Conditions | Yield |
---|---|
With sodium hydroxide; hydrogen; nickel In water at 135℃; under 14251.4 Torr; for 3h; | 98.2% |
With [Ru(H)(BH4)(CO)(PPh3)(3-(di-tert-butylphosphino)-N-((1-methyl-1H-imidazol-2 yl)methyl)propylamine)]; hydrogen In isopropyl alcohol at 70℃; for 3h; Inert atmosphere; Autoclave; | 88% |
With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); {[(phenylphosphinediyl)bis(2,1-phenylene)]bis(methylene)}bis(di-tert-butylphosphine); hydrogen In isopropyl alcohol at 70℃; under 11251.1 Torr; for 17h; Inert atmosphere; Autoclave; | 72% |
2-octadecylisoindoline-1,3-dione
1-aminooctadecane
Conditions | Yield |
---|---|
With hydrazine hydrate In methanol at 95℃; for 1h; Gabriel Amine Synthesis; | 95% |
N-trityloctadecan-1-amine
1-aminooctadecane
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; water; acetic acid In dichloromethane at 20℃; for 40h; Inert atmosphere; | 93% |
N-Boc-octadecylamine
1-aminooctadecane
Conditions | Yield |
---|---|
With 3-butyl-l-methyl-1H-imidazol-3-iumtrifloroacetate In 1,4-dioxane; water at 80℃; for 1.5h; | 92% |
With methanol; Amberlyst 15; ammonia 1.) CH2Cl2, 25 deg C, 14 h, 2.) 50 min; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
Stage #1: N-octadecylacetamide With Schwartz's reagent In tetrahydrofuran at 20℃; for 0.0333333h; Inert atmosphere; Stage #2: With water In tetrahydrofuran Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With ammonia; hydrogen; catalyst formed by supporting 2percent by mass of ruthenium on zirconia surface-treated with sulfur at 220℃; under 120012 Torr; for 2.8h; Product distribution / selectivity; Autoclave; | A 7.4% B 84.8% |
Stage #1: 1-octadecanol With hydrogen; catalyst with 35weight percent Ni, 6weight percent Cu, 27weight percent Zr, 0.4weight percent La at 200℃; for 2h; Gas phase; Stage #2: With ammonia; hydrogen; catalyst with 35weight percent Ni, 6weight percent Cu, 27weight percent Zr, 0.4weight percent La at 220℃; for 6h; Product distribution / selectivity; | |
Stage #1: 1-octadecanol With hydrogen; catalyst with 31weight percent Ni, 12weight percent Cu at 200℃; for 2h; Gas phase; Stage #2: With ammonia; hydrogen; catalyst with 31weight percent Ni, 12weight percent Cu at 220℃; for 9h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With ammonia at 50℃; |
Conditions | Yield |
---|---|
With ammonia; hydrogen; cobalt at 270℃; under 147102 - 183877 Torr; | |
With ammonia; hydrogen; cobalt; decalin at 270℃; under 147102 - 183877 Torr; | |
With ammonia; cobalt at 270℃; under 147102 - 183877 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With aluminium oxide hydrate-kaolin; ammonia at 380℃; under 147102 Torr; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether | |
With lithium aluminium tetrahydride In tetrahydrofuran | |
With lithium aluminium tetrahydride In tetrahydrofuran for 1h; |
Conditions | Yield |
---|---|
With copper manganese; cyclohexane; ammonia at 270℃; under 220652 Torr; Hydrogenation; | |
With copper manganese; cyclohexane; ammonia at 270℃; under 220652 Torr; Hydrogenation; |
octadecanal oxime
1-aminooctadecane
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene at 140℃; for 4h; |
Conditions | Yield |
---|---|
With potassium carbonate und Erwaermen des Reaktionsprodukts mit Hydrazin-hydrat und Aethanol; |
Conditions | Yield |
---|---|
With silica-alumina; ammonia at 360℃; |
Conditions | Yield |
---|---|
at 90℃; under 29420.3 Torr; an Raney-Nickel.Hydrogenation; |
Conditions | Yield |
---|---|
at 35 - 77℃; bei der Reduktion an Kupfer-Kathoden verschiedener Stromdichte und verschiedenen Reaktionszeite; |
Conditions | Yield |
---|---|
