Dodecanamine supplier | CasNO.124-22-1

Name
Dodecylamine
EINECS 204-690-6
CAS No. 124-22-1
Article Data128
CAS DataBase
Density 0.804 g/cm³
Solubility water: 78 mg/L (25 ºC)
Melting Point 28-32 ºC
Formula C₁₂H₂₇N
Boiling Point 258.6ºC at 760 mmHg
Molecular Weight 185.353
Flash Point 100.4ºC
Transport Information UN 3259 8/PG 3
Appearance white solid
Safety 26-36/37/39-45-60-61
Risk Codes 22-34-50/53-20/21/22
Molecular Structure
Hazard Symbols C,N
Synonyms Lauramine;Laurinamine;Laurylamine;Monododecylamine;Monolaurylamine;Nissan Amine BB;n-Dodecylamine;n-Laurylamine;1-Aminododecane;1-Dodecylamine;Alamine 4;Amine BB;Armeen 12D;Farmin20D;HAN 12;Kemamine P 690;
PSA 26.02000
LogP 4.56630

Synthetic route

: 2437-25-4
undecyl cyanide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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

A: 124-22-1
n-Dodecylamine

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

Conditions

Conditions	Yield
With samarium diiodide; water; triethylamine In tetrahydrofuran at 23℃; for 3h; Inert atmosphere; chemoselective reaction;	A 99% B 88%

: 13733-78-3
dodecyl azide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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%

: 33140-65-7
N-dodecylbenzamide

A: 124-22-1
n-Dodecylamine

B: 65-85-0
benzoic acid

Conditions

Conditions	Yield
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

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With benzyltriethylammonium tetrathiomolybdate In acetonitrile at 28℃; for 0.5h;	95%

: 158773-38-7
N-(allyloxycarbonyl)-dodecyl amine

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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%

: 128038-36-8
C14H27NO2

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With hydrogenchloride In ethanol; water for 2h; Heating;	93%

: 112-53-8
1-dodecyl alcohol

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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;

: 848129-47-5
N-trityldodecan-1-amine

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With ammonium cerium (IV) nitrate; water; acetic acid In dichloromethane at 20℃; for 33h; Inert atmosphere;	90%

: 148773-52-8
12-(phenylthio)dodecanenitrile

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With sodium tetrahydroborate; nickel dichloride In tetrahydrofuran; methanol at 0℃; for 0.25h;	86%

: 2437-25-4
undecyl cyanide

A: 124-22-1
n-Dodecylamine

B: 3007-31-6
N,N-didodecylamine

Conditions

Conditions	Yield
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

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With PPA at 160℃; for 1h;	74%

: 143-07-7
lauric acid

A: 124-22-1
n-Dodecylamine

B: 1120-21-4
n-Undecane

C: 1120-16-7
lauric acid amide

D: 3007-31-6
N,N-didodecylamine

E: 33422-43-4
N-dodecanoyldodecanylamide

Conditions

Conditions	Yield
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%

...Expand

: 59590-10-2
2-chlorododecan-1-amine

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With tert-butyl alcohol at 30℃; regioselective reaction;	70%

: 143-07-7
lauric acid

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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

: 136918-14-4
phthalimide

: 143-15-7
1-dodecylbromide

A: 124-22-1
n-Dodecylamine

B: 112-53-8
1-dodecyl alcohol

C: 4542-57-8
dilauryl ether

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

E 1-dodecan: 1-dodecan

Conditions

Conditions	Yield
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

...Expand

: 1120-16-7
lauric acid amide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
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

: 1120-16-7
lauric acid amide

A: 124-22-1
n-Dodecylamine

B: 3007-31-6
N,N-didodecylamine

Conditions

Conditions	Yield
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.

: 111-82-0
methyl n-dodecanoate

A: 124-22-1
n-Dodecylamine

B: 3007-31-6
N,N-didodecylamine

Conditions

Conditions	Yield
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;

: 34778-57-9
tridecanoic acid[2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-piperidin-4-yl]-amide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With 1,4-dioxane; sodium hypochlorite

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

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With potassium hydroxide durch Schmelzen;

: N-dodecyl-N'-tridecanoyl-urea

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With potassium hydroxide

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

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

: 124-22-1
n-Dodecylamine

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

: dodecyl isocyanide; compound with dodecyl bromide

A: 124-22-1
n-Dodecylamine

B: 3007-31-6
N,N-didodecylamine

...Expand

: 143-15-7
1-dodecylbromide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With ammonia
With ethanol; ammonia
With ammonia; sodium amide at -50℃;

: 124-40-3
dimethyl amine

: 74-89-5
methylamine

: 2437-25-4
undecyl cyanide

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
Hydrogenation;

