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Pentaerythritol triacrylate is a viscous, thick, clear yellow liquid that is a versatile monomer used in various applications due to its ability to bind both covalently and irreversibly to outer cell membrane surfaces.

3524-68-3

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3524-68-3 Usage

Uses

Used in Adhesives, Coatings, and Inks Industry:
Pentaerythritol triacrylate is used as a reactive diluent and crosslinking agent for [application reason] enhanced adhesion, durability, and performance in adhesives, coatings, inks, photoresists, castings, and other products cured by UV radiation.
Used in Organic Synthesis:
Pentaerythritol triacrylate is used as a key intermediate in [application type] organic synthesis for [application reason] the production of various chemicals and materials that require its unique properties.
Used in Lithographic Printing Plate Industry:
Pentaerythritol triacrylate is used as a precursor for [application type] lithographic printing plates for [application reason] improving the quality and durability of the plates, as well as enhancing the printing process.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Pentaerythritol triacrylate is explosively unstable at temperatures near its boiling point .

Fire Hazard

The flash point of Pentaerythritol triacrylate has not been determined, but Pentaerythritol triacrylate is probably combustible.

Safety Profile

Moderately toxic by ingestion and skin contact. Skin and severe eye irritant. Questionable carcinogen with experimentaltumorigenic data. Used for radiation-cured adhesives, coatings, inks, textiles, photo resists, and coatings. When heated to decompositio

Check Digit Verification of cas no

The CAS Registry Mumber 3524-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3524-68:
(6*3)+(5*5)+(4*2)+(3*4)+(2*6)+(1*8)=83
83 % 10 = 3
So 3524-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O7/c1-4-11(16)19-8-14(7-15,9-20-12(17)5-2)10-21-13(18)6-3/h4-6,15H,1-3,7-10H2

3524-68-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (15705)  Pentaerythritol triacrylate, stab. with 300-400ppm 4-methoxyphenol   

  • 3524-68-3

  • 500g

  • 467.0CNY

  • Detail
  • Aldrich

  • (246794)  Pentaerythritoltriacrylate  technical grade

  • 3524-68-3

  • 246794-100G

  • 862.29CNY

  • Detail
  • Aldrich

  • (246794)  Pentaerythritoltriacrylate  technical grade

  • 3524-68-3

  • 246794-500G

  • 1,614.60CNY

  • Detail

3524-68-3Synthetic route

Pentaerythritol
115-77-5

Pentaerythritol

acrylic acid
79-10-7

acrylic acid

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

Conditions
ConditionsYield
Stage #1: Pentaerythritol; acrylic acid With IR-120 strong acid type ion exchange resin at 100℃; for 0.5h;
Stage #2: In benzene at 100℃; for 3h; Temperature;
88%
pentaerythritol triallyl ether
1471-17-6

pentaerythritol triallyl ether

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

Conditions
ConditionsYield
With triethylamine; trichlorophosphate In (2S)-N-methyl-1-phenylpropan-2-amine hydrate
Pentaerythritol
115-77-5

Pentaerythritol

2-methoxyethyl acrylate
3121-61-7

2-methoxyethyl acrylate

A

2,2-bis(hydroxymethyl)-1,3-propanediyl diacrylate

2,2-bis(hydroxymethyl)-1,3-propanediyl diacrylate

B

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

Conditions
ConditionsYield
With zinc diacetate; oxygen; 4-methoxy-phenol; 1,8-diazabicyclo[5.4.0]undec-7-ene at 105 - 120℃; for 5h; Reagent/catalyst; Inert atmosphere; Overall yield = 48 %;
Pentaerythritol
115-77-5