at 65℃; under 15200 Torr; Hydrogenation; |
ammonia
stearonitrile
A
Dioctadecylamine
B
trioctadecylamine
C
1-aminooctadecane
Conditions | Yield |
---|---|
at 280℃; under 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 50℃; |
Conditions | Yield |
---|---|
at 380℃; |
Conditions | Yield |
---|---|
at 270℃; under 147102 Torr; |
Conditions | Yield |
---|---|
at 270℃; under 147102 Torr; |
Conditions | Yield |
---|---|
With cobalt-aluminium barium at 130 - 140℃; under 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: SOCl2 2: NH3 3: LiAlH4 / tetrahydrofuran View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NH3 2: LiAlH4 / tetrahydrofuran View Scheme |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 30℃; under 6000.6 Torr; for 4h; | |
With platinum; hydrogen under 750.075 Torr; |
1-octadecylammonium 1-octadecylcarbamate
1-aminooctadecane
Conditions | Yield |
---|---|
for 0.166667h; Inert atmosphere; Heating; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: oxalyl dichloride / benzene / 72 h 2: ammonia / benzene 3: lithium aluminium tetrahydride / tetrahydrofuran / 1 h View Scheme |
perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride
1-aminooctadecane
N,N’-bis(octadecyl)-3,4:9,10-perylenebis(dicarboximide)
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 8h; Reflux; | 100% |
With 1H-imidazole at 140℃; for 3h; | 89% |
63% |
2-(vinyloxy)ethyl isothiocyanate
1-aminooctadecane
Conditions | Yield |
---|---|
at 45℃; for 2h; other primary and secondary amines; | 100% |
In tetrachloromethane at 45℃; for 2h; | 100% |
3-Thietanyl isothiocyanate
1-aminooctadecane
Conditions | Yield |
---|---|
100% | |
Selfheating; | 91% |
methyl 15-hydroxypentadecanoate
1-aminooctadecane
15-hydroxy-pentadecanoic acid octadecylamide
Conditions | Yield |
---|---|
at 148℃; | 100% |
4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester
1-aminooctadecane
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 3h; | 100% |
Conditions | Yield |
---|---|
With Desmodur W In hexane for 1h; Reflux; | 100% |
In hexane for 1h; Reflux; | 100% |
Conditions | Yield |
---|---|
for 72h; Heating; | 100% |
di-o-tolyl carbonate
1-aminooctadecane
n-octadecylcarbamate methyl ester
Conditions | Yield |
---|---|
With hydrogenchloride In toluene | 99.5% |
Conditions | Yield |
---|---|
at 150℃; for 18.5h; Temperature; Green chemistry; | 99.4% |
2,5-hexanedione
1-aminooctadecane
2,5-dimethyl-1-n-octadecyl-1H-pyrrole
Conditions | Yield |
---|---|
With sulfated anatase In neat (no solvent) at 20℃; for 0.333333h; Paal-Knorr Pyrrole Synthesis; Milling; Green chemistry; | 99% |
N-<2-(acetylamino)-2-deoxy-3,4,6-triacetyl-β-D-glucopyranosyl>-N2-<(1,1-dimethylethoxy)carbonyl>-L-asparagine
1-aminooctadecane
N4-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-N2-(tert-butoxycarbonyl)-L-asparagine octadecylamide
Conditions | Yield |
---|---|
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline In chloroform for 48h; Ambient temperature; | 99% |
4-(N,N-dimethylamino)-1,8-naphthalic anhydride
1-aminooctadecane
4-N,N-dimethylamino-N'-octadecylnaphthalimide
Conditions | Yield |
---|---|
In xylene Heating; | 99% |
1-aminooctadecane
4-ethoxy-3-nitropyridine
3-nitro-4-octadecylaminopyridine
Conditions | Yield |
---|---|
at 150 - 155℃; for 2h; | 99% |
1-aminooctadecane
4-fluorocarbonyltetrathiafulvalene
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.25h; Substitution; | 99% |
1-aminooctadecane
BocNHCys[S-S-cholesteryl]-OH
BocNHCys[S-S-cholesteryl]-NH(CH2)17CH3
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h; | 99% |
Conditions | Yield |
---|---|
at 130 - 160℃; Inert atmosphere; | 99% |
S-dodecyl heptanethioate
