Dodecyl acrylate supplier | CasNO.2156-97-0

Name
Dodecyl acrylate
EINECS 218-463-4
CAS No. 2156-97-0
Article Data22
CAS DataBase
Density 0.875 g/cm³
Solubility 1μg/L at 20℃
Melting Point 4oC
Formula C₁₅H₂₈O₂
Boiling Point 306.2 °C at 760 mmHg
Molecular Weight 240.386
Flash Point 110.4 °C
Transport Information UN 3082 9/PG 3
Appearance
Safety 26-28-61
Risk Codes 36/37/38-51/53
Molecular Structure
Hazard Symbols Xi, N
Synonyms Acrylicacid, dodecyl ester (6CI,7CI,8CI);Ageflex FA 12;Blemmer LA;KU-LA;LA;Lauryl acrylate;Light Acrylate L-A;NK Ester LA;NSC 24177;Photomer 4812;SR 335;SR 498D;Sartomer 335;Viscoat LA;n-Dodecyl acrylate;
PSA 26.30000
LogP 4.63650

Synthetic route

: 112-53-8
1-dodecyl alcohol

: 79-10-7
acrylic acid

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With 10H-phenothiazine; hydroquinone at 110 - 130℃; for 4h;	95.8%
With toluene-4-sulfonic acid; hydroquinone In toluene at 130℃; for 3h; Inert atmosphere;	85%
With toluene-4-sulfonic acid; hydroquinone In toluene at 130℃; for 4h; Inert atmosphere;	76%
With phosphoric acid; (p-tolueneslfonic acid, sulfosalicylic acid, resin KU-2x8); hydroquinone In toluene Heating;
With hydroquinone In cyclohexane at 120 - 140℃; for 6h;

: 112-53-8
1-dodecyl alcohol

: 814-68-6
acryloyl chloride

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 10 - 20℃; for 3h;	84%
With triethylamine In dichloromethane at 0℃; for 3h;	65%
With triethylamine In dichloromethane at 20℃;
In dichloromethane at 0 - 20℃; Inert atmosphere; Alkaline conditions;

: 112-53-8
1-dodecyl alcohol

: 2043-21-2
acryloyl-1,3-oxazolidin-2-one

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With ytterbium(III) triflate In acetonitrile at 90℃; for 48h; Sealed tube; Inert atmosphere;	70%

: 109182-98-1
Acrylic acid 12-iodo-dodecyl ester

A: 106-02-5
pentadecanolide

B: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With 2,2'-azobis(isobutyronitrile); tertbutyltin hydride In benzene for 3h; Heating;	A 55% B 21%

: 112-53-8
1-dodecyl alcohol

: 79-10-7
acrylic acid

A: 2156-97-0
lauryl acrylate

B: 3-(dodecyloxy)-3-oxopropyl acrylate

Conditions

Conditions	Yield
With sodium hydrogen sulfate at 110℃; for 2h;	A 36% B 40.5%

...Expand

: 112-53-8
1-dodecyl alcohol

: 292638-85-8
acrylic acid methyl ester

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With toluene-4-sulfonic acid; hydroquinone Abdestillieren des entstandenen Methanols als Azeotrop mit Methylacrylat;
at 60 - 70℃;

: 112-53-8
1-dodecyl alcohol

: 74-86-2
acetylene

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With hydrogenchloride; tetracarbonyl nickel

: 112-53-8
1-dodecyl alcohol

: 74-86-2
acetylene

carbon monoxide: carbon monoxide

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With tetrahydrofuran; copper(ll) bromide; nickel dibromide at 200℃; under 40 - 50 Torr;
With hydrogenchloride; tetracarbonyl nickel

...Expand

diethyl ether dicarboxylic acid-(2.2')-didodecyl ester: diethyl ether dicarboxylic acid-(2.2')-didodecyl ester

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
With sulfuric acid; β-naphthol at 288 - 310℃; under 21 Torr;

: 5675-51-4
1,12-dodecandiol

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 38 percent / carbon tetrabromide, triphenylphosphine / tetrahydrofuran / 20 h / Ambient temperature 2: 2.3 g / triethylamine / CH2Cl2 / Ambient temperature 3: 2.7 g / sodium iodide / butan-2-one / 3 h / Heating 4: 21 percent / tertbutyltin hydride, AIBN / benzene / 3 h / Heating View Scheme

: 3344-77-2
12-bromododecanol

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 2.3 g / triethylamine / CH2Cl2 / Ambient temperature 2: 2.7 g / sodium iodide / butan-2-one / 3 h / Heating 3: 21 percent / tertbutyltin hydride, AIBN / benzene / 3 h / Heating View Scheme

: 112231-59-1
12-bromododecanyl acrylate

: 2156-97-0
lauryl acrylate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 2.7 g / sodium iodide / butan-2-one / 3 h / Heating 2: 21 percent / tertbutyltin hydride, AIBN / benzene / 3 h / Heating View Scheme