Pentaerythritol

2-methoxyethyl acrylate
3121-61-7

2-methoxyethyl acrylate

A

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

B

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

Conditions
ConditionsYield
With 1,4-diaza-bicyclo[2.2.2]octane; zinc diacetate; oxygen; 4-methoxy-phenol at 105 - 120℃; under 130 - 760 Torr; for 30h; Inert atmosphere; Overall yield = 96 %;
With 1,4-diaza-bicyclo[2.2.2]octane; zinc diacetate; oxygen; 4-methoxy-phenol at 105 - 120℃; under 130 - 760 Torr; for 30h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Overall yield = 88 %;
With 1,4-diaza-bicyclo[2.2.2]octane; zinc diacetate; oxygen; 4-methoxy-phenol at 105 - 120℃; under 130 - 760 Torr; for 30h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Overall yield = 88 %;
succinic acid anhydride
108-30-5

succinic acid anhydride

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C19H22O11

C19H22O11

Conditions
ConditionsYield
With triphenylphosphine at 90℃; for 8h;99.9%
cyclopenta-1,3-diene
542-92-7

cyclopenta-1,3-diene

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C29H36O7

C29H36O7

Conditions
ConditionsYield
In toluene for 3h; Diels-Alder Cycloaddition; Inert atmosphere; Schlenk technique;97%
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

polymer resin; monomer(s): pentaerythritol triacrylate

polymer resin; monomer(s): pentaerythritol triacrylate

Conditions
ConditionsYield
With acetic acid butyl ester; hydroxyethyl cellulose; dibenzoyl peroxide In water at 80℃; for 8h; Product distribution; Further Variations:; Reagents;96.6%
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

teroxirone
2451-62-9

teroxirone

C66H81N3O36

C66H81N3O36

Conditions
ConditionsYield
With 4-methoxy-phenol; triphenylphosphine at 95℃; for 14h;94.58%
4-methyl-hexahydrophthalic anhydride
19438-60-9

4-methyl-hexahydrophthalic anhydride

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C22H28O10

C22H28O10

Conditions
ConditionsYield
With 4-methoxy-phenol; triphenylphosphine at 90℃; for 8h;91.2%
C29H22O4

C29H22O4

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C57H54O16

C57H54O16

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 20h;85%
3-(triethoxypropyl) isocyanate
24801-88-5

3-(triethoxypropyl) isocyanate

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C24H39NO11Si

C24H39NO11Si

Conditions
ConditionsYield
With dibutyltin dilaurate at 50℃; Reagent/catalyst; Temperature;82%
With dibutyltin dilaurate at 40℃; for 16h;
With dibutyltin dilaurate; 4-methoxy-phenol at 60℃; for 5h;
3-(trimethoxysilyl)propyl isocyanate
15396-00-6

3-(trimethoxysilyl)propyl isocyanate

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C21H33NO11Si

C21H33NO11Si

Conditions
ConditionsYield
With triethylamine at 50℃; Temperature; Reagent/catalyst;81%
With octyl sulfoxide; pentaerythritol tetraacrylate at 80℃; for 2h;
4,4'-(9-fluorenylidene)-bis-benzoic acid
54941-51-4

4,4'-(9-fluorenylidene)-bis-benzoic acid

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C55H50O16

C55H50O16

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 20h;80%
sebacoyl chloride
111-19-3

sebacoyl chloride

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C38H50O16

C38H50O16

Conditions
ConditionsYield
With pyridine In dichloromethane at 26℃; for 2h; Reflux;73%
C28H31N2O3(1+)*C24BF20(1-)

C28H31N2O3(1+)*C24BF20(1-)

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C42H47N2O9(1+)*C24BF20(1-)

C42H47N2O9(1+)*C24BF20(1-)

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 25℃; for 3h;21%
C29H31N2O5(1+)*C24BF20(1-)

C29H31N2O5(1+)*C24BF20(1-)

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C57H67N2O14(1+)*C24BF20(1-)

C57H67N2O14(1+)*C24BF20(1-)

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 25℃; for 8h;18%
ethyleneimine
151-56-4

ethyleneimine

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

pentaerythritol tris(3-(1-aziridinyl)propionate)
57116-45-7

pentaerythritol tris(3-(1-aziridinyl)propionate)

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

polymer; monomer(s): pentaerythritol triacrylate

polymer; monomer(s): pentaerythritol triacrylate

Conditions
ConditionsYield
With 1-hydroxycyclohexyl phenyl ketone; sodium dodecyl-sulfate In water UV-irradiation;
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

poly[pentaerythritol triacrylate], photocured stereolithography; monomer(s): pentaerythritol triacrylate

poly[pentaerythritol triacrylate], photocured stereolithography; monomer(s): pentaerythritol triacrylate

