Welcome to LookChem.com Sign In|Join Free
  • or
Acryloyloxyethyltrimethyl ammonium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

44992-01-0

Post Buying Request

44992-01-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

44992-01-0 Usage

Safety Profile

A severe eye irritant. When heated to decomposition it emits toxic vapors of NOx and Clí

Check Digit Verification of cas no

The CAS Registry Mumber 44992-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,4,9,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 44992-01:
(7*4)+(6*4)+(5*9)+(4*9)+(3*2)+(2*0)+(1*1)=140
140 % 10 = 0
So 44992-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H16NO2.ClH/c1-5-8(10)11-7-6-9(2,3)4;/h5H,1,6-7H2,2-4H3;1H/q+1;/p-1

44992-01-0 Well-known Company Product Price

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

  • (496146)  [2-(Acryloyloxy)ethyl]trimethylammoniumchloridesolution  80 wt. % in H2O, contains 600 ppm monomethyl ether hydroquinone as inhibitor

  • 44992-01-0

  • 496146-200ML

  • 407.16CNY

  • Detail

44992-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(2-prop-2-enoyloxyethyl)azanium,chloride

1.2 Other means of identification

Product number -
Other names ADAMQUAT 80 MC

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:44992-01-0 SDS

44992-01-0Synthetic route

2-(dimethylamino)ethyl methacrylate
2439-35-2

2-(dimethylamino)ethyl methacrylate

methylene chloride
74-87-3

methylene chloride

A

acrylic acid
79-10-7

acrylic acid

B

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

Conditions
ConditionsYield
With water; 4-methoxy-phenol at 55℃; under 375.038 - 900.09 Torr; for 4.5 - 5.5h; Product distribution / selectivity;
2-(dimethylamino)ethyl methacrylate
2439-35-2

2-(dimethylamino)ethyl methacrylate

methylene chloride
74-87-3

methylene chloride

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

Conditions
ConditionsYield
With water at 50 - 55℃; under 1125.11 Torr; for 6.5h; Product distribution / selectivity;
In water at 60℃; under 1575.16 - 1800.18 Torr; Product distribution / selectivity;
In water at 50℃; under 3102.97 Torr; for 1.25h; Product distribution / selectivity;
With hydrogenchloride; 4-methoxy-phenol In dichloromethane; water at 25 - 30℃; pH=7; Reagent/catalyst; Concentration;
2-(dimethylamino)ethyl methacrylate
2439-35-2

2-(dimethylamino)ethyl methacrylate

methylene chloride
74-87-3

methylene chloride

A

ADAMQUAT MC

ADAMQUAT MC

B

acrylic acid
79-10-7

acrylic acid

C

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

Conditions
ConditionsYield
In water at 40 - 47℃; under 4500.45 Torr; for 4 - 5.25h; Product distribution / selectivity;
4-Chloro-2-methylphenoxyacetic acid potassium salt
5221-16-9

4-Chloro-2-methylphenoxyacetic acid potassium salt

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium (4-chloro-2-methylphenoxy)acetate

[2-(acryloyloxy)ethyl]trimethylammonium (4-chloro-2-methylphenoxy)acetate

Conditions
ConditionsYield
In methanol at 20℃; for 1.5h; Green chemistry;99%
potassium 3,6-dichloro-2-methoxybenzoate
10007-85-9

potassium 3,6-dichloro-2-methoxybenzoate

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium 3,6-dichloro-2-methoxybenzoate

[2-(acryloyloxy)ethyl]trimethylammonium 3,6-dichloro-2-methoxybenzoate

Conditions
ConditionsYield
In methanol at 20℃; for 1.5h; Green chemistry;97%
mecoprop, potassium salt

mecoprop, potassium salt

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium 2-(4-chloro-2-methylphenoxy)propioniate

[2-(acryloyloxy)ethyl]trimethylammonium 2-(4-chloro-2-methylphenoxy)propioniate

Conditions
ConditionsYield
In methanol at 20℃; for 1.5h; Green chemistry;96%
bis(trifluoromethane)sulfonimide lithium
90076-65-6

bis(trifluoromethane)sulfonimide lithium

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium bis-(trifluoromethane)sulfonimide
827027-31-6

[2-(acryloyloxy)ethyl]trimethylammonium bis-(trifluoromethane)sulfonimide

Conditions
ConditionsYield
In water at 20℃; for 3h; Large scale;93.6%
In acetonitrile at 20℃; for 48h;80%
In water at 0℃; for 1h;
2,4-dichlorophenoxyacetic acid potassium
14214-89-2

2,4-dichlorophenoxyacetic acid potassium

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium (2,4-dichlorophenoxy)acetate

