceutical and biotechnological research.
CAS:
131-17-9
Molecular Formula:
C14H14O4
Molecular Weight (g/mol):
246.26
MDL Number:
MFCD00008646
InChI Key:
QUDWYFHPNIMBFC-UHFFFAOYSA-N
Synonym:
Diallyl phthalate (DAP), allyl phthalate, diallylphthalate, dapon r, phthalic acid diallyl ester, dapon 35, phthalic acid, diallyl ester, o-phthalic acid, diallyl ester, 1,2-benzenedicarboxylic acid, di-2-propenyl ester, unii-f79l0ul6st
PubChem CID:
8560
IUPAC Name:
bis(prop-2-enyl) benzene-1,2-dicarboxylate
SMILES:
C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C
Diallyl phthalate (DAP) and diallyl iso-phthalate (DAIP) are thermosetting ester resins produced by the reaction of allyl alcohol with ortho-phthalic anhydride and meta-phthalic anhydride, respectively.
The cured resins have excellent electrical insulating properties including high insulation resistance and low electrical losses, even when subjected to to high heat and humidity over long periods of time.
They also have excellent dimensional stability and do not warp in high-heat applications.
Furthermore, they have low moisture absorption, excellent weathering properties, and good chemical resistance to many chemicals and solvents including aliphatic hydrocarbons, oils, alcohols, acids, and alkalis.
The monomers are often used as cross-linking agents in unsaturated (alkyd) polyester resins.
As polymers, Diallyl phthalate (DAP) and DAIP prepolymers are mainly used as molding resins for electrical and electronic parts such as switches, connectors, control panels, circuit breakers, terminal boards, resistors, and insulators.
Other (potential) applications include laminates, prepregs, headlight lamp reflectors, bathtubs, sinks, appliance handles and control knobs.
Applications of Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is used as a reagent in ring-closing ruthenium based reactions.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package.
PROPERTIES of Diallyl phthalate (DAP):
vapor density:
8.3 (vs air)
Quality Level:
100
vapor pressure:
2.3 mmHg ( 150 °C)
Assay:
97%
form:
liquid
autoignition temp.:
725 °F
refractive index:
n20/D 1.519 (lit.)
bp:
165-167 °C/5 mmHg (lit.)
density:
1.121 g/mL at 25 °C (lit.)
SMILES string:
C=CCOC(=O)c1ccccc1C(=O)OCC=C
InChI:
1S/C14H14O4/c1-3-9-17-13(15)11-7-5-6-8-12(11)14(16)18-10-4-2/h3-8H,1-2,9-10H2
InChI key:
QUDWYFHPNIMBFC-UHFFFAOYSA-N
The bulk polymerization of Diallyl phthalate (DAP) was carried out at high temperature (190 °C) without using any initiator, and the reaction was stopped before the gelation point in order to get the prepolymer of DAP.
The mixture for the prepolymer and the monomer was successfully separated by a novel ultrasonic method for the first time, and the separation efficiency for the new method was obviously higher than that for the traditional reprecipitation.
The product obtained by ultrasonic separation was characterized by infrared spectroscopy (IR), gel permeation chromatography (GPC) and iodine number measurement.
It was shown that the average molecular weight of the prepolymer got by the ultrasonic method was lower than that of the prepolymer got by the multi-precipitation, moreover, the molecular weight distribution of the prepolymer got by the ultrasonic separation was broader.
Besides, the residual unsaturation degree of the prepolymer separated by ultrasonic was slightly higher than that of prepolymer separated by reprecipitation.
Linear Formula:
C6H4-1,2-(CO2CH2CH=CH2)2
CAS Number:
131-17-9
Molecular Weight:
246.26
Beilstein:
1880877
EC Number:
205-016-3
MDL number:
MFCD00008646
PubChem Substance ID:
24856324
NACRES:
NA.22
Diallyl phthalate (DAP) is a filled thermoset resin recommended for mounting moderately hard materials and provides good edge retention.
Diallyl phthalate (DAP) is available as either glass or mineral filled.
Diallyl phthalate (DAP) is used as a reagent in ring-closing ruthenium based reactions.
Diallyl phthalate (DAP) is combustible.
Diallyl phthalate (DAP) can react with oxidizers.
Diallyl phthalate (DAP) can also react with acids and alkalis.
Diallyl phthalate (DAP) is incompatible with water and oxygen.
About Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Diallyl phthalate (DAP) is used in articles, in formulation or re-packing and at industrial sites.
Consumer Uses of Diallyl phthalate (DAP):
ECHA has no public registered data indicating whether or in which chemical products Diallyl phthalate (DAP) might be used.