Conditions
ConditionsYield
With Camphorquinone UV-irradiation;
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

Hexamethylene diisocyanate
822-06-0

Hexamethylene diisocyanate

C36H48N2O16
77001-81-1

C36H48N2O16

Conditions
ConditionsYield
dibutyltin dilaurate In methylpentan-2-one, 4- at 70℃; for 4h; Heating / reflux;
With dibutyltin dilaurate at 75℃; for 6h;
isophorone diisocyanate
4098-71-9

isophorone diisocyanate

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C40H54N2O16
101162-60-1

C40H54N2O16

Conditions
ConditionsYield
dibutyltin dilaurate In methylpentan-2-one, 4- at 70℃; for 4h; Heating / reflux;
With dibutyltin dilaurate; 4-methoxy-phenol at 70 - 80℃; for 6h;
N-propyl-perfluorooctylethylamine

N-propyl-perfluorooctylethylamine

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C27H30F17NO7
852876-56-3

C27H30F17NO7

Conditions
ConditionsYield
triethylamine at 50℃; for 3h; Michael Condensation;
glutaric anhydride,
108-55-4

glutaric anhydride,

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C19H24O10

C19H24O10

Conditions
ConditionsYield
With 2,6-di-tert-butyl-4-methyl-phenol; sulfuric acid at 20 - 50℃;
1,4-Divinylbenzene
105-06-6

1,4-Divinylbenzene

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

polymer; monomer(s): pentaerythritol triacrylate; 4-divinylbenzene

polymer; monomer(s): pentaerythritol triacrylate; 4-divinylbenzene

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; toluene at 60℃; for 6h;
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

poly(pentaerythritol triacrylate); monomer(s): pentaerythritol triacrylate

poly(pentaerythritol triacrylate); monomer(s): pentaerythritol triacrylate

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; toluene at 60℃;
Butane-1,4-diol
110-63-4

Butane-1,4-diol

2-methoxy-ethanol
109-86-4

2-methoxy-ethanol

(2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate
3779-63-3

(2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate

2-amino-6-methylpyrimidin-4-ol
3977-29-5

2-amino-6-methylpyrimidin-4-ol

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

1,4-butanediol; DESMODUR N-100; 2-methoxyethanol; methyl isocytocine; PETA; mixture of, heated

1,4-butanediol; DESMODUR N-100; 2-methoxyethanol; methyl isocytocine; PETA; mixture of, heated

Conditions
ConditionsYield
Stage #1: Butane-1,4-diol; (2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate; dibutyltin dilaurate In ISOPROPYLAMIDE at 40℃; for 0.5h;
Stage #2: 2-amino-6-methylpyrimidin-4-ol In ISOPROPYLAMIDE at 40 - 87℃;
Stage #3: 2-methoxy-ethanol; pentaerythritol triacrylate With hydroquinone more than 3 stages;
Butane-1,4-diol
110-63-4

Butane-1,4-diol

(2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate
3779-63-3

(2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate

2-amino-6-methylpyrimidin-4-ol
3977-29-5

2-amino-6-methylpyrimidin-4-ol

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

1,4-butanediol; DESMODUR N-100; methyl isocytocine; PETA; mixture of, heated

1,4-butanediol; DESMODUR N-100; methyl isocytocine; PETA; mixture of, heated

Conditions
ConditionsYield
Stage #1: (2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene)isocyanate; 2-amino-6-methylpyrimidin-4-ol In ISOPROPYLAMIDE at 87 - 90℃;
Stage #2: pentaerythritol triacrylate With hydroquinone; dibutyltin dilaurate In ISOPROPYLAMIDE at 40 - 60℃; for 5.5h;
Stage #3: Butane-1,4-diol In ISOPROPYLAMIDE at 50℃; for 5.5h;
pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

(hexanediol diacrylate)-co-(hydroxyethyl acrylat)-co-(pentaerythritol triacrylate)

