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124-22-1

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124-22-1 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 124-22-1 differently. You can refer to the following data:
1. white solid
2. Dodecylamine is a solid.

Uses

Different sources of media describe the Uses of 124-22-1 differently. You can refer to the following data:
1. Dodecylamine was used in preparation of novel surfactant copper(II) complexes.Intercalation of dodecylamine into the layer space of kaolinite was investigated. Dodecylamine was investigated as inhibitor of mild steel hydrochloric acid corrosion.
2. Dodecylamine was used in preparation of novel surfactant copper(II) complexes. It is used as a catalyst and template agent in the sol-gel process for the fabrication of monodispersed mesoporous bioactive glass sub-micron spheres.
3. Dodecylamine (DDA) can be used: As a modifier in the preparation of dodecylamine incorporated sodium montmorillonite. It is used as an adsorbent for hexavalent chromium.In the synthesis of DDA-poly(aspartic acid) as a biodegradable water-soluble polymeric material.As an organic surfactant in the synthesis of Sn(IV)-containing layered double hydroxide (LDHs), which can be further used as ion exchangers, absorbents, ion conductors, and catalysts.As a complexing, reducing and capping agent in the synthesis of pentagonal silver nanowires.

General Description

A yellow liquid with an ammonia-like odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

DODECANAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion. A severe skin and eye irritant. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.

Check Digit Verification of cas no

The CAS Registry Mumber 124-22-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124-22:
(5*1)+(4*2)+(3*4)+(2*2)+(1*2)=31
31 % 10 = 1
So 124-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H27N.H2O4S/c1-2-3-4-5-6-7-8-9-10-11-12-13;1-5(2,3)4/h2-13H2,1H3;(H2,1,2,3,4)

124-22-1 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (A15515)  1-Dodecylamine, 97%   

  • 124-22-1

  • 100g

  • 284.0CNY

  • Detail
  • Alfa Aesar

  • (A15515)  1-Dodecylamine, 97%   

  • 124-22-1

  • 500g

  • 638.0CNY

  • Detail
  • Alfa Aesar

  • (A15515)  1-Dodecylamine, 97%   

  • 124-22-1

  • 1kg

  • 1088.0CNY

  • Detail

124-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Dodecanamine

1.2 Other means of identification

Product number -
Other names Dibenzo[b,e][1,4]dioxin-1-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Processing aids, not otherwise listed,Surface active agents
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:124-22-1 SDS

124-22-1Synthetic route

undecyl cyanide
2437-25-4

undecyl cyanide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With hydrogen In methanol at 80℃; under 37503.8 Torr; for 3h; Catalytic behavior; Reagent/catalyst; Autoclave;100%
With lithium borohydride; diisopropopylaminoborane In tetrahydrofuran for 18h; Reflux;99%
With samarium diiodide; water; triethylamine In tetrahydrofuran at 20℃; for 0.0833333h; Reagent/catalyst; Time; Inert atmosphere;93%
N-dodecyl-3-phenylpropanamide

N-dodecyl-3-phenylpropanamide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

3-Phenyl-1-propanol
122-97-4

3-Phenyl-1-propanol

Conditions
ConditionsYield
With samarium diiodide; water; triethylamine In tetrahydrofuran at 23℃; for 3h; Inert atmosphere; chemoselective reaction;A 99%
B 88%
dodecyl azide
13733-78-3

dodecyl azide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With (Sn(SPh)3)(Et3N) In benzene at 15℃; for 0.0833333h;98%
With tellurium; water at 275℃; for 4h;87%
With dichloroborane-dimethyl sulfide In dichloromethane for 1h; Heating;78%
N-dodecylbenzamide
33140-65-7

