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Pentaerythritol tetraacrylate (PETA) is a hydrophobic tetrafunctional monomer that serves as a crosslinking agent, enhancing the surface morphology of polymeric materials. It is synthesized by suspending pentaerythritol in a solution of triethylamine and dichloromethane.

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  • 4986-89-4 Structure
  • Basic information

    1. Product Name: Pentaerythritol tetraacrylate
    2. Synonyms: TETRACROYLPENTA;PENTATETRAACRYLATE;PENTAERYTHRITOL TETRAACRYLATE;2-Propenoicacid,2,2-bis[[(1-oxo-2-propenyl)oxy]methyl]-1,3-propanediylester;2,2-bis[[(1-oxoallyl)oxy]methyl]-1,3-propanediyl diacrylate;PENTAERYTHRITOLTETRAAERYLATE;Pentaerythrityl tetraacrylate;PENTAERYTHRITOL TETRACRYLATE
    3. CAS NO:4986-89-4
    4. Molecular Formula: C17H20O8
    5. Molecular Weight: 352.34
    6. EINECS: 225-644-1
    7. Product Categories: Functional Monomer;Acrylic Monomers;C12 to C63Monomers;Carbonyl Compounds;Esters;Polyfunctional Acrylics
    8. Mol File: 4986-89-4.mol
  • Chemical Properties

    1. Melting Point: 18°C
    2. Boiling Point: 450.3 ºC at 760 mmHg
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.19 g/mL at 25 °C(lit.)
    6. Refractive Index: n20/D 1.487(lit.)
    7. Storage Temp.: Amber Vial, Refrigerator, Under inert atmosphere
    8. Solubility: Chloroform, Methanol (Sparingly)
    9. Stability: Light Sensitive
    10. CAS DataBase Reference: Pentaerythritol tetraacrylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Pentaerythritol tetraacrylate(4986-89-4)
    12. EPA Substance Registry System: Pentaerythritol tetraacrylate(4986-89-4)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/38-43
    3. Safety Statements: 26-39-36/37
    4. WGK Germany: 1
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4986-89-4(Hazardous Substances Data)

4986-89-4 Usage

Uses

Used in Research Chemicals:
Pentaerythritol tetraacrylate is used as a research chemical for various scientific investigations and experiments, contributing to the advancement of polymer chemistry and material science.
Used in Lithium-Sulfur Batteries:
Pentaerythritol tetraacrylate is used as a component in the synthesis of gel polymer electrolyte for the fabrication of lithium-sulfur batteries. Its role in the electrolyte formulation helps improve the performance and stability of these batteries, making them more efficient and reliable for energy storage applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4986-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4986-89:
(6*4)+(5*9)+(4*8)+(3*6)+(2*8)+(1*9)=144
144 % 10 = 4
So 4986-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O8/c1-7-12(18)22-11-16(5,6)17(23-13(19)8-2,24-14(20)9-3)25-15(21)10-4/h7-10H,1-4,11H2,5-6H3

4986-89-4 Well-known Company Product Price

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  • Aldrich

  • (408263)  Pentaerythritoltetraacrylate  contains 350 ppm monomethyl ether hydroquinone as inhibitor

  • 4986-89-4

  • 408263-100ML

  • 538.20CNY

  • Detail
  • Aldrich

  • (408263)  Pentaerythritoltetraacrylate  contains 350 ppm monomethyl ether hydroquinone as inhibitor

  • 4986-89-4

  • 408263-250ML

  • 1,081.08CNY

  • Detail

4986-89-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Pentaerythritol tetraacrylate

1.2 Other means of identification

Product number -
Other names tetramethylolmethane tetraacrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Paint additives and coating additives not described by other categories,Photosensitive chemicals
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4986-89-4 SDS

4986-89-4Synthetic route

Pentaerythritol
115-77-5

Pentaerythritol

acryloyl chloride
814-68-6

acryloyl chloride

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 2.5h;96.6%
With triethylamine In dichloromethane at 0℃; Inert atmosphere;
(E)-but-2-enol
504-61-0

(E)-but-2-enol

Pentaerythritol
115-77-5

Pentaerythritol

4-methoxy-phenol
150-76-5

4-methoxy-phenol

acrylic acid
79-10-7

acrylic acid

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
In Petroleum ether
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 %;
Pentaerythritol
115-77-5