(hexanediol diacrylate)-co-(hydroxyethyl acrylat)-co-(pentaerythritol triacrylate)

Conditions
ConditionsYield
With 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one In isopropyl alcohol; toluene UV-irradiation;
3,5-bis(1,1-dimethylethyl)-4-hydroxy-N-(4-hydroxy-3-methylphenyl)-benzenepropanamide

3,5-bis(1,1-dimethylethyl)-4-hydroxy-N-(4-hydroxy-3-methylphenyl)-benzenepropanamide

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C86H117N3O16
1001078-10-9

C86H117N3O16

Conditions
ConditionsYield
Stage #1: 3,5-bis(1,1-dimethylethyl)-4-hydroxy-N-(4-hydroxy-3-methylphenyl)-benzenepropanamide With potassium tert-butylate In tetrahydrofuran Michael Addition;
Stage #2: pentaerythritol triacrylate In tetrahydrofuran
C67H108N6O27

C67H108N6O27

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

C109H162N6O45

C109H162N6O45

Conditions
ConditionsYield
In acetone for 40 - 50h; Inert atmosphere;

3524-68-3Relevant academic research and scientific papers

Piezoelectric pH sensors. AT-cut quartz resonators with amphoteric polymer films

Wang,Ward,Ebersole,Foss

, p. 2553 - 2562 (1993)

Piezoelectric AT-cut quartz resonators immersed in aqueous media, coated with cross-linked films of the random copolymer-{[CH2CH(CO2H)]a-[CH2C(CH3) (CO2CH3)]b-[CH2C(CH3) (CO2CH2CH3-NMe2)]c}n (1), exhibit large frequency changes when the pH is changed in the vicinity of the isoelectric point of the polymer film. The frequency changes are attributed to changes in the viscoelastic properties of the films that occur during phase transitions between the isoelectric form and the cationic polymer (1-NMe2H+) present at low pH or the anionic polymer (1-CO2-) present at high pH. These phase transitions are accompanied by dramatic changes in acoustic energy attenuation, film thickness changes, and film surface energy, as indicated by acoustic impedance analysis, phase measurement interferometric microscopy, and contact angle measurements. The results are consistent with pH-dependent segregation of the isolectric and ionic phases within the bulk and between the bulk and the surface. The unique pH-sensing capabilities of the coated resonators, combined with their robustness, ease of fabrication, and low cost, provide a convenient approach for the measurement of 'threshold' pH changes. Real-time measurements of enzymatic activity and microbe metabolism are demonstrated as examples of potential applications of these sensors.

Preparation method of pentaerythritol triacrylate

-

Paragraph 0029-0032; 0039-0042; 0046; 0049-0052; 0054, (2018/10/19)

The invention discloses a preparation method of pentaerythritol triacrylate. The method comprises the following steps: adding acrylic acid and pentaerythritol into an esterification reactor, adding anion exchange resin acid catalyst, an ion exchange resin supported polymerization inhibitor and a dehydrating agent, performing a reaction under a certain temperature condition, filtering out the superfluous ion exchange resin acid catalyst and the superfluous supported polymerization inhibitor, and performing reduced pressure distillation to remove the superfluous dehydrating agent and acrylic acid and a small amount of water to obtain the pentaerythritol triacrylate product. Compared with the prior art, the method has the advantages of omission of a acid-base neutralization water washing step, great reduction of industrial wastewater discharge, high recovering and recycling rate of the solid catalyst and the polymerization inhibitor, reduction of environmental pollution, and improvementof the yield and the product quality.

METHOD FOR PRODUCING (METH)ACRYLATE

-

Paragraph 0097-0109, (2018/04/26)

A method for producing a (meth) acrylate comprises transesterification reaction of an alcohol and a monofunctional (meth) acrylate with catalysts in combination being cyclic tertiary amines having an azabicyclo structure and compounds containing zinc, separating a solid that contains the catalysts from a reaction product containing a (meth) acrylate, and producing a (meth) acrylate by transesterification reaction of an alcohol and a monofunctional (meth) acrylate, while using the recovered solid catalyst.