N-dodecylbenzamide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

benzoic acid
65-85-0

benzoic acid

Conditions
ConditionsYield
With 40% potassium fluoride/alumina for 0.0666667h; Microwave irradiation; Neat (no solvent);A 93%
B 96%
dodecyl-carbamic acid 4-dodecylcarbamoyloxy-but-2-ynyl ester

dodecyl-carbamic acid 4-dodecylcarbamoyloxy-but-2-ynyl ester

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With benzyltriethylammonium tetrathiomolybdate In acetonitrile at 28℃; for 0.5h;95%
N-(allyloxycarbonyl)-dodecyl amine
158773-38-7

N-(allyloxycarbonyl)-dodecyl amine

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With trisodium tris(3-sulfophenyl)phosphine; water; diethylamine; palladium diacetate; heptakis(2,6-di-O-methyl)cyclomaltoheptaose In toluene at 20℃; for 15h; Substitution;94%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In methanol at 20℃; for 12h;88%
C14H27NO2
128038-36-8

C14H27NO2

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water for 2h; Heating;93%
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With sodium azide; triphenylphosphine In dichloromethane; N,N-dimethyl-formamide at 90℃; for 5h; Substitution; Mitsunobu reaction; Staudinger reaction;91%
With aluminum oxide; ammonia; magnesium oxide at 400℃; under 95616 Torr;
With L-alanin; L-alanine dehydrogenase; ω-transaminase from Chromobacterium violaceum; alcohol dehydrogenase from Bacillus stearothermophilus; pyridoxal 5'-phosphate; NAD; ammonium chloride; sodium hydroxide In 1,2-dimethoxyethane; water at 20℃; for 24h; pH=8.5; Enzymatic reaction;10 %Chromat.
With ammonia In 5,5-dimethyl-1,3-cyclohexadiene under 7500.75 Torr; for 12h; Reflux;59 %Chromat.
With aluminum oxide; ammonia; magnesium oxide at 400℃; under 95616 Torr;
N-trityldodecan-1-amine
848129-47-5

N-trityldodecan-1-amine

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With ammonium cerium (IV) nitrate; water; acetic acid In dichloromethane at 20℃; for 33h; Inert atmosphere;90%
12-(phenylthio)dodecanenitrile
148773-52-8

12-(phenylthio)dodecanenitrile

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With sodium tetrahydroborate; nickel dichloride In tetrahydrofuran; methanol at 0℃; for 0.25h;86%
undecyl cyanide
2437-25-4

undecyl cyanide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

Conditions
ConditionsYield
With hydrogen In methanol at 80℃; under 37503.8 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Autoclave;A 75.8%
B 24.2%
With hydrogen; potassium hydroxide In water at 119.84℃; under 15001.5 Torr; for 0.833333h;
N-dodecylmethanesulfonamide

N-dodecylmethanesulfonamide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With PPA at 160℃; for 1h;74%
lauric acid
143-07-7

lauric acid

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

n-Undecane
1120-21-4

n-Undecane

C

lauric acid amide
1120-16-7

lauric acid amide

D

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

E

N-dodecanoyldodecanylamide
33422-43-4

N-dodecanoyldodecanylamide

Conditions
ConditionsYield
Stage #1: lauric acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry;
Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6.5h; Cooling with ice; Green chemistry;
A 74%
B 1%
C 3%
D 15%
E 5%
2-chlorododecan-1-amine
59590-10-2

2-chlorododecan-1-amine

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With tert-butyl alcohol at 30℃; regioselective reaction;70%
lauric acid
143-07-7

lauric acid

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With D-glucose; pyridoxal 5'-phosphate; glucose dehydrogenase (CDX-901) from Codexis; NADP; isopropylamine; magnesium chloride In n-heptane; dimethyl sulfoxide at 30℃; for 20h; pH=8; Green chemistry; Enzymatic reaction;61%
With methanol; ammonia; hydrogen; Cu/Cr/Ca; titanium(IV) oxide at 300℃; under 37503 Torr;27.0 % Chromat.
Multi-step reaction with 3 steps
1: oxalyl dichloride / benzene / 1 h
2: ammonia / dichloromethane
3: lithium aluminium tetrahydride / tetrahydrofuran / 1 h
View Scheme
Multi-step reaction with 3 steps
1: ammonia / 0.5 h / 145 °C
2: 1 h / 290 °C
3: hydrogen / ethanol / 0.5 h / 95 °C / 52505.3 Torr
View Scheme
phthalimide
136918-14-4