[2-(acryloyloxy)ethyl]trimethylammonium (2,4-dichlorophenoxy)acetate

Conditions
ConditionsYield
In methanol at 20℃; for 1.5h; Green chemistry;91%
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium hexafluorophosphate

[2-(acryloyloxy)ethyl]trimethylammonium hexafluorophosphate

Conditions
ConditionsYield
With potassium hexafluorophosphate In water at 20℃; for 48h;82%
sodium tetrafluoroborate
13755-29-8

sodium tetrafluoroborate

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium tetrafluoroborate

[2-(acryloyloxy)ethyl]trimethylammonium tetrafluoroborate

Conditions
ConditionsYield
In acetonitrile at 20℃; for 48h;78%
sodium hexafluoroantimonate

sodium hexafluoroantimonate

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium hexafluoroantimonate

[2-(acryloyloxy)ethyl]trimethylammonium hexafluoroantimonate

Conditions
ConditionsYield
In acetonitrile at 20℃; for 48h;74%
sodium triflate
2926-30-9

sodium triflate

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

[2-(acryloyloxy)ethyl]trimethylammonium trifluoromethanesulfonate

[2-(acryloyloxy)ethyl]trimethylammonium trifluoromethanesulfonate

Conditions
ConditionsYield
In acetonitrile at 20℃; for 48h;55%
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

poly((2-(acryloyloxy)ethyl)trimethylammonium chloride); monomer(s): (2-(acryloyloxy)ethyl)trimethylammonium choride

poly((2-(acryloyloxy)ethyl)trimethylammonium chloride); monomer(s): (2-(acryloyloxy)ethyl)trimethylammonium choride

Conditions
ConditionsYield
With 2,2'-azobis(2-aminopropane) dihydrochloride; 2-[p-(OH-2-Me-propiphenone)]ethylene glycolmethacrylate; cetyltrimethylammonim bromide In water UV-irradiation;
2-(2-thiobenzoylsulfanylpropionylamino)naphthalene-6,8-disulfonic acid dipotassium salt

2-(2-thiobenzoylsulfanylpropionylamino)naphthalene-6,8-disulfonic acid dipotassium salt

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

polymer; monomer(s): (2-acryloyloxyethyl)trimethylammonium chloride; 2-(2-thiobenzoylsulfanylpropionylamino)naphthalene-6,8-disulfonic acid dipotassium salt

polymer; monomer(s): (2-acryloyloxyethyl)trimethylammonium chloride; 2-(2-thiobenzoylsulfanylpropionylamino)naphthalene-6,8-disulfonic acid dipotassium salt

Conditions
ConditionsYield
With 2,2'-azobis(2-methyl-N-phenylpropionamidine) dihydrochloride; potassium chloride at 48℃;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

N-dodecyl methacrylamide
1191-39-5

N-dodecyl methacrylamide

Reaxys ID: 15742269

Reaxys ID: 15742269

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; water at 76℃; for 72.5h; Heating / reflux;
CHEMDEX SO

CHEMDEX SO

2-propenamide
79-06-1

2-propenamide

acrylic acid
79-10-7

acrylic acid

sodium 2-acrylamido-2-methylpropane-1-sulfonate
5165-97-9

sodium 2-acrylamido-2-methylpropane-1-sulfonate

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

poly(AM-co-AA-co-NaAMPS-co-AETAC) soyamidopropyldimethylamine complex

poly(AM-co-AA-co-NaAMPS-co-AETAC) soyamidopropyldimethylamine complex

Conditions
ConditionsYield
Stage #1: CHEMDEX SO; 2-propenamide; acrylic acid; sodium 2-acrylamido-2-methylpropane-1-sulfonate; [2-(acryloyloxy)ethyl]trimethylammonium chloride With sodium hydroxide; ethylene diamine tetraacetic acid tetrasodium salt In water at 65℃; for 0.5h;
Stage #2: With sodium metabisulfite; sodium persulfate In water for 0.75h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 3% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 85% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 3% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 85% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 6% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 82% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 6% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 82% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 12% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 76% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 12% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 76% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 24% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 64% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 24% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 64% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 50% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 38% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 50% wt; 2-acryloxyethyltrimethylammonium chloride, 12% wt; 2-hydroxyethyl acrylate, 38% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 3% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 72% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 3% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 72% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 6% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 69% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 6% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 69% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 12% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 63% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 12% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 63% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 24% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 51% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 24% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 51% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

undeca-ethylene glycol diacrylate
17831-71-9

undeca-ethylene glycol diacrylate

2-hydroxyethyl acrylate
818-61-1

2-hydroxyethyl acrylate

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 50% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 25% wt