: 2156-97-0
lauryl acrylate

: 111-42-2
2,2'-iminobis[ethanol]

: 3-[bis-(2-hydroxy-ethyl)-amino]-propionic acid dodecyl ester

Conditions

Conditions	Yield
at 50℃; Michael addition;	100%

: 111-88-6
Octanethiol

: 2156-97-0
lauryl acrylate

: dodecyl 3-(octylthio)propanoate

Conditions

Conditions	Yield
With 2,2'-azobis(isobutyronitrile) at 115℃; for 24h; Sealed tube;	99%

: 872-85-5
pyridine-4-carbaldehyde

: 2156-97-0
lauryl acrylate

: C21H33NO3

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In toluene at 20℃; for 8h;	95%

: 2156-97-0
lauryl acrylate

: 192884-89-2, 1013643-92-9
dimethyl 3-phenylcyclohexa-1,4-diene-1,2-dicarboxylate

A: 6221-93-8
1-dodecyl propionate

B: 50402-81-8
biphenyl-2,3-dicarboxylic acid dimethyl ester

Conditions

Conditions	Yield
With palladium 10% on activated carbon In water at 120℃; for 6h;	A 0.077 mmol B 95%

...Expand

: 2156-97-0
lauryl acrylate

: 6284-40-8
1-deoxy-1-(methylamino)-D-glucitol

: C22H45NO7

Conditions

Conditions	Yield
In 1,4-dioxane; water at 50℃; for 5h;	91%

: 1121-60-4
pyridine-2-carbaldehyde

: 2156-97-0
lauryl acrylate

: C21H33NO3

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In toluene at 20℃; for 8h;	90%

: 2156-97-0
lauryl acrylate

: 609-36-9
rac-Pro-OH

: C20H37NO4

Conditions

Conditions	Yield
In ethanol at 75℃; for 8h; Michael Addition;	88%

: 2156-97-0
lauryl acrylate

: 54-42-2
5-Iodo-2'-deoxyuridine

: dodecyl (E)-3-(1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)-tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate

Conditions

Conditions	Yield
Stage #1: 5-Iodo-2'-deoxyuridine With C26H32N8O6P2PdS2 In acetonitrile at 80℃; for 0.0833333h; Heck Reaction; Inert atmosphere; Stage #2: lauryl acrylate With triethylamine In acetonitrile at 80℃; for 8h; Heck Reaction; Inert atmosphere;	86%

: 2156-97-0
lauryl acrylate

: 99970-84-0
[2,2']bipyridinyl-4,4'-dicarbaldehyde

: C42H64N2O6

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In methanol at 20℃; for 12h; Reagent/catalyst; Morita-Baylis-Hillman Alkylation;	84%

: 2156-97-0
lauryl acrylate

: 71182-37-1
N-(3-methoxyphenyl)-2-methylpropanamide

: 1222482-64-5
C26H41NO4

Conditions

Conditions	Yield
With tetrakis(acetonitrile)palladium(II) tetrafluoroborate; silver nitrate; p-benzoquinone In water at 20℃; for 20h; Fujiwara-Moritani reaction; regiospecific reaction;	80%

: 500-22-1
3-pyridinecarboxaldehyde

: 2156-97-0
lauryl acrylate

: dodecyl 2-(hydroxy(pyridine-3-yl)methyl)acrylate

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In toluene at 20℃; for 8h;	78%
With 1,4-diaza-bicyclo[2.2.2]octane In octanol at 20℃; for 22h; Baylis-Hillman Reaction;	71%

: 2156-97-0
lauryl acrylate

: 104704-09-8
4'-methyl-2,2'-bipyridine-4-carboxylaldehyde

: C27H38N2O3

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In methanol at 20℃; for 12.4h; Morita-Baylis-Hillman Alkylation;	78%

: 591-50-4
iodobenzene

: 2156-97-0
lauryl acrylate

: 146354-36-1
trans-dodecyl-3-phenylprop-2-enoate

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl acetamide at 90℃; for 9h;	77%
With triethylamine In dimethyl sulfoxide at 90℃; for 9h; Reagent/catalyst;

: 2156-97-0
lauryl acrylate

: N,8-dimethylindolizine-2-carboxamide

: dodecyl (E)-3-(8-methyl-2-(methylcarbamoyl)indolizin-3-yl)acrylate

Conditions

Conditions	Yield
With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; copper(II) acetate monohydrate In tetrahydrofuran at 20℃; Inert atmosphere; regioselective reaction;	76%

: 1070-83-3
tert-Butylacetic acid

: 2156-97-0
lauryl acrylate

: C19H34O4

Conditions

Conditions	Yield
With disodium hydrogenphosphate; palladium(II) trifluoroacetate; N-acetyl-L-valine; silver carbonate at 120℃; for 12h;	76%