phthalimide

1-dodecylbromide
143-15-7

1-dodecylbromide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

C

dilauryl ether
4542-57-8

dilauryl ether

D

2-dodecylisoindoline-1,3-dione
27646-77-1

2-dodecylisoindoline-1,3-dione

E

1-dodecan

1-dodecan

Conditions
ConditionsYield
With sodium hydroxide; Methyl methyltrioctylammonium sulfate In toluene at 95℃; for 4h; Product distribution; different bases, other temperatures;A 3.7%
B 41.7%
C 7.9%
D 3.5%
E n/a
lauric acid amide
1120-16-7

lauric acid amide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride; diethyl ether
With ethanol; sodium
With pentan-1-ol; sodium
With lithium aluminium tetrahydride In tetrahydrofuran for 1h;
Multi-step reaction with 2 steps
1: 1 h / 290 °C
2: hydrogen / ethanol / 0.5 h / 95 °C / 52505.3 Torr
View Scheme
lauric acid amide
1120-16-7

lauric acid amide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

Conditions
ConditionsYield
With 1,4-dioxane; copper chromite at 250℃; under 147102 - 220652 Torr; Hydrogenation;
With 1,4-dioxane; copper chromite at 250℃; under 147102 - 220652 Torr; Hydrogenation;
With ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6h; Catalytic behavior;A 80 %Chromat.
B 14 %Chromat.
methyl n-dodecanoate
111-82-0

methyl n-dodecanoate

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

Conditions
ConditionsYield
With copper-aluminium oxide barium oxide; ammonia; hydrogen at 270℃; under 147102 Torr;
With copper-aluminium oxide barium oxide; ammonia; hydrogen at 270℃; under 147102 Torr;
tridecanoic acid[2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-piperidin-4-yl]-amide
34778-57-9

tridecanoic acid[2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-piperidin-4-yl]-amide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With 1,4-dioxane; sodium hypochlorite
N-acetyl-1-dodecylamine
3886-80-4

N-acetyl-1-dodecylamine

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With potassium hydroxide durch Schmelzen;
N-dodecyl-N'-tridecanoyl-urea

N-dodecyl-N'-tridecanoyl-urea

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With potassium hydroxide
1-methyl-4-nitrosobenzene
623-11-0

1-methyl-4-nitrosobenzene

dodecyl isocyanide; compound with methyl chloride
4562-31-6

dodecyl isocyanide; compound with methyl chloride

n-Dodecylamine
124-22-1

n-Dodecylamine

1-methyl-4-nitrosobenzene
623-11-0

1-methyl-4-nitrosobenzene

dodecyl isocyanide; compound with dodecyl bromide

dodecyl isocyanide; compound with dodecyl bromide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

1-dodecylbromide
143-15-7

1-dodecylbromide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With ammonia
With ethanol; ammonia
With ammonia; sodium amide at -50℃;
dimethyl amine
124-40-3

dimethyl amine

methylamine
74-89-5

methylamine

undecyl cyanide
2437-25-4

undecyl cyanide

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
Hydrogenation;
dimethyl amine
124-40-3

dimethyl amine

undecyl cyanide
2437-25-4

undecyl cyanide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-dimethylaminododecane
112-18-5

N,N-dimethylaminododecane

Conditions
ConditionsYield
With nickel Fuller's earth; hydrogen at 180℃; under 147102 Torr;
1-chlorododecane
112-52-7

1-chlorododecane

n-Dodecylamine
124-22-1

n-Dodecylamine

Conditions
ConditionsYield
With methanol; ammonia; sodium carbonate fluessiges Ammoniak;
1-chlorododecane
112-52-7