(METH)ACRYLATE MANUFACTURING METHOD

-

Paragraph 0103-0104, (2018/05/17)

The present invention provides a (meth)acrylate manufacturing method characterized in that when manufacturing a (meth) acrylate by an ester exchange reaction between an alcohol and a monofunctional (meth)acrylate using catalyst A and catalyst B together, contact treatment of the ester exchange reaction product with adsorbent C is performed. Catalyst A: One or more kinds of compounds selected from a group consisting of cyclic tertiary amines with an azabicyclo structure and salts or complexes thereof, amidine and salts or complexes thereof, compounds with a pyridine ring and salts or complexes thereof, phosphines and salts or complexes thereof, and compounds with a tertiary diamine structure and salts or complexes thereof. Catalyst B: One or more kinds of compounds selected from a group consisting of compounds comprising zinc. Adsorbent C: One or more kinds of compounds selected from a group consisting of oxides and hydroxides comprising at least one of magnesium, aluminum and silicon.

MULTIFUNCTIONAL (METH)ACRYLATE MANUFACTURING METHOD

-

Paragraph 0087; 0088, (2017/08/07)

[Problem] The purpose of the present invention is to obtain a multifunctional (meth)acrylate with good yield by an ester exchange reaction of a polyhydric alcohol such as pentaerythritol or dipentaerythritol with a monofunctional (meth)acrylate. [Solution] A multifunctional (meth)acrylate manufacturing method characterized in that when manufacturing a multifunctional (meth)acrylate by an ester exchange reaction of a polyhydric alcohol with a monofunctional (meth)acrylate, catalyst (A) and catalyst (B) are used together. Catalyst (A): One or more kinds of compounds selected from a group consisting of cyclic tertiary amines with an azabicyclo structure or salts or complexes thereof, amidines or salts or complexes thereof, and compounds with a pyridine ring or salts or complexes thereof. Catalyst (B): One or more kinds of compounds selected from a group consisting of zinc-containing compounds.

COMPOSITION FOR POLYELECTROLYTES, POLYELECTROLYTES, ELECTRICAL DOUBLE LAYER CAPACITORS AND NONAQUEOUS ELECTROLYTE SECONDARY CELLS

-

, (2008/06/13)

A polymer electrolyte-forming composition containing (A) a quaternary ammonium salt of general formula (1) below and (B) an ionic liquid can be converted into a polymer without compromising the excellent properties of the ionic liquid, thus enabling an electrolyte having an excellent safety and electrical conductivity and also a broad potential window to be obtained. In formula (1), R1 to R3 are each independently an alkyl group of 1 to 5 carbons or a substituent having a reactive unsaturated bond and any two from among R1 to R3 may together form a ring, and R4 is methyl, ethyl or a substituent having a reactive unsaturated bond, with the proviso that at least one of R1 to R4 is a substituent having a reactive unsaturated bond. X is a monovalent anion, the letter m is an integer from 1 to 8, and the letter n is an integer from 1 to 4.

Composite materials and adhesion promoters for dental applications

-

, (2008/06/13)

Composite materials particularly suitable in the dental art as a tooth filling material including a polymer matrix, a metal, metal alloy, metal oxide particulate, or combinations thereof, in the presence or absence of colloidal silica, and a coupling agent to adhere the particulate to the polymer matrix. Adhesion can also be facilitated by cleaning and/or coating the particulates prior to incorporation into the polymer matrix. One or two paste systems of the composition with suitable initiators, accelerators, etc. can be formulated.

Liquid oligomers containing acrylate unsaturation

-

, (2008/06/13)

The liquid oligomeric compositions of this invention are made by the Michael addition reaction of acetoacetate functional donor compounds with multifunctional acrylate receptor compounds where the equivalent ratios of multifunctional acrylate to acetoacetate vary from >/=1:1 to >/=13.2:1 depending on the functionality of both multifunctional acrylate and acetoacetate. Unuseable gelled or solid oligomer products occur below the claimed ranges. The liquid oligomers of this invention are further crosslinked to make coatings, laminates and adhesives.

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