Polymer; Monomers: poly(ethylene glycol) diacrylate, n=11, 50% wt; 2-acryloxyethyltrimethylammonium chloride, 25% wt; 2-hydroxyethyl acrylate, 25% wt

Conditions
ConditionsYield
With 2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol; ethylhexylperoxydicarbonate In n-heptane at 20℃; for 12h;
2-propenamide
79-06-1

2-propenamide

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 14%, Mv (viscosity-average) = 1.51E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 14%, Mv (viscosity-average) = 1.51E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; water at 75℃;
2-propenamide
79-06-1

2-propenamide

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 23%, Mv (viscosity-average) = 1.58E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 23%, Mv (viscosity-average) = 1.58E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

Conditions
ConditionsYield
In ethanol; water at 75℃;
2-propenamide
79-06-1

2-propenamide

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 42%, Mv (viscosity-average) = 1.72E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 42%, Mv (viscosity-average) = 1.72E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; water at 75℃;
2-propenamide
79-06-1

2-propenamide

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 54%, Mv (viscosity-average) = 2.00E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

cationic copolymer (acrylamide-trimethylaminoethyl acrylate), synthesized with AIBN as initiator, charge density 54%, Mv (viscosity-average) = 2.00E4 dL/g; monomer(s): 2-(dimethylamino)ethyl acrylate methyl cloride; acrylamide

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In ethanol; water at 75℃;
1,3-bis(trimethylammonium)-2-propyl acrylate chloride

1,3-bis(trimethylammonium)-2-propyl acrylate chloride

2-propenamide
79-06-1

2-propenamide

[2-(acryloyloxy)ethyl]trimethylammonium chloride
44992-01-0

[2-(acryloyloxy)ethyl]trimethylammonium chloride

Reaxys ID: 11379662

Reaxys ID: 11379662

Conditions
ConditionsYield
Stage #1: 1,3-bis(trimethylammonium)-2-propyl acrylate chloride; 2-propenamide; [2-(acryloyloxy)ethyl]trimethylammonium chloride With potassium bromate; LACTIC ACID; Adipic acid; polyoxyethylene sorbital hexaoleate; sorbitan mono isostearate; ethylenediaminetetraacetic acid In isoparaffinic solvent; water for 0.758333h;
Stage #2: 2,2'-azobis-(2,4-dimethylvaleronitrile) In isoparaffinic solvent; water; xylene at 40 - 55℃; for 6h; Reactivity;

44992-01-0Downstream Products

44992-01-0Relevant academic research and scientific papers

METHOD FOR PREPARING A BIOCIDAL, BACTERIOCIDAL AND/OR BACTERIOSTATIC MATERIAL

-

, (2022/03/02)

A process for preparing a biocidal, bactericidal and/or bacteriostatic material including the preparation of a polymer precursor solution that has (a) at least one monomer A having a porphyrin group and at least one radical polymerizable function, (b) at least one radical polymerizable monomer B, a photoinitiator, and (c) at least one of the monomers chosen from a monomer C having a quaternary amine and a radical polymerizable function; and/or a monomer D having copper and a radical polymerizable function. Also, the material obtainable by the process and its uses.

Organic monomer for synthesizing amphoteric polycarboxylic superplasticizer and preparation method

-

Paragraph 0027; 0028; 0029; 0030; 0031; 0032; 0033, (2016/11/21)

The invention discloses an organic monomer for synthesizing an amphoteric polycarboxylic superplasticizer, which has a molecular structure shown in the description. The invention further discloses a preparation method of the organic monomer for synthesizing the amphoteric polycarboxylic superplasticizer and comprises the following steps: preparing a dimethylaminoethyl acrylate intermediate and a cationic active organic monomer; adopting one-time charging at the normal temperature; and selecting a reasonable type of catalyst to prepare the organic monomer. The method has reduced cost, plays an important part in process simplification, and has characteristics of high reaction conversion rate, high yield, and high purity. Compared with an anionic polycarboxylic superplasticizer sold in the market, under a condition of a relatively low mixing amount, the amphoteric polycarboxylic superplasticizer enables neat cement paste or concrete to have excellent performance of good water reduction, high dispersion, good plasticity preservation, and high early-stage compressive strength.

PROCESS FOR UNSATURATED QUATERNARY AMMONIUM SALT

-

Page/Page column 5, (2011/02/18)

An unsaturated quaternary ammonium salt is produced by a process that includes reacting methyl chloride in a first vessel with a stoichiometric excess of an unsaturated tertiary amine in the presence of water to form a reaction mixture that includes the unsaturated quaternary ammonium salt and residual unsaturated tertiary amine. The reaction mixture is transferred to a second vessel and phase separated to yield a first fraction in which the unsaturated quaternary ammonium salt is concentrated, and a second fraction in which the residual unsaturated tertiary amine is concentrated. At least a portion of the second fraction is recycled from the second vessel to the first vessel for use in the reaction with methyl chloride. The process, which is preferably operated continuously, allows the use of reduced reaction pressures compared to processes utilizing a stoichiometric excess of methyl chloride, and it also reduces or eliminates the problems associated with recycling methyl chloride and removing methyl chloride from the unsaturated quaternary ammonium salt product.