1-chlorododecane

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N,N-didodecylamine
3007-31-6

N,N-didodecylamine

Conditions
ConditionsYield
With ammonia at 75 - 80℃;
methylamine
74-89-5

methylamine

undecyl cyanide
2437-25-4

undecyl cyanide

A

n-Dodecylamine
124-22-1

n-Dodecylamine

B

N-methyldodecylamine
7311-30-0

N-methyldodecylamine

Conditions
ConditionsYield
With hydrogen; tungsten trisulfide at 270℃; under 147102 Torr;
n-Dodecylamine
124-22-1

n-Dodecylamine

formic acid ethyl ester
109-94-4

formic acid ethyl ester

N-(dodecyl)formamide
7402-57-5

N-(dodecyl)formamide

Conditions
ConditionsYield
for 20h; Inert atmosphere; Reflux;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

bromocyane
506-68-3

bromocyane

dodecyl cyanamide
13463-96-2

dodecyl cyanamide

Conditions
ConditionsYield
100%
n-Dodecylamine
124-22-1

n-Dodecylamine

2-(chloroseleno)benzoyl chloride
1441-85-6

2-(chloroseleno)benzoyl chloride

2-dodecyl-1,2-benzisoselenazol-3(2H)-one
106966-84-1

2-dodecyl-1,2-benzisoselenazol-3(2H)-one

Conditions
ConditionsYield
In chloroform for 4h; Ambient temperature;100%
In dichloromethane at 20℃;96%
In dichloromethane
n-Dodecylamine
124-22-1

n-Dodecylamine

D-Ribono-1,4-lactone
5336-08-3

D-Ribono-1,4-lactone

N-(1-dodecyl)-D-ribonamide

N-(1-dodecyl)-D-ribonamide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 1h;100%
In methanol93%
In methanol93%
n-Dodecylamine
124-22-1

n-Dodecylamine

2-chloro-3-methyl-1-oxa-3-aza-2-phosphacyclopentane 2-oxide
66046-61-5

2-chloro-3-methyl-1-oxa-3-aza-2-phosphacyclopentane 2-oxide

Dodecyl-(3-methyl-2-oxo-2λ5-[1,3,2]oxazaphospholidin-2-yl)-amine

Dodecyl-(3-methyl-2-oxo-2λ5-[1,3,2]oxazaphospholidin-2-yl)-amine

Conditions
ConditionsYield
With triethylamine In dichloromethane for 17h; Ambient temperature;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

1,1'-carbonyldiimidazole
530-62-1

1,1'-carbonyldiimidazole

5-methoxy-2-phenylsulfonylbenzyl alcohol

5-methoxy-2-phenylsulfonylbenzyl alcohol

dodecyl-carbamic acid 2-benzenesulfonyl-5-methoxy-benzyl ester

dodecyl-carbamic acid 2-benzenesulfonyl-5-methoxy-benzyl ester

Conditions
ConditionsYield
Stage #1: 1,1'-carbonyldiimidazole; 5-methoxy-2-phenylsulfonylbenzyl alcohol In dichloromethane at 20℃; for 1h;
Stage #2: n-Dodecylamine at 20℃; for 6h;
100%
n-Dodecylamine
124-22-1

n-Dodecylamine

L-lysine methyl ester diisocyanate

L-lysine methyl ester diisocyanate

Nα,Nε-bis(dodecylaminocarbonyl)-L-lysine methyl ester

Nα,Nε-bis(dodecylaminocarbonyl)-L-lysine methyl ester

Conditions
ConditionsYield
In toluene Heating;100%
In toluene at 100℃; for 0.166667h;97%
In toluene at 0 - 80℃;91%
5-(2-bromo-ethyl)-phenanthridinium bromide

5-(2-bromo-ethyl)-phenanthridinium bromide

n-Dodecylamine
124-22-1

n-Dodecylamine

1-dodecyl-2,3-dihydro-1H-imidazo[1,2-f]phenanthridin-4-ylium bromide

1-dodecyl-2,3-dihydro-1H-imidazo[1,2-f]phenanthridin-4-ylium bromide

Conditions
ConditionsYield
Stage #1: 5-(2-bromo-ethyl)-phenanthridinium bromide; n-Dodecylamine With sodium carbonate In ethyl acetate at 20℃; for 3h;
Stage #2: With N-Bromosuccinimide In ethyl acetate at 20℃; for 3h;
100%
4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester
948995-62-8

4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

n-Dodecylamine
124-22-1

n-Dodecylamine

4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-N-(dodecyl)-4-oxobutyramide

4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-N-(dodecyl)-4-oxobutyramide

Conditions
ConditionsYield
In dichloromethane at 20℃; for 3h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

acetic acid
64-19-7

acetic acid

4-methoxy-2,2'-bipyrrole-5-carboxaldehyde
10476-41-2

4-methoxy-2,2'-bipyrrole-5-carboxaldehyde

C22H35N3O*C2H4O2

C22H35N3O*C2H4O2

Conditions
ConditionsYield
In 1,2-dichloro-ethane at 50℃; for 3h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

cis,cis-Muconic acid
1119-72-8

cis,cis-Muconic acid

(Z,Z)-muconic dodecylammonium

(Z,Z)-muconic dodecylammonium

Conditions
ConditionsYield
at 20℃; for 0.5h; Neat (no solvent); Trituration;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

acetyl chloride
75-36-5

acetyl chloride

N-acetyl-1-dodecylamine
3886-80-4

N-acetyl-1-dodecylamine

Conditions
ConditionsYield
at 100℃; for 0.05h; microwave irradiation;100%
With triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere;88%
With triethylamine In dichloromethane
N,N-dimethylacetamide dimethyl acetal
18871-66-4

N,N-dimethylacetamide dimethyl acetal

n-Dodecylamine
124-22-1

n-Dodecylamine

N’-dodecyl-N,N-dimethylacetamidine

N’-dodecyl-N,N-dimethylacetamidine

Conditions
ConditionsYield
With dimethyl amine In tetrahydrofuran at 20℃; for 18.25h; Darkness; chemoselective reaction;100%
With dimethyl amine In tetrahydrofuran for 18h; Darkness;100%
at 70℃; for 1h;
n-Dodecylamine
124-22-1

n-Dodecylamine

C36H56N2O5S2
1252598-47-2

C36H56N2O5S2

C48H83N3O4S2

C48H83N3O4S2

Conditions
ConditionsYield
Stage #1: n-Dodecylamine; C36H56N2O5S2 With acetic acid In chloroform at 40℃; for 1h;
Stage #2: With sodium tris(acetoxy)borohydride In chloroform at 20℃; for 18h; chemoselective reaction;
100%
n-Dodecylamine
124-22-1

n-Dodecylamine

1,7-lactobioamidoheptanoic acid
1210930-89-4

1,7-lactobioamidoheptanoic acid

C12H27N*C19H35NO13
1256959-78-0

C12H27N*C19H35NO13

Conditions
ConditionsYield
In water at 20℃; for 24h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

C23H43NO13
790637-33-1

C23H43NO13

C12H27N*C23H43NO13
1131531-07-1

C12H27N*C23H43NO13

Conditions
ConditionsYield
In water at 20℃; for 24h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

C17H31NO13
1256959-72-4

C17H31NO13

C12H27N*C17H31NO13
1256959-75-7

C12H27N*C17H31NO13

Conditions
ConditionsYield
In water at 20℃; for 24h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

2-Bromoacetyl bromide
598-21-0

2-Bromoacetyl bromide

2-bromo-N-dodecyl-acetamide
15537-87-8

2-bromo-N-dodecyl-acetamide

Conditions
ConditionsYield
With potassium carbonate In dichloromethane; water at 5 - 20℃; for 2.5h;100%
With potassium carbonate In dichloromethane; water at 5 - 20℃; for 4h;100%
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;93.3%
n-Dodecylamine
124-22-1

n-Dodecylamine

dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

bis(n-dodecylamino)dimethylsilane
1384112-03-1

bis(n-dodecylamino)dimethylsilane

Conditions
ConditionsYield
In hexane at 20℃; for 24h; Cooling;100%
With triethylamine In pentane at -0.16 - 19.84℃; Inert atmosphere;
n-Dodecylamine
124-22-1

n-Dodecylamine

(7-(carboxymethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl)-acetic acid
5880-06-8

(7-(carboxymethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl)-acetic acid

C18H10N2O8*2C12H27N

C18H10N2O8*2C12H27N

Conditions
ConditionsYield
In methanol at 20℃;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

(R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid
72925-16-7

(R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid

tert-butyl (R)-3-(dodecylcarbamoyl)pyrrolidine-1-carboxylate

tert-butyl (R)-3-(dodecylcarbamoyl)pyrrolidine-1-carboxylate

Conditions
ConditionsYield
Stage #1: n-Dodecylamine; (R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid With 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole In N,N-dimethyl-formamide for 0.0833333h;
Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 3.5h;
100%
With 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 3.5h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

3-(benzo[d] thiazol-2-yl)-4-hydroxy-5-methylbenzaldehyde

3-(benzo[d] thiazol-2-yl)-4-hydroxy-5-methylbenzaldehyde

(E)-1-(3-(benzo[d]thiazol-2-yl)-4-hydroxy-5-methylphenyl)-N-dodecylmethanimine

(E)-1-(3-(benzo[d]thiazol-2-yl)-4-hydroxy-5-methylphenyl)-N-dodecylmethanimine

Conditions
ConditionsYield
With acetic acid In isopropyl alcohol at 80℃; pH=Ca. 4;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

palladium diacetate
3375-31-3

palladium diacetate

bis(dodecylamine)palladium(II) acetate

bis(dodecylamine)palladium(II) acetate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 2h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

palladium dodecanoate

palladium dodecanoate

bis(dodecylamine)palladium(II) laurate

bis(dodecylamine)palladium(II) laurate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 2h;100%
n-Dodecylamine
124-22-1

n-Dodecylamine

benzaldehyde
100-52-7

benzaldehyde

N-(benzylidene)dodecylimine
20172-42-3

N-(benzylidene)dodecylimine

Conditions
ConditionsYield
In methanol for 3h; Ambient temperature;99.5%
With 3 A molecular sieve In dichloromethane at 40℃; for 6h; Condensation;91%
With diethyl ether at 20℃;
n-Dodecylamine
124-22-1

n-Dodecylamine

acetic anhydride
108-24-7

acetic anhydride

N-acetyl-1-dodecylamine
3886-80-4

N-acetyl-1-dodecylamine

Conditions
ConditionsYield
With triethylamine In acetonitrile at 0℃; for 0.75h;99%
With N,N'-dimethyl-N,N'-di(pyridin-4-yl)ferrocene-1,1'-dicarboxamide at 20℃; for 0.583333h;81%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 2h;80%
n-Dodecylamine
124-22-1

n-Dodecylamine

1-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-2-methyl-1H-pyrrole-3-carbonyl chloride

1-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-2-methyl-1H-pyrrole-3-carbonyl chloride

1-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid dodecylamide

1-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid dodecylamide

Conditions
ConditionsYield
In benzene for 1h; Heating;99%
n-Dodecylamine
124-22-1

n-Dodecylamine

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

N-Monododecyl-o-nitraniline
94208-22-7

N-Monododecyl-o-nitraniline

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 6h;99%
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 2h; Inert atmosphere;95%
In nitrobenzene at 190 - 200℃; for 6h;46%
n-Dodecylamine
124-22-1

n-Dodecylamine

4-nitro-benzoyl chloride
122-04-3

4-nitro-benzoyl chloride

N-dodecyl-p-nitrobenzamide
64026-23-9

N-dodecyl-p-nitrobenzamide

Conditions
ConditionsYield
With pyridine In toluene at 80℃; for 3h; Inert atmosphere;99%
In chloroform Heating;

124-22-1Related news

Full Length ArticleIntensify Dodecylamine (cas 124-22-1) adsorption on magnesite and dolomite surfaces by monohydric alcohols09/29/2019

The flotation of magnesite and dolomite were investigated with the presence of single dodecylamine (DDA) and combined mixtures of DDA and monohydric alcohols, respectively. The adsorption behavior of DDA, butanol, hexanol and octanol on the surface of the two minerals were shown by molecular dyn...detailed

Dynamic surface tension measurement of Dodecylamine (cas 124-22-1) solutions—a pendant bubble tensiometer with modified cell system09/28/2019

A pendant bubble tensiometer was modified for the dynamic surface tension (ST) measurement of a dodecylamine (DDA) surfactant solution. The dynamic STs of DDA solutions showed a peculiar relaxation: the ST relaxed from the ST of the solvent, reached a minimum, and then increased to ∼72 mN/m. Th...detailed

Intercalation of Dodecylamine (cas 124-22-1) into kaolinite and its layering structure investigated by molecular dynamics simulation10/01/2019

Dodecylamine was successfully intercalated into the layer space of kaolinite by utilizing the methanol treated kaolinite–dimethyl sulfoxide (DMSO) intercalation complex as an intermediate. The basal spacing of kaolinite, measured by X-ray diffraction (XRD), increased from 0.72 nm to 4.29 nm aft...detailed

Full length articleApplication of ToF-SIMS and PCA to study interaction mechanism of Dodecylamine (cas 124-22-1) and smithsonite09/27/2019

Although dodecylamine (DDA) is a conventional collector for the flotation of smithsonite, the interaction mechanism between DDA and smithsonite is still unclear. In this study, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and principal component analysis (PCA) were used to investiga...detailed

Tribological behavior of Dodecylamine (cas 124-22-1) functionalized graphene nanosheets dispersed engine oil nanolubricants09/26/2019

The present study investigates the tribological properties of nanolubricants dispersed with dodecylamine functionalized graphene (DAG) in commercial engine oil. Standard techniques were used to determine the morphology of the DAG and the worn surfaces. The tribological properties of the nanolubr...detailed

A study of adsorption mechanism of Dodecylamine (cas 124-22-1) on sphalerite09/25/2019

Long-chain primary amines are not only good collectors for silicate minerals, but, they can also float some metallic sulfides. However, the flotation mechanism of sulfide minerals using long-chain primary amines as collector is uncertain. In this paper, the flotation performance and adsorption m...detailed

Full Length ArticleEffect of pH on the adsorption of Dodecylamine (cas 124-22-1) on montmorillonite: Insights from experiments and molecular dynamics simulations09/24/2019

The hydrophobic aggregation in cationic surfactant suspension is an effective method to enhance the dewatering of clay-rich tailing. The solution pH can affect the adsorption behavior of cationic surfactant on clay mineral. The effect of pH on the adsorption of dodecylamine (DDA) on montmorillon...detailed

Full Length ArticleThe adsorption of Dodecylamine (cas 124-22-1) and oleic acid on kaolinite surfaces: Insights from DFT calculation and experimental investigation09/09/2019

The interaction of hydrophobic modifiers with clay mineral surfaces plays an important role in the hydrophobic aggregation sedimentation for the treatment of clay-rich tailing. The adsorption of dodecylamine and oleic acid on kaolinite was investigated at the atomic level by using density functi...detailed

Intensification of interfacial adsorption of Dodecylamine (cas 124-22-1) onto quartz by ultrasonic method09/08/2019

Besides being a versatile mineral resource, quartz is also a common gangue mineral in mineral separation. The separation and enrichment of quartz minerals are particularly important in industrial production. Cationic surfactants of dodecylamine (DDA) is mainly used as collector in the quartz flo...detailed

124-22-1Relevant articles and documents

Surface properties of Ni/MgO catalysts for the hydrogenation of lauronitrile

Chen, Hui,Xue, Mingwei,Shen, Jianyi

, p. 246 - 255 (2010)

60%Ni/MgO (wt%) catalysts were prepared by the co-precipitation method and the influence of n-butanol treatment was investigated. The results showed that the treatment with n-butanol improved the dispersion and reducibility of supported nickel, resulted in an increase of H2 uptake from 410 to 582 μmol/g, corresponding to an increase of active Ni surface area from 32 to 46 m2/g (increased by 42%). Accordingly, the catalytic activity for the hydrogenation of toluene to methyl cyclohexane was significantly increased. Microcalorimetric adsorption of H2 and CO indicated that the treatment with n-butanol increased the amount of active metal sites on the surface, without the change of electron densities of supported nickel surface. Microcalorimetric adsorption of CO2 and NH3 revealed the strong surface basicity and weak surface acidity for the Ni/MgO catalysts, especially for the reduced ones. The initial heat for the adsorption of acetonitrile was measured to be about 130 kJ/mol on the Ni/MgO catalysts, indicating the strong interaction between acetonitrile and the supported nickel, which might be an important factor determining the activity of nickel for the hydrogenation of aliphatic nitriles. The surface basicity of the Ni/MgO catalysts might play a role in inhibiting the formation of secondary and tertiary amines and therefore improved the selectivity to primary amine during the hydrogenation of lauronitrile to laurylamine. In addition, the Ni/MgO-B catalyst prepared with n-butanol treatment seemed more active for the hydrogenation of lauronitrile.

Broome, F. K.,Ralstone, A. W.,Thornton, M. H.

, p. 67 - 69 (1946)

MATERIALS COMPRISING CARBON-EMBEDDED IRON NANOPARTICLES, PROCESSES FOR THEIR MANUFACTURE, AND USE AS HETEROGENEOUS CATALYSTS

-

Page/Page column 14, (2021/03/13)

201900257 Ausland 18 Abstract The present invention relates to catalytically active material, comprising grains of non-graphitizing carbon with iron nanoparticles dispersed therein, wherein dp, the average diameter of iron nanoparticles in the non-graphitizing carbon grains, is in the range of 1 nm to 20 nm, D, the average distance between iron nanoparticles in the non-graphitizing carbon grains, is in the range 5 of 2 nm to 150 nm, and ω, the combined total mass fraction of metal in the non-graphitizing carbon grains, is in the range of 30 wt% to 70 wt% of the total mass of the non-graphitizing carbon grains, and wherein dp, D and ω conform to the following relation: 4.5 dp / ω > D ≥ 0.25 dp / ω. The present invention, further, relates to a process for the manufacture of material according to the invention, as well as its use as a catalyst. 10

Direct Enzymatic Synthesis of Fatty Amines from Renewable Triglycerides and Oils

Bevinakatti, Han,Citoler, Joan,Finnigan, William,Turner, Nicholas J.

, (2021/11/30)

Fatty amines represent an important class of commodity chemicals which have broad applicability in different industries. The synthesis of fatty amines starts from renewable sources such as vegetable oils or animal fats, but the process has multiple drawbacks that compromise the overall effectiveness and efficiency of the synthesis. Herein, we report a proof-of-concept biocatalytic alternative towards the synthesis of primary fatty amines from renewable triglycerides and oils. By coupling a lipase with a carboxylic acid reductase (CAR) and a transaminase (TA), we have accomplished the direct synthesis of multiple medium and long chain primary fatty amines in one pot with analytical yields as high as 97 %. We have also performed a 75 mL preparative scale reaction for the synthesis of laurylamine from trilaurin, obtaining 73 % isolated yield.

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