Pentaerythritol

ethyl acrylate
140-88-5

ethyl acrylate

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With 2CF3O3S(1-)*(x)C7H8*C26H42Hf(2+) In acetonitrile at 20℃; for 12h; Green chemistry;
carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

A

C14H20O11

C14H20O11

B

C16H20O9

C16H20O9

C

C15H20O10

C15H20O10

D

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 0.5h; Inert atmosphere; Overall yield = 3.8 g;
Pentaerythritol
115-77-5

Pentaerythritol

acrylic acid
79-10-7

acrylic acid

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With methanesulfonic acid; hypophosphorous acid; copper(l) chloride In toluene at 70℃; Inert atmosphere;
With hypophosphorous acid; toluene-4-sulfonic acid; 4-methoxy-phenol In toluene at 82℃; under 225.023 Torr;
Pentaerythritol
115-77-5

Pentaerythritol

acetic anhydride
108-24-7

acetic anhydride

acrylic acid
79-10-7

acrylic acid

A

Pentaerithrit-triacetat-acrylat
51690-75-6

Pentaerithrit-triacetat-acrylat

B

C15H20O8

C15H20O8

C

C16H20O8

C16H20O8

D

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
Stage #1: Pentaerythritol; acrylic acid With methanesulfonic acid; 4-methoxy-phenol; copper(l) chloride In water; toluene at 75℃; under 1125.11 Torr; for 15h; Inert atmosphere;
Stage #2: acetic anhydride With methanesulfonic acid; 4-methoxy-phenol In toluene at 35 - 40℃; for 1h; Inert atmosphere;
acetic anhydride
108-24-7

acetic anhydride

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

A

Pentaerithrit-triacetat-acrylat
51690-75-6

Pentaerithrit-triacetat-acrylat

B

C15H20O8

C15H20O8

C

C16H20O8

C16H20O8

D

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2.5h; Inert atmosphere;
acetic anhydride
108-24-7

acetic anhydride

pentaerythritol triacrylate
3524-68-3

pentaerythritol triacrylate

A

C15H20O8

C15H20O8

B

C16H20O8

C16H20O8

C

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

Conditions
ConditionsYield
With methanesulfonic acid at 20℃; for 0.5h; Inert atmosphere;
morpholine
110-91-8

morpholine

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C62H104N6O20

C62H104N6O20

Conditions
ConditionsYield
Stage #1: 1,12-Diaminododecane; pentaerythritol tetraacrylate In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
99%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

1-dodecylthiol
112-55-0

1-dodecylthiol

pentaerythritol tetrakis(3-n-dodecylthiopropionate)

pentaerythritol tetrakis(3-n-dodecylthiopropionate)

Conditions
ConditionsYield
With potassium tert-butylate; acetic acid at 40 - 55℃; for 8h; pH=6 - 7; Reagent/catalyst; Inert atmosphere;97.8%
morpholine
110-91-8

morpholine

1,6-Hexanediamine
124-09-4

1,6-Hexanediamine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C122H204N14O44

C122H204N14O44

Conditions
ConditionsYield
Stage #1: 1,6-Hexanediamine; pentaerythritol tetraacrylate In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 19h; Further stages.;
97%
morpholine
110-91-8

morpholine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

1,4-diaminobutane
110-60-1

1,4-diaminobutane

C120H200N14O44

C120H200N14O44

Conditions
ConditionsYield
Stage #1: pentaerythritol tetraacrylate; 1,4-diaminobutane In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
96%
rac-3-sulfanylpropane-1,2-diol
96-27-5

rac-3-sulfanylpropane-1,2-diol

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C25H44O16S4

C25H44O16S4

Conditions
ConditionsYield
With triethylamine In dimethyl sulfoxide at 20℃; for 0.5h;95.9%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

ethylenediamine
107-15-3

ethylenediamine

C53H68N2O24

C53H68N2O24

Conditions
ConditionsYield
In methanol at 30℃; for 18h; Michael addition;95%
morpholine
110-91-8

morpholine

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C128H216N14O44

C128H216N14O44

Conditions
ConditionsYield
Stage #1: 1,12-Diaminododecane; pentaerythritol tetraacrylate In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
94%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

polymer resin; monomer(s): pentaerythritol tetraacrylate

polymer resin; monomer(s): pentaerythritol tetraacrylate

Conditions
ConditionsYield
With hydroxyethyl cellulose; xylene; dibenzoyl peroxide In water at 80℃; for 8h; Product distribution; Further Variations:; Reagents;93%
morpholine
110-91-8

morpholine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

1,4-diaminobutane
110-60-1

1,4-diaminobutane

C54H88N6O20

C54H88N6O20

Conditions
ConditionsYield
Stage #1: pentaerythritol tetraacrylate; 1,4-diaminobutane In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
93%
morpholine
110-91-8

morpholine

1,6-Hexanediamine
124-09-4

1,6-Hexanediamine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C93H157N11O33