: 2058-74-4
1-methyl-1H-indole-2,3-dione

: 2156-97-0
lauryl acrylate

: C24H35NO4

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In toluene at 20℃; for 8h;	72%

: 2156-97-0
lauryl acrylate

: 140652-55-7
di-tert-butyl ((butane-1,4-diylbis(azanediyl))bis(propane-3,1-diyl))dicarbamate

: C50H98N4O8

Conditions

Conditions	Yield
In isopropyl alcohol at 90℃; for 2h;	72%

: 2156-97-0
lauryl acrylate

: dodecyl acrylate-d3

Conditions

Conditions	Yield
With platinum on carbon; water-d2; hydroquinone; isopropyl alcohol at 120℃; for 24h; Reagent/catalyst; Time; Sealed tube; Inert atmosphere;	71%

: 2156-97-0
lauryl acrylate

: 256425-12-4
N-(3-isopropoxyphenyl)acetamide

: 1222482-60-1
C26H41NO4

Conditions

Conditions	Yield
With tetrakis(acetonitrile)palladium(II) tetrafluoroborate; silver nitrate; p-benzoquinone In water at 20℃; for 20h; Fujiwara-Moritani reaction; regiospecific reaction;	70%

: 487-89-8
Indole-3-carboxaldehyde

: 2156-97-0
lauryl acrylate

: (E)-dodecyl 3-(3-formyl-1H-indol-4-yl)acrylate

Conditions

Conditions	Yield
With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; copper diacetate at 110℃; for 4h; Inert atmosphere; regioselective reaction;	64%

: 2156-97-0
lauryl acrylate

: 110-60-1
1,4-diaminobutane

: dilauryl spermate

Conditions

Conditions	Yield
In tetrahydrofuran for 36h; Ambient temperature;	58%

: 1-octyloxy-2,2,6,6-tetramethylpiperidin-4-one oxime

: 2156-97-0
lauryl acrylate

: lauryl 3-[N-(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-N-hydroxyamino]propionate

Conditions

Conditions	Yield
With hydrogenchloride; platinum In methanol	52%

: 2156-97-0
lauryl acrylate

: C17H27NO5

: 10-(5'-(dodecyloxycarbonyl)-4',5'-dihydroisoxazol-3'-yl)methyldeoxoartemisinin

Conditions

Conditions	Yield
With sodium hypochlorite; triethylamine In dichloromethane at 20℃;	46%

: 498-60-2
furan-3-carboxaldehyde

: 2156-97-0
lauryl acrylate

: dodecyl 2-(furan-3-yl(hydroxy)methyl)acrylate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene at 20℃; for 48h; Baylis-Hillman reaction;	40%

: 98-01-1
furfural

: 2156-97-0
lauryl acrylate

: 1092799-80-8
dodecyl 2-[(furan-2-yl)(hydroxy)methyl]acrylate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene at 0 - 25℃; Baylis-Hillman reaction;	36%

Dodecyl acrylate Chemical Properties

Molecular structure of 2-Propenoic acid, dodecyl ester (CAS NO.2156-97-0) is:

Product Name: 2-Propenoic acid, dodecyl ester
CAS Registry Number: 2156-97-0
IUPAC Name: Dodecyl prop-2-enoate
Molecular Weight: 240.38162 [g/mol]
Molecular Formula: C₁₅H₂₈O₂
XLogP3: 6.2
H-Bond Donor: 0
H-Bond Acceptor: 2
EINECS: 218-463-4
Refractive index: 1.445
Surface Tension: 29.9 dyne/cm
Density: 0.875 g/cm³
Flash Point: 110.4 °C
Enthalpy of Vaporization: 54.67 kJ/mol
Boiling Point: 306.2 °C at 760 mmHg
Vapour Pressure: 0.000784 mmHg at 25°C
Other Registry Number: 199685-42-2
Product Categories: Functional Monomer; Monomer

Dodecyl acrylate Safety Profile

Safty information about 2-Propenoic acid, dodecyl ester (CAS NO.2156-97-0) is:
Hazard Codes: Irritant Xi; Dangerous N
Risk Statements: 36/37/38-51/53
Safety Statements: 26-28-61
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S28:After contact with skin, wash immediately with plenty of soap-suds.
S51/53:Use only in well ventilated areas and avoid exposure - obtain special instructions before use.
RIDADR: UN 3082 9/PG 3
WGK Germany: 2

Dodecyl acrylate Specification

2-Propenoic acid, dodecyl ester , its cas register number is 2156-97-0. It also can be called AI3-03198 ; Acrylic acid, dodecyl ester ; Dodecyl acrylate ; Lauryl acrylate ; NSC 24177 ; n-Dodecyl acrylate ; n-Lauryl acrylate .

Product Name

Dodecyl acrylate

Synthetic route

Dodecyl acrylate Chemical Properties

Dodecyl acrylate Safety Profile

Dodecyl acrylate Specification

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