1-aminooctadecane
N-octadecylheptanamide
Conditions | Yield |
---|---|
In water for 3h; Reflux; | 99% |
1-cyano-cyclopropanecarboxylic acid
1-aminooctadecane
1-cyano-N-octadecylcyclopropanecarboxamide
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 4h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In ethyl acetate at 5℃; Inert atmosphere; | 99% |
In ethyl acetate at 5 - 50℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
Stage #1: cycl-isopropylidene malonate; trimethyl orthoformate for 1h; Reflux; Stage #2: 1-aminooctadecane for 2h; Reflux; | 99% |
acrylic acid methyl ester
1-aminooctadecane
methyl 3-(octadecylamino)propionate
Conditions | Yield |
---|---|
at 65℃; for 7h; Michael Addition; | 98.55% |
1-aminooctadecane
Conditions | Yield |
---|---|
In toluene at 100℃; for 0.166667h; | 98% |
Conditions | Yield |
---|---|
In methanol Reflux; | 98% |
Conditions | Yield |
---|---|
In methanol at 65℃; for 2h; | 98% |
Conditions | Yield |
---|---|
With iron(II) triflate In N,N-dimethyl-formamide at 80℃; for 2h; | 98% |
1-aminooctadecane
Conditions | Yield |
---|---|
With acetic acid In isopropyl alcohol at 80℃; pH=Ca. 4; | 98% |
1-aminooctadecane
BocNHCys[S-S-(CH2)17CH3]-OH
BocNHCys[S-S-(CH2)17CH3]-NH(CH2)17CH3
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h; | 97% |
Conditions | Yield |
---|---|
In butan-1-ol at 70℃; for 19h; | 97% |
Conditions | Yield |
---|---|
In methanol at 20℃; Inert atmosphere; | 96.9% |
Product Name: Octadecanamine (CAS NO.124-30-1)
Molecular Formula: C18H39N
Molar mass: 269.51 g/mol
Flash Point: 148 °C
Melting point: 50-60 °C
Boiling Point: 349°C
Vapour Pressure: 10 mm Hg ( 72 °C)
Density: 0.862 g/cm3
Refractive index 1.4522
FreezingPoint: 53.1°C
Water solubility: practically insoluble
Appearance: White prills
Surface Tension: 31 dyne/cm
Enthalpy of Vaporization: 59.33 kJ/mol
Vapour Pressure: 4.88E-05 mmHg at 25°C
Index of Refraction: 1.452
Molar Refractivity: 88.97 cm3
Molar Volume: 329.3 cm3
XLogP3-AA: 8.5
H-Bond Donor: 1
H-Bond Acceptor: 1
Structure Descriptors of Octadecanamine (CAS NO.124-30-1):
IUPAC Name: octadecan-1-amine
Canonical SMILES: CCCCCCCCCCCCCCCCCCN
InChI: InChI=1S/C18H39N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-19H2,1H3
InChIKey: REYJJPSVUYRZGE-UHFFFAOYSA-N
Product Categories: Alkylamines; Monofunctional & alpha,omega-Bifunctional Alkanes; Monofunctional Alkanes
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 250mg/kg (250mg/kg) | National Technical Information Service. Vol. AD691-490, | |
mouse | LD50 | oral | 3gm/kg (3000mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(11), Pg. 31, 1973. |
rat | LD50 | oral | 2395mg/kg (2395mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(11), Pg. 31, 1973. |
Reported in EPA TSCA Inventory.
Poison by intraperitoneal route. Moderately toxic by ingestion. A skin irritant. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.
Safety Information of Octadecanamine (CAS NO.124-30-1):
Hazard Codes:Xi
Risk Statements:
36: Irritating to the eyes
37: Irritating to the respiratory system
38: Irritating to the skin
41: Risk of serious damage to eyes
Safety Statements:
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
28: After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer)
36: Wear suitable protective clothing
37: Wear suitable gloves
39: Wear eye/face protection
RIDADR: 3259
WGK Germany: 2
RTECS: RG4150000
HazardClass: 8
PackingGroup: III
HS Code: 29211980
Octadecanamine , its CAS NO. is 124-30-1, the synonyms are Adogenen 142 ; 1-Octadecanamine ; adogenen142 ; Alamine 7 ; Alamine 7D ; Amine 18-90 .
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