C93H157N11O33

Conditions
ConditionsYield
Stage #1: 1,6-Hexanediamine; pentaerythritol tetraacrylate In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 19h; Further stages.;
89%
morpholine
110-91-8

morpholine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

C120H201N15O44

C120H201N15O44

Conditions
ConditionsYield
Stage #1: pentaerythritol tetraacrylate; 3-azapentane-1,5-diamine In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
84%
1-aza-18-crown-6
33941-15-0

1-aza-18-crown-6

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

3-(1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl)-propionic acid 3-(3-1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl-propionyloxy)-2,2-bis-(3-1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl-propionyloxymethyl)-propyl ester

3-(1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl)-propionic acid 3-(3-1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl-propionyloxy)-2,2-bis-(3-1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl-propionyloxymethyl)-propyl ester

Conditions
ConditionsYield
In methanol at 50℃; for 24h; Michael addition;82.5%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

1,4,7,10-tetraoxa-15-azacyclopentadecane
66943-05-3

1,4,7,10-tetraoxa-15-azacyclopentadecane

3-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-propionic acid 3-(3-1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl-propionyloxy)-2,2-bis-(3-1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl-propionyloxymethyl)-propyl ester

3-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-propionic acid 3-(3-1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl-propionyloxy)-2,2-bis-(3-1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl-propionyloxymethyl)-propyl ester

Conditions
ConditionsYield
In methanol at 50℃; for 24h; Michael addition;82.1%
trichlorogermane etherate

trichlorogermane etherate

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

(Cl3GeC2H4CO2CH2)4C
742108-47-0

(Cl3GeC2H4CO2CH2)4C

Conditions
ConditionsYield
In neat (no solvent) acrylate was added dropwise to Ge compd.; mixt. was stirred at room temp. overnight;77%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

diphenylphosphane
829-85-6

diphenylphosphane

C65H64O8P4

C65H64O8P4

Conditions
ConditionsYield
In 2-methyltetrahydrofuran at 90℃; for 12h; Inert atmosphere; Sealed tube; Green chemistry; regioselective reaction;72%
4'-aminobenzo-15-crown-5-ether
60835-71-4

4'-aminobenzo-15-crown-5-ether

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C73H104N4O28

C73H104N4O28

Conditions
ConditionsYield
With triethylamine In methanol at 50℃; for 144h; Michael addition;68%
2-(aminomethyl)-18-crown-6
83585-61-9

2-(aminomethyl)-18-crown-6

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

3-[(1,4,7,10,13,16-Hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionic acid 3-{3-[(1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionyloxy}-2,2-bis-{3-[(1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionyloxymethyl}-propyl ester

3-[(1,4,7,10,13,16-Hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionic acid 3-{3-[(1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionyloxy}-2,2-bis-{3-[(1,4,7,10,13,16-hexaoxa-cyclooctadec-2-ylmethyl)-amino]-propionyloxymethyl}-propyl ester

Conditions
ConditionsYield
In methanol at 50℃; for 24h; Michael addition;67.5%
2-aminomethyl-15-crown-5
83585-56-2

2-aminomethyl-15-crown-5

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

3-[(1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionic acid 3-{3-[(1,4,7,10,13-pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionyloxy}-2,2-bis-{3-[(1,4,7,10,13-pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionyloxymethyl}-propyl ester

3-[(1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionic acid 3-{3-[(1,4,7,10,13-pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionyloxy}-2,2-bis-{3-[(1,4,7,10,13-pentaoxa-cyclopentadec-2-ylmethyl)-amino]-propionyloxymethyl}-propyl ester

Conditions
ConditionsYield
In methanol at 50℃; for 24h; Michael addition;66%
4-aminobenzo-18-crown-6
68941-06-0

