Product Name

  • Name

    N'-Laruoyl-L-lysine

  • EINECS 257-843-4
  • CAS No. 52315-75-0
  • Article Data3
  • CAS DataBase
  • Density 0.994 g/cm3
  • Solubility
  • Melting Point 229-231 °C
  • Formula C18H36N2O3
  • Boiling Point 528 °C at 760 mmHg
  • Molecular Weight 328.495
  • Flash Point 273.1 °C
  • Transport Information
  • Appearance White to off-white solid with characteristic faint odor
  • Safety 22-24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 52315-75-0 (N'-Laruoyl-L-lysine)
  • Hazard Symbols
  • Synonyms Lysine,N6-lauroyl-, L- (6CI);Amihope LL;Famex L 12;N-Lauroyl-L-lysine;N6-Lauroyl-L-lysine;Ne-Lauroyl-L-lysine;Ne-Lauroyllysine;Ne-Lauroyllysine;
  • PSA 92.42000
  • LogP 4.69690

Synthetic route

lauric acid
143-07-7

lauric acid

L-lysine
56-87-1

L-lysine

A

N-lauroyl-L-lysine
59409-41-5

N-lauroyl-L-lysine

B

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Conditions
ConditionsYield
With Streptomyces mobaraensis NBRC 13819 acylase In glycerol at 37℃; for 48h; pH=7.5;A 5%
B 44%
tetrabutylphosphonium lysinate

tetrabutylphosphonium lysinate

methyl n-dodecanoate
111-82-0

methyl n-dodecanoate

A

N-lauroyl-L-lysine
59409-41-5

N-lauroyl-L-lysine

B

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Conditions
ConditionsYield
at 80℃; for 54h; Inert atmosphere;A 32%
B 23%
ethanol
64-17-5

ethanol

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-L-lysine ethyl ester
292140-08-0

Nε-lauroyl-L-lysine ethyl ester

Conditions
ConditionsYield
With hydrogenchloride at 20℃;96%
n-dodecanoyl chloride
112-16-3

n-dodecanoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nε-bis(1-oxododecyl)-L-lysine
14379-54-5

Nα,Nε-bis(1-oxododecyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;96%
With sodium hydroxide In diethyl ether at 0 - 20℃;
suberoyl chloride
10027-07-3

suberoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-suberoyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-suberoyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;96%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;82%
isononanoyl chloride
36727-29-4

isononanoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-(1-oxododecyl)-Nα-(3,5,5-trimethyl-1-oxohexyl)-L-lysine
783304-20-1

Nε-(1-oxododecyl)-Nα-(3,5,5-trimethyl-1-oxohexyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;94%
With sodium hydroxide In diethyl ether at 0 - 20℃;
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

2-heptyl-1-undecanoyl chloride

2-heptyl-1-undecanoyl chloride

Nα-(2-heptyl-1-oxoundecyl)-Nε-(1-oxododecyl)-L-lysine

Nα-(2-heptyl-1-oxoundecyl)-Nε-(1-oxododecyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;94%
With sodium hydroxide In diethyl ether at 0 - 20℃;
1-Decanol
112-30-1

1-Decanol

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-L-lysine decyl ester
521974-57-2

Nε-lauroyl-L-lysine decyl ester

Conditions
ConditionsYield
Stage #1: 1-Decanol; Nε-lauroyl-L-lysine With toluene-4-sulfonic acid In benzene at 130℃; for 48h;
Stage #2: With morpholine In methanol Further stages.;
93%
With toluene-4-sulfonic acid for 48h; Heating;91%
gloutaric dichloride
2873-74-7

gloutaric dichloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-glutaryl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-glutaryl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;93%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;79%
sebacoyl chloride
111-19-3

sebacoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-sebacoyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-sebacoyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;93%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;83%
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

hexan-1-ol
111-27-3

hexan-1-ol

Nε-lauroyl-L-lysine hexyl ester

Nε-lauroyl-L-lysine hexyl ester

Conditions
ConditionsYield
With hydrogenchloride at 20℃;93%
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

cyclohexanylcarbonyl chloride
2719-27-9

cyclohexanylcarbonyl chloride

Nα-(cyclohexylcarbonyl)-Nε-(1-oxododecyl)-L-lysine
755752-92-2

Nα-(cyclohexylcarbonyl)-Nε-(1-oxododecyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;92%
With sodium hydroxide In diethyl ether at 0 - 20℃;
pimeloyl chloride
142-79-0

pimeloyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-pimeloyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-pimeloyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;92%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;82%
azelaoyl chloride
123-98-8

azelaoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-azelaoyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-azelaoyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;92%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;82%
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-L-lysine 3,5,5-trimethylhexyl ester

Nε-lauroyl-L-lysine 3,5,5-trimethylhexyl ester

Conditions
ConditionsYield
90%
Adipic acid dichloride
111-50-2

Adipic acid dichloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-adipoyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-adipoyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;90%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;80%
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-L-lysine dodecyl ester
340811-55-4

Nε-lauroyl-L-lysine dodecyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid for 48h; Heating;89%
succinoyl dichloride
543-20-4

succinoyl dichloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-succinyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-succinyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;88%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;68%
Hexanoyl chloride
142-61-0

Hexanoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα-hexanoyl-Nε-lauroyl-L-lysine
817203-60-4

Nα-hexanoyl-Nε-lauroyl-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;88%
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;85%
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

2-ethylhexanoic acid chloride
760-67-8

2-ethylhexanoic acid chloride

Nα-(2-ethyl-1-oxohexyl)-Nε-(1-oxododecyl)-L-lysine

Nα-(2-ethyl-1-oxohexyl)-Nε-(1-oxododecyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;86%
With sodium hydroxide In diethyl ether at 0 - 20℃;
11-bromoundecanoyl chloride
15949-84-5

11-bromoundecanoyl chloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-Nα-(11-bromoundecanoyl)-L-lysine

Nε-lauroyl-Nα-(11-bromoundecanoyl)-L-lysine

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; under 24 Torr;85%
With sodium hydroxide In diethyl ether; water at 0 - 20℃; for 24h;85%
1-Bromo-11-hydroxyundecane
1611-56-9

1-Bromo-11-hydroxyundecane

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-L-lysine 11-bromoundecyl ester
611610-44-7

Nε-lauroyl-L-lysine 11-bromoundecyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid In benzene at 130℃; for 48h;80%
1,12-dodecanedioyl dichloride
4834-98-4

1,12-dodecanedioyl dichloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-dodecanedioyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-dodecanedioyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;80%
oxalyl dichloride
79-37-8

oxalyl dichloride

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 20℃; for 23h;79%
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;65%
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

malonoyl dichloride
1663-67-8

malonoyl dichloride

Nα,Nα'-malonyl-bis(Nε-lauroyl-L-lysine)

Nα,Nα'-malonyl-bis(Nε-lauroyl-L-lysine)

Conditions
ConditionsYield
With sodium hydroxide In diethyl ether at 0 - 20℃; for 24h;70%
ethyl 6-chloro-6-oxohexanoate
1071-71-2

ethyl 6-chloro-6-oxohexanoate

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nepsilon-lauroyl-Nalpha-(5-carboxypentanoyl)-L-lysine

Nepsilon-lauroyl-Nalpha-(5-carboxypentanoyl)-L-lysine

Conditions
ConditionsYield
With water; sodium hydroxide at 20℃; for 24h;66%
methanol
67-56-1

methanol

Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-Nα-Cbz-lysine methyl ester hydrochloride

Nε-lauroyl-Nα-Cbz-lysine methyl ester hydrochloride

Conditions
ConditionsYield
With hydrogenchloride at 0 - 20℃;
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nε-lauroyl-Nα-(11-pyridiniumdecanoyl)-L-lysine bromide

Nε-lauroyl-Nα-(11-pyridiniumdecanoyl)-L-lysine bromide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 85 percent / aq. NaOH / diethyl ether / 0 - 20 °C / 24 Torr
2: 98 percent / 24 h / 100 °C
View Scheme
Multi-step reaction with 2 steps
1: 85 percent / NaOH / H2O; diethyl ether / 24 h / 0 - 20 °C
2: 98 percent / 24 h / 100 °C
View Scheme
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine hexyl ester)

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine hexyl ester)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / HCl / 20 °C
2: 91 percent / Et3N / tetrahydrofuran / 24 h / 20 °C
View Scheme
Nε-lauroyl-L-lysine
52315-75-0

Nε-lauroyl-L-lysine

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine 3,5,5-trimethylhexyl ester)

Nα,Nα'-oxalyl-bis(Nε-lauroyl-L-lysine 3,5,5-trimethylhexyl ester)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / Et3N / tetrahydrofuran / 24 h / 20 °C
View Scheme

N'-Laruoyl-L-lysine Specification

The N'-Laruoyl-L-lysine with the cas number 52315-75-0 is also called N6-(1-Oxododecyl)-L-lysine. The IUPAC name is (2S)-2-amino-6-(dodecanoylamino)hexanoic acid. Its EINECS registry number is 257-843-4. The molecular formula of this chemical is C18H36N2O3. This chemical is a kind of organics. It should be stored in dry and cool environment.

The properties of the chemical are: (1)ACD/LogP: 3.89; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.39; (4)ACD/LogD (pH 7.4): 1.39; (5)ACD/BCF (pH 5.5): 1.69; (6)ACD/BCF (pH 7.4): 1.68; (7)ACD/KOC (pH 5.5): 9.86; (8)ACD/KOC (pH 7.4): 9.83; (9)#H bond acceptors: 5; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 17; (12)Polar Surface Area: 49.85Å2; (13)Index of Refraction: 1.481; (14)Molar Refractivity: 94.12 cm3; (15)Molar Volume: 330.2 cm3; (16)Polarizability: 37.31×10-24cm3; (17)Surface Tension: 39.7 dyne/cm; (18)Enthalpy of Vaporization: 87.81 kJ/mol; (19)Vapour Pressure: 1.48×10-12 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(NCCCC[C@H](N)C(=O)O)CCCCCCCCCCC
(2)InChI: InChI=1/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1
(3)InChIKey: GYDYJUYZBRGMCC-INIZCTEOBA

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