ECHA has no public registered data on the routes by which Diallyl phthalate (DAP) is most likely to be released to the environment.
Article service life of Diallyl phthalate (DAP):
Other release to the environment of Diallyl phthalate (DAP) is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).
Diallyl phthalate (DAP) can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones).
Widespread uses by professional workers of Diallyl phthalate (DAP):
ECHA has no public registered data indicating whether or in which chemical products Diallyl phthalate (DAP) might be used.
ECHA has no public registered data on the types of manufacture using Diallyl phthalate (DAP).
ECHA has no public registered data on the routes by which Diallyl phthalate (DAP) is most likely to be released to the environment.
Formulation or re-packing of Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is used in the following products: coating products.
Release to the environment of Diallyl phthalate (DAP) can occur from industrial use: formulation of mixtures.
Uses at industrial sites of Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is used in the following products: adhesives and sealants, coating products and polymers.
Diallyl phthalate (DAP) is used for the manufacture of: electrical, electronic and optical equipment, rubber products and plastic products.
Release to the environment of Diallyl phthalate (DAP) can occur from industrial use: in processing aids at industrial sites, in the production of articles and as processing aid.
Manufacture of Diallyl phthalate (DAP):
ECHA has no public registered data on the routes by which Diallyl phthalate (DAP) is most likely to be released to the environment.
Physical Description of Diallyl phthalate (DAP):
Diallyl phthalate (DAP) is a clear pale-yellow liquid.
Diallyl phthalate (DAP) is odorless.
Molecular Weight: 246.26
XLogP3: 3.2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 8
Exact Mass: 246.08920892
Monoisotopic Mass: 246.08920892
Topological Polar Surface Area: 52.6 Ų
Heavy Atom Count: 18
Formal Charge: 0
Complexity: 290
Isotope Atom Count : 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
The uses of phthalates as plasticizers are widely spread and growing rapidly in the manufacture of various PVC products, textiles, toys as well as medicinal products.
Moreover, they can be applied in various industries such as insect repellents, propellants and many cosmetics manufacture.
Due to its low cost production and its versatile chemical properties, phthalates attracted innumerable industrialists towards plastic-based productions throughout the world.
Being widely used as plasticizers and not bounded to polymer mesh, they easily pass from plastic products to surrounding environments and consequently pollute water, soil, air and last but not least food products.
Rainfall transfers phthalates and phthalate esters in the atmosphere, which lead to their accumulation in water depending on geographic locations.
Discharge of phthalate esters into the atmospheric and aquatic regions has therefore increased as a reason of urbanization.
Using agricultural plastics has enormously caused contamination to the soil in rural areas.
Hence, phthalates are very toxic, carcinogenic and can cause serious diseases in human beings.
They are considered as toxic environmental priority pollutants and endocrine disruptor chemicals.
In addition, it has toxic effects on the liver, kidney, and reproductive organs and act partly as endocrine disrupting agents.
Thus far, a number of phthalates have been reported such as Dibutyl Phthalate (DBP), Diethyl Phthalate (DEP), Diethyl Hexyl Phthalate (DEHP), Diallyl phthalates (DAP) and identified in environmental water samples.
This compound can pause environmental and health problems.
Diallyl phthalate (DAP) is largely used as plastilizers in PVC plastic containers, packaging and medical devices.
It can be released during longtime storage in warm conditions and contaminate water bodies.
Nevertheless, despite its high toxicity, no valuable information on the decontamination of wastewaters containing DAP exists.
Production of Diallyl phthalate (DAP) during 2002 is estimated at 4400 tonnes worldwide.
Annual production at the two manufacturing sites in Japan is estimated at 3900 tonnes.
Diallyl phthalate (DAP) is produced either by the esterification reaction between allyl alcohol and phthalic anhydride, or by the condensation between allyl chloride and disodium phthalate.
Diallyl phthalate (DAP) functions as a crosslinking agent.
The functionality is ascribed to the two highly reactive allyl groups in the molecule.
The allyl groups are able to react with other unsaturated organic chemicals to form C-C covalent bonds.
Diallyl phthalate (DAP) also functions as a plasticizer.
However, unlike other phthalate esters, such as di-butyl phthalate (DBP), di-(2-ethylhexyl) phthalate (DEHP), etc., Diallyl phthalate (DAP) is used as a reactive plasticizer.
Diallyl phthalate (DAP) is added to polymer and prepolymer systems in order to make them softer and more easily moulded during the curing process and then it binds covalently into the polymer matrix to produce rigid thermoset plastics.
The other phthalate esters, such as DBP and DEHP are normally added to the polymer in order to make the end products softer or more flexible.