4-aminobenzo-18-crown-6

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C81H120N4O32

C81H120N4O32

Conditions
ConditionsYield
With triethylamine In methanol at 50℃; for 144h; Michael addition;65%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

polymer, photopolymerization; monomer(s): pentaerythritol tetraacrylate

polymer, photopolymerization; monomer(s): pentaerythritol tetraacrylate

Conditions
ConditionsYield
With 2,2-dimethoxy-2-phenylacetophenone under 56704.5 Torr; for 0.168333h; Kinetics; Product distribution; UV-irradiation;38.6%
pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

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

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

Conditions
ConditionsYield
With Synperonic(R) F-68 In acetone at 60℃; for 0.75h; UV-irradiation;
With 2,2'-azobis(isobutyronitrile) In ethanol; toluene at 60℃;
1-undecylamine
7307-55-3

1-undecylamine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

A

C28H45NO8

C28H45NO8

B

C45H65NO16

C45H65NO16

Conditions
ConditionsYield
In methanol at 4 - 20℃; Product distribution; Further Variations:; educt ratio; Michael addition;
1-pentanamine
110-58-7

1-pentanamine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C22H33NO8

C22H33NO8

Conditions
ConditionsYield
In methanol at 4 - 20℃; Michael addition;
1-pentanamine
110-58-7

1-pentanamine

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

A

C22H33NO8

C22H33NO8

B

C39H53NO16

C39H53NO16

Conditions
ConditionsYield
In methanol at 4 - 20℃; Product distribution; Further Variations:; educt ratio; Michael addition;
thiomalic acid di(perfluorohexylethylester)

thiomalic acid di(perfluorohexylethylester)

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C37H32F26O12S

C37H32F26O12S

Conditions
ConditionsYield
triethylamine In ethyl acetate at 50℃; for 3h; Michael Condensation;
2-benzyl-2-N,N-dimethylamino-1-[4-piperazinophenyl]-1-butanone
886463-08-7

2-benzyl-2-N,N-dimethylamino-1-[4-piperazinophenyl]-1-butanone

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C109H144N12O12

C109H144N12O12

Conditions
ConditionsYield
1,8-diazabicyclo[5.4.0]undec-7-ene In toluene for 6h; Heating / reflux;
2-methyl-2-morpholin-4-yl-1-(4-piperazinylphenyl)propan-1-one
886463-09-8

2-methyl-2-morpholin-4-yl-1-(4-piperazinylphenyl)propan-1-one

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C89H128N12O16

C89H128N12O16

Conditions
ConditionsYield
1,8-diazabicyclo[5.4.0]undec-7-ene In toluene for 6h; Heating / reflux;

4986-89-4Relevant articles and documents

Facile synthesis of polyester dendrimers as drug delivery carriers

Ma, Xinpeng,Zhou, Zhuxian,Jin, Erlei,Sun, Qihang,Zhang, Bo,Tang, Jianbin,Shen, Youqing

, p. 37 - 42 (2013)

Aliphatic polyester dendrimers are attractive carriers for in vivo delivery of bioactive molecules due to their biocompatibility and biodegradability, but efficient precision synthesis of these dendrimers without tedious purifications remains challenging. Herein, we report an efficient synthesis approach to polyester dendrimers from two AB2-type monomers via combining a click reaction of thiol/acrylate Michael addition with esterification. The reaction solution of each generation contains only the targeted dendrimer macromolecules; thus, the only required separation is simple precipitation. The resulting hydroxyl-terminated fifth-generation dendrimer is thermoresponsive with a LCST of 41 C. The dendrimer could be further pegylated to obtain a water-soluble biocompatible dendrimer capable of encapsulation and controlled release of a hydrophobic anticancer drug, doxorubicin.

Low-viscosity acrylate type compound and compounding application system thereof

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Paragraph 0087-0093, (2019/08/01)

The present invention relates to the field of new materials and fine chemicals, particularly to a class of low-viscosity acrylate type compounds, and a new preparation technology thereof, and applications in alkene-containing unsaturated radiation polymerization systems.