...Expand

: 124-40-3
dimethyl amine

: 2437-25-4
undecyl cyanide

A: 124-22-1
n-Dodecylamine

B: 112-18-5
N,N-dimethylaminododecane

Conditions

Conditions	Yield
With nickel Fuller's earth; hydrogen at 180℃; under 147102 Torr;

...Expand

: 112-52-7
1-chlorododecane

: 124-22-1
n-Dodecylamine

Conditions

Conditions	Yield
With methanol; ammonia; sodium carbonate fluessiges Ammoniak;

: 112-52-7
1-chlorododecane

A: 124-22-1
n-Dodecylamine

B: 3007-31-6
N,N-didodecylamine

Conditions

Conditions	Yield
With ammonia at 75 - 80℃;

: 74-89-5
methylamine

: 2437-25-4
undecyl cyanide

A: 124-22-1
n-Dodecylamine

B: 7311-30-0
N-methyldodecylamine

Conditions

Conditions	Yield
With hydrogen; tungsten trisulfide at 270℃; under 147102 Torr;

...Expand

: 124-22-1
n-Dodecylamine

: 109-94-4
formic acid ethyl ester

: 7402-57-5
N-(dodecyl)formamide

Conditions

Conditions	Yield
for 20h; Inert atmosphere; Reflux;	100%

: 124-22-1
n-Dodecylamine

: 506-68-3
bromocyane

: 13463-96-2
dodecyl cyanamide

Conditions

Conditions	Yield
	100%

: 124-22-1
n-Dodecylamine

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

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

Conditions

Conditions	Yield
In chloroform for 4h; Ambient temperature;	100%
In dichloromethane at 20℃;	96%
In dichloromethane

: 124-22-1
n-Dodecylamine

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

: N-(1-dodecyl)-D-ribonamide

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 20℃; for 1h;	100%
In methanol	93%
In methanol	93%

: 124-22-1
n-Dodecylamine

: 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

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 17h; Ambient temperature;	100%

: 124-22-1
n-Dodecylamine

: 530-62-1
1,1'-carbonyldiimidazole

: 5-methoxy-2-phenylsulfonylbenzyl alcohol

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

Conditions

Conditions	Yield
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%

...Expand

: 124-22-1
n-Dodecylamine

: L-lysine methyl ester diisocyanate

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

Conditions

Conditions	Yield
In toluene Heating;	100%
In toluene at 100℃; for 0.166667h;	97%
In toluene at 0 - 80℃;	91%

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

: 124-22-1
n-Dodecylamine

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

Conditions

Conditions	Yield
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%

: 948995-62-8
4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

: 124-22-1
n-Dodecylamine

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

Conditions

Conditions	Yield
In dichloromethane at 20℃; for 3h;	100%

: 124-22-1
n-Dodecylamine

: 64-19-7
acetic acid

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

: C22H35N3O*C2H4O2

Conditions

Conditions	Yield
In 1,2-dichloro-ethane at 50℃; for 3h;	100%

...Expand

: 124-22-1
n-Dodecylamine

: 1119-72-8
cis,cis-Muconic acid

: (Z,Z)-muconic dodecylammonium

Conditions

Conditions	Yield
at 20℃; for 0.5h; Neat (no solvent); Trituration;	100%

: 124-22-1
n-Dodecylamine

: 75-36-5
acetyl chloride

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

Conditions

Conditions	Yield
at 100℃; for 0.05h; microwave irradiation;	100%
With triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere;	88%
With triethylamine In dichloromethane

: 18871-66-4
N,N-dimethylacetamide dimethyl acetal

: 124-22-1
n-Dodecylamine

: N’-dodecyl-N,N-dimethylacetamidine

Conditions

Conditions	Yield
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;

: 124-22-1
n-Dodecylamine

: 1252598-47-2
C36H56N2O5S2

: C48H83N3O4S2

Conditions

Conditions	Yield
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%

: 124-22-1
n-Dodecylamine

: 1210930-89-4
1,7-lactobioamidoheptanoic acid

: 1256959-78-0
C12H27N*C19H35NO13

Conditions

Conditions	Yield
In water at 20℃; for 24h;	100%

: 124-22-1
n-Dodecylamine

: 790637-33-1
C23H43NO13

: 1131531-07-1
C12H27N*C23H43NO13

Conditions

Conditions	Yield
In water at 20℃; for 24h;	100%

: 124-22-1
n-Dodecylamine

: 1256959-72-4
C17H31NO13

: 1256959-75-7
C12H27N*C17H31NO13

Conditions

Conditions	Yield
In water at 20℃; for 24h;	100%

: 124-22-1
n-Dodecylamine

: 598-21-0
2-Bromoacetyl bromide

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

Conditions

Conditions	Yield
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%

: 124-22-1
n-Dodecylamine

: 75-78-5
dimethylsilicon dichloride

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

Conditions

Conditions	Yield
In hexane at 20℃; for 24h; Cooling;	100%
With triethylamine In pentane at -0.16 - 19.84℃; Inert atmosphere;

: 124-22-1
n-Dodecylamine

: 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

Conditions

Conditions	Yield
In methanol at 20℃;	100%

: 124-22-1
n-Dodecylamine

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

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

Conditions

Conditions	Yield
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%

: 124-22-1
n-Dodecylamine

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

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

Conditions

Conditions	Yield
With acetic acid In isopropyl alcohol at 80℃; pH=Ca. 4;	100%

: 124-22-1
n-Dodecylamine

: 3375-31-3
palladium diacetate

: bis(dodecylamine)palladium(II) acetate

Conditions

Conditions	Yield
In dichloromethane at 40℃; for 2h;	100%

: 124-22-1
n-Dodecylamine

: palladium dodecanoate

: bis(dodecylamine)palladium(II) laurate

Conditions

Conditions	Yield
In dichloromethane at 40℃; for 2h;	100%

: 124-22-1
n-Dodecylamine

: 100-52-7
benzaldehyde

: 20172-42-3
N-(benzylidene)dodecylimine

Conditions

Conditions	Yield
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℃;

: 124-22-1
n-Dodecylamine

: 108-24-7
acetic anhydride

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

Conditions

Conditions	Yield
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%

: 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-carboxylic acid dodecylamide

Conditions

Conditions	Yield
In benzene for 1h; Heating;	99%

: 124-22-1
n-Dodecylamine

: 88-73-3
2-Chloronitrobenzene

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

Conditions

Conditions	Yield
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%

: 124-22-1
n-Dodecylamine

: 122-04-3
4-nitro-benzoyl chloride

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

Conditions

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

Dodecanamine Chemical Properties

The Molecular Structure of Dodecanamine (CAS NO.124-22-1):

Empirical Formula: C₁₂H₂₇N
Molecular Weight: 185.3495
IUPAC Name: dodecan-1-amine
Appearance: white solid
Nominal Mass: 185 Da
Average Mass: 185.3495 Da
Monoisotopic Mass: 185.21435 Da
Index of Refraction: 1.444
Molar Refractivity: 61.17 cm³
Molar Volume: 230.2 cm³
Surface Tension: 29.9 dyne/cm
Density: 0.804 g/cm³
Flash Point: 100.4 °C
Enthalpy of Vaporization: 49.63 kJ/mol
Boiling Point: 258.6 °C at 760 mmHg
Vapour Pressure: 0.0136 mmHg at 25°C
Synonyms: 1-Aminododecan ; 1-Dideanamine ; 1-Dodecanamin ; 1-Dodecanamine ; 1-Dodecylamin ; Alamine 4 ; alamine4 ; aminebb
Product Categories: Alkylamines;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes
Water Solubility: 78 mg/L (25 °C )
Stability: Stable. Combustible. Incompatible with acid chlorides, acids, acid anhydrides, oxidizing agents

Dodecanamine Uses

Dodecanamine (CAS NO.124-22-1) can be used in the production of medicines, pesticides, dyestuff, mineral flotation agent, emulsifier and intermediates of fine chemical ,etc.

Dodecanamine Toxicity Data With Reference

1.	skn-rbt 500 mg/24H SEV	28ZPAK Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku Marhold, J.V.,Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha,Czechoslovakia.: 1972,62.
2.	eye-rbt 50 µg/24H SEV	28ZPAK Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku Marhold, J.V.,Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha,Czechoslovakia.: 1972,52.
3.	eye-rbt 2 mg	AEPPAE Naunyn-Schmiedebergs Archiv fuer Experimentelle Pathologie und Pharmakologie. 219 (1953),119.
4.	orl-rat LD50:1020 mg/kg	AEPPAE Naunyn-Schmiedebergs Archiv fuer Experimentelle Pathologie und Pharmakologie. 219 (1953),119.
5.	orl-mus LD50:1160 mg/kg	AEPPAE Naunyn-Schmiedebergs Archiv fuer Experimentelle Pathologie und Pharmakologie. 219 (1953),119.
6.	ipr-mus LD50:50 mg/kg	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) AD691-490 .

Dodecanamine Consensus Reports

Reported in EPA TSCA Inventory.

Dodecanamine 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 NO_x. See also AMINES.
Hazard Codes: Corrosive C Dangerous N
Risk Statements: 22-34-50/53-20/21/22
R22: Harmful if swallowed
R34: Causes burns
R50/53: Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed
Safety Statements: 26-36/37/39-45-60-61
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S60: This material and its container must be disposed of as hazardous waste
S61: Avoid release to the environment. Refer to special instructions / safety data sheets
RIDADR: UN 3259 8/PG 3
WGK Germany: 2
RTECS: JR6475000
F: 10-34
HazardClass: 8
PackingGroup: II
HS Code: 29211980

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