CONTINUOUS PRODUCTION OF DMAEA QUATERNARY SALTS

-

Page/Page column 3-4, (2011/08/04)

The invention provides a method of continuously producing high quality quaternized N,N-dialkylaminoethyl (meth)acrylates (DMAEA.MCQ) that has a long shelf life and which is stable in water. The method involves placing starting materials into a continuously stirred tank reactor in the presence of less than 6% water. This low amount of water causes two liquid phases to form and prevents unwanted side reactions. The denser liquid phase contains DMAEA.MCQ and the lighter phase contains the starting materials. Liquid from the denser phase is removed from a position where little of the lighter phase has been mixed in. The removed liquid then has any last traces of the starting materials reacted into DMAEA.MCQ and strips away any starting materials with a gas flow. The resulting liquid is high purity DMAEA.MCQ. Water can then safely be added to ease in the transport and use of the produced DMAEA.MCQ.

Method for making aqueous solutions of unsaturated quaternary ammonium salts

-

Page/Page column 4-5, (2008/06/13)

The invention concerns a method for making aqueous solutions of unsaturated quaternary ammonium salts of formula (I) by reacting, in the presence of water, N,N-dimethylaminoethyl acrylate with a quaternizing agent of formula (II): R—Cl, said method is characterized in that it consists in: (a) in a closed reactor containing 5 60 wt. % of N,N-dimethylaminoethyl acrylate required for the reaction and which has been pressurized with air or depleted air at 0.5 to 3 bars, carrying out the reaction by continuously introducing, at a temperature ranging between 35 to 65° C., the quaternizing agent (II), and water, and finally the remaining N,N-dimethylaminoethyl acrylate, until the desired concentration of salt (I) in the water is reached, the water being introduced only when 0–20 wt. % of the amount required for the quaternizing agent (II) reaction has been added; the introduction of the remaining N,N-dimethylaminoethyl acrylate starting only when 20–80 wt. % required for the quaternizing agent (II) reaction has been added; and the pressure at the end of the reaction capable of reaching 9 bars; then (b) in depressurizing while maintaining the oxygen content constant by simultaneous introduction of air and, after returning to atmospheric pressure, eliminating the residual quaternizing agent. In formule (I) and (II). R=methyl or benzyl.

METHOD FOR PRODUCING UNSATURATED QUATERNARY AMMONIUM SALT

-

Page/Page column 10-11, (2008/06/13)

PROBLEM TO BE SOLVED: To provide a method for producing an unsaturated quaternary ammonium salt, capable of producing the salt in a short time, without causing deposition of crystals, nor formation of slurry, in reaction of quarternizing a vinyl monomer having a tertiary amino group with a halogenated alkyl. SOLUTION: This method for producing the unsaturated quaternary ammonium salt expressed by formula (3) comprises sequentially conducting processes (a) to (c) as follows: (a) a process for feeding a reactor with the vinyl monomer having the tertiary amino group and water in an amount of 0-20% based on the total amount of the water to be supplied; (b) a process (reaction former process) for continuously or intermittently supplying the reactor with the water and the halogenated alkyl in a mass ratio X of the water to the halogenated alkyl (provided that, X > 0); and (c) a process (reaction latter process) for continuously or intermittently supplying the reactor with the water and the halogenated alkyl in such a mass ratio X of the water to the halogenated alkyl as to be larger than in the process (b).

METHOD FOR PRODUCING UNSATURATED QUATERNARY AMMONIUM SALT AQUEOUS SOLUTION

-

Page/Page column 7-8, (2008/06/13)

PROBLEM TO BE SOLVED: To provide a method for producing an unsaturated quaternary ammonium salt aqueous solution that causes no blockade of a pipe for feeding a halogenated alkyl, when the quaternary ammonium salt is produced. SOLUTION: This invention is a method for producing the unsaturated quaternary ammonium salt aqueous solution by using a (meth)acrylic alkylaminoester, a halogenated alkyl and water, as starting materials, wherein the halogenated alkyl is directly introduced through the halogenated alkyl-introducing pipe into the (meth)acrylic alkylaminoester only or into a mixed solution containing the (meth)acrylic alkylaminoester. In addition, the water is added through the halogenated alkyl-introducing pipe, as the reaction advances.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 44992-01-0