Due to their lack of functionality, these other phthalate esters do not bind chemically into the polymer matrix, and, therefore, there is the potential for them to leach out.
Whereas other phthalate esters are used at up to levels greater than 50% to plasticize final products, no use of Diallyl phthalate (DAP) where it functions to plasticize the final product is known (therefore, DAP is an intermediate).
Sources of Environmental Exposure:
The environmental exposure to Diallyl phthalate (DAP) may occur by emission to aquatic compartment from waste water at production and user sites and evaporative emissions associated with its use as building and household materials, etc., and disposal of consumer products.
Environmental exposure is also expected from formulation and industrial use.
Monitoring of wastewater from the Diallyl phthalate (DAP) manufacturing plant in Matsuyama, Japan found that levels of DAP were in the range of 0.3-0.5 µg/L (DAISO, 2003b).
Sampling was conducted for the wastewater in the outfall facing the bay in Seto Inland Sea in Matsuyama-shi, Ehime Prefecture.
The annual estimated emission from the plant is considered to be 5.3 kg/year (equivalent to 2.7x10-3 kg/tonne Diallyl phthalate (DAP) produced) (DAISO 2003b).
A Japanese study showed that no Diallyl phthalate (DAP) was detected in either the sediment or hydrosphere of 27 monitoring points in Japan in 1985.
The lower limits of detection were 0.0002 µg/mL in water (0.2 ppb) and 0.02 µg/g in dry sediment (0.02 ppm).
Synonyms:
Diallyl phthalate (DAP)
131-17-9
Allyl phthalate
Diallylphthalate
Dapon 35
Dapon R
Phthalic Acid Diallyl Ester
Phthalic acid, diallyl ester
1,2-Benzenedicarboxylic acid, di-2-propenyl ester
o-Phthalic acid, diallyl ester
NCI-C50657
NSC 7667
bis(prop-2-enyl) benzene-1,2-dicarboxylate
Diallylester kyseliny ftalove
1,2-Benzenedicarboxylic acid, 1,2-di-2-propen-1-yl ester
Di-2-propenyl 1,2-benzenedicarboxylate
phthalic acid, bis-allyl ester
F79L0UL6ST
143318-73-4
25053-15-0
DTXSID7020392
DIPROP-2-ENYL BENZENE-1,2-DICARBOXYLATE
NSC-7667
DTXCID70392
CAS-131-17-9
CCRIS 1361
HSDB 4169
Diallylester phthalic acid
EINECS 205-016-3
Diallylester kyseliny ftalove [Czech]
UNII-F79L0UL6ST
BRN 1880877
AI3-02574
DAP monomer
di-allyl phthalate
MFCD00008646
Phthalic acid diallyl
Diallyl phthalate (DAP), 97%
1,2-Benzenedicarboxylicaciddi-2-propenylester
EC 205-016-3
SCHEMBL15174
4-09-00-03188 (Beilstein Handbook Reference)
Diallyl ester o-phthalic acid
MLS002415725
Diallyl ester of phthalic acid
WLN: 1U2OVR BVO2U1
Diallyl phthalate (DAP) Monomer, DAP
RX 1-501N (Salt/Mix)
CHEMBL1329372
Diallyl phthalate (DAP) [HSDB]
NSC7667
HMS2267F17
RX 3-1-530 (Salt/Mix)
ZINC1688261
Tox21_201961
Tox21_300135
Nonflammable decobest DA (Salt/Mix)
Diallyl phthalate (DAP), analytical standard
AKOS015891274
NCGC00091365-01
NCGC00091365-02
NCGC00091365-03
NCGC00091365-04
NCGC00254197-01
NCGC00259510-01
BS-14891
SMR001253767
FT-0624597
P0290
J-005948
Q2161731
1,2-bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate
1,2-benzenedicarboxylic acid, di-2-propen-1-yl ester
1,2-benzenedicarboxylic acid, di-2-propenyl ester
diallylester phthalic acid
diallylphthalate
diprop-2-en-1-yl benzene-1,2-dicarboxylate
phthalic acid diallyl ester
o-phthalic acid diallyl ester
phthalic acid, diallyl ester
o-phthalic acid, diallyl ester
phthalic acid, diallyl ester (8CI)
prop-2-enyl 2-(prop-2-enyloxycarbonyl)benzoate
bis(prop-2-enyl) benzene-1,2-dicarboxylate
1,2-Benzenedicarboxylic acid, di-2-propen-1-yl ester [ACD/Index Name]
1,2-Bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate
131-17-9 [RN]
205-016-3 [EINECS]
25053-15-0 [RN]
CZ4200000
Diallyl phthalate (DAP) [ACD/IUPAC Name]
Diallyl phthalate (DAP) resin
Diallyl-phthalat [German] [ACD/IUPAC Name]
diprop-2-en-1-yl benzene-1,2-dicarboxylate
MFCD00008646 [MDL number]
Phtalate de diallyle [French] [ACD/IUPAC Name]
Phthalic acid, diallyl ester (8CI)
[131-17-9] [RN]
1,2-Benzenedicarboxylic acid 1,2-di-2-propen-1-yl ester
1,2-Benzenedicarboxylic acid, 1,2-di-2-propen-1-yl ester
1,2-Benzenedicarboxylic acid, di-2-propenyl ester
1,2-Benzenedicarboxylicaciddi-2-propenylester
124743-27-7 [RN]
143318-73-4 [RN]
3,5-diiodo-2-methyl benzoic acid
3,5-Diiodo-2-methylbenzoic acid [ACD/IUPAC Name]
4-09-00-03188 [Beilstein]
4-09-00-03188 (Beilstein Handbook Reference) [Beilstein]
ALLYL PHTHALATE
benzene-1,2-dicarboxylic acid diallyl ester
bis(prop-2-enyl) benzene-1,2-dicarboxylate
C049098
Dap
DAP monomer
Dapon R
dapon r.