Modified acrylate, preparation method thereof and application of modified acrylate in preparation of conductive adhesive

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Paragraph 0072-0077, (2019/11/28)

The invention discloses modified acrylate, a preparation method thereof and application of modified acrylate in preparation of a conductive adhesive. Hydroxyl groups in a polyol acrylate monomer is converted into alpha-H-containing acetal groups so as to obtain the modified acrylate. The modified acrylate obtained through reduction of hydroxyl groups has low viscosity, and can be effectively usedas a reactive diluent in a photo-cured coating formula, and since the modified acrylate contains the alpha-H-containing acetal groups which can promote photopolymerization activity, the photo-curing activity can be improved, so that photocrosslinking is promoted without addition of a hydrogenation donor assistant, and the problem of oxygen inhibition is avoided. When the modified acrylate is applied to preparation of a photo-cured composition, the prepared photo-cured composition has easy curing and fast surface drying; and the invention also provides a method for preparing the alpha-H-containing acetal groups through a reaction between enol ether and hydroxyl groups of the polyol acrylate monomer, and provides application of the modified acrylate in preparation of the photo-cured composition and the conductive adhesive of the photo-cured composition.

Carbonated polyols and acrylate-based compound thereof

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Paragraph 0091-0093, (2019/08/01)

The invention relates to the field of new materials and fine chemicals, particularly to a class of novel carbonated polyols and (meth)acrylate-based compounds thereof, and a preparation method thereof, and applications in an olefin-containing unsaturated radiation-polymerizable systems.

METHOD FOR PRODUCING (METH)ACRYLATE

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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

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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.

A containing 2, 6 - di-tert-butyl phenol anti-oxidant and its preparation method

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Paragraph 0020; 0087; 0088, (2017/09/26)

The invention reveals a 2,6-di-tert-butylphenol-containing anti-oxidant and a novel preparation method thereof. The method takes titanium, zirconium, hafnium, bismuth, antimony metal complexes as green catalysts, a two-step system is substituted by a series reaction one step method technology, and a high efficiency metal complex catalyst capable of simultaneously catalyzing a direct esterification reaction and a Michael addition reaction is employed to prepare the novel anti-oxidant. The method takes acrylic acid (or acrylic acid ester), pentaerythritol and 2,6-di-tert-butylphenol as main raw materials, under organic solvent or solvent-free condition, the titanium, zirconium, hafnium, bismuth, antimony metal complex green catalysts are reacted to obtain the novel anti-oxidant with high yield. The method has the advantages of low cost, high yield, simple operation and no pollution, and has certain feasibility for realizing industrial production. The preparation method is the green approach with low cost.

MULTIFUNCTIONAL (METH)ACRYLATE MANUFACTURING METHOD

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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.

Photo-initiated thiol-ene "click" hydrogels from RAFT-synthesized poly(N-isopropylacrylamide)

Ooi, Huey Wen,Jack, Kevin S.,Whittaker, Andrew K.,Peng, Hui

, p. 4626 - 4636 (2013/10/21)

Despite the efficiency and robustness of the widely used copper-catalyzed 1,3-dipolar cycloaddition reaction, the use of copper as a catalyst is often not attractive, particularly for materials intended for biological systems. The use of photo-initiated thiol-ene as an alternative "click" reaction to synthesize "model networks" is investigated here. Poly(N- isopropylacrylamide) precursors were synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization and were designed to have trithiocarbonate moieties as end groups. This structure design provides opportunity for subsequent end-group modifications in preparation for thiol-ene "click." Two reaction routes have been proposed and studied to yield thiol and ene moieties. The advantages and disadvantages of each reaction path were investigated to propose a simple but efficient route to prepare copper-free "click" hydrogels.

POLYOL DERIVED ANTI-MICROBIAL AGENTS AND COMPOSITIONS

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Page/Page column 13, (2009/12/05)

Anti-microbial compositions are provided which comprise as an antimicrobial agent at least one compound derived from a select polyol containing at least 3 hydroxy groups wherein one or more, and often two or more, of the hydroxyls are derivitized to form certain ether, ester, carbonate or carbamate groups which groups may bear additional functionality. Novel antimicrobial compounds of this class are also provided. The compositions are effective against a variety of pathogens including fungi, Gram positive bacteria and Gram negative bacteria and are expected to have low human toxicity. Applications for the polyglycerol anti-microbial agents and compositions include those involving human and plant contact, such as cosmetics, hair care products, textiles and plant protections, as well as in applications with much less human contact, such as plastics, coatings, wood, paper and other materials of construction.

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