Di-2-propenyl 1,2-benzenedicarboxylate
diallyl benzene-1,2-dicarboxylate
Diallyl ester of phthalic acid
Diallyl ester o-phthalic acid
Diallyl phthalate (DAP) Monomer, DAP
Diallyl phthalic acid
Diallylester kyseliny ftalove [Czech]
Diallylester kyseliny ftalove
Diallylester kyseliny ftalove [Czech]
diallylester phthalic acid
DIALLYLPHTHALATE
diprop-2-enyl benzene-1,2-dicarboxylate
EINECS 205-016-3
NCGC00091365-02
Nonflammable decobest da
Nonflammable decobest DA (Salt/Mix)
o-phthalic acid diallyl ester
o-Phthalic acid, diallyl ester
phthalic acid diallyl ester
Phthalic acid, bis-allyl ester
Phthalic acid, diallyl ester
POLY(Diallyl phthalate (DAP))
prop-2-enyl 2-(prop-2-enyloxycarbonyl)benzoate
RX 1-501N (Salt/Mix)
RX 3-1-530 (Salt/Mix)
ST5405391
WLN: 1U2OVR BVO2U1
Regulatory process names:
1,2-Benzenedicarboxylic acid, 1,2-di-2-propen-1-yl ester
1,2-Benzenedicarboxylic acid, di-2-propenyl ester
Allyl phthalate
Dapon 35
Dapon R
Di-2-propenyl 1,2-benzenedicarboxylate
Diallyl phthalate (DAP)
Diallyl phthalate (DAP)
Diallylester kyseliny ftalove
o-Phthalic acid, diallyl ester
Phthalic acid, diallyl ester
phthalic acid, diallyl ester
Phthalic acid, diallyl ester (8CI)
Translated names:
dialil ftalat (ro)
dialil ftalat (sl)
dialil-ftalat (hr)
dialilftalatas (lt)
diallil-ftalát (hu)
diallyl-ftalát (cs)
diallylftalaat (nl)
diallylftalat (no)
diallylftalat (sv)
diallylphthalat (da)
Diallylphthalat (de)
diallyyliftalaatti (fi)
Diallüülftalaat (et)
dialyl-ftalát (sk)
ester diallilowy kwasu ftalowego (pl)
ftalan diallilu (pl)
ftalan diallilu ester diallilowy kwasu ftalowego (pl)
ftalato de dialilo (es)
ftalato de dialilo (pt)
ftalato di diallile (it)
phtalate de diallyle (fr)
dialilftalāts (lv)
φθαλικό διαλλύλιο (el)
диалил фталат (bg)
CAS names:
1,2-Benzenedicarboxylic acid, 1,2-di-2-propen-1-yl ester
IUPAC names:
1,2-Benzenedicarboxylic acid di-2-propenyl ester
1,2-Benzenedicarboxylic acid, di-2-propenyl ester
1,2-bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate
bis(prop-2-enyl) benzene-1,2-dicarboxylate
DAP Monomer
Diallyl phthalate (DAP)
Diallyl phthalate (DAP)
Diallyl phthalate (DAP)
Diallyl phthalate (DAP) MONOMER
diallyl-phthalate-
Diallylphthalat
Diallylphthalate
diprop-2-enyl benzene-1,2-dicarboxylate
Trade names:
DAP monomer
Other identifiers:
124743-27-7
124743-27-7
131-17-9
143318-73-4
143318-73-4